Kenneth Kidd, PhD
Research & Publications
Biography
News
Research Summary
The majority of the work in my laboratory is currently focused on human genome diversity: the patterns of normal genetic variation among four dozen populations (~2500 individuals) from around the world, the variation in those patterns along the genome, and the inference of recent human evolutionary processes. The research involves both molecular and biostatistical components. Because of longstanding interest in neuropsychiatric disorders that fail to show a Mendelian pattern but do "run in families," our genome diversity studies include sequence variation at several genes with important neurologic functions, candidate genes for various neuropsychiatric disorders, and genes demonstrated to be associated with alcoholism. Managing these genotype and allele frequency data and making them publicly available has also involved us in a major bioinformatics effort: ALFRED, the allele frequency database we have developed. That database, illustrations of our human evolution findings, recent publications, and other material can be accessed through the Lab’s website.
Specialized Terms: Complex Human Disorders; Neuropsychiatric Disorders; Human Population ; Genetics; Human Evolution
Extensive Research Description
For the past several years my laboratory has studied the genetics of complex human disorders, those disorders that fail to show a Mendelian pattern but do "run in families". DNA polymorphisms are now being used to search for the genetic loci of major effect in behavioral and other complex disorders. Our previous efforts focused on finding genes responsible for neuropsychiatric disorders, especially Giles de la Tourette Syndrome and schizophrenia. While no locus appears to account for all cases of Tourette Syndrome, we have strong evidence of a predisposing genetic factor on the distal long arm of chromosome 17. Studies are ongoing through collaborations to narrow the region and identify the relevant variant.
We are studying the population genetics of expressed and non-expressed genetic variation at several genes of known neurologic relevance, such as the dopamine receptors D2 and D4 and the enzyme COMT, Catechol-O-methyl transferase. Also, because of their demonstrated relevance to alcoholism we are studying the genes involved in ethanol metabolism, the ADH genes and ALDH2. Understanding the nature of the common normal variation at these loci provides a background for investigating how they might influence normal and abnormal neurologic/metabolic function and susceptibility to psychiatric disorders. The duplicated ADH Class 1 genes are unique to primates and are the focus of molecular evolution studies. Several more evolution-oriented projects are also being pursued. These include theoretical studies as well as studying samples from diverse human populations for DNA polymorphisms. For some genes of interest we are also collecting DNA sequence of other great apes to examine the origins of the human lineage.
The lab's efforts are currently focused on genome diversity among world populations and understanding how that diversity arose. We have accumulated cell lines on individuals from over 45 different populations and plan to increase this resource in the coming years. On a global basis we are finding that the majority of alleles for nuclear DNA polymorphisms are present in most populations around the world, though sub-Saharan African populations have more genetic variation (alleles), in general, than indigenous populations in any other part of the world. We interpret the data to mean that there was a major founder effect and loss of variation associated with the expansion of modern humans out of Africa. Haplotype data collected on all of the populations we are studying are beginning to reveal patterns that provide a better understanding of that founder effect and the recent evolutionary history of modern humans. Recent studies have used these resources to select SNPs that can be useful in forensics, both for individual identification (matching the DNA at a crime scene with a suspect's DNA). Other SNPs are being selected for their value in inference of ancestry from an individual's DNA.
Bioinformatics research, in collaboration with the Yale Center for Medical Informatics, is ongoing in two areas. We are working to improve data management for the extensive marker typing results accumulating on many of the projects. We are also working to improve the utility of data in ALFRED through new search and display modes as well as relevant links to other online sources
- Gene study using polymorphism of the DNA for several inherited disorders
- Collaborative study to narrow the region and identify the chromosome involved in Tourette syndrome and Schizophrenia
- Population genetics of expressed and non-expressed genetic variation at several genes of known neurologic relevance
- Bioinformatics research to improve data management for extensive marker typing results and improve the utility of data in ALFRED
Coauthors
Research Interests
Africa; China; Gambia; Genetics; India; Psychiatry; Global Health; Neuropsychiatry
Selected Publications
- A multipurpose panel of microhaplotypes for caseworkKidd K, Pakstis A, Gandotra N, Scharfe C, Podini D. A multipurpose panel of microhaplotypes for casework Forensic Science International Genetics Supplement Series 2022, 8: 202-204. DOI: 10.1016/j.fsigss.2022.10.035.
- Metabolic diversity in human populations and correlation with genetic and ancestral geographic distancesPeng G, Pakstis AJ, Gandotra N, Cowan TM, Zhao H, Kidd KK, Scharfe C. Metabolic diversity in human populations and correlation with genetic and ancestral geographic distances Molecular Genetics And Metabolism 2022, 137: 292-300. PMID: 36252453, DOI: 10.1016/j.ymgme.2022.10.002.
- State of the Art for MicrohaplotypesKidd KK, Pakstis AJ. State of the Art for Microhaplotypes Genes 2022, 13: 1322. PMID: 35893059, PMCID: PMC9329722, DOI: 10.3390/genes13081322.
- Ancient DNA reveals five streams of migration into Micronesia and matrilocality in early Pacific seafarers.Liu YC, Hunter-Anderson R, Cheronet O, Eakin J, Camacho F, Pietrusewsky M, Rohland N, Ioannidis A, Athens JS, Douglas MT, Ikehara-Quebral RM, Bernardos R, Culleton BJ, Mah M, Adamski N, Broomandkhoshbacht N, Callan K, Lawson AM, Mandl K, Michel M, Oppenheimer J, Stewardson K, Zalzala F, Kidd K, Kidd J, Schurr TG, Auckland K, Hill AVS, Mentzer AJ, Quinto-Cortés CD, Robson K, Kennett DJ, Patterson N, Bustamante CD, Moreno-Estrada A, Spriggs M, Vilar M, Lipson M, Pinhasi R, Reich D. Ancient DNA reveals five streams of migration into Micronesia and matrilocality in early Pacific seafarers. Science (New York, N.Y.) 2022, 377: 72-79. PMID: 35771911, DOI: 10.1126/science.abm6536.
- A multipurpose panel of microhaplotypes for use with STR markers in caseworkKidd KK, Pakstis AJ, Gandotra N, Scharfe C, Podini D. A multipurpose panel of microhaplotypes for use with STR markers in casework Forensic Science International Genetics 2022, 60: 102729. PMID: 35696960, DOI: 10.1016/j.fsigen.2022.102729.
- North Asian population relationships in a global contextKidd KK, Evsanaa B, Togtokh A, Brissenden JE, Roscoe JM, Dogan M, Neophytou PI, Gurkan C, Bulbul O, Cherni L, Speed WC, Murtha M, Kidd JR, Pakstis AJ. North Asian population relationships in a global context Scientific Reports 2022, 12: 7214. PMID: 35508562, PMCID: PMC9068624, DOI: 10.1038/s41598-022-10706-x.
- New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3, CSMD1 and NRG1 genesMestiri S, Boussetta S, Pakstis AJ, Kamel S, Gaaied A, Kidd KK, Cherni L. New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3, CSMD1 and NRG1 genes Molecular Genetics & Genomic Medicine 2022, 10: e1871. PMID: 35128830, PMCID: PMC8922960, DOI: 10.1002/mgg3.1871.
- A Distinctive Pattern of Diversity for the TAS2R38 Gene in North AfricaMourali-Chebil S, Elkamel S, Boussetta S, Pakstis A, Kidd K, Benammar-Elgaaied A, Cherni L. A Distinctive Pattern of Diversity for the TAS2R38 Gene in North Africa Human Biology 2022 DOI: 10.1353/hub.2017.0106.
- The population genetics characteristics of a 90 locus panel of microhaplotypesPakstis AJ, Gandotra N, Speed WC, Murtha M, Scharfe C, Kidd KK. The population genetics characteristics of a 90 locus panel of microhaplotypes Human Genetics 2021, 140: 1753-1773. PMID: 34643790, PMCID: PMC8553733, DOI: 10.1007/s00439-021-02382-0.
- STAT3 polymorphisms in North Africa and its implication in breast cancerZiadi W, Boussetta S, Elkamel S, Pakstis AJ, Kidd KK, Medimegh I, Elgaaied A, Cherni L. STAT3 polymorphisms in North Africa and its implication in breast cancer Molecular Genetics & Genomic Medicine 2021, 9: e1744. PMID: 34251094, PMCID: PMC8404238, DOI: 10.1002/mgg3.1744.
- Editorial: Current and Emerging Trends in Human Identification and Molecular AnthropologyGurkan C, Bulbul O, Kidd KK. Editorial: Current and Emerging Trends in Human Identification and Molecular Anthropology Frontiers In Genetics 2021, 12: 708222. PMID: 34249111, PMCID: PMC8262838, DOI: 10.3389/fgene.2021.708222.
- A Distinctive Pattern of Diversity for the TAS2R38 Gene in North AfricaMourali-Chebil* S, Elkamel S, Boussetta S, Pakstis A, Kidd K, Benammar-Elgaaied A, Cherni L. A Distinctive Pattern of Diversity for the TAS2R38 Gene in North Africa Human Biology 2021, 93: 163-177. DOI: 10.1353/hub.2021.0009.
- Genetic relationships of Southwest Asian and Mediterranean populationsKidd KK, Bulbul O, Gurkan C, Dogan M, Dogan S, Neophytou PI, Cherni L, Gurwitz D, Speed WC, Murtha M, Kidd JR, Pakstis AJ. Genetic relationships of Southwest Asian and Mediterranean populations Forensic Science International Genetics 2021, 53: 102528. PMID: 34020230, DOI: 10.1016/j.fsigen.2021.102528.
- Genetic diversity of the North African population revealed by the typing of SNPs in the DRD2/ANKK1 genomic regionMestiri S, Boussetta S, Pakstis AJ, Elkamel S, Elgaaied ABA, Kidd KK, Cherni L. Genetic diversity of the North African population revealed by the typing of SNPs in the DRD2/ANKK1 genomic region Gene 2021, 777: 145466. PMID: 33524518, DOI: 10.1016/j.gene.2021.145466.
- Forensic Ancestry Inference: Data Requirements, Analysis Methods, and Interpretation of ResultsBulbul O, Kidd K. Forensic Ancestry Inference: Data Requirements, Analysis Methods, and Interpretation of Results 2021, 225-240. DOI: 10.1201/9781003043027-12.
- Population genetic data of 74 microhaplotypes in four major U.S. population groupsOldoni F, Yoon L, Wootton SC, Lagacé R, Kidd KK, Podini D. Population genetic data of 74 microhaplotypes in four major U.S. population groups Forensic Science International Genetics 2020, 49: 102398. PMID: 33045522, DOI: 10.1016/j.fsigen.2020.102398.
- The distinctive geographic patterns of common pigmentation variants at the OCA2 geneKidd KK, Pakstis AJ, Donnelly MP, Bulbul O, Cherni L, Gurkan C, Kang L, Li H, Yun L, Paschou P, Meiklejohn KA, Haigh E, Speed WC. The distinctive geographic patterns of common pigmentation variants at the OCA2 gene Scientific Reports 2020, 10: 15433. PMID: 32963319, PMCID: PMC7508881, DOI: 10.1038/s41598-020-72262-6.
- A sequence-based 74plex microhaplotype assay for analysis of forensic DNA mixturesOldoni F, Bader D, Fantinato C, Wootton SC, Lagacé R, Kidd KK, Podini D. A sequence-based 74plex microhaplotype assay for analysis of forensic DNA mixtures Forensic Science International Genetics 2020, 49: 102367. PMID: 32919300, DOI: 10.1016/j.fsigen.2020.102367.
- Validation of novel forensic DNA markers using multiplex microhaplotype sequencingGandotra N, Speed WC, Qin W, Tang Y, Pakstis AJ, Kidd KK, Scharfe C. Validation of novel forensic DNA markers using multiplex microhaplotype sequencing Forensic Science International Genetics 2020, 47: 102275. PMID: 32305739, DOI: 10.1016/j.fsigen.2020.102275.
- FrogAncestryCalc: A Standalone Batch Likelihood Computation Tool for Ancestry Inference Panels catalogued in FROG-kbRajeevan H, Soundararajan U, Pakstis AJ, Kidd KK. FrogAncestryCalc: A Standalone Batch Likelihood Computation Tool for Ancestry Inference Panels catalogued in FROG-kb Forensic Science International Genetics 2020, 46: 102237. PMID: 31991337, DOI: 10.1016/j.fsigen.2020.102237.
- Population relationships based on 170 ancestry SNPs from the combined Kidd and Seldin panelsPakstis AJ, Speed WC, Soundararajan U, Rajeevan H, Kidd JR, Li H, Kidd KK. Population relationships based on 170 ancestry SNPs from the combined Kidd and Seldin panels Scientific Reports 2019, 9: 18874. PMID: 31827153, PMCID: PMC6906462, DOI: 10.1038/s41598-019-55175-x.
- A massively parallel sequencing assay of microhaplotypes for mixture deconvolutionOldoni F, Bader D, Fantinato C, Wootton S, Lagacé R, Hasegawa R, Chang J, Kidd K, Podini D. A massively parallel sequencing assay of microhaplotypes for mixture deconvolution Forensic Science International Genetics Supplement Series 2019, 7: 522-524. DOI: 10.1016/j.fsigss.2019.10.075.
- Genetic relationships of European, Mediterranean, and SW Asian populations using a panel of 55 AISNPsPakstis AJ, Gurkan C, Dogan M, Balkaya HE, Dogan S, Neophytou PI, Cherni L, Boussetta S, Khodjet-El-Khil H, Ben Ammar ElGaaied A, Salvo NM, Janssen K, Olsen GH, Hadi S, Almohammed EK, Pereira V, Truelsen DM, Bulbul O, Soundararajan U, Rajeevan H, Kidd JR, Kidd KK. Genetic relationships of European, Mediterranean, and SW Asian populations using a panel of 55 AISNPs European Journal Of Human Genetics 2019, 27: 1885-1893. PMID: 31285530, PMCID: PMC6871633, DOI: 10.1038/s41431-019-0466-6.
- MAPlex - A massively parallel sequencing ancestry analysis multiplex for Asia-Pacific populationsPhillips C, McNevin D, Kidd K, Lagacé R, Wootton S, de la Puente M, Freire-Aradas A, Mosquera-Miguel A, Eduardoff M, Gross T, Dagostino L, Power D, Olson S, Hashiyada M, Oz C, Parson W, Schneider P, Lareu M, Daniel R. MAPlex - A massively parallel sequencing ancestry analysis multiplex for Asia-Pacific populations Forensic Science International Genetics 2019, 42: 213-226. PMID: 31377479, DOI: 10.1016/j.fsigen.2019.06.022.
- Genetic history of the population of CreteDrineas P, Tsetsos F, Plantinga A, Lazaridis I, Yannaki E, Razou A, Kanaki K, Michalodimitrakis M, Perez‐Jimenez F, De Silvestro G, Renda MC, Stamatoyannopoulos JA, Kidd KK, Browning BL, Paschou P, Stamatoyannopoulos G. Genetic history of the population of Crete Annals Of Human Genetics 2019, 83: 373-388. PMID: 31192450, PMCID: PMC6851683, DOI: 10.1111/ahg.12328.
- Correction to: Mixture deconvolution by massively parallel sequencing of microhaplotypesBennett L, Oldoni F, Long K, Cisana S, Maddela K, Wootton S, Chang J, Hasegawa R, Lagacé R, Kidd KK, Podini D. Correction to: Mixture deconvolution by massively parallel sequencing of microhaplotypes International Journal Of Legal Medicine 2019, 133: 731-731. PMID: 30834970, DOI: 10.1007/s00414-019-02031-2.
- Usefulness of COMT gene polymorphisms in North African populationsBoussetta S, Cherni L, Pakstis AJ, Ben Salem N, Elkamel S, Khodjet-El-Khil H, Kidd KK, Elgaaied ABA. Usefulness of COMT gene polymorphisms in North African populations Gene 2019, 696: 186-196. PMID: 30790653, DOI: 10.1016/j.gene.2019.02.021.
- Mixture deconvolution by massively parallel sequencing of microhaplotypesBennett L, Oldoni F, Long K, Cisana S, Madella K, Wootton S, Chang J, Hasegawa R, Lagacé R, Kidd KK, Podini D. Mixture deconvolution by massively parallel sequencing of microhaplotypes International Journal Of Legal Medicine 2019, 133: 719-729. PMID: 30758713, DOI: 10.1007/s00414-019-02010-7.
- In Remembrance of: Luigi Luca Cavalli-Sforza (1922–2018)Kidd K. In Remembrance of: Luigi Luca Cavalli-Sforza (1922–2018) American Journal Of Human Genetics 2019, 104: 11-12. DOI: 10.1016/j.ajhg.2018.12.003.
- Microhaplotypes in forensic geneticsOldoni F, Kidd KK, Podini D. Microhaplotypes in forensic genetics Forensic Science International Genetics 2018, 38: 54-69. PMID: 30347322, DOI: 10.1016/j.fsigen.2018.09.009.
- Recent Selection on a Class I ADH Locus Distinguishes Southwest Asian Populations Including Ashkenazi JewsGu S, Li H, Pakstis AJ, Speed WC, Gurwitz D, Kidd JR, Kidd KK. Recent Selection on a Class I ADH Locus Distinguishes Southwest Asian Populations Including Ashkenazi Jews Genes 2018, 9: 452. PMID: 30205534, PMCID: PMC6162407, DOI: 10.3390/genes9090452.
- Microhaplotypes for ancestry predictionOldoni F, Hart R, Long K, Maddela K, Cisana S, Schanfield M, Wootton S, Chang J, Lagace R, Hasegawa R, Kidd K, Podini D. Microhaplotypes for ancestry prediction Forensic Science International Genetics Supplement Series 2017, 6: e513-e515. DOI: 10.1016/j.fsigss.2017.09.209.
- Increasing the reference populations for the 55 AISNP panel: the need and benefitsPakstis AJ, Kang L, Liu L, Zhang Z, Jin T, Grigorenko EL, Wendt FR, Budowle B, Hadi S, Al Qahtani MS, Morling N, Mogensen HS, Themudo GE, Soundararajan U, Rajeevan H, Kidd JR, Kidd KK. Increasing the reference populations for the 55 AISNP panel: the need and benefits International Journal Of Legal Medicine 2017, 131: 913-917. PMID: 28070634, PMCID: PMC5491587, DOI: 10.1007/s00414-016-1524-z.
- Genetic and neural predictors of behavioral weight loss treatment: A preliminary study.Chen EY, Olino TM, Conklin CJ, Mohamed FB, Hoge WS, Foster GD, Arlt JM, Eneva K, Kidd JR, Kidd KR, Lent MR, Murray S, Newberg A, Tewksbury C, VanderVeur SS, Yiu A. Genetic and neural predictors of behavioral weight loss treatment: A preliminary study. Obesity (Silver Spring, Md.) 2017, 25: 66-75. PMID: 27804228, PMCID: PMC5381816, DOI: 10.1002/oby.21691.
- Thoughts on Estimating AncestryKidd K. Thoughts on Estimating Ancestry 2016, 2: 131-144. DOI: 10.1142/9781786340788_0007.
- Proposed nomenclature for microhaplotypesKidd KK. Proposed nomenclature for microhaplotypes Human Genomics 2016, 10: 16. PMID: 27316555, PMCID: PMC4912715, DOI: 10.1186/s40246-016-0078-y.
- Genetic markers for massively parallel sequencing in forensicsKidd K, Speed W, Wootton S, Lagace R, Langit R, Haigh E, Chang J, Pakstis A. Genetic markers for massively parallel sequencing in forensics Forensic Science International Genetics Supplement Series 2015, 5: e677-e679. DOI: 10.1016/j.fsigss.2015.12.004.
- Criteria for selecting microhaplotypes: mixture detection and deconvolutionKidd KK, Speed WC. Criteria for selecting microhaplotypes: mixture detection and deconvolution Investigative Genetics 2015, 6: 1. PMID: 25750707, PMCID: PMC4351693, DOI: 10.1186/s13323-014-0018-3.
- Mongolians in the Genetic Landscape of Central Asia: Exploring the Genetic Relations among Mongolians and Other World PopulationsBrissenden JE, Kidd JR, Evsanaa B, Togtokh AJ, Pakstis AJ, Friedlaender F, Kidd KK, Roscoe JM. Mongolians in the Genetic Landscape of Central Asia: Exploring the Genetic Relations among Mongolians and Other World Populations Human Biology 2015, 87: 73-91. PMID: 26829292, DOI: 10.13110/humanbiology.87.2.0005.
- Inferring population structure and demographic history using Y-STR data from worldwide populationsXu H, Wang CC, Shrestha R, Wang LX, Zhang M, He Y, Kidd JR, Kidd KK, Jin L, Li H. Inferring population structure and demographic history using Y-STR data from worldwide populations Molecular Genetics And Genomics 2014, 290: 141-150. PMID: 25159112, DOI: 10.1007/s00438-014-0903-8.
- Current sequencing technology makes microhaplotypes a powerful new type of genetic marker for forensicsKidd KK, Pakstis AJ, Speed WC, Lagacé R, Chang J, Wootton S, Haigh E, Kidd JR. Current sequencing technology makes microhaplotypes a powerful new type of genetic marker for forensics Forensic Science International Genetics 2014, 12: 215-224. PMID: 25038325, DOI: 10.1016/j.fsigen.2014.06.014.
- Maritime route of colonization of EuropePaschou P, Drineas P, Yannaki E, Razou A, Kanaki K, Tsetsos F, Padmanabhuni SS, Michalodimitrakis M, Renda MC, Pavlovic S, Anagnostopoulos A, Stamatoyannopoulos JA, Kidd KK, Stamatoyannopoulos G. Maritime route of colonization of Europe Proceedings Of The National Academy Of Sciences Of The United States Of America 2014, 111: 9211-9216. PMID: 24927591, PMCID: PMC4078858, DOI: 10.1073/pnas.1320811111.
- A Form of the Metabolic Syndrome Associated with Mutations in DYRK1BKeramati AR, Fathzadeh M, Go GW, Singh R, Choi M, Faramarzi S, Mane S, Kasaei M, Sarajzadeh-Fard K, Hwa J, Kidd KK, Babaee Bigi MA, Malekzadeh R, Hosseinian A, Babaei M, Lifton RP, Mani A. A Form of the Metabolic Syndrome Associated with Mutations in DYRK1B New England Journal Of Medicine 2014, 370: 1909-1919. PMID: 24827035, PMCID: PMC4069260, DOI: 10.1056/nejmoa1301824.
- Extensive sequence variation in the 3′ untranslated region of the KRAS gene in lung and ovarian cancer casesKim M, Chen X, Chin L, Paranjape T, Speed W, Kidd K, Zhao H, Weidhaas J, Slack FJ. Extensive sequence variation in the 3′ untranslated region of the KRAS gene in lung and ovarian cancer cases Cell Cycle 2014, 13: 1030-1040. PMID: 24552817, PMCID: PMC3984301, DOI: 10.4161/cc.27941.
- Progress toward an efficient panel of SNPs for ancestry inferenceKidd KK, Speed WC, Pakstis AJ, Furtado MR, Fang R, Madbouly A, Maiers M, Middha M, Friedlaender FR, Kidd JR. Progress toward an efficient panel of SNPs for ancestry inference Forensic Science International Genetics 2014, 10: 23-32. PMID: 24508742, DOI: 10.1016/j.fsigen.2014.01.002.
- Application of six IrisPlex SNPs and comparison of two eye color prediction systems in diverse Eurasia populationsYun L, Gu Y, Rajeevan H, Kidd KK. Application of six IrisPlex SNPs and comparison of two eye color prediction systems in diverse Eurasia populations International Journal Of Legal Medicine 2014, 128: 447-453. PMID: 24395150, DOI: 10.1007/s00414-013-0953-1.
- An historical perspective on “The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus”Kidd KK, Pakstis AJ, Yun L. An historical perspective on “The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus” Human Genetics 2013, 133: 431-433. PMID: 24162668, DOI: 10.1007/s00439-013-1386-0.
- Haplotype structure and positive selection at TLR1Heffelfinger C, Pakstis AJ, Speed WC, Clark AP, Haigh E, Fang R, Furtado MR, Kidd KK, Snyder MP. Haplotype structure and positive selection at TLR1 European Journal Of Human Genetics 2013, 22: 551-557. PMID: 24002163, PMCID: PMC3953919, DOI: 10.1038/ejhg.2013.194.
- Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panelNievergelt CM, Maihofer AX, Shekhtman T, Libiger O, Wang X, Kidd KK, Kidd JR. Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel Investigative Genetics 2013, 4: 13. PMID: 23815888, PMCID: PMC3699392, DOI: 10.1186/2041-2223-4-13.
- Worldwide Population Variation and Haplotype Analysis at the Serotonin Transporter Gene SLC6A4 and Implications for Association StudiesMurdoch JD, Speed WC, Pakstis AJ, Heffelfinger CE, Kidd KK. Worldwide Population Variation and Haplotype Analysis at the Serotonin Transporter Gene SLC6A4 and Implications for Association Studies Biological Psychiatry 2013, 74: 879-889. PMID: 23510579, DOI: 10.1016/j.biopsych.2013.02.006.
- Microhaplotype loci are a powerful new type of forensic markerKidd K, Pakstis A, Speed W, Lagace R, Chang J, Wootton S, Ihuegbu N. Microhaplotype loci are a powerful new type of forensic marker Forensic Science International Genetics Supplement Series 2013, 4: e123-e124. DOI: 10.1016/j.fsigss.2013.10.063.
- High diversity and no significant selection signal of human ADH1B gene in TibetLu Y, Kang L, Hu K, Wang C, Sun X, Chen F, Kidd JR, Kidd KK, Li H. High diversity and no significant selection signal of human ADH1B gene in Tibet Investigative Genetics 2012, 3: 23. PMID: 23176670, PMCID: PMC3528464, DOI: 10.1186/2041-2223-3-23.
- Genome-wide association study of Tourette's syndromeScharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, Davis LK, Han B, Crane J, Moorjani P, Crenshaw AT, Parkin MA, Reus VI, Lowe TL, Rangel-Lugo M, Chouinard S, Dion Y, Girard S, Cath DC, Smit JH, King RA, Fernandez TV, Leckman JF, Kidd KK, Kidd JR, Pakstis AJ, State MW, Herrera LD, Romero R, Fournier E, Sandor P, Barr CL, Phan N, Gross-Tsur V, Benarroch F, Pollak Y, Budman CL, Bruun RD, Erenberg G, Naarden AL, Lee PC, Weiss N, Kremeyer B, Berrío GB, Campbell DD, Cardona Silgado JC, Ochoa WC, Mesa Restrepo SC, Muller H, Valencia Duarte AV, Lyon GJ, Leppert M, Morgan J, Weiss R, Grados MA, Anderson K, Davarya S, Singer H, Walkup J, Jankovic J, Tischfield JA, Heiman GA, Gilbert DL, Hoekstra PJ, Robertson MM, Kurlan R, Liu C, Gibbs JR, Singleton A, Hardy J, Strengman E, Ophoff R, Wagner M, Moessner R, Mirel D, Posthuma D, Sabatti C, Eskin E, Conti D, Knowles J, Ruiz-Linares A, Rouleau G, Purcell S, Heutink P, Oostra B, McMahon W, Freimer N, Cox N, Pauls D. Genome-wide association study of Tourette's syndrome Molecular Psychiatry 2012, 18: 721-728. PMID: 22889924, PMCID: PMC3605224, DOI: 10.1038/mp.2012.69.
- Reconstructing Native American population historyReich D, Patterson N, Campbell D, Tandon A, Mazieres S, Ray N, Parra MV, Rojas W, Duque C, Mesa N, García LF, Triana O, Blair S, Maestre A, Dib JC, Bravi CM, Bailliet G, Corach D, Hünemeier T, Bortolini MC, Salzano FM, Petzl-Erler ML, Acuña-Alonzo V, Aguilar-Salinas C, Canizales-Quinteros S, Tusié-Luna T, Riba L, Rodríguez-Cruz M, Lopez-Alarcón M, Coral-Vazquez R, Canto-Cetina T, Silva-Zolezzi I, Fernandez-Lopez JC, Contreras AV, Jimenez-Sanchez G, Gómez-Vázquez MJ, Molina J, Carracedo Á, Salas A, Gallo C, Poletti G, Witonsky DB, Alkorta-Aranburu G, Sukernik RI, Osipova L, Fedorova SA, Vasquez R, Villena M, Moreau C, Barrantes R, Pauls D, Excoffier L, Bedoya G, Rothhammer F, Dugoujon JM, Larrouy G, Klitz W, Labuda D, Kidd J, Kidd K, Di Rienzo A, Freimer NB, Price AL, Ruiz-Linares A. Reconstructing Native American population history Nature 2012, 488: 370-374. PMID: 22801491, PMCID: PMC3615710, DOI: 10.1038/nature11258.
- Structural diversity and African origin of the 17q21.31 inversion polymorphismSteinberg KM, Antonacci F, Sudmant PH, Kidd JM, Campbell CD, Vives L, Malig M, Scheinfeldt L, Beggs W, Ibrahim M, Lema G, Nyambo TB, Omar SA, Bodo JM, Froment A, Donnelly MP, Kidd KK, Tishkoff SA, Eichler EE. Structural diversity and African origin of the 17q21.31 inversion polymorphism Nature Genetics 2012, 44: 872-880. PMID: 22751100, PMCID: PMC3408829, DOI: 10.1038/ng.2335.
- Mini-haplotypes as lineage informative SNPs and ancestry inference SNPsPakstis AJ, Fang R, Furtado MR, Kidd JR, Kidd KK. Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs European Journal Of Human Genetics 2012, 20: 1148-1154. PMID: 22535184, PMCID: PMC3476707, DOI: 10.1038/ejhg.2012.69.
- Expanding data and resources for forensic use of SNPs in individual identificationKidd KK, Kidd JR, Speed WC, Fang R, Furtado MR, Hyland FC, Pakstis AJ. Expanding data and resources for forensic use of SNPs in individual identification Forensic Science International Genetics 2012, 6: 646-652. PMID: 22445421, DOI: 10.1016/j.fsigen.2012.02.012.
- Crohn's Disease Risk Alleles on the NOD2 Locus Have Been Maintained by Natural Selection on Standing VariationNakagome S, Mano S, Kozlowski L, Bujnicki JM, Shibata H, Fukumaki Y, Kidd JR, Kidd KK, Kawamura S, Oota H. Crohn's Disease Risk Alleles on the NOD2 Locus Have Been Maintained by Natural Selection on Standing Variation Molecular Biology And Evolution 2012, 29: 1569-1585. PMID: 22319155, PMCID: PMC3697811, DOI: 10.1093/molbev/mss006.
- Duplicated Gene Evolution of the Primate Alcohol Dehydrogenase FamilyOota H, Oota H, Kidd K. Duplicated Gene Evolution of the Primate Alcohol Dehydrogenase Family 2011, 149-161. DOI: 10.1007/978-4-431-54011-3_9.
- A global view of the OCA2-HERC2 region and pigmentationDonnelly MP, Paschou P, Grigorenko E, Gurwitz D, Barta C, Lu RB, Zhukova OV, Kim JJ, Siniscalco M, New M, Li H, Kajuna SL, Manolopoulos VG, Speed WC, Pakstis AJ, Kidd JR, Kidd KK. A global view of the OCA2-HERC2 region and pigmentation Human Genetics 2011, 131: 683-696. PMID: 22065085, PMCID: PMC3325407, DOI: 10.1007/s00439-011-1110-x.
- ALFRED: an allele frequency resource for research and teachingRajeevan H, Soundararajan U, Kidd JR, Pakstis AJ, Kidd KK. ALFRED: an allele frequency resource for research and teaching Nucleic Acids Research 2011, 40: d1010-d1015. PMID: 22039151, PMCID: PMC3245092, DOI: 10.1093/nar/gkr924.
- Intelligence, Race, and GeneticsSternberg R, Grigorenko E, Kidd K, Stemler S. Intelligence, Race, and Genetics 2011, 195-238. DOI: 10.7312/columbia/9780231156974.003.0010.
- Single nucleotide polymorphisms and haplotypes in Native American populationsKidd JR, Friedlaender F, Pakstis AJ, Furtado M, Fang R, Wang X, Nievergelt CM, Kidd KK. Single nucleotide polymorphisms and haplotypes in Native American populations American Journal Of Biological Anthropology 2011, 146: 495-502. PMID: 21913176, PMCID: PMC3658315, DOI: 10.1002/ajpa.21560.
- High altitude adaptation in Daghestani populations from the CaucasusPagani L, Ayub Q, MacArthur DG, Xue Y, Baillie JK, Chen Y, Kozarewa I, Turner DJ, Tofanelli S, Bulayeva K, Kidd K, Paoli G, Tyler-Smith C. High altitude adaptation in Daghestani populations from the Caucasus Human Genetics 2011, 131: 423-433. PMID: 21904933, PMCID: PMC3312735, DOI: 10.1007/s00439-011-1084-8.
- The Molecular Origin and Consequences of Escape from miRNA Regulation by HLA-C AllelesO'hUigin C, Kulkarni S, Xu Y, Deng Z, Kidd J, Kidd K, Gao X, Carrington M. The Molecular Origin and Consequences of Escape from miRNA Regulation by HLA-C Alleles American Journal Of Human Genetics 2011, 89: 424-431. PMID: 21907013, PMCID: PMC3169826, DOI: 10.1016/j.ajhg.2011.07.024.
- Selecting SNPs to Identify AncestrySampson JN, Kidd KK, Kidd JR, Zhao H. Selecting SNPs to Identify Ancestry Annals Of Human Genetics 2011, 75: 539-553. PMID: 21668909, PMCID: PMC3141729, DOI: 10.1111/j.1469-1809.2011.00656.x.
- Selection on the Human Bitter Taste Gene, TAS2R16, in Eurasian PopulationsLi H, Pakstis AJ, Kidd JR, Kidd KK. Selection on the Human Bitter Taste Gene, TAS2R16, in Eurasian Populations Human Biology 2011, 83: 363-377. PMID: 21740153, DOI: 10.3378/027.083.0303.
- Diversification of the ADH1B Gene during Expansion of Modern HumansLi H, Gu S, Han Y, Xu Z, Pakstis AJ, Jin L, Kidd JR, Kidd KK. Diversification of the ADH1B Gene during Expansion of Modern Humans Annals Of Human Genetics 2011, 75: 497-507. PMID: 21592108, PMCID: PMC3722864, DOI: 10.1111/j.1469-1809.2011.00651.x.
- Hunter-gatherer genomic diversity suggests a southern African origin for modern humansHenn BM, Gignoux CR, Jobin M, Granka JM, Macpherson JM, Kidd JM, Rodríguez-Botigué L, Ramachandran S, Hon L, Brisbin A, Lin AA, Underhill PA, Comas D, Kidd KK, Norman PJ, Parham P, Bustamante CD, Mountain JL, Feldman MW. Hunter-gatherer genomic diversity suggests a southern African origin for modern humans Proceedings Of The National Academy Of Sciences Of The United States Of America 2011, 108: 5154-5162. PMID: 21383195, PMCID: PMC3069156, DOI: 10.1073/pnas.1017511108.
- 10. Intelligence, Race, and GeneticsSternberg R, Grigorenko E, Kidd K, Stemler S. 10. Intelligence, Race, and Genetics 2011, 195-238. DOI: 10.7312/krim15696-011.
- An Application of the Elastic Net for an Endophenotype AnalysisPalejev D, Hwang W, Landi N, Eastman M, Frost SJ, Fulbright RK, Kidd JR, Kidd KK, Mason GF, Mencl WE, Yrigollen C, Pugh KR, Grigorenko EL. An Application of the Elastic Net for an Endophenotype Analysis Behavior Genetics 2011, 41: 120-124. PMID: 21229297, PMCID: PMC3613288, DOI: 10.1007/s10519-011-9443-8.
- Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samplesKidd JR, Friedlaender FR, Speed WC, Pakstis AJ, De La Vega FM, Kidd KK. Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples Investigative Genetics 2011, 2: 1. PMID: 21208434, PMCID: PMC3025953, DOI: 10.1186/2041-2223-2-1.
- Rare BRCA1 haplotypes including 3’UTR SNPs associated with breast cancer riskPelletier C, Speed WC, Paranjape T, Keane K, Blitzblau R, Hollestelle A, Safavi K, van den Ouweland A, Zelterman D, Slack FJ, Kidd KK, Weidhaas JB. Rare BRCA1 haplotypes including 3’UTR SNPs associated with breast cancer risk Cell Cycle 2011, 10: 90-99. PMID: 21191178, PMCID: PMC3048078, DOI: 10.4161/cc.10.1.14359.
- A Variant in a MicroRNA complementary site in the 3′ UTR of the KIT oncogene increases risk of acral melanomaGodshalk SE, Paranjape T, Nallur S, Speed W, Chan E, Molinaro AM, Bacchiocchi A, Hoyt K, Tworkoski K, Stern DF, Sznol M, Ariyan S, Lazova R, Halaban R, Kidd KK, Weidhaas JB, Slack FJ. A Variant in a MicroRNA complementary site in the 3′ UTR of the KIT oncogene increases risk of acral melanoma Oncogene 2010, 30: 1542-1550. PMID: 21119596, PMCID: PMC3069149, DOI: 10.1038/onc.2010.536.
- Vegetable Intake in College-Aged Adults Is Explained by Oral Sensory Phenotypes and TAS2R38 GenotypeDuffy VB, Hayes JE, Davidson AC, Kidd JR, Kidd KK, Bartoshuk LM. Vegetable Intake in College-Aged Adults Is Explained by Oral Sensory Phenotypes and TAS2R38 Genotype Chemosensory Perception 2010, 3: 137-148. PMID: 21157576, PMCID: PMC3000691, DOI: 10.1007/s12078-010-9079-8.
- Using a Pharmacokinetic Model to Relate an Individual’s Susceptibility to Alcohol Dependence to GenotypesMustavich LF, Miller P, Kidd KK, Zhao H. Using a Pharmacokinetic Model to Relate an Individual’s Susceptibility to Alcohol Dependence to Genotypes Human Heredity 2010, 70: 177-193. PMID: 20714161, PMCID: PMC3164201, DOI: 10.1159/000317056.
- A variant of the endothelial nitric oxide synthase gene (NOS3) associated with AMS susceptibility is less common in the Quechua, a high altitude Native population.Wang P, Ha AY, Kidd KK, Koehle MS, Rupert JL. A variant of the endothelial nitric oxide synthase gene (NOS3) associated with AMS susceptibility is less common in the Quechua, a high altitude Native population. High Altitude Medicine & Biology 2010, 11: 27-30. PMID: 20367485, DOI: 10.1089/ham.2009.1054.
- Additional support for the association of SLITRK1 var321 and Tourette syndromeO'Roak B, Morgan T, Fishman D, Saus E, Alonso P, Gratacòs M, Estivill X, Teltsh O, Kohn Y, Kidd K, Cho J, Lifton R, State M. Additional support for the association of SLITRK1 var321 and Tourette syndrome Molecular Psychiatry 2010, 15: 447-450. PMID: 20351724, PMCID: PMC3292207, DOI: 10.1038/mp.2009.105.
- The Distribution and Most Recent Common Ancestor of the 17q21 Inversion in HumansDonnelly MP, Paschou P, Grigorenko E, Gurwitz D, Mehdi SQ, Kajuna SL, Barta C, Kungulilo S, Karoma NJ, Lu RB, Zhukova OV, Kim JJ, Comas D, Siniscalco M, New M, Li P, Li H, Manolopoulos VG, Speed WC, Rajeevan H, Pakstis AJ, Kidd JR, Kidd KK. The Distribution and Most Recent Common Ancestor of the 17q21 Inversion in Humans American Journal Of Human Genetics 2010, 86: 161-171. PMID: 20116045, PMCID: PMC2820164, DOI: 10.1016/j.ajhg.2010.01.007.
- Genetic Landscape of Eurasia and “Admixture” in UyghursLi H, Cho K, Kidd JR, Kidd KK. Genetic Landscape of Eurasia and “Admixture” in Uyghurs American Journal Of Human Genetics 2009, 85: 934-937. PMID: 20004770, PMCID: PMC2790568, DOI: 10.1016/j.ajhg.2009.10.024.
- Multiplexed SNP detection panels for human identificationFang R, Pakstis A, Hyland F, Wang D, Shewale J, Kidd J, Kidd K, Furtado M. Multiplexed SNP detection panels for human identification Forensic Science International Genetics Supplement Series 2009, 2: 538-539. DOI: 10.1016/j.fsigss.2009.08.161.
- Low Allele Frequency of ADH1B∗47His in West China and Different ADH1B Haplotypes in Western and Eastern AsiaLi H, Kidd K. Low Allele Frequency of ADH1B∗47His in West China and Different ADH1B Haplotypes in Western and Eastern Asia American Journal Of Human Genetics 2009, 84: 92-94. PMCID: PMC2668049, DOI: 10.1016/j.ajhg.2008.12.006.
- Report on ISFG SNP Panel DiscussionButler J, Budowle B, Gill P, Kidd K, Phillips C, Schneider P, Vallone P, Morling N. Report on ISFG SNP Panel Discussion Forensic Science International Genetics Supplement Series 2008, 1: 471-472. DOI: 10.1016/j.fsigss.2007.10.159.
- SNPs for individual identificationPakstis A, Speed W, Kidd J, Kidd K. SNPs for individual identification Forensic Science International Genetics Supplement Series 2008, 1: 479-481. DOI: 10.1016/j.fsigss.2007.10.200.
- Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 geneLee M, Mukherjee N, Pakstis A, Khaliq S, Mohyuddin A, Mehdi S, Speed W, Kidd J, Kidd K. Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene The Pharmacogenomics Journal 2008, 8: 349-356. PMID: 18663376, PMCID: PMC2782390, DOI: 10.1038/tpj.2008.9.
- The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferaseMukherjee N, Kidd K, Pakstis A, Speed W, Li H, Tarnok Z, Barta C, Kajuna S, Kidd J. The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase Molecular Psychiatry 2008, 15: 216-225. PMID: 18574484, PMCID: PMC2811226, DOI: 10.1038/mp.2008.64.
- Correction: The Genetic Structure of Pacific IslandersFriedlaender J, Friedlaender F, Reed F, Kidd K, Kidd J, Chambers G, Lea R, Loo J, Koki G, Hodgson J, Merriwether D, Weber J. Correction: The Genetic Structure of Pacific Islanders PLOS Genetics 2008, 4: 10.1371/annotation/cbdd11a0-4a29-4e7c-9e4e-c00a184c7777. PMCID: PMC2637087, DOI: 10.1371/annotation/cbdd11a0-4a29-4e7c-9e4e-c00a184c7777.
- Human genetic variation of medical significanceKidd K, Kidd J. Human genetic variation of medical significance 2007, 51-62. DOI: 10.1093/acprof:oso/9780199207466.003.0005.
- 4-OR: Global diversity of KIR and HLA: Population-level evidence for co-evolution, natural selection, and signatures of demographic historySingle R, Martin M, Gao X, Meyer D, Yeager M, Kidd J, Kidd K, Carrington M. 4-OR: Global diversity of KIR and HLA: Population-level evidence for co-evolution, natural selection, and signatures of demographic history Human Immunology 2007, 68: s10. DOI: 10.1016/j.humimm.2007.08.009.
- Searching for Major Genes for Psychiatric DisordersKidd K. Searching for Major Genes for Psychiatric Disorders 2007, 184-196. DOI: 10.1002/9780470513507.ch11.
- Motoneuron-specific NR3B gene: No association with ALS and evidence for a common null alleleSYMBOLNiemann S, Landers J, Churchill M, Hosler B, Sapp P, Speed W, Lahn B, Kidd K, Brown R, Hayashi Y. Motoneuron-specific NR3B gene: No association with ALS and evidence for a common null alleleSYMBOL Neurology 2007, 70: 666-676. PMID: 17687115, DOI: 10.1212/01.wnl.0000271078.51280.17.
- Erratum: Significant variation in haplotype block structure but conservation in tagSNP patterns among global populationsGu S, Pakstis A, Li H, Speed W, Kidd J, Kidd K. Erratum: Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations European Journal Of Human Genetics 2007, 15: 818-818. DOI: 10.1038/sj.ejhg.5201862.
- Racing Toward the Finish LineSternberg R, Grigorenko E, Kidd K. Racing Toward the Finish Line American Psychologist 2006, 61: 178-179. DOI: 10.1037/0003-066x.61.2.178.
- DESIGN AND ANALYSIS OF GENETIC STUDIES AFTER THE HAPMAP PROJECT: SESSION INTRODUCTIONDE LA VEGA F, CLARK A, COLLINS A, KIDD K. DESIGN AND ANALYSIS OF GENETIC STUDIES AFTER THE HAPMAP PROJECT: SESSION INTRODUCTION 2005, 451-453. DOI: 10.1142/9789812701626_0041.
- Normal DNA sequence variations in humansKidd K. Normal DNA sequence variations in humans 2005 DOI: 10.1002/047001153x.g206101.
- Human genome diversity projectWeiss K, Kidd K, Kidd J. Human genome diversity project Evolutionary Anthropology Issues News And Reviews 2005, 1: 80-82. DOI: 10.1002/evan.1360010303.
- ALFRED: An Allele Frequency Database for Microevolutionary StudiesRajeevan H, Cheung K, Gadagkar R, Stein S, Soundararajan U, Kidd J, Pakstis A, Miller P, Kidd K. ALFRED: An Allele Frequency Database for Microevolutionary Studies Evolutionary Bioinformatics 2005, 1: 117693430500100006. DOI: 10.1177/117693430500100006.
- Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility RegionPaschou P, Feng Y, Pakstis A, Speed W, DeMille M, Kidd J, Jaghori B, Kurlan R, Pauls D, Sandor P, Barr C, Kidd K. Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility Region American Journal Of Human Genetics 2004, 75: 545-560. PMID: 15303240, PMCID: PMC1182043, DOI: 10.1086/424389.
- The Genetic Architecture of Selection at the Human Dopamine Receptor D4 (DRD4) Gene LocusWang E, Ding Y, Flodman P, Kidd J, Kidd K, Grady D, Ryder O, Spence M, Swanson J, Moyzis R. The Genetic Architecture of Selection at the Human Dopamine Receptor D4 (DRD4) Gene Locus American Journal Of Human Genetics 2004, 74: 931-944. PMID: 15077199, PMCID: PMC1181986, DOI: 10.1086/420854.
- COMT haplotypes suggest P2 promoter region relevance for schizophreniaPalmatier M, Pakstis A, Speed W, Paschou P, Goldman D, Odunsi A, Okonofua F, Kajuna S, Karoma N, Kungulilo S, Grigorenko E, Zhukova O, Bonne-Tamir B, Lu R, Parnas J, Kidd J, DeMille M, Kidd K. COMT haplotypes suggest P2 promoter region relevance for schizophrenia Molecular Psychiatry 2004, 9: 859-870. PMID: 15098000, DOI: 10.1038/sj.mp.4001496.
- COMPUTATIONAL TOOLS FOR COMPLEX TRAIT GENE MAPPINGDE LA VEGA F, KIDD K, COLLINS A. COMPUTATIONAL TOOLS FOR COMPLEX TRAIT GENE MAPPING 2003, 89-92. DOI: 10.1142/9789812704856_0009.
- Selective Pressure has not Acted Against Hypercoagulability Alleles in High‐Altitude AmerindiansRupert J, Monsalve M, Kidd K, Tan C, Hochachka P, Devine D. Selective Pressure has not Acted Against Hypercoagulability Alleles in High‐Altitude Amerindians Annals Of Human Genetics 2003, 67: 426-432. PMID: 12940916, DOI: 10.1046/j.1469-1809.2003.00043.x.
- Response to Comment on "Genetic Structure of Human Populations"Rosenberg N, Pritchard J, Weber J, Cann H, Kidd K, Zhivotovsky L, Feldman M. Response to Comment on "Genetic Structure of Human Populations" Science 2003, 300: 1877c-1877. DOI: 10.1126/science.1084688.
- Genetic Polymorphisms in the Renin‐Angiotensin System in High‐Altitude and Low‐Altitude Native American PopulationsRupert J, Kidd K, Norman L, Monsalve M, Hochachka P, Devine D. Genetic Polymorphisms in the Renin‐Angiotensin System in High‐Altitude and Low‐Altitude Native American Populations Annals Of Human Genetics 2003, 67: 17-25. PMID: 12556231, DOI: 10.1046/j.1469-1809.2003.00004.x.
- Mitochondrial and nuclear DNA estimates of divergence between western and eastern gorillasJensen-Seaman M, Deinard A, Kidd K. Mitochondrial and nuclear DNA estimates of divergence between western and eastern gorillas 2002, 247-268. DOI: 10.1017/cbo9780511542558.011.
- Session IntroductionDE LA VEGA F, KIDD K, KOHANE I. Session Introduction 2002, 463-465. DOI: 10.1142/9789812776303_0043.
- Reply to WhitfieldKidd K, Osier M, Pakstis A, Kidd J. Reply to Whitfield American Journal Of Human Genetics 2002, 71: 1250-1251. DOI: 10.1086/344288.
- Modern African Ape Populations as Genetic and Demographic Models of the Last Common Ancestor of Humans, Chimpanzees, and GorillasJensen-Seaman M, Deinard A, Kidd K. Modern African Ape Populations as Genetic and Demographic Models of the Last Common Ancestor of Humans, Chimpanzees, and Gorillas Journal Of Heredity 2001, 92: 475-480. PMID: 11948214, DOI: 10.1093/jhered/92.6.475.
- Comparisons of Two Methods for Haplotype Reconstruction and Haplotype Frequency Estimation from Population DataZhang S, Pakstis A, Kidd K, Zhao H. Comparisons of Two Methods for Haplotype Reconstruction and Haplotype Frequency Estimation from Population Data American Journal Of Human Genetics 2001, 69: 906-912. PMID: 11536083, PMCID: PMC1226079, DOI: 10.1086/323622.
- Insertional polymorphisms of full-length endogenous retroviruses in humansTurner G, Barbulescu M, Su M, Jensen-Seaman M, Kidd K, Lenz J. Insertional polymorphisms of full-length endogenous retroviruses in humans Current Biology 2001, 11: 1531-1535. PMID: 11591322, DOI: 10.1016/s0960-9822(01)00455-9.
- Mitochondrial DNA variation and biogeography of eastern gorillasJensen‐Seaman M, Kidd K. Mitochondrial DNA variation and biogeography of eastern gorillas Molecular Ecology 2001, 10: 2241-2247. PMID: 11555266, DOI: 10.1046/j.0962-1083.2001.01365.x.
- A HERV-K provirus in chimpanzees, bonobos and gorillas, but not humansBarbulescu M, Turner G, Su M, Kim R, Jensen-Seaman M, Deinard A, Kidd K, Lenz J. A HERV-K provirus in chimpanzees, bonobos and gorillas, but not humans Current Biology 2001, 11: 779-783. PMID: 11378389, DOI: 10.1016/s0960-9822(01)00227-5.
- Worldwide Genetic Analysis of the CFTR RegionMateu E, Calafell F, Lao O, Bonné-Tamir B, Kidd J, Pakstis A, Kidd K, Bertranpetit J. Worldwide Genetic Analysis of the CFTR Region American Journal Of Human Genetics 2000, 68: 103-117. PMID: 11104661, PMCID: PMC1234903, DOI: 10.1086/316940.
- Reply to Kong and NicolaeZhao H, Merikangas K, Kidd K. Reply to Kong and Nicolae American Journal Of Human Genetics 2000, 67: 1355-1356. DOI: 10.1016/s0002-9297(07)62968-1.
- Haplotype Evolution and Linkage Disequilibrium: A Simulation StudyCalafell F, Grigorenko E, Chikanian A, Kidd K. Haplotype Evolution and Linkage Disequilibrium: A Simulation Study Human Heredity 2000, 51: 85-96. PMID: 11096275, DOI: 10.1159/000022963.
- Short Tandem-Repeat Polymorphism/Alu Haplotype Variation at the PLAT Locus: Implications for Modern Human OriginsTishkoff S, Pakstis A, Stoneking M, Kidd J, Destro-Bisol G, Sanjantila A, Lu R, Deinard A, Sirugo G, Jenkins T, Kidd K, Clark A. Short Tandem-Repeat Polymorphism/Alu Haplotype Variation at the PLAT Locus: Implications for Modern Human Origins American Journal Of Human Genetics 2000, 67: 901-925. PMID: 10986042, PMCID: PMC1287905, DOI: 10.1086/303068.
- Transmission/Disequilibrium Tests Using Multiple Tightly Linked MarkersZhao H, Zhang S, Merikangas K, Trixler M, Wildenauer D, Sun F, Kidd K. Transmission/Disequilibrium Tests Using Multiple Tightly Linked Markers American Journal Of Human Genetics 2000, 67: 936-946. PMID: 10968775, PMCID: PMC1287895, DOI: 10.1086/303073.
- A primate genome project deserves high priority.McConkey E, Varki A, Allman J, Benirschke K, Crick F, Deacon T, de Waal F, Dugaiczyk A, Gagneux P, Goodman M, Grossman L, Gumucio D, Insel T, Kidd K, King M, Krauter K, Kucherlapati R, Motulsky A, Nelson D, Oefner P, Palade G, Palade G, Ryder O, Stewart C, Sikela J, Stone A, Woodruff D. A primate genome project deserves high priority. Science 2000, 289: 1295-6. PMID: 10979852, DOI: 10.1126/science.289.5483.1295b.
- The Accuracy of Statistical Methods for Estimation of Haplotype Frequencies: An Example from the CD4 LocusTishkoff S, Pakstis A, Ruano G, Kidd K. The Accuracy of Statistical Methods for Estimation of Haplotype Frequencies: An Example from the CD4 Locus American Journal Of Human Genetics 2000, 67: 518-522. PMID: 10859209, PMCID: PMC1287198, DOI: 10.1086/303000.
- Haplotypes and Linkage Disequilibrium at the Phenylalanine Hydroxylase Locus, PAH, in a Global Representation of PopulationsKidd J, Pakstis A, Zhao H, Lu R, Okonofua F, Odunsi A, Grigorenko E, Tamir B, Friedlaender J, Schulz L, Parnas J, Kidd K. Haplotypes and Linkage Disequilibrium at the Phenylalanine Hydroxylase Locus, PAH, in a Global Representation of Populations American Journal Of Human Genetics 2000, 66: 1882-1899. PMID: 10788337, PMCID: PMC1378054, DOI: 10.1086/302952.
- Evolution of exon 1 of the dopamine D4 receptor (DRD4) gene in primatesSeaman M, Chang F, Deinard A, Quiñones A, Kidd K. Evolution of exon 1 of the dopamine D4 receptor (DRD4) gene in primates Journal Of Experimental Zoology 2000, 288: 32-38. PMID: 10750051, DOI: 10.1002/(sici)1097-010x(20000415)288:1<32::aid-jez4>3.0.co;2-g.
- Identifying conservation units within captive chimpanzee populationsDeinard A, Kidd K. Identifying conservation units within captive chimpanzee populations American Journal Of Biological Anthropology 2000, 111: 25-44. PMID: 10618587, DOI: 10.1002/(sici)1096-8644(200001)111:1<25::aid-ajpa3>3.0.co;2-r.
- Tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4)Seaman M, Fisher J, Chang F, Kidd K. Tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4) American Journal Of Medical Genetics 1999, 88: 705-709. PMID: 10581493, DOI: 10.1002/(sici)1096-8628(19991215)88:6<705::aid-ajmg22>3.0.co;2-f.
- ALFRED: A WEB-ACCESSIBLE ALLELE FREQUENCY DATABASECHEUNG K, MILLER P, KIDD J, KIDD K, OSIER M, PAKSTIS A. ALFRED: A WEB-ACCESSIBLE ALLELE FREQUENCY DATABASE 1999, 639-650. DOI: 10.1142/9789814447331_0062.
- On a Randomization Procedure in Linkage AnalysisZhao H, Merikangas K, Kidd K. On a Randomization Procedure in Linkage Analysis American Journal Of Human Genetics 1999, 65: 1449-1456. PMID: 10521312, PMCID: PMC1288298, DOI: 10.1086/302607.
- Experience and Preliminary Results in Human Genome Diversity ResearchKidd K, Kidd J. Experience and Preliminary Results in Human Genome Diversity Research Politics And The Life Sciences 1999, 18: 314-316. PMID: 12561788, DOI: 10.1017/s0730938400021572.
- Many human endogenous retrovirus K (HERV-K) proviruses are unique to humansBarbulescu M, Turner G, Seaman M, Deinard A, Kidd K, Lenz J. Many human endogenous retrovirus K (HERV-K) proviruses are unique to humans Current Biology 1999, 9: 861-s1. PMID: 10469592, DOI: 10.1016/s0960-9822(99)80390-x.
- Global variation in the frequencies of functionally different catechol-O-methyltransferase allelesPalmatier M, Kang A, Kidd K. Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles Biological Psychiatry 1999, 46: 557-567. PMID: 10459407, DOI: 10.1016/s0006-3223(99)00098-0.
- Evolution of the HOXB6 intergenic region: Motif conservation at the lateral plate mesoderm (LPM) enhancer elementDeinard A, Dorit R, Castiglione C, Jiang Z, Becker D, Ruddle F, Schugart K, Kidd K. Evolution of the HOXB6 intergenic region: Motif conservation at the lateral plate mesoderm (LPM) enhancer element Journal Of Experimental Zoology 1999, 285: 170-176. PMID: 10440728, DOI: 10.1002/(sici)1097-010x(19990815)285:2<170::aid-jez9>3.0.co;2-j.
- A paradigm for finding genes for a complex human trait: Polycystic ovary syndrome and follistatinOdunsi K, Kidd K. A paradigm for finding genes for a complex human trait: Polycystic ovary syndrome and follistatin Proceedings Of The National Academy Of Sciences Of The United States Of America 1999, 96: 8315-8317. PMID: 10411866, PMCID: PMC33617, DOI: 10.1073/pnas.96.15.8315.
- Genome scan for linkage to Gilles de la Tourette syndromeBarr C, Wigg K, Pakstis A, Kurlan R, Pauls D, Kidd K, Tsui L, Sandor P. Genome scan for linkage to Gilles de la Tourette syndrome American Journal Of Medical Genetics 1999, 88: 437-445. PMID: 10402514, DOI: 10.1002/(sici)1096-8628(19990820)88:4<437::aid-ajmg24>3.0.co;2-e.
- Global variation of a 40-bp VNTR in the 3′-untranslated region of the dopamine transporter gene (SLC6A3)Kang A, Palmatier M, Kidd K. Global variation of a 40-bp VNTR in the 3′-untranslated region of the dopamine transporter gene (SLC6A3) Biological Psychiatry 1999, 46: 151-160. PMID: 10418689, DOI: 10.1016/s0006-3223(99)00101-8.
- Evolution of a HOXB6 intergenic region within the great apes and humansDeinard A, Kidd K. Evolution of a HOXB6 intergenic region within the great apes and humans Journal Of Human Evolution 1999, 36: 687-703. PMID: 10330333, DOI: 10.1006/jhev.1999.0298.
- No Association Between DRD2 Locus and Alcoholism After Controlling the ADH and ALDH Genotypes in Chinese Han PopulationLee J, Lu R, Ko H, Chang F, Yin S, Pakstis A, Kidd K. No Association Between DRD2 Locus and Alcoholism After Controlling the ADH and ALDH Genotypes in Chinese Han Population Alcoholism Clinical And Experimental Research 1999, 23: 592-599. PMID: 10235293, DOI: 10.1111/j.1530-0277.1999.tb04159.x.
- Linkage Disequilibrium at the ADH2 and ADH3 Loci and Risk of AlcoholismOsier M, Pakstis A, Kidd J, Lee J, Yin S, Ko H, Edenberg H, Lu R, Kidd K. Linkage Disequilibrium at the ADH2 and ADH3 Loci and Risk of Alcoholism American Journal Of Human Genetics 1999, 64: 1147-1157. PMID: 10090900, PMCID: PMC1377839, DOI: 10.1086/302317.
- Genealogy reconstruction from short tandem repeat genotypes in an Amazonian populationCalafell F, Shuster A, Speed W, Kidd J, Black F, Kidd K. Genealogy reconstruction from short tandem repeat genotypes in an Amazonian population American Journal Of Biological Anthropology 1999, 108: 137-146. PMID: 9988377, DOI: 10.1002/(sici)1096-8644(199902)108:2<137::aid-ajpa1>3.0.co;2-k.
- Allele Frequencies in a Worldwide Survey of a CA Repeat in the First Intron of the CFTR GeneMateu E, Calafell F, Bonné-Tamir B, Kidd J, Casals T, Kidd K, Bertranpetit J. Allele Frequencies in a Worldwide Survey of a CA Repeat in the First Intron of the CFTR Gene Human Heredity 1999, 49: 15-20. PMID: 9858852, DOI: 10.1159/000022834.
- A more powerful method to evaluate p‐values in GENEHUNTERZhao H, Sheffield L, Pakstis A, Knauert M, Kidd K. A more powerful method to evaluate p‐values in GENEHUNTER Genetic Epidemiology 1999, 17: s415-s420. PMID: 10597472, DOI: 10.1002/gepi.1370170770.
- No Association Between DRD2 Locus and Alcoholism After Controlling the ADH and ALDH Genotypes in Chinese Han PopulationLee J, Lu R, Ko H, Chang F, Yin S, Pakstis A, Kidd K. No Association Between DRD2 Locus and Alcoholism After Controlling the ADH and ALDH Genotypes in Chinese Han Population Alcoholism Clinical And Experimental Research 1999, 23: 592. DOI: 10.1097/00000374-199904001-00004.
- A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locusKidd K, Morar B, Castiglione C, Zhao H, Pakstis A, Speed W, Bonne-Tamir B, Lu R, Goldman D, Lee C, Nam Y, Grandy D, Jenkins T, Kidd J. A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus Human Genetics 1998, 103: 211-227. PMID: 9760208, DOI: 10.1007/s004390050809.
- Hominid phylogeny: inferences from a sub-terminal minisatellite analyzed by repeat expansion detection (RED)Deinard A, Sirugo G, Kidd K. Hominid phylogeny: inferences from a sub-terminal minisatellite analyzed by repeat expansion detection (RED) Journal Of Human Evolution 1998, 35: 321-325. PMID: 9782100, DOI: 10.1006/jhev.1998.0245.
- Network Analyses of Y-Chromosomal Types in Europe, Northern Africa, and Western Asia Reveal Specific Patterns of Geographic DistributionMalaspina P, Cruciani F, Ciminelli B, Terrenato L, Santolamazza P, Alonso A, Banyko J, Brdicka R, García O, Gaudiano C, Guanti G, Kidd K, Lavinha J, Avila M, Mandich P, Moral P, Qamar R, Mehdi S, Ragusa A, Stefanescu G, Caraghin M, Tyler-Smith C, Scozzari R, Novelletto A. Network Analyses of Y-Chromosomal Types in Europe, Northern Africa, and Western Asia Reveal Specific Patterns of Geographic Distribution American Journal Of Human Genetics 1998, 63: 847-860. PMID: 9718330, PMCID: PMC1377388, DOI: 10.1086/301999.
- Hominoid phylogeny: inferences from a sub-terminal minisatellite analyzed by repeat expansion detection (RED)Deinard A, Sirugo G, Kidd K. Hominoid phylogeny: inferences from a sub-terminal minisatellite analyzed by repeat expansion detection (RED) Journal Of Human Evolution 1998, 35: 313-7. PMID: 9749409.
- Genetic Structure of the Ancestral Population of Modern HumansZiętkiewicz E, Yotova V, Jarnik M, Korab-Laskowska M, Kidd K, Modiano D, Scozzari R, Stoneking M, Tishkoff S, Batzer M, Labuda D. Genetic Structure of the Ancestral Population of Modern Humans Journal Of Molecular Evolution 1998, 47: 146-155. PMID: 9694663, DOI: 10.1007/pl00006371.
- Repeat Expansion–Detection Analysis of Telomeric Uninterrupted (TTAGGG) n ArraysSirugo G, Kidd K. Repeat Expansion–Detection Analysis of Telomeric Uninterrupted (TTAGGG) n Arrays American Journal Of Human Genetics 1998, 63: 648-651. PMID: 9683592, PMCID: PMC1377302, DOI: 10.1086/301961.
- Reply to Dr. GoodmanSirugo G, Pakstis A, Kidd K. Reply to Dr. Goodman American Journal Of Medical Genetics 1998, 81: 348-348. DOI: 10.1002/(sici)1096-8628(19980710)81:4<348::aid-ajmg14>3.0.co;2-l.
- A Global Haplotype Analysis of the Myotonic Dystrophy Locus: Implications for the Evolution of Modern Humans and for the Origin of Myotonic Dystrophy MutationsTishkoff S, Goldman A, Calafell F, Speed W, Deinard A, Bonne-Tamir B, Kidd J, Pakstis A, Jenkins T, Kidd K. A Global Haplotype Analysis of the Myotonic Dystrophy Locus: Implications for the Evolution of Modern Humans and for the Origin of Myotonic Dystrophy Mutations American Journal Of Human Genetics 1998, 62: 1389-1402. PMID: 9585589, PMCID: PMC1377140, DOI: 10.1086/301861.
- Long CAG/CTG repeats in miceKing B, Sirugo G, Nadeau J, Hudson T, Kidd K, Kacinski B, Schalling M. Long CAG/CTG repeats in mice Mammalian Genome 1998, 9: 392-393. PMID: 9545500, DOI: 10.1007/s003359900778.
- OA1 Mutations and Deletions in X-Linked Ocular AlbinismSchnur R, Gao M, Wick P, Keller M, Benke P, Edwards M, Grix A, Hockey A, Jung J, Kidd K, Kistenmacher M, Levin A, Lewis R, Musarella M, Nowakowski R, Orlow S, Pagon R, Pillers D, Punnett H, Quinn G, Tezcan K, Wagstaff J, Weleber R. OA1 Mutations and Deletions in X-Linked Ocular Albinism American Journal Of Human Genetics 1998, 62: 800-809. PMID: 9529334, PMCID: PMC1377018, DOI: 10.1086/301776.
- Short tandem repeat polymorphism evolution in humansCalafell F, Shuster A, Speed W, Kidd J, Kidd K. Short tandem repeat polymorphism evolution in humans European Journal Of Human Genetics 1998, 6: 38-49. PMID: 9781013, DOI: 10.1038/sj.ejhg.5200151.
- Analyses of Cross Species Polymerase Chain Reaction Products to Infer the Ancestral State of Human PolymorphismsIyengar S, Seaman M, Deinard A, Rosenbaum H, Sirugo G, Castiglione C, Kidd J, Kidd K. Analyses of Cross Species Polymerase Chain Reaction Products to Infer the Ancestral State of Human Polymorphisms Mitochondrial DNA Part A 1998, 8: 317-327. PMID: 10993602, DOI: 10.3109/10425179809034076.
- Evolution of a D2 Dopamine Receptor Intron Within the Great Apes and HumansDeinard A, Kidd K. Evolution of a D2 Dopamine Receptor Intron Within the Great Apes and Humans Mitochondrial DNA Part A 1998, 8: 289-301. PMID: 10993600, DOI: 10.3109/10425179809034074.
- Nuclear DNA diversity in worldwide distributed human populationsZigtkiewicz E, Yotova V, Jarnik M, Korab-Laskowska M, Kídd K, Modiano D, Scozzari R, Stoneking M, Tishkoff S, Batzer M, Labuda D. Nuclear DNA diversity in worldwide distributed human populations Gene 1997, 205: 161-171. PMID: 9461390, DOI: 10.1016/s0378-1119(97)00408-3.
- A Novel, Heritable, Expanding CTG Repeat in an Intron of the SEF2-1 Gene on Chromosome 18q21.1Breschel T, McInnis M, Margolis R, Sirugo G, Corneliussen B, Simpson S, McMahon F, MacKinnon D, Xu J, Pleasant N, Huo Y, Ashworth R, Grundstrom C, Grundstrom T, Kidd K, DePaulo J, Ross C. A Novel, Heritable, Expanding CTG Repeat in an Intron of the SEF2-1 Gene on Chromosome 18q21.1 Human Molecular Genetics 1997, 6: 1855-1863. PMID: 9302263, DOI: 10.1093/hmg/6.11.1855.
- Detection of a large CTG/CAG trinucleotide repeat expansion in a Danish schizophrenia kindredSirugo G, Pakstis A, Kidd K, Matthysse S, Levy D, Holzman P, Párnas J, McInnis M, Breschel T, Ross C. Detection of a large CTG/CAG trinucleotide repeat expansion in a Danish schizophrenia kindred American Journal Of Medical Genetics 1997, 74: 546-548. PMID: 9342210, DOI: 10.1002/(sici)1096-8628(19970919)74:5<546::aid-ajmg19>3.0.co;2-c.
- Differential Structuring of Human Populations for Homologous X and Y Microsatellite LociScozzari R, Cruciani F, Malaspina P, Santolamazza P, Ciminelli B, Torroni A, Modiano D, Wallace D, Kidd K, Olckers A, Moral P, Terrenato L, Akar N, Qamar R, Mansoor A, Mehdi S, Meloni G, Vona G, Cole D, Cai W, Novelletto A. Differential Structuring of Human Populations for Homologous X and Y Microsatellite Loci American Journal Of Human Genetics 1997, 61: 719-733. PMID: 9326337, PMCID: PMC1715969, DOI: 10.1086/515500.
- Population genetics of a functional variant of the dopamine β‐hydroxylase gene (DBH)Cubells J, Kobayashi K, Nagatsu T, Kidd K, Kidd J, Calafell F, Kranzler H, Ichinose H, Gelernter J. Population genetics of a functional variant of the dopamine β‐hydroxylase gene (DBH) American Journal Of Medical Genetics 1997, 74: 374-379. PMID: 9259372, DOI: 10.1002/(sici)1096-8628(19970725)74:4<374::aid-ajmg7>3.0.co;2-p.
- Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.Iyengar S, Kalinsky H, Weiss S, Korostishevsky M, Sadeh M, Zhao Y, Kidd K, Bonne-Tamir B. Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease. Journal Of Medical Genetics 1997, 34: 391. PMID: 9152836, PMCID: PMC1050946, DOI: 10.1136/jmg.34.5.391.
- Survey of Maximum CTG/CAG Repeat Lengths in Humans and Non-Human Primates: Total Genome Scan in Populations Using the Repeat Expansion Detection MethodSirugo G, Deinard A, Kidd J, Kidd K. Survey of Maximum CTG/CAG Repeat Lengths in Humans and Non-Human Primates: Total Genome Scan in Populations Using the Repeat Expansion Detection Method Human Molecular Genetics 1997, 6: 403-408. PMID: 9147643, DOI: 10.1093/hmg/6.3.403.
- Editorial: Can we find genes for schizophrenia?Kidd K. Editorial: Can we find genes for schizophrenia? American Journal Of Medical Genetics 1997, 74: 104-111. PMID: 9034016, DOI: 10.1002/(sici)1096-8628(19970221)74:1<104::aid-ajmg21>3.0.co;2-u.
- Rapid molecular haplotyping of the first exon of the human dopamine D4 receptor gene by heteroduplex analysisChang F, Kidd K. Rapid molecular haplotyping of the first exon of the human dopamine D4 receptor gene by heteroduplex analysis American Journal Of Medical Genetics 1997, 74: 91-94. PMID: 9034013, DOI: 10.1002/(sici)1096-8628(19970221)74:1<91::aid-ajmg18>3.0.co;2-m.
- The dopamine D4 receptor gene (DRD4) is not associated with alcoholism in three Taiwanese populations: Six polymorphisms tested separately and as haplotypesChang F, Ko H, Lu R, Pakstis A, Kidd K. The dopamine D4 receptor gene (DRD4) is not associated with alcoholism in three Taiwanese populations: Six polymorphisms tested separately and as haplotypes Biological Psychiatry 1997, 41: 394-405. PMID: 9034534, DOI: 10.1016/s0006-3223(96)00248-x.
- Concerted evolution of the tandemly repeated genes encoding human U2 snRNA (the RNU2 locus) involves rapid intrachromosomal homogenization and rare interchromosomal gene conversionLiao D, Pavelitz T, Kidd J, Kidd K, Weiner A. Concerted evolution of the tandemly repeated genes encoding human U2 snRNA (the RNU2 locus) involves rapid intrachromosomal homogenization and rare interchromosomal gene conversion The EMBO Journal 1997, 16: 588-598. PMID: 9034341, PMCID: PMC1169662, DOI: 10.1093/emboj/16.3.588.
- Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemesIyengar S, Calafell F, Kidd K. Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemes Genetic Epidemiology 1997, 14: 809-814. PMID: 9433582, DOI: 10.1002/(sici)1098-2272(1997)14:6<809::aid-gepi41>3.0.co;2-r.
- Proposed model ethical protocol for collecting DNA samples.Weiss K, Cavalli-Sforza L, Dunston G, Feldman M, Greely H, Kidd K, King M, Moore J, Szathmary E, Twinn C. Proposed model ethical protocol for collecting DNA samples. Houston Law Review 1997, 33: 1431-74. PMID: 12627556.
- Dynamics of the haplotype frequencies in populations: study using the Monte Carlo method.Grigorenko E, Shikanian A, Kidd D, Dorig R, Kidd K. Dynamics of the haplotype frequencies in populations: study using the Monte Carlo method. Генетика 1996, 32: 1705-13. PMID: 9102365.
- Molecular Haplotyping of Genetic Markers 10 kb Apart by Allele-Specific Long-Range PCRMichalatos-Beloin S, Tishkoff S, Bentley K, Kidd K, Ruano G. Molecular Haplotyping of Genetic Markers 10 kb Apart by Allele-Specific Long-Range PCR Nucleic Acids Research 1996, 24: 4841-4843. PMID: 8972876, PMCID: PMC146303, DOI: 10.1093/nar/24.23.4841.
- Response: Genetic Data and the African Origin of HumansRisch N, Kidd K, Tishkoff S. Response: Genetic Data and the African Origin of Humans Science 1996, 274: 1548-1549. PMID: 17816998, DOI: 10.1126/science.274.5292.1548b.
- Response: Genetic Data and the African Origin of HumansRisch N, Kidd K, Tishkoff S. Response: Genetic Data and the African Origin of Humans Science 1996, 274: 1548-1549. DOI: 10.1126/science.274.5292.1548-b.
- Response: Interpretations of Multiregional EvolutionTishkoff S, Kidd K, Risch N. Response: Interpretations of Multiregional Evolution Science 1996, 274: 706-707. PMID: 17735319, DOI: 10.1126/science.274.5288.706.
- Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: Implications for therapyGill J, Reyes-Múgica M, Iyengar S, Kidd K, Touloukian R, Smith C, Keller M, Genel M. Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: Implications for therapy The Journal Of Pediatrics 1996, 129: 459-464. PMID: 8804341, DOI: 10.1016/s0022-3476(96)70084-7.
- PhenoDB: An Integrated Client/Server Database for Linkage and Population GeneticsCheung K, Nadkarni P, Silverstein S, Kidd J, Pakstis A, Miller P, Kidd K. PhenoDB: An Integrated Client/Server Database for Linkage and Population Genetics Journal Of Biomedical Informatics 1996, 29: 327-337. PMID: 8812078, DOI: 10.1006/cbmr.1996.0024.
- Distribution and frequency of a polymorphicAlu insertion at the plasminogen activator locus in humansTishkoff S, Ruano G, Kidd J, Kidd K. Distribution and frequency of a polymorphicAlu insertion at the plasminogen activator locus in humans Human Genetics 1996, 97: 759-764. PMID: 8641693, DOI: 10.1007/bf02346186.
- Minisatellite diversity supports a recent African origin for modern humansArmour J, Anttinen T, May C, Vega E, Sajantila A, Kidd J, Kidd K, Bertranpetit J, Pääbo S, Jeffreys A. Minisatellite diversity supports a recent African origin for modern humans Nature Genetics 1996, 13: 154-160. PMID: 8640220, DOI: 10.1038/ng0696-154.
- DRD2 Haplotypes Containing the TaqI A1 Allele: Implications for Alcoholism ResearchKidd K, Pakstis A, Castiglione C, Kidd J, Speed W, Goldman D, Knowler W, Lu R, Bonne‐Tamir B. DRD2 Haplotypes Containing the TaqI A1 Allele: Implications for Alcoholism Research Alcoholism Clinical And Experimental Research 1996, 20: 697-705. PMID: 8800387, DOI: 10.1111/j.1530-0277.1996.tb01674.x.
- The world-wide distribution of allele frequencies at the human dopamine D4 receptor locusChang F, Kidd J, Livak K, Pakstis A, Kidd K. The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus Human Genetics 1996, 98: 91-101. PMID: 8682515, DOI: 10.1007/s004390050166.
- Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human OriginsTishkoff S, Dietzsch E, Speed W, Pakstis A, Kidd J, Cheung K, Bonné-Tamir B, Santachiara-Benerecetti A, Moral P, Krings M, Pääbo S, Watson E, Risch N, Jenkins T, Kidd K. Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins Science 1996, 271: 1380-1387. PMID: 8596909, DOI: 10.1126/science.271.5254.1380.
- Anthropology's Role in the HGDPKidd K. Anthropology's Role in the HGDP Anthropology News 1996, 37: 2-2. DOI: 10.1111/an.1996.37.3.2.3.
- No association between alcoholism and multiple polymorphisms at the dopamine D2 receptor gene (DRD2) in three distinct taiwanese populationsLu R, Ko H, Chang F, Castiglione C, Schoolfield G, Pakstis A, Kidd J, Kidd K. No association between alcoholism and multiple polymorphisms at the dopamine D2 receptor gene (DRD2) in three distinct taiwanese populations Biological Psychiatry 1996, 39: 419-429. PMID: 8679787, DOI: 10.1016/0006-3223(95)00182-4.
- Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridizationHaaf T, Sirugo G, Kidd K, Ward D. Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization Nature Genetics 1996, 12: 183-185. PMID: 8563757, DOI: 10.1038/ng0296-183.
- DNA Workbench: A Database Package to Manage Regional Physical MappingNadkarni P, Cheung K, Castiglione C, Miller P, Kidd K. DNA Workbench: A Database Package to Manage Regional Physical Mapping Journal Of Computational Biology 1996, 3: 319-329. PMID: 8811490, DOI: 10.1089/cmb.1996.3.319.
- Nucleotide polymorphism, effective population size, and dispersal distances in the yellow baboons (Papio hamadryas cynocephalus) of Mikumi National Park, TanzaniaRogers J, Kidd K. Nucleotide polymorphism, effective population size, and dispersal distances in the yellow baboons (Papio hamadryas cynocephalus) of Mikumi National Park, Tanzania American Journal Of Primatology 1996, 38: 157-168. PMID: 31918472, DOI: 10.1002/(sici)1098-2345(1996)38:2<157::aid-ajp4>3.0.co;2-y.
- Conserved regulatory element involved in the early onset of Hoxb6 gene expressionBecker D, Jiang Z, Knödler P, Deinard A, Eid R, Kidd K, Shashikant C, Ruddle F, Schughart K. Conserved regulatory element involved in the early onset of Hoxb6 gene expression Developmental Dynamics 1996, 205: 73-81. PMID: 8770553, DOI: 10.1002/(sici)1097-0177(199601)205:1<73::aid-aja7>3.0.co;2-2.
- The Dopamine Transporter Protein Gene (SLC6A3): Primary Linkage Mapping and Linkage Studies in Tourette SyndromeGelernter J, Vandenbergh D, Kruger S, Pauls D, Kurlan R, Pakstis A, Kidd K, Uhl G. The Dopamine Transporter Protein Gene (SLC6A3): Primary Linkage Mapping and Linkage Studies in Tourette Syndrome Genomics 1995, 30: 459-463. PMID: 8825631, DOI: 10.1006/geno.1995.1265.
- Internet-based Support for Bioscience Research: A Collaborative Genome center for Human Chromosome 12Miller P, Nadkarni P, Kidd K, Cheung K, Ward D, Banks A, Bray-Ward P, Cupelli L, Herdman V, Marondel I, Montcomery K, Renault B, Yoon S, Krauter K, Kucherlapati R. Internet-based Support for Bioscience Research: A Collaborative Genome center for Human Chromosome 12 Journal Of The American Medical Informatics Association 1995, 2: 351-364. PMID: 8581551, PMCID: PMC116278, DOI: 10.1136/jamia.1995.96157828.
- HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes.Hawley M, Kidd K. HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. Journal Of Heredity 1995, 86: 409-11. PMID: 7560877, DOI: 10.1093/oxfordjournals.jhered.a111613.
- Dopamine D2 Receptor and Tourette's Syndrome-ReplyGelernter J, Leckman J, Pauls D, Kidd K, Kurlan R. Dopamine D2 Receptor and Tourette's Syndrome-Reply JAMA Neurology 1995, 52: 442-443. DOI: 10.1001/archneur.1995.00540290019005.
- The CEPH Consortium Linkage Map of Human Chromosome 11Litt M, Kramer P, Kort E, Fain P, Cox S, Root D, White R, Weissenbach J, Donis-Keller H, Gatti R, Weber J, Nakamura Y, Julier C, Hayashi K, Spurr N, Dean M, Mandel J, Kidd K, Kruse T, Retief A, Bale A, Meo T, Vergnaud G, Warren S, Willard H. The CEPH Consortium Linkage Map of Human Chromosome 11 Genomics 1995, 27: 101-112. PMID: 7665156, DOI: 10.1006/geno.1995.1011.
- Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with tourette syndromeGelernter J, Rao P, Pauls D, Hamblin M, Sibley D, Kidd K. Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with tourette syndrome Genomics 1995, 26: 207-209. PMID: 7601444, DOI: 10.1016/0888-7543(95)80202-w.
- Apparent monomorphism of ALDH2 in seven American Indian populationsNovoradovsky A, Kidd J, Kidd K, Goldman D. Apparent monomorphism of ALDH2 in seven American Indian populations Alcohol 1995, 12: 163-167. PMID: 7772269, DOI: 10.1016/0741-8329(94)00086-7.
- Network-based informatics support of research collaborations in the Human Genome Project and the Human Brain Project.Miller P, Nadkarni P, Kucherlapati R, Krauter K, Kidd K, Ward D, Shepherd G, Berkowicz D. Network-based informatics support of research collaborations in the Human Genome Project and the Human Brain Project. Medinfo. 1995, 8 Pt 2: 1541-4. PMID: 8591495.
- The CEPH consortium linkage map of human chromosome 16Kozman H, Keith T, Donis-keller H, White R, Weissenbach J, Dean M, Vergnaud G, Kidd K, Gusella J, Royle N, Sutherland G, Mulley J. The CEPH consortium linkage map of human chromosome 16 Genomics 1995, 25: 44-58. PMID: 7774955, DOI: 10.1016/0888-7543(95)80108-x.
- Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.Baldwin C, Weiss S, Farrer L, De Stefano A, Adair R, Franklyn B, Kidd K, Korostishevsky M, Bonné-Tamir B. Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. Human Molecular Genetics 1995, 4: 1637-42. PMID: 8541853, DOI: 10.1093/hmg/4.9.1637.
- Progress in a genome scan for linkage in schizophrenia in a large Swedish kindredBarr C, Kennedy J, Pakstis A, Wetterberg L, Sjögren B, Bierut L, Wadelius C, Wahlström J, Martinsson T, Giuffra L, Gelernter J, Hallmayer J, Moises H, Kurth J, Cavalli‐Sforza L, Kidd K. Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred American Journal Of Medical Genetics 1994, 54: 51-58. PMID: 7909991, DOI: 10.1002/ajmg.1320540110.
- Detection of DNA sequence variation via deliberate heteroduplex formation from genomic DNAs amplified en masse in "population tubes".Ruano G, Deinard A, Tishkoff S, Kidd K. Detection of DNA sequence variation via deliberate heteroduplex formation from genomic DNAs amplified en masse in "population tubes". Genome Research 1994, 3: 225-231. PMID: 8173512, DOI: 10.1101/gr.3.4.225.
- Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region.Barr C, Kennedy J, Pakstis A, Castiglione C, Kidd J, Wetterberg L, Kidd K. Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region. Schizophrenia Bulletin 1994, 20: 277-286. PMID: 8085132, DOI: 10.1093/schbul/20.2.277.
- Computer-assisted restriction mapping: an integrated approach to handling experimental uncertainty.Wright L, Lichter J, Reinitz J, Shifman M, Kidd K, Miller P. Computer-assisted restriction mapping: an integrated approach to handling experimental uncertainty. Bioinformatics 1994, 10: 435-42. PMID: 7804876, DOI: 10.1093/bioinformatics/10.4.435.
- Alleles at the dopamine D4 receptor locus do not contribute to the genetic susceptibility to schizophrenia in a large Swedish kindredBarr C, Kennedy J, Lichter J, Van Tol H, Wetterberg L, Livak K, Kidd K. Alleles at the dopamine D4 receptor locus do not contribute to the genetic susceptibility to schizophrenia in a large Swedish kindred American Journal Of Medical Genetics 1993, 48: 218-222. PMID: 8135305, DOI: 10.1002/ajmg.1320480409.
- Assignment of the norepinephrine transporter protein (NET1) locusto chromosome 16Gelernter J, Kruger S, Pakstis A, Pacholczyk T, Sparkes R, Kidd K, Amara S. Assignment of the norepinephrine transporter protein (NET1) locusto chromosome 16 Genomics 1993, 18: 690-692. PMID: 7905857, DOI: 10.1016/s0888-7543(05)80375-1.
- Genetic and Physical Mapping of the Treacher Collins Syndrome Locus with Respect to Loci in the Chromosome 5q3 RegionJabs E, Li X, Lovett M, Yamaoka L, Taylor E, Speer M, Coss C, Cadle R, Hall B, Brown K, Kidd K, Dolganov G, Polymeropoulos M, Meyers D. Genetic and Physical Mapping of the Treacher Collins Syndrome Locus with Respect to Loci in the Chromosome 5q3 Region Genomics 1993, 18: 7-13. PMID: 8276417, DOI: 10.1006/geno.1993.1420.
- Genomic and Yeast Artificial Chromosome Long-Range Regular Article Linking Six Loci in 10q11.2 and Spanning the Multiple Endocrine Neoplasia Type 2A (MEN2A) RegionBrooks-Wilson A, Lichter J, Ward D, Kidd K, Goodfellow P. Genomic and Yeast Artificial Chromosome Long-Range Regular Article Linking Six Loci in 10q11.2 and Spanning the Multiple Endocrine Neoplasia Type 2A (MEN2A) Region Genomics 1993, 17: 611-617. PMID: 7902324, DOI: 10.1006/geno.1993.1380.
- Population frequencies of the A1 allele at the dopamine D2 receptor locusBarr C, Kidd K. Population frequencies of the A1 allele at the dopamine D2 receptor locus Biological Psychiatry 1993, 34: 204-209. PMID: 8399816, DOI: 10.1016/0006-3223(93)90073-m.
- Associations of disease with genetic markers: Déjà vu all over againKidd K. Associations of disease with genetic markers: Déjà vu all over again American Journal Of Medical Genetics 1993, 48: 71-73. PMID: 8362928, DOI: 10.1002/ajmg.1320480202.
- Physical and Genetic Maps for Chromosome 10Lichter J, Difilippantonio M, Pakstis A, Goodfellow P, Ward D, Kidd K. Physical and Genetic Maps for Chromosome 10 Genomics 1993, 16: 320-324. PMID: 8314570, DOI: 10.1006/geno.1993.1192.
- Nuclear DNA polymorphisms in a wild population of yellow baboons (Papio hamadryas cynocephalus) from Mikumi National Park, TanzaniaRogers J, Kidd K. Nuclear DNA polymorphisms in a wild population of yellow baboons (Papio hamadryas cynocephalus) from Mikumi National Park, Tanzania American Journal Of Biological Anthropology 1993, 90: 477-486. PMID: 8097371, DOI: 10.1002/ajpa.1330900407.
- Human genome diversity initiative.Kidd J, Kidd K, Weiss K. Human genome diversity initiative. Human Biology 1993, 65: 1-6. PMID: 8436383.
- A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locusLichter J, Wu J, Brooks-Wilson A, Difillipantonio M, Brewster S, Ward D, Goodfellow P, Kidd K. A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus Human Genetics 1993, 90: 516-520. PMID: 8094065, DOI: 10.1007/bf00217451.
- A hypervariable segment in the human dopamine receptor D4 (DRD4) gene.Lichter J, Barr C, Kennedy J, Van Tol H, Kidd K, Livak K. A hypervariable segment in the human dopamine receptor D4 (DRD4) gene. Human Molecular Genetics 1993, 2: 767-73. PMID: 8353495, DOI: 10.1093/hmg/2.6.767.
- The CEPH consortium linkage map of human chromosome 2Spurr N, Cox S, Bryant S, Attwood J, Robson E, Shields D, Steinbrueck T, Jenkins T, Murray J, Kidd K, Summar M, Tsipouras P, Retief A, Kruse T, Bale A, Vergnaud G, Weber J, McBride O, Donis-Keller H, White R. The CEPH consortium linkage map of human chromosome 2 Genomics 1992, 14: 1055-1063. PMID: 1478647, DOI: 10.1016/s0888-7543(05)80129-6.
- Modeling of heteroduplex formation during PCR from mixtures of DNA templates.Ruano G, Kidd K. Modeling of heteroduplex formation during PCR from mixtures of DNA templates. Genome Research 1992, 2: 112-116. PMID: 1362127, DOI: 10.1101/gr.2.2.112.
- A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10Lichter J, Wu J, Miller D, Goodfellow P, Kidd K. A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10 Genomics 1992, 13: 607-612. PMID: 1353475, DOI: 10.1016/0888-7543(92)90131-b.
- Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10Miller D, Dill F, Lichter J, Kidd K, Goodfellow P. Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10 Genomics 1992, 13: 601-606. PMID: 1353474, DOI: 10.1016/0888-7543(92)90130-k.
- DNA sequence polymorphism within hominoid species exceeds the number of phylogenetically informative characters for a HOX2 locus.Ruano G, Rogers J, Ferguson-Smith A, Kidd K. DNA sequence polymorphism within hominoid species exceeds the number of phylogenetically informative characters for a HOX2 locus. Molecular Biology And Evolution 1992, 9: 575-86. PMID: 1352841, DOI: 10.1093/oxfordjournals.molbev.a040743.
- Exclusion of Linkage Between the Serotonin2 Receptor and Schizophrenia in a Large Swedish KindredHallmayer J, Kennedy J, Wetterberg L, Sjögren B, Kidd K, Cavalli-Sforza L. Exclusion of Linkage Between the Serotonin2 Receptor and Schizophrenia in a Large Swedish Kindred JAMA Psychiatry 1992, 49: 216-219. PMID: 1348924, DOI: 10.1001/archpsyc.1992.01820030048006.
- Response: Forensic DNA TypingChakraborty R, Kidd K. Response: Forensic DNA Typing Science 1992, 255: 1053-1054. PMID: 17817770, DOI: 10.1126/science.255.5048.1053.
- Response: Forensic DNA TypingChakraborty R, Kidd K. Response: Forensic DNA Typing Science 1992, 255: 1052-1053. DOI: 10.1126/science.1052-c.
- Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A.Lichter J, Wu J, Genel M, Flynn S, Pakstis A, Kidd J, Kidd K. Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A. The Journal Of Clinical Endocrinology & Metabolism 1992, 74: 368-73. PMID: 1346145, DOI: 10.1210/jcem.74.2.1346145.
- Two RFLPs near HOX2@INGFR at locus D17S444EKennedy J, Honer W, Kaufmann C, Martignetti J, Brosius J, Kidd K. Two RFLPs near HOX2@INGFR at locus D17S444E Nucleic Acids Research 1992, 20: 1171-1171. PMID: 1372406, PMCID: PMC312148, DOI: 10.1093/nar/20.5.1171.
- A dinucleotide repeat polymorphism at the HOX2B locusDeinard A, Ruano G, Kidd K. A dinucleotide repeat polymorphism at the HOX2B locus Nucleic Acids Research 1992, 20: 1171-1171. PMID: 1347934, PMCID: PMC312149, DOI: 10.1093/nar/20.5.1171-a.
- Variability in nuclear DNA among nonhuman primates: Application of molecular genetic techniques to intra‐ and inter‐species genetic analysesRogers J, Ruano G, Kidd K. Variability in nuclear DNA among nonhuman primates: Application of molecular genetic techniques to intra‐ and inter‐species genetic analyses American Journal Of Primatology 1992, 27: 93-105. PMID: 31948144, DOI: 10.1002/ajp.1350270205.
- Genetics of Gilles de la tourette syndromeKidd K, Pakstis A, Heutink P, Pauls D, Kurlan R, Weber J, Wilkie P, van de Wetering B, Oostra B. Genetics of Gilles de la tourette syndrome Movement Disorders 1992, 7: 3-3. DOI: 10.1002/mds.870070504.
- Localization of the gene for MEN 2A.Lichter J, Difilippantonio M, Wu J, Miller D, Ward D, Goodfellow P, Kidd K. Localization of the gene for MEN 2A. Henry Ford Hospital Medical Journal 1992, 40: 199-204. PMID: 1362405.
- The Utility of DNA Typing in Forensic WorkChakraborty R, Kidd K. The Utility of DNA Typing in Forensic Work Science 1991, 254: 1735-1739. PMID: 1763323, DOI: 10.1126/science.1763323.
- A linkage map spanning the locus for diastrophic dysplasia (DTD)Hästbacka J, Sistonen P, Kaitila I, Weiffenbach B, Kidd K, de la Chapelle A. A linkage map spanning the locus for diastrophic dysplasia (DTD) Genomics 1991, 11: 968-973. PMID: 1783404, DOI: 10.1016/0888-7543(91)90021-6.
- Study of an additional 58 DNA markers in five human populations from four continents.Bowcock A, Hebert J, Mountain J, Kidd J, Rogers J, Kidd K, Cavalli-Sforza L. Study of an additional 58 DNA markers in five human populations from four continents. Gene Geography 1991, 5: 151-73. PMID: 1841601.
- Trials and tribulations in the search for genes causing neuropsychiatric disordersKidd K. Trials and tribulations in the search for genes causing neuropsychiatric disorders Biodemography And Social Biology 1991, 38: 163-178. PMID: 1801198, DOI: 10.1080/19485565.1991.9988785.
- Report of the Chromosome 5 WorkshopWestbrook C, Neuman W, Hewitt J, Kidd K, Le Beau M, Williamson R. Report of the Chromosome 5 Workshop Genomics 1991, 10: 1105-1109. PMID: 1916818, DOI: 10.1016/0888-7543(91)90211-v.
- Status of the search for a major genetic locus for affective disorder in the Old Order AmishPakstis A, Kidd J, Castiglione C, Kidd K. Status of the search for a major genetic locus for affective disorder in the Old Order Amish Human Genetics 1991, 87: 475-483. PMID: 1879834, DOI: 10.1007/bf00197172.
- No Linkage Between D2 Dopamine Receptor Gene Region and SchizophreniaMoises H, Gelernter J, Giuffra L, Zarcone V, Wetterberg L, Civelli O, Kidd K, Cavalli-Sforza L, Grandy D, Kennedy J, Vinogradov S, Mauer J, Litt M, Sjögren B. No Linkage Between D2 Dopamine Receptor Gene Region and Schizophrenia JAMA Psychiatry 1991, 48: 643-647. PMID: 2069495, DOI: 10.1001/archpsyc.1991.01810310061011.
- Parallelizing genetic linkage analysis: A case study for applying parallel computation in molecular biologyMiller P, Nadkarni P, Gelernter J, Carriero N, Pakstis A, Kidd K. Parallelizing genetic linkage analysis: A case study for applying parallel computation in molecular biology Journal Of Biomedical Informatics 1991, 24: 234-248. PMID: 1868693, DOI: 10.1016/0010-4809(91)90046-y.
- Progress towards completing the human linkage mapKidd K. Progress towards completing the human linkage map Current Opinion In Genetics & Development 1991, 1: 99-104. PMID: 1840885, DOI: 10.1016/0959-437x(91)80049-r.
- From antibody to gene in schizophrenia: Methodology and progress reportHoner W, Kennedy J, Martignetti J, Brosius J, Kaufmann C, Kidd K, Davies P. From antibody to gene in schizophrenia: Methodology and progress report Schizophrenia Research 1991, 4: 278-279. DOI: 10.1016/0920-9964(91)90145-h.
- Coupled amplification and sequencing of genomic DNA.Ruano G, Kidd K. Coupled amplification and sequencing of genomic DNA. Proceedings Of The National Academy Of Sciences Of The United States Of America 1991, 88: 2815-2819. PMID: 1672768, PMCID: PMC51330, DOI: 10.1073/pnas.88.7.2815.
- Rearrangement of the retinoic acid receptor gene in acute promyelocytic leukemia.Chang K, Trujillo J, Ogura T, Castiglione C, Kidd K, Zhao S, Freireich E, Stass S. Rearrangement of the retinoic acid receptor gene in acute promyelocytic leukemia. Leukemia 1991, 5: 200-4. PMID: 1849600.
- Drift, admixture, and selection in human evolution: a study with DNA polymorphisms.Bowcock A, Kidd J, Mountain J, Hebert J, Carotenuto L, Kidd K, Cavalli-Sforza L. Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. Proceedings Of The National Academy Of Sciences Of The United States Of America 1991, 88: 839-843. PMID: 1992475, PMCID: PMC50909, DOI: 10.1073/pnas.88.3.839.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 11 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 11 of 27) Cytogenetic And Genome Research 1991, 58: 1510-1549. DOI: 10.1159/000317223.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 18 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 18 of 27) Cytogenetic And Genome Research 1991, 58: 1724-1734. DOI: 10.1159/000317230.
- A Hindi RFLP In the human D4 dopamine receptor locus (DRD4)Kennedy J, Sidenberg D, Van Tol H, Kidd K. A Hindi RFLP In the human D4 dopamine receptor locus (DRD4) Nucleic Acids Research 1991, 19: 5801-5801. PMID: 1682888, PMCID: PMC329013, DOI: 10.1093/nar/19.20.5801.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 21 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 21 of 27) Cytogenetic And Genome Research 1991, 58: 1764-1767. DOI: 10.1159/000317233.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 16 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 16 of 27) Cytogenetic And Genome Research 1991, 58: 1685-1705. DOI: 10.1159/000317228.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 7 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 7 of 27) Cytogenetic And Genome Research 1991, 58: 1368-1399. DOI: 10.1159/000317219.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 9 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 9 of 27) Cytogenetic And Genome Research 1991, 58: 1440-1474. DOI: 10.1159/000317221.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 3 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 3 of 27) Cytogenetic And Genome Research 1991, 58: 1236-1264. DOI: 10.1159/000317215.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 8 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 8 of 27) Cytogenetic And Genome Research 1991, 58: 1400-1439. DOI: 10.1159/000317220.
- Genotyping and haplotyping of polymorphisms directly from genomic DNA via coupled amplification and sequencing(CAS)Ruano G, Kidd K. Genotyping and haplotyping of polymorphisms directly from genomic DNA via coupled amplification and sequencing(CAS) Nucleic Acids Research 1991, 19: 6877-6882. PMID: 1684844, PMCID: PMC329323, DOI: 10.1093/nar/19.24.6877.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 19 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 19 of 27) Cytogenetic And Genome Research 1991, 58: 1735-1756. DOI: 10.1159/000317231.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 24 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 24 of 27) Cytogenetic And Genome Research 1991, 58: 1790-1800. DOI: 10.1159/000317237.
- Two RFLPs at the HOX2G locusOgura T, Castiglione C, Pakstis A, Kidd K. Two RFLPs at the HOX2G locus Nucleic Acids Research 1991, 19: 1716-1716. PMID: 1674132, PMCID: PMC333946, DOI: 10.1093/nar/19.7.1716-a.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 1 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 1 of 27) Cytogenetic And Genome Research 1991, 58: 1190-1211. DOI: 10.1159/000133727.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 26 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 26 of 27) Cytogenetic And Genome Research 1991, 58: 1812-1822. DOI: 10.1159/000317239.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 22 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 22 of 27) Cytogenetic And Genome Research 1991, 58: 1768-1778. DOI: 10.1159/000317234.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 2 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 2 of 27) Cytogenetic And Genome Research 1991, 58: 1212-1235. DOI: 10.1159/000317214.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 5 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 5 of 27) Cytogenetic And Genome Research 1991, 58: 1300-1333. DOI: 10.1159/000317217.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 25 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 25 of 27) Cytogenetic And Genome Research 1991, 58: 1801-1811. DOI: 10.1159/000317238.
- An Mspl polymorphism for the HOX2F geneOgura T, Castiglione C, Pakstis A, Kidd K. An Mspl polymorphism for the HOX2F gene Nucleic Acids Research 1991, 19: 1716-1716. PMID: 1709280, PMCID: PMC333945, DOI: 10.1093/nar/19.7.1716.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 10 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 10 of 27) Cytogenetic And Genome Research 1991, 58: 1475-1509. DOI: 10.1159/000317253.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 13 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 13 of 27) Cytogenetic And Genome Research 1991, 58: 1590-1629. DOI: 10.1159/000317225.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 23 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 23 of 27) Cytogenetic And Genome Research 1991, 58: 1779-1789. DOI: 10.1159/000317235.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 20 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 20 of 27) Cytogenetic And Genome Research 1991, 58: 1757-1763. DOI: 10.1159/000317232.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 17 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 17 of 27) Cytogenetic And Genome Research 1991, 58: 1706-1723. DOI: 10.1159/000317229.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 27 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 27 of 27) Cytogenetic And Genome Research 1991, 58: 1823-1832. DOI: 10.1159/000317240.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 4 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 4 of 27) Cytogenetic And Genome Research 1991, 58: 1265-1299. DOI: 10.1159/000317216.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 15 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 15 of 27) Cytogenetic And Genome Research 1991, 58: 1664-1684. DOI: 10.1159/000317227.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 6 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 6 of 27) Cytogenetic And Genome Research 1991, 58: 1334-1367. DOI: 10.1159/000317218.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 14 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 14 of 27) Cytogenetic And Genome Research 1991, 58: 1630-1663. DOI: 10.1159/000317226.
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 12 of 27)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, Hewett D, Linch C, Maslen G. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 12 of 27) Cytogenetic And Genome Research 1991, 58: 1550-1589. DOI: 10.1159/000317224.
- Modeling uncertainty in a database for physical gene mapping data.Miller P, Shifman M, Kidd K. Modeling uncertainty in a database for physical gene mapping data. AMIA Annual Symposium Proceedings 1991, 409-13. PMID: 1807633, PMCID: PMC2247564.
- The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.Carson N, Wu J, Jackson C, Kidd K, Simpson N. The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10. American Journal Of Human Genetics 1990, 47: 946-51. PMID: 1978560, PMCID: PMC1683917.
- A refined linkage map for DNA markers around the pericentromeric region of chromosome 10Wu J, Myers S, Carson N, Kidd J, Anderson L, Castiglione C, Hoyle L, Lichter J, Sukhatme V, Simpson N, Kidd K. A refined linkage map for DNA markers around the pericentromeric region of chromosome 10 Genomics 1990, 8: 461-468. PMID: 1981049, DOI: 10.1016/0888-7543(90)90032-p.
- The Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1Dudley C, Giuffra L, Tippett P, Kidd K, Reeders S. The Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1 Human Genetics 1990, 86: 79-83. PMID: 1979310, DOI: 10.1007/bf00205179.
- The Human Genome Map 1990Stephens J, Mador M, Cavanaugh M, Gradie M, Kidd K. The Human Genome Map 1990 Science 1990, 250: suppl-4. PMID: 2218516, DOI: 10.1126/science.2218516.
- Mapping the Human Genome: Current StatusStephens J, Cavanaugh M, Gradie M, Mador M, Kidd K. Mapping the Human Genome: Current Status Science 1990, 250: 237-244. PMID: 2218527, DOI: 10.1126/science.2218527.
- Genetic and physical mapping and population studies of a fibronectin receptor β-subunit-like sequence on human chromosome 19Giuffra L, Lichter P, Wu J, Kennedy J, Pakstis A, Rogers J, Kidd J, Harley H, Jenkins T, Ward D, Kidd K. Genetic and physical mapping and population studies of a fibronectin receptor β-subunit-like sequence on human chromosome 19 Genomics 1990, 8: 340-346. PMID: 1979054, DOI: 10.1016/0888-7543(90)90291-2.
- Chromosome plotbooks and diskettes available from the human gene mapping libraryKidd K. Chromosome plotbooks and diskettes available from the human gene mapping library American Journal Of Medical Genetics 1990, 37: 292-292. PMID: 2248303, DOI: 10.1002/ajmg.1320370231.
- Haplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules.Ruano G, Kidd K, Stephens J. Haplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules. Proceedings Of The National Academy Of Sciences Of The United States Of America 1990, 87: 6296-6300. PMID: 1974719, PMCID: PMC54520, DOI: 10.1073/pnas.87.16.6296.
- Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20.Summar M, Phillips J, Battey J, Castiglione C, Kidd K, Maness K, Weiffenbach B, Gravius T. Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20. Endocrinology 1990, 4: 947-50. PMID: 1978246, DOI: 10.1210/mend-4-6-947.
- Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundary.Ellis N, Kidd J, Goodfellow P, Kidd K, Goodfellow P. Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundary. American Journal Of Human Genetics 1990, 46: 950-5. PMID: 2339693, PMCID: PMC1683589.
- Segregation and Linkage Analyses of Tourette's Syndrome and Related DisordersPAULS D, PAKSTIS A, KURLAN R, KIDD K, LECKMAN J, COHEN D, KIDD J, COMO P, SPARKES R. Segregation and Linkage Analyses of Tourette's Syndrome and Related Disorders Journal Of The American Academy Of Child & Adolescent Psychiatry 1990, 29: 195-203. PMID: 2324061, DOI: 10.1097/00004583-199003000-00007.
- The CEPH consortium primary linkage map of human chromosome 10White R, Lalouel J, Nakamura Y, Donis-Keller H, Green P, Bowden D, Mathew C, Easton D, Robson E, Morton N, Gusella J, Haines J, Retief A, Kidd K, Murray J, Lathrop G, Cann H. The CEPH consortium primary linkage map of human chromosome 10 Genomics 1990, 6: 393-412. PMID: 1970325, DOI: 10.1016/0888-7543(90)90469-b.
- Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric regionWu J, Kidd K. Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region Human Genetics 1990, 84: 279-282. PMID: 1968036, DOI: 10.1007/bf00200575.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 14 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 14 of 14) Cytogenetic And Genome Research 1990, 55: 769-778. DOI: 10.1159/000317054.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 3 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 3 of 14) Cytogenetic And Genome Research 1990, 55: 502-532. DOI: 10.1159/000317043.
- Monomorphism in humans and sequence differences among higher primates for a sequence tagged site (STS) in homeo box cluster 2 as assayed by denaturing gradient electrophoresisRuano G, Gray M, Miki T, Ferguson-Smith A, Ruddle F, Kidd K. Monomorphism in humans and sequence differences among higher primates for a sequence tagged site (STS) in homeo box cluster 2 as assayed by denaturing gradient electrophoresis Nucleic Acids Research 1990, 18: 1314-1314. PMID: 1969622, PMCID: PMC330476, DOI: 10.1093/nar/18.5.1314.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 8 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 8 of 14) Cytogenetic And Genome Research 1990, 55: 662-692. DOI: 10.1159/000317048.
- Search for the Gene for Multiple Endocrine Neoplasia Type 2AKIDD K, SIMPSON N. Search for the Gene for Multiple Endocrine Neoplasia Type 2A 1990, 305-343. DOI: 10.1016/b978-0-12-571146-3.50015-8.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 5 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 5 of 14) Cytogenetic And Genome Research 1990, 55: 564-598. DOI: 10.1159/000317045.
- An EcoRI polymorphism identified by KW6 (D10S97) on chromosome 10Wu J, Kidd K. An EcoRI polymorphism identified by KW6 (D10S97) on chromosome 10 Nucleic Acids Research 1990, 18: 1316-1316. PMID: 1969624, PMCID: PMC330479, DOI: 10.1093/nar/18.5.1316.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 1 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 1 of 14) Cytogenetic And Genome Research 1990, 55: 457-472. PMID: 2073845, DOI: 10.1159/000133027.
- High frequency Pvull and Pstl polymorphisms identified by KW31 (D10S96) on chromosome 10Wu J, Kidd K. High frequency Pvull and Pstl polymorphisms identified by KW31 (D10S96) on chromosome 10 Nucleic Acids Research 1990, 18: 1316-1316. PMID: 1969625, PMCID: PMC330480, DOI: 10.1093/nar/18.5.1316-a.
- The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphicKidd J, Matsubara Y, Castiglione C, Tanaka K, Kidd K. The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic Genomics 1990, 6: 89-93. PMID: 1968047, DOI: 10.1016/0888-7543(90)90451-y.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 4 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 4 of 14) Cytogenetic And Genome Research 1990, 55: 533-563. DOI: 10.1159/000317044.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 7 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 7 of 14) Cytogenetic And Genome Research 1990, 55: 629-661. DOI: 10.1159/000317047.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 10 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 10 of 14) Cytogenetic And Genome Research 1990, 55: 714-726. DOI: 10.1159/000317050.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 6 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 6 of 14) Cytogenetic And Genome Research 1990, 55: 599-628. DOI: 10.1159/000317046.
- Hincll polymorphism at the D10S95 locusWu J, Kidd K. Hincll polymorphism at the D10S95 locus Nucleic Acids Research 1990, 18: 4965-4965. PMID: 1975682, PMCID: PMC332037, DOI: 10.1093/nar/18.16.4965-a.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 13 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 13 of 14) Cytogenetic And Genome Research 1990, 55: 757-768. DOI: 10.1159/000317053.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 11 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 11 of 14) Cytogenetic And Genome Research 1990, 55: 727-742. DOI: 10.1159/000317051.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 9 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 9 of 14) Cytogenetic And Genome Research 1990, 55: 693-713. DOI: 10.1159/000317049.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 2 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 2 of 14) Cytogenetic And Genome Research 1990, 55: 473-501. DOI: 10.1159/000317042.
- Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 12 of 14)Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, Trumper S, Walley A. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 12 of 14) Cytogenetic And Genome Research 1990, 55: 743-756. DOI: 10.1159/000317052.
- Search for the Gene for Multiple Endocrine Neoplasia Type 2AKIDD K, SIMPSON N. Search for the Gene for Multiple Endocrine Neoplasia Type 2A 1990, 46: 305-343. PMID: 2281187, DOI: 10.1016/b978-0-12-571146-3.50015-8.
- Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order AmishKelsoe J, Ginns E, Egeland J, Gerhard D, Goldstein A, Bale S, Pauls D, Long R, Kidd K, Conte G, Housman D, Paul S. Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish Nature 1989, 342: 238-243. PMID: 2682265, DOI: 10.1038/342238a0.
- The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studiesWu J, Giuffra L, Goodfellow P, Myers S, Carson N, Anderson L, Hoyle L, Simpson N, Kidd K. The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies Human Genetics 1989, 83: 383-390. PMID: 2572537, DOI: 10.1007/bf00291386.
- Estimation of segregation and linkage parameters in simulated data. I. Segregation analyses with different ascertainment schemes.Kramer P, Pauls D, Price R, Kidd K. Estimation of segregation and linkage parameters in simulated data. I. Segregation analyses with different ascertainment schemes. American Journal Of Human Genetics 1989, 45: 83-94. PMID: 2741953, PMCID: PMC1683375.
- Estimation of segregation and linkage parameters in simulated data. II. Simultaneous estimation with one linked marker.Price R, Kramer P, Pauls D, Kidd K. Estimation of segregation and linkage parameters in simulated data. II. Simultaneous estimation with one linked marker. American Journal Of Human Genetics 1989, 45: 95-105. PMID: 2741954, PMCID: PMC1683382.
- One Form of Bipolar Affective Disorder is Mapped to Chromosome 11Kidd K, Egeland J, Gerhard D, Pauls D, Sussex J, Allen C, Hostetter A, Kidd J, Pakstis A, Housman D. One Form of Bipolar Affective Disorder is Mapped to Chromosome 11 1989, 184-187. DOI: 10.1007/978-1-4612-3524-8_41.
- Direct haplotyping of chromosomal segments from multiple heterozygotes via allele-specific PCR amplificationRuano G, Kidd K. Direct haplotyping of chromosomal segments from multiple heterozygotes via allele-specific PCR amplification Nucleic Acids Research 1989, 17: 8392-8392. PMID: 2573038, PMCID: PMC334997, DOI: 10.1093/nar/17.20.8392.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 862–891Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 862–891 Cytogenetic And Genome Research 1989, 51: 862-891. DOI: 10.1159/000227797.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 922–947Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 922–947 Cytogenetic And Genome Research 1989, 51: 922-947. DOI: 10.1159/000227799.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 702–731Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 702–731 Cytogenetic And Genome Research 1989, 51: 702-731. DOI: 10.1159/000227791.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 807–831Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 807–831 Cytogenetic And Genome Research 1989, 51: 807-831. DOI: 10.1159/000227795.
- The HGM10 information management systemMador M, Cavanaugh M, Chan H, Alles W, Hawley M, Miller R, Schiff G, Ruddle F, Kidd K. The HGM10 information management system Cytogenetic And Genome Research 1989, 51: 3-7. PMID: 2791654, DOI: 10.1159/000132774.
- Linkage Analysis in PsychiatryGiuffra L, Kidd K. Linkage Analysis in Psychiatry International Review Of Psychiatry 1989, 1: 231-242. DOI: 10.3109/09540268909089417.
- Biphasic amplification of very dilute DNA samples via ‘booster‘ PCRRuano G, Fenton W, Kidd K. Biphasic amplification of very dilute DNA samples via ‘booster‘ PCR Nucleic Acids Research 1989, 17: 5407-5407. PMID: 2762140, PMCID: PMC318146, DOI: 10.1093/nar/17.13.5407.
- The Human Gene Mapping Workshops in transitionRuddle F, Kidd K. The Human Gene Mapping Workshops in transition Cytogenetic And Genome Research 1989, 51: 1-2. PMID: 2791652, DOI: 10.1159/000132773.
- Linkage Analysis Approach to Hereditary Movement DisordersKurlan R, Kidd K, Pauls D. Linkage Analysis Approach to Hereditary Movement Disorders Journal Of Neurogenetics 1989, 5: 161-171. PMID: 2569508, DOI: 10.3109/01677068909066206.
- Molecular Genetic Studies in Schizophrenia.Kennedy J, Giuffra L, Moises H, Wetterberg L, Sjögren B, Cavalli-Sforza L, Pakstis A, Kidd J, Kidd K. Molecular Genetic Studies in Schizophrenia. Schizophrenia Bulletin 1989, 15: 383-391. PMID: 2573149, DOI: 10.1093/schbul/15.3.383.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 758–781Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 758–781 Cytogenetic And Genome Research 1989, 51: 758-781. DOI: 10.1159/000227793.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 892–921Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 892–921 Cytogenetic And Genome Research 1989, 51: 892-921. DOI: 10.1159/000227798.
- EDIT10: a database interface for HGM10Miller R, Chan H, Cavanaugh M, Alles W, Mador M, Kidd K. EDIT10: a database interface for HGM10 Cytogenetic And Genome Research 1989, 51: 9-10. PMID: 2791657, DOI: 10.1159/000132776.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 677–701Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 677–701 Cytogenetic And Genome Research 1989, 51: 677-701. DOI: 10.1159/000227790.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 832–861Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 832–861 Cytogenetic And Genome Research 1989, 51: 832-861. DOI: 10.1159/000227796.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 644–676Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 644–676 Cytogenetic And Genome Research 1989, 51: 644-676. DOI: 10.1159/000227789.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 782–806Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 782–806 Cytogenetic And Genome Research 1989, 51: 782-806. DOI: 10.1159/000227794.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 732–757Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 732–757 Cytogenetic And Genome Research 1989, 51: 732-757. DOI: 10.1159/000227792.
- The mapping of the locus for multiple endocrine neoplasia type 2A by linkage with chromosome 10 markers.Simpson N, Kidd K. The mapping of the locus for multiple endocrine neoplasia type 2A by linkage with chromosome 10 markers. Hormone And Metabolic Research. Supplement Series 1989, 21: 5-9. PMID: 2572529.
- The Genetics of Affective DisordersKidd K, Kennedy J. The Genetics of Affective Disorders 1989, 191-198. DOI: 10.1007/978-1-349-10729-2_17.
- Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigreeKennedy J, Giuffra L, Moises H, Cavalli-Sforza L, Pakstis A, Kidd J, Castiglione C, Sjogren B, Wetterberg L, Kidd K. Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree Nature 1988, 336: 167-170. PMID: 2903450, DOI: 10.1038/336167a0.
- The human “interferon-β2/hepatocyte stimulating factor/interleukin-6” gene: DNA polymorphism studies and localization to chromosome 7p21Bowcock A, Kidd J, Lathrop G, Daneshvar L, May L, Ray A, Sehgal P, Kidd K, Cavalli-Sforza L. The human “interferon-β2/hepatocyte stimulating factor/interleukin-6” gene: DNA polymorphism studies and localization to chromosome 7p21 Genomics 1988, 3: 8-16. PMID: 2906047, DOI: 10.1016/0888-7543(88)90152-8.
- A linkage group of five DNA markers on human chromosome 10Farrer L, Castiglione C, Kidd J, Myers S, Carson N, Simpson N, Kidd K. A linkage group of five DNA markers on human chromosome 10 Genomics 1988, 3: 72-77. PMID: 2906045, DOI: 10.1016/0888-7543(88)90162-0.
- D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4Miki T, Nishisho I, Tateishi H, Chen Y, Kidd J, Wu J, Pravtcheva D, Pakstis A, Takai S, Ruddle F, Kidd K. D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4 Genomics 1988, 3: 78-81. PMID: 2906046, DOI: 10.1016/0888-7543(88)90163-2.
- Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's diseaseFarrer L, Bonne-Tamir B, Frydman M, Magazanik A, Kidd K, Bowcock A, Cavalli-Sforza L. Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease Human Genetics 1988, 79: 109-117. PMID: 3164701, DOI: 10.1007/bf00280547.
- Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 lociXue F, Kidd J, Pakstis A, Castiglione C, Mallet J, Kidd K. Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 loci Genomics 1988, 2: 288-293. PMID: 2906039, DOI: 10.1016/0888-7543(88)90016-x.
- Report of the committee on human gene mapping by recombinant DNA techniques (Part 4 of 6)Kidd K, Bowcock A, Pearson P, Schmidtke J, Willard H, Track R, Ricciuti F. Report of the committee on human gene mapping by recombinant DNA techniques (Part 4 of 6) Cytogenetic And Genome Research 1988, 49: 176-191. DOI: 10.1159/000317006.
- Report of the committee on human gene mapping by recombinant DNA techniques (Part 3 of 6)Kidd K, Bowcock A, Pearson P, Schmidtke J, Willard H, Track R, Ricciuti F. Report of the committee on human gene mapping by recombinant DNA techniques (Part 3 of 6) Cytogenetic And Genome Research 1988, 49: 162-175. DOI: 10.1159/000317005.
- The Anonymous RFLP Locus D1S2 Is Close to PGMl on Chromosome 1Kidd K, Kidd J, Castiglione C, Sparkes R, Egeland J, Bakker E. The Anonymous RFLP Locus D1S2 Is Close to PGMl on Chromosome 1 Human Heredity 1988, 38: 22-26. PMID: 2895061, DOI: 10.1159/000153749.
- Report of the committee on human gene mapping by recombinant DNA techniques (Part 6 of 6)Kidd K, Bowcock A, Pearson P, Schmidtke J, Willard H, Track R, Ricciuti F. Report of the committee on human gene mapping by recombinant DNA techniques (Part 6 of 6) Cytogenetic And Genome Research 1988, 49: 206-218. DOI: 10.1159/000317008.
- Report of the committee on human gene mapping by recombinant DNA techniques (Part 5 of 6)Kidd K, Bowcock A, Pearson P, Schmidtke J, Willard H, Track R, Ricciuti F. Report of the committee on human gene mapping by recombinant DNA techniques (Part 5 of 6) Cytogenetic And Genome Research 1988, 49: 192-205. DOI: 10.1159/000317007.
- An MPO cDNA clone identifies an RFLP with PstIMiki T, Weil S, Rosner G, Reid M, Kidd K. An MPO cDNA clone identifies an RFLP with PstI Nucleic Acids Research 1988, 16: 1649-1649. PMID: 2894639, PMCID: PMC336369, DOI: 10.1093/nar/16.4.1649.
- Some effects of selection strategies on linkage analysisCox N, Hodge S, Marazita M, Spence M, Kidd K, Rao D. Some effects of selection strategies on linkage analysis Genetic Epidemiology 1988, 5: 289-297. PMID: 3049227, DOI: 10.1002/gepi.1370050410.
- Glucocorticoid receptor maps to the distal long arm of chromosome 5Giuffra L, Kennedy J, Castiglione C, Evans R, Wasmuth J, Kidd K. Glucocorticoid receptor maps to the distal long arm of chromosome 5 Cytogenetic And Genome Research 1988, 49: 313-314. PMID: 2907873, DOI: 10.1159/000132686.
- The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10Wu J, Ramesh V, Kidd J, Castiglione C, Myers S, Carson N, Anderson L, Gusella J, Simpson N, Kidd K. The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10 Cytogenetic And Genome Research 1988, 48: 126-127. PMID: 3197452, DOI: 10.1159/000132606.
- Report of the committee on human gene mapping by recombinant DNA techniques (Part 2 of 6)Kidd K, Bowcock A, Pearson P, Schmidtke J, Willard H, Track R, Ricciuti F. Report of the committee on human gene mapping by recombinant DNA techniques (Part 2 of 6) Cytogenetic And Genome Research 1988, 49: 146-161. DOI: 10.1159/000317004.
- A polymorphic DNA marker on chromosome 10 linked to RBP3 on the MEN2A sideWu J, Cavenee W, Miki T, Kidd K. A polymorphic DNA marker on chromosome 10 linked to RBP3 on the MEN2A side Cytogenetic And Genome Research 1988, 48: 246-247. PMID: 2907872, DOI: 10.1159/000132639.
- Report of the committee on human gene mapping by recombinant DNA techniques (Part 1 of 6)Kidd K, Bowcock A, Pearson P, Schmidtke J, Willard H, Track R, Ricciuti F. Report of the committee on human gene mapping by recombinant DNA techniques (Part 1 of 6) Cytogenetic And Genome Research 1988, 49: 132-145. PMID: 2904880, DOI: 10.1159/000132664.
- Migraine and depression: Association and familial transmissionMerikangas K, Risch N, Merikangas J, Weissman M, Kidd K. Migraine and depression: Association and familial transmission Journal Of Psychiatric Research 1988, 22: 119-129. PMID: 3404480, DOI: 10.1016/0022-3956(88)90076-3.
- A HindIII polymorphism identified by the human early growth response gene 2 (EGR2) on chromosome 10Wu J, Loren J, Sukhatme V, Kidd K. A HindIII polymorphism identified by the human early growth response gene 2 (EGR2) on chromosome 10 Nucleic Acids Research 1988, 16: 11855-11855. PMID: 2905450, PMCID: PMC339153, DOI: 10.1093/nar/16.24.11855.
- Molecular genetics of an autosomal dominant form of torsion dystonia.Kramer P, Ozelius L, Brin M, Fahn S, Kidd K, Gusella J, Breakefield X. Molecular genetics of an autosomal dominant form of torsion dystonia. Advances In Neurology 1988, 50: 57-66. PMID: 2899954.
- Tourette's Syndrome and Attention Deficit Disorder With Hyperactivity-ReplyPauls D, Hurst C, Leckman J, Cohen D, Kruger S, Kidd K. Tourette's Syndrome and Attention Deficit Disorder With Hyperactivity-Reply JAMA Psychiatry 1987, 44: 1025-1026. DOI: 10.1001/archpsyc.1987.01800230105018.
- Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkageSimpson N, Kidd K, Goodfellow P, McDermid H, Myers S, Kidd J, Jackson C, Duncan A, Farrer L, Brasch K, Castiglione C, Genel M, Gertner J, Greenberg C, Gusella J, Holden J, White B. Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage Nature 1987, 328: 528-530. PMID: 2886918, DOI: 10.1038/328528a0.
- Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: Evidence against syntenyFarrer L, Goodfellow P, White B, Holden J, Kidd J, Simpson N, Kidd K. Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: Evidence against synteny Cancer Genetics 1987, 27: 327-334. PMID: 2885081, DOI: 10.1016/0165-4608(87)90015-x.
- Family-Genetic Studies and Identification of Valid Diagnostic Categories in Adult and Child PsychiatryLeckman J, Weissman M, Pauls D, Kidd K. Family-Genetic Studies and Identification of Valid Diagnostic Categories in Adult and Child Psychiatry The British Journal Of Psychiatry 1987, 151: 39-44. PMID: 3315088, DOI: 10.1192/bjp.151.1.39.
- Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.Bowcock A, Farrer L, Cavalli-Sforza L, Hebert J, Kidd K, Frydman M, Bonne-Tamir B. Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. American Journal Of Human Genetics 1987, 41: 27-35. PMID: 3474893, PMCID: PMC1684171.
- Population genetics of a diseaseKidd K. Population genetics of a disease Nature 1987, 327: 282-283. PMID: 2884567, DOI: 10.1038/327282a0.
- Early Onset (Under Age 30 Years) and Panic Disorder as Markers for Etiologic Homogeneity in Major DepressionPrice R, Kidd K, Weissman M. Early Onset (Under Age 30 Years) and Panic Disorder as Markers for Etiologic Homogeneity in Major Depression JAMA Psychiatry 1987, 44: 434-440. PMID: 3472494, DOI: 10.1001/archpsyc.1987.01800170048008.
- An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.Farrer L, Goodfellow P, Lamarche C, Franjkovic I, Myers S, White B, Holden J, Kidd J, Simpson N, Kidd K. An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13. American Journal Of Human Genetics 1987, 40: 329-37. PMID: 2883889, PMCID: PMC1684085.
- Study of 47 DNA markers in five populations from four continents.Bowcock A, Bucci C, Hebert J, Kidd J, Kidd K, Friedlaender J, Cavalli-Sforza L. Study of 47 DNA markers in five populations from four continents. Gene Geography 1987, 1: 47-64. PMID: 2908691.
- Severity of Tourette's Syndrome in One Large Kindred: Implication for Determination of Disease Prevalence RateKurlan R, Behr J, Medved L, Shoulson I, Pauls D, Kidd K. Severity of Tourette's Syndrome in One Large Kindred: Implication for Determination of Disease Prevalence Rate JAMA Neurology 1987, 44: 268-269. PMID: 3469941, DOI: 10.1001/archneur.1987.00520150024013.
- Bipolar affective disorders linked to DNA markers on chromosome 11Egeland J, Gerhard D, Pauls D, Sussex J, Kidd K, Alien C, Hostetter A, Housman D. Bipolar affective disorders linked to DNA markers on chromosome 11 Nature 1987, 325: 783-787. PMID: 2881209, DOI: 10.1038/325783a0.
- One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map.Pakstis A, Kidd J, Castiglione C, Pletcher B, Murphy P, Farrer L, Genel M, Kidd K. One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map. Henry Ford Hospital Medical Journal 1987, 35: 164-7. PMID: 2891651.
- The anonymous RFLP locus D11S16 is tightly linked to catalase on 11pKidd J, Castiglione C, Pakstis A, Kidd K. The anonymous RFLP locus D11S16 is tightly linked to catalase on 11p Cytogenetic And Genome Research 1987, 45: 63-64. PMID: 2885154, DOI: 10.1159/000132428.
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 9 of 9)Pearson P, Kidd K, Willard H. Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 9 of 9) Cytogenetic And Genome Research 1987, 46: 551-566. DOI: 10.1159/000316988.
- A moderately frequent RFLP identified by both SacI and BanII with a probe from the HOX2 locus in man (17q11–17q22)Murphy P, Ferguson-Smith A, Miki T, Feinberg A, Ruddle F, Kidd K. A moderately frequent RFLP identified by both SacI and BanII with a probe from the HOX2 locus in man (17q11–17q22) Nucleic Acids Research 1987, 15: 6311-6311. PMID: 2888083, PMCID: PMC306101, DOI: 10.1093/nar/15.15.6311.
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 6 of 9)Pearson P, Kidd K, Willard H. Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 6 of 9) Cytogenetic And Genome Research 1987, 46: 508-520. DOI: 10.1159/000316985.
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 1 of 9)Pearson P, Kidd K, Willard H. Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 1 of 9) Cytogenetic And Genome Research 1987, 46: 390-408. PMID: 3507285, DOI: 10.1159/000132487.
- Localization and linkage of three polymorphic DNA sequences on human chromosome 20Goodfellow P, Duncan A, Farrer L, Holden J, White B, Kidd J, Kidd K, Simpson N. Localization and linkage of three polymorphic DNA sequences on human chromosome 20 Cytogenetic And Genome Research 1987, 44: 112-117. PMID: 2882953, DOI: 10.1159/000132354.
- A new human RFLP identified by 7D2 places D13S10 proximal to esterase DBowcock A, Farrer L, Hebert J, Bonne-Tamir B, Frydman M, Kidd K, Cavalli-Sforza L. A new human RFLP identified by 7D2 places D13S10 proximal to esterase D Cytogenetic And Genome Research 1987, 44: 236-237. PMID: 2884079, DOI: 10.1159/000132379.
- Searching for a major genetic locus for affective disorder in the old order AmishKidd J, Egeland J, Pakstis A, Castiglione C, Pletcher B, Morton L, Kidd K. Searching for a major genetic locus for affective disorder in the old order Amish Journal Of Psychiatric Research 1987, 21: 577-580. PMID: 2894461, DOI: 10.1016/0022-3956(87)90107-5.
- Research design considerations for linkage studies of affective disorders using recombinant DNA markersKidd K. Research design considerations for linkage studies of affective disorders using recombinant DNA markers Journal Of Psychiatric Research 1987, 21: 551-557. PMID: 3326941, DOI: 10.1016/0022-3956(87)90104-x.
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 2 of 9)Pearson P, Kidd K, Willard H. Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 2 of 9) Cytogenetic And Genome Research 1987, 46: 409-431. DOI: 10.1159/000316981.
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 3 of 9)Pearson P, Kidd K, Willard H. Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 3 of 9) Cytogenetic And Genome Research 1987, 46: 432-454. DOI: 10.1159/000316982.
- Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi‐point linkage analysisKramer P, Ozelius L, Gusella J, Fahn S, Kidd K, Breakefield X, Boerecki I. Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi‐point linkage analysis Genetic Epidemiology 1987, 4: 377-386. PMID: 3692135, DOI: 10.1002/gepi.1370040506.
- MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA cloneWu J, Riordan J, Willard H, Milner R, Kidd K. MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone Nucleic Acids Research 1987, 15: 1882-1882. PMID: 2434933, PMCID: PMC340598, DOI: 10.1093/nar/15.4.1882.
- A second useful polymorphism for the cytosolic thymidine kinase gene (TK1) with the enzyme BstEII which will allow haplotying at this locus on chromosome 17 (q21-q22)Murphy P, Lin P, Ruddle F, Kidd K. A second useful polymorphism for the cytosolic thymidine kinase gene (TK1) with the enzyme BstEII which will allow haplotying at this locus on chromosome 17 (q21-q22) Nucleic Acids Research 1987, 15: 7212-7212. PMID: 2889186, PMCID: PMC306236, DOI: 10.1093/nar/15.17.7212.
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 4 of 9)Pearson P, Kidd K, Willard H. Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 4 of 9) Cytogenetic And Genome Research 1987, 46: 455-479. DOI: 10.1159/000316983.
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 8 of 9)Pearson P, Kidd K, Willard H. Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 8 of 9) Cytogenetic And Genome Research 1987, 46: 539-550. DOI: 10.1159/000316987.
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 5 of 9)Pearson P, Kidd K, Willard H. Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 5 of 9) Cytogenetic And Genome Research 1987, 46: 480-507. DOI: 10.1159/000316984.
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 7 of 9)Pearson P, Kidd K, Willard H. Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 7 of 9) Cytogenetic And Genome Research 1987, 46: 521-537. DOI: 10.1159/000316986.
- Where is the locus for multiple endocrine neoplasia type 2A?Simpson N, Kidd K. Where is the locus for multiple endocrine neoplasia type 2A? Henry Ford Hospital Medical Journal 1987, 35: 168-71. PMID: 2891652.
- Searching for Major Genes for Psychiatric DisordersKidd K. Searching for Major Genes for Psychiatric Disorders 1987, 130: 184-196. PMID: 2894929, DOI: 10.1002/9780470513507.ch11.
- Gilles de la Tourette's Syndrome and Attention Deficit Disorder With Hyperactivity: Evidence Against a Genetic RelationshipPauls D, Hurst C, Kruger S, Leckman J, Kidd K, Cohen D. Gilles de la Tourette's Syndrome and Attention Deficit Disorder With Hyperactivity: Evidence Against a Genetic Relationship JAMA Psychiatry 1986, 43: 1177-1179. PMID: 3465279, DOI: 10.1001/archpsyc.1986.01800120063012.
- DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia.Breakefield X, Ozelius L, Bothwell M, Chao M, Axelrod F, Kramer P, Kidd K, Lanahan A, Johnson D, Ross A. DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia. Molecular Biology & Medicine 1986, 3: 483-94. PMID: 2886891.
- Family-Genetic Studies of Psychiatric Disorders: Developing TechnologiesWeissman M, Merikangas K, John K, Wickramaratne P, Prusoff B, Kidd K. Family-Genetic Studies of Psychiatric Disorders: Developing Technologies JAMA Psychiatry 1986, 43: 1104-1116. PMID: 3532996, DOI: 10.1001/archpsyc.1986.01800110090012.
- Genetics of a wild population of rhesus monkeys (Macaca mulatta): II. The Dunga Gali population in species‐wide perspectiveMelnick D, Jolly C, Kidd K. Genetics of a wild population of rhesus monkeys (Macaca mulatta): II. The Dunga Gali population in species‐wide perspective American Journal Of Biological Anthropology 1986, 71: 129-140. PMID: 3799822, DOI: 10.1002/ajpa.1330710202.
- Familial Tourette's syndrome: report of a large pedigree and potential for linkage analysis.Kurlan R, Behr J, Medved L, Shoulson I, Pauls D, Kidd J, Kidd K. Familial Tourette's syndrome: report of a large pedigree and potential for linkage analysis. Neurology 1986, 36: 772-6. PMID: 3458031, DOI: 10.1212/wnl.36.6.772.
- Understanding the Clinical Heterogeneity of Major Depression Using Family DataWeissman M, Merikangas K, Priya W, Kidd K, Prusoff B, Leckman J, Pauls D. Understanding the Clinical Heterogeneity of Major Depression Using Family Data JAMA Psychiatry 1986, 43: 430-434. PMID: 3964021, DOI: 10.1001/archpsyc.1986.01800050028003.
- Linkage Analyses of Multiple Endocrine Neoplasia, Type 2 (MEN-2) with 23 Classical Genetic PolymorphismsKruger S, Gertner J, Sparkes R, Haedt L, Crist M, Sparkes M, Genel M, Kidd K. Linkage Analyses of Multiple Endocrine Neoplasia, Type 2 (MEN-2) with 23 Classical Genetic Polymorphisms Human Heredity 1986, 36: 6-11. PMID: 2868987, DOI: 10.1159/000153592.
- Linkage Analyses of Multiple Endocrine Neoplasia, Type 2A (MEN-2A) with 20 DNA Polymorphisms: 5% of the Genome ExcludedKidd K, Kidd J, Castiglione C, Genel M, Darby J, Cavalli-Sforza L, Gusella J. Linkage Analyses of Multiple Endocrine Neoplasia, Type 2A (MEN-2A) with 20 DNA Polymorphisms: 5% of the Genome Excluded Human Heredity 1986, 36: 243-249. PMID: 2875939, DOI: 10.1159/000153634.
- Development of a map of chromosome 11pKramer P, Farrer L, Pakstis A, Kidd K. Development of a map of chromosome 11p Genetic Epidemiology. Supplement 1986, 3: 153-158. PMID: 3471659, DOI: 10.1002/gepi.1370030724.
- Recurrence risks in an oligogenic threshold model: the effect of alterations in allele frequencyKENDLER K, KIDD K. Recurrence risks in an oligogenic threshold model: the effect of alterations in allele frequency Annals Of Human Genetics 1986, 50: 83-91. PMID: 3426150, DOI: 10.1111/j.1469-1809.1986.tb01941.x.
- Linkage Analysis in a Family with Dominantly Inherited Torsion Dystonia: Exclusion of the Pro-Opiomelanocortin and Glutamic Acid Decarboxylase Genes and Other Chromosomal Regions Using DNA PolymorphismsBreakefield X, Bressman S, Kramer P, Ozelius L, Moskowitz C, Tanzi R, Brin M, Hobbs W, Kaufman D, Tobin A, Kidd K, Fahn S, Gusella J. Linkage Analysis in a Family with Dominantly Inherited Torsion Dystonia: Exclusion of the Pro-Opiomelanocortin and Glutamic Acid Decarboxylase Genes and Other Chromosomal Regions Using DNA Polymorphisms Journal Of Neurogenetics 1986, 3: 159-175. PMID: 3016220, DOI: 10.3109/01677068609106846.
- A PvuII RFLP for the human liver arginase (ARG1) geneKidd J, Dizikes G, Grody W, Cederbaum S, Kidd K. A PvuII RFLP for the human liver arginase (ARG1) gene Nucleic Acids Research 1986, 14: 9544-9544. PMID: 2879271, PMCID: PMC311993, DOI: 10.1093/nar/14.23.9544.
- Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group‐specific loci: Use of restriction fragment length polymorphisms extends exclusion regionKidd K, Kidd J, Castiglione C, Pakstis A, Sparkes R, Rao D. Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group‐specific loci: Use of restriction fragment length polymorphisms extends exclusion region Genetic Epidemiology 1986, 3: 195-200. PMID: 2873080, DOI: 10.1002/gepi.1370030306.
- A frequent polymorphism for the cytosolic thymidine kinase gene, TK1, (17q21-q22) detected by the enzyme TaqlMurphy P, Kidd J, Castiglione C, Lin P, Ruddle F, Kidd K. A frequent polymorphism for the cytosolic thymidine kinase gene, TK1, (17q21-q22) detected by the enzyme Taql Nucleic Acids Research 1986, 14: 4381-4381. PMID: 3012471, PMCID: PMC339879, DOI: 10.1093/nar/14.10.4381.
- Close linkage of MT2P1 with GC on chromosome 4Pakstis A, Kidd J, Castiglione C, Sparkes R, Kidd K. Close linkage of MT2P1 with GC on chromosome 4 Cytogenetic And Genome Research 1986, 41: 189-190. PMID: 3956270, DOI: 10.1159/000132226.
- DNA markers and genetic variation in the human species.Cavalli-Sforza L, Kidd J, Kidd K, Bucci C, Bowcock A, Hewlett B, Friedlaender J. DNA markers and genetic variation in the human species. Cold Spring Harbor Symposia On Quantitative Biology 1986, 51 Pt 1: 411-7. PMID: 2884067, DOI: 10.1101/sqb.1986.051.01.049.
- Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.Goodfellow P, White B, Holden J, Duncan A, Sears E, Wang H, Berlin L, Kidd K, Simpson N. Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A. American Journal Of Human Genetics 1985, 37: 890-7. PMID: 2864854, PMCID: PMC1684696.
- A Twin Study of Tourette SyndromePrice R, Kidd K, Cohen D, Pauls D, Leckman J. A Twin Study of Tourette Syndrome JAMA Psychiatry 1985, 42: 815-820. PMID: 3860194, DOI: 10.1001/archpsyc.1985.01790310077011.
- Validity of RDC and DSM-III-ReplyLeckman J, Weissman M, Prusoff B, Caruso K, Merikangas K, Pauls D, Kidd K. Validity of RDC and DSM-III-Reply JAMA Psychiatry 1985, 42: 634-634. DOI: 10.1001/archpsyc.1985.01790290116016.
- Genetic and evolutionary relationships among Asian MacaquesMelnick1 D, Kidd K. Genetic and evolutionary relationships among Asian Macaques International Journal Of Primatology 1985, 6: 333-333. DOI: 10.1007/bf02745504.
- Genetic and evolutionary relationships among Asian MacaquesMelnick1 D, Kidd K. Genetic and evolutionary relationships among Asian Macaques International Journal Of Primatology 1985, 6: 123-160. DOI: 10.1007/bf02693650.
- Drug response as a predictor of transmission of non-bipolar major depression within familiesPrusoff B, Weissman M, Merikangas K, Leckman J, Kidd K. Drug response as a predictor of transmission of non-bipolar major depression within families Journal Of Affective Disorders 1985, 8: 171-176. PMID: 3157727, DOI: 10.1016/0165-0327(85)90041-2.
- Genetic analysis workshop III: Sampling considerations and assumptions in gene mappingPrice R, Kramer P, Pakstis A, Kidd K. Genetic analysis workshop III: Sampling considerations and assumptions in gene mapping Genetic Epidemiology 1985, 2: 219-220. DOI: 10.1002/gepi.1370020220.
- Report of the committee on methods of linkage analysis and reportingConneally P, Edwards J, Kidd K, Lalouel J, Morton N, Ott J, White R. Report of the committee on methods of linkage analysis and reporting Cytogenetic And Genome Research 1985, 40: 356-359. PMID: 3864600, DOI: 10.1159/000132186.
- Multiple threshold models for the affective disorders: The Yale-NIMH collaborative family studyPrice R, Kidd K, Pauls D, Gershon E, Prusoff B, Weissman M, Goldin L. Multiple threshold models for the affective disorders: The Yale-NIMH collaborative family study Journal Of Psychiatric Research 1985, 19: 533-546. PMID: 4078756, DOI: 10.1016/0022-3956(85)90071-8.
- An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79]Murphy P, Kidd J, Breg W, Ruddle F, Kidd K. An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79] Nucleic Acids Research 1985, 13: 3015-3015. PMID: 4000970, PMCID: PMC341211, DOI: 10.1093/nar/13.8.3015.
- Onset of Major Depression in Early Adulthood: Increased Familial Loading and SpecificityWeissman M, Wickramaratne P, Merikangas K, Leckman J, Prusoff B, Caruso K, Kidd K, Gammon G. Onset of Major Depression in Early Adulthood: Increased Familial Loading and Specificity JAMA Psychiatry 1984, 41: 1136-1143. PMID: 6508504, DOI: 10.1001/archpsyc.1984.01790230022003.
- Some Environmental Factors and Hypotheses for Stuttering in Families with Several StutterersCox N, Seider R, Kidd K. Some Environmental Factors and Hypotheses for Stuttering in Families with Several Stutterers Journal Of Speech Language And Hearing Research 1984, 27: 543-548. PMID: 6521460, DOI: 10.1044/jshr.2704.543.
- Identification of a recent recombination event within the human beta-globin gene cluster.Gerhard D, Kidd K, Kidd J, Egeland J, Housman D. Identification of a recent recombination event within the human beta-globin gene cluster. Proceedings Of The National Academy Of Sciences Of The United States Of America 1984, 81: 7875-7879. PMID: 6096866, PMCID: PMC392255, DOI: 10.1073/pnas.81.24.7875.
- Subtypes of Depression: Family Study PerspectiveLeckman J, Weissman M, Prusoff B, Caruso K, Merikangas K, Pauls D, Kidd K. Subtypes of Depression: Family Study Perspective JAMA Psychiatry 1984, 41: 833-838. PMID: 6466042, DOI: 10.1001/archpsyc.1984.01790200015002.
- Amish study, IV: Genetic linkage study of pedigrees of bipolar probandsKidd K, Egeland J, Molthan L, Pauls D, Kruger S, Messner K. Amish study, IV: Genetic linkage study of pedigrees of bipolar probands American Journal Of Psychiatry 1984, 141: 1042-1048. PMID: 6331772, DOI: 10.1176/ajp.141.9.1042.
- Amish study, V: Lithium-sodium countertransport and catechol O- methyltransferase in pedigrees of bipolar probandsEgeland J, Kidd J, Frazer A, Kidd K, Neuhauser V. Amish study, V: Lithium-sodium countertransport and catechol O- methyltransferase in pedigrees of bipolar probands American Journal Of Psychiatry 1984, 141: 1049-1054. PMID: 6589966, DOI: 10.1176/ajp.141.9.1049.
- RECOMBINANT DNA METHODS IN GENETIC STUDIES OF AFFECTIVE DISORDERS.Kidd K, Gerhard D, Kidd J, Housman D, Egeland J. RECOMBINANT DNA METHODS IN GENETIC STUDIES OF AFFECTIVE DISORDERS. Clinical Neuropharmacology 1984, 7: s104. DOI: 10.1097/00002826-198406001-00099.
- Outcomes on lithium treatment as a tool for genetic studies in affective disordersSmeraldi E, Petroccione A, Gasperini M, Macciardi F, Orsini A, Kidd K. Outcomes on lithium treatment as a tool for genetic studies in affective disorders Journal Of Affective Disorders 1984, 6: 139-151. PMID: 6233346, DOI: 10.1016/0165-0327(84)90019-3.
- The genetics of a wild population of rhesus monkeys (Macaca mulatta). I. Genetic variability within and between social groupsMelnick D, Jolly C, Kidd K. The genetics of a wild population of rhesus monkeys (Macaca mulatta). I. Genetic variability within and between social groups American Journal Of Biological Anthropology 1984, 63: 341-360. DOI: 10.1002/ajpa.1330630402.
- The Risk of Tourette's Syndrome and Chronic Multiple Tics among Relatives of Tourette's Syndrome Patients Obtained by Direct InterviewPAULS D, KRUGER S, LECKMAN J, COHEN D, KIDD K. The Risk of Tourette's Syndrome and Chronic Multiple Tics among Relatives of Tourette's Syndrome Patients Obtained by Direct Interview Journal Of The American Academy Of Child & Adolescent Psychiatry 1984, 23: 134-137. PMID: 6585415, DOI: 10.1097/00004583-198403000-00003.
- Utilizing automated methods to improve estimates of recurrence risk with linked genetic markersPrice R, Kidd K, Opitz J. Utilizing automated methods to improve estimates of recurrence risk with linked genetic markers American Journal Of Medical Genetics 1984, 17: 621-625. PMID: 6585143, DOI: 10.1002/ajmg.1320170311.
- Psychiatric Disorders in the Relatives of Probands With Affective Disorders: The Yale University—National Institute of Mental Health Collaborative StudyWeissman M, Gershon E, Kidd K, Prusoff B, Leckman J, Dibble E, Hamovit J, Thompson W, Pauls D, Guroff J. Psychiatric Disorders in the Relatives of Probands With Affective Disorders: The Yale University—National Institute of Mental Health Collaborative Study JAMA Psychiatry 1984, 41: 13-21. PMID: 6691780, DOI: 10.1001/archpsyc.1984.01790120015003.
- Psychopathology in the Children (Ages 6–18) of Depressed and Normal ParentsWEISSMAN M, PRUSOFF B, GAMMON G, MERIKANGAS K, LECKMAN J, KIDD K. Psychopathology in the Children (Ages 6–18) of Depressed and Normal Parents Journal Of The American Academy Of Child & Adolescent Psychiatry 1984, 23: 78-84. PMID: 6693680, DOI: 10.1097/00004583-198401000-00011.
- Linkage data excluding a locus for multiple endocrine neoplasia type 2 syndromes from the distal part of the short arm of chromosome 11.Kidd K, Kruger S, Gerhard D, Kidd J, Housman D, Gertner J. Linkage data excluding a locus for multiple endocrine neoplasia type 2 syndromes from the distal part of the short arm of chromosome 11. Henry Ford Hospital Medical Journal 1984, 32: 262-5. PMID: 6152463.
- Estimating the Recombination Frequency for the MN and the Ss LociSpence A, Field L, Marazita M, Joseph J, Sparkes M, Crist M, Crandall B, Anderson C, Bateman J, Rotter J, Kidd K, Hodge S, Sparkes R. Estimating the Recombination Frequency for the MN and the Ss Loci Human Heredity 1984, 34: 343-347. PMID: 6510930, DOI: 10.1159/000153494.
- Genetic analysis workshop II: Further consideration of segregation and linkage analyses in problem 3Kramer P, Altmann D, Kidd K. Genetic analysis workshop II: Further consideration of segregation and linkage analyses in problem 3 Genetic Epidemiology 1984, 1: 189-193. PMID: 14971372, DOI: 10.1002/gepi.1370010213.
- The detection of major loci by segregation and linkage analysis: A simulation studyGoldin L, Cox N, Pauls D, Gershon E, Kidd K, Rao D. The detection of major loci by segregation and linkage analysis: A simulation study Genetic Epidemiology 1984, 1: 285-296. PMID: 6599402, DOI: 10.1002/gepi.1370010307.
- Segregation analyses of stutteringCox N, Kramer P, Kidd K, Rao D. Segregation analyses of stuttering Genetic Epidemiology 1984, 1: 245-253. PMID: 6549563, DOI: 10.1002/gepi.1370010304.
- Recovery and Persistence of Stuttering among Relatives of StutterersSeider R, Kidd K, Gladstien K. Recovery and Persistence of Stuttering among Relatives of Stutterers Journal Of Speech-language & Hearing Disorders 1983, 48: 402-409. PMID: 6645435, DOI: 10.1044/jshd.4804.402.
- The genetic consequences of social group fission in a wild population of rhesus monkeys (Macaca mulatta)Melnick D, Kidd K. The genetic consequences of social group fission in a wild population of rhesus monkeys (Macaca mulatta) Behavioral Ecology And Sociobiology 1983, 12: 229-236. DOI: 10.1007/bf00290775.
- Can recovery from stuttering be considered a genetically milder subtype of stuttering?Cox N, Kidd K. Can recovery from stuttering be considered a genetically milder subtype of stuttering? Behavior Genetics 1983, 13: 129-139. PMID: 6860250, DOI: 10.1007/bf01065662.
- Variability in Rates of Affective Disorders in Relatives of Depressed and Normal ProbandsWeissman M, Kidd K, Prusoff B. Variability in Rates of Affective Disorders in Relatives of Depressed and Normal Probands JAMA Psychiatry 1982, 39: 1397-1403. PMID: 7149900, DOI: 10.1001/archpsyc.1982.04290120033006.
- Language Onset and Concomitant Speech and Language Problems in Subgroups of Stutterers and Their SiblingsSeider R, Gladstien K, Kidd K. Language Onset and Concomitant Speech and Language Problems in Subgroups of Stutterers and Their Siblings Journal Of Speech Language And Hearing Research 1982, 25: 482-486. PMID: 7162147, DOI: 10.1044/jshr.2504.482.
- The effects of requisite assumptions on linkage analyses of manic-depressive illness with HLA.Kruger S, Turner W, Kidd K. The effects of requisite assumptions on linkage analyses of manic-depressive illness with HLA. Biological Psychiatry 1982, 17: 1081-99. PMID: 6959652.
- An analysis of the genetics of schizophreniaKidd K, Cavalli‐Sforza L. An analysis of the genetics of schizophrenia Biodemography And Social Biology 1982, 29: 276-286. DOI: 10.1080/19485565.1982.9988500.
- Comparison of the family history method to direct interview Factors affecting the diagnosis of depressionOrvaschel H, Thompson W, Belanger A, Prusoff B, Kidd K. Comparison of the family history method to direct interview Factors affecting the diagnosis of depression Journal Of Affective Disorders 1982, 4: 49-59. PMID: 6461687, DOI: 10.1016/0165-0327(82)90019-2.
- HLA-linkage in affective disorderMatthysse S, Kidd K. HLA-linkage in affective disorder Trends In Neurosciences 1982, 5: 104-105. DOI: 10.1016/0166-2236(82)90065-0.
- The epidemiology of Tourette's syndrome: A pilot study.Jagger J, Prusoff B, Cohen D, Kidd K, Carbonari C, John K. The epidemiology of Tourette's syndrome: A pilot study. Schizophrenia Bulletin 1982, 8: 267-278. PMID: 6955942, DOI: 10.1093/schbul/8.2.267.
- Recombinant DNA approach to neurogenetic disordersHousman D, Kidd K, Gusella J. Recombinant DNA approach to neurogenetic disorders Trends In Neurosciences 1982, 5: 320-323. DOI: 10.1016/0166-2236(82)90192-8.
- Genetic strategies for the analysis of childhood behavioral traits.Pauls D, Kidd K. Genetic strategies for the analysis of childhood behavioral traits. Schizophrenia Bulletin 1982, 8: 253-266. PMID: 6955941, DOI: 10.1093/schbul/8.2.253.
- LIST OF PARTICIPANTSAbell C, Anton R, Blass J, Bowers M, Brown P, Buchsbaum M, Cancro R, Comings D, Coryell W, Coursey R, Davis J, Delisi L, Duffy J, Dunner D, Ehrensing R, Extein I, Feinberg M, Finney J, Fullerton D, Gaines R, Garver D, Gilder D, Giller E, Goodwin D, Greden J, Hanin I, Henn F, Hetrick E, Hirschowitz J, Hitzemann R, Janowsky D, Karson C, Kidd K, Kleinman J, Koslow S, Kupfer D, Lewy A, Loosen P, Lowe T, Luchins D, Major L, Mallinger A, Manberg P, Mandell A, Mathura C, McKinney W, Meltzer H, Morihisa J, Murphy D, Nies A, Ostrow D, Paul S, Potkin S, Risch S, Ryback R, Schaffer C, Schildkraut J, Schuckit M, Seeman P, Siever L, Sitaram N, Steinhauer S, U′Prichard D, Usdin E, Vaughan G, Weinberger D, Weiss K, Werner G, White K, Zahn T, Zubin J. LIST OF PARTICIPANTS 1982, xi-xiv. DOI: 10.1016/b978-0-08-027987-9.50005-6.
- GENETIC LINKAGE MARKERS IN THE STUDY OF PSYCHIATRIC DISORDERSKidd K. GENETIC LINKAGE MARKERS IN THE STUDY OF PSYCHIATRIC DISORDERS 1982, 459-466. DOI: 10.1016/b978-0-08-027987-9.50049-4.
- An Evaluation of the Family History Method for Ascertaining Psychiatric DisordersThompson W, Orvaschel H, Prusoff B, Kidd K. An Evaluation of the Family History Method for Ascertaining Psychiatric Disorders JAMA Psychiatry 1982, 39: 53-58. PMID: 7055408, DOI: 10.1001/archpsyc.1982.04290010031006.
- Genetic hypotheses for Tourette syndrome.Kidd K, Pauls D. Genetic hypotheses for Tourette syndrome. Advances In Neurology 1982, 35: 243-9. PMID: 6959493.
- Evidence of HLA Linkage in Depressive DisordersMatthysse S, Kidd K. Evidence of HLA Linkage in Depressive Disorders New England Journal Of Medicine 1981, 305: 1340-1341. PMID: 7290155, DOI: 10.1056/nejm198111263052209.
- Familial Pattern and Transmission of Gilles de la Tourette Syndrome and Multiple TicsPauls D, Cohen D, Heimbuch R, Detlor J, Kidd K. Familial Pattern and Transmission of Gilles de la Tourette Syndrome and Multiple Tics JAMA Psychiatry 1981, 38: 1091-1093. PMID: 6945827, DOI: 10.1001/archpsyc.1981.01780350025002.
- Analysis of the Sibship Patterns of StutterersGladstien K, Seider R, Kidd K. Analysis of the Sibship Patterns of Stutterers Journal Of Speech Language And Hearing Research 1981, 24: 460-462. PMID: 7300289, DOI: 10.1044/jshr.2403.460.
- An easy-to-use maximum-likelihood method of estimating the ascertainment probability.Gladstien K, Kidd K. An easy-to-use maximum-likelihood method of estimating the ascertainment probability. American Journal Of Human Genetics 1981, 33: 785-801. PMID: 7294027, PMCID: PMC1685118.
- Familial patterns and possible modes of inheritance of primary affective disordersSmeraldi E, Negri F, Heimbuch R, Kidd K. Familial patterns and possible modes of inheritance of primary affective disorders Journal Of Affective Disorders 1981, 3: 173-182. PMID: 6454711, DOI: 10.1016/0165-0327(81)90042-2.
- A Comparison of Methods for Reconstructing Evolutionary TreesAstolfi P, Kidd K, Cavalli-Sforza L. A Comparison of Methods for Reconstructing Evolutionary Trees Systematic Biology 1981, 30: 156-169. DOI: 10.1093/sysbio/30.2.156.
- A Comparison of Methods for Reconstructing Evolutionary TreesAstolfi P, Kidd K, Cavalli-Sforza L. A Comparison of Methods for Reconstructing Evolutionary Trees Systematic Biology 1981, 30: 156. DOI: 10.2307/2992414.
- Vertical transmission of susceptibility to stuttering with sex-modified expression.Kidd K, Heimbuch R, Records M. Vertical transmission of susceptibility to stuttering with sex-modified expression. Proceedings Of The National Academy Of Sciences Of The United States Of America 1981, 78: 606-610. PMID: 6941261, PMCID: PMC319103, DOI: 10.1073/pnas.78.1.606.
- Dermo‐distortive urticaria: An autosomal dominant dermatologic disorderEpstein P, Kidd K, Opitz J. Dermo‐distortive urticaria: An autosomal dominant dermatologic disorder American Journal Of Medical Genetics 1981, 9: 307-315. PMID: 7294069, DOI: 10.1002/ajmg.1320090407.
- Genetic linkage analysis of dermo‐distortive urticariaEpstein P, Kidd K, Sparkes R, Opitz J. Genetic linkage analysis of dermo‐distortive urticaria American Journal Of Medical Genetics 1981, 9: 317-321. PMID: 6945804, DOI: 10.1002/ajmg.1320090408.
- Hand usage in a colony of bonnett monkeys,Macaca radiataBrooker R, Lehman R, Heimbuch R, Kidd K. Hand usage in a colony of bonnett monkeys,Macaca radiata Behavior Genetics 1981, 11: 49-56. PMID: 7259722, DOI: 10.1007/bf01065827.
- Genetics of Childhood Behavior DisordersPauls D, Kidd K. Genetics of Childhood Behavior Disorders 1981, 331-362. DOI: 10.1007/978-1-4613-9808-0_9.
- Familial Pattern of Gilles de la Tourette SyndromeKidd K, Prusoff B, Cohen D. Familial Pattern of Gilles de la Tourette Syndrome JAMA Psychiatry 1980, 37: 1336-1339. PMID: 6934712, DOI: 10.1001/archpsyc.1980.01780250022001.
- Familial Stuttering Patterns Are Not Related to One Measure of SeverityKidd K, Heimbuch R, Records M, Oehlert G, Webster R. Familial Stuttering Patterns Are Not Related to One Measure of Severity Journal Of Speech Language And Hearing Research 1980, 23: 539-545. PMID: 7421157, DOI: 10.1044/jshr.2303.539.
- Genetic models of stutteringKidd K. Genetic models of stuttering Journal Of Fluency Disorders 1980, 5: 187-201. DOI: 10.1016/0094-730x(80)90028-5.
- Estimating age-of-onset distributions for disorders with variable onset.Heimbuch R, Matthysse S, Kidd K. Estimating age-of-onset distributions for disorders with variable onset. American Journal Of Human Genetics 1980, 32: 564-74. PMID: 7395869, PMCID: PMC1686126.
- Children and depression The children of depressed parents; The childhood of depressed patients; Depression in childrenOrvaschel H, Weissman M, Kidd K. Children and depression The children of depressed parents; The childhood of depressed patients; Depression in children Journal Of Affective Disorders 1980, 2: 1-16. PMID: 6448876, DOI: 10.1016/0165-0327(80)90017-8.
- The effects of variable age‐of‐onset and diagnostic criteria on the estimates of linkage: An example using manic‐depressive illness and color blindnessMorton L, Kidd K. The effects of variable age‐of‐onset and diagnostic criteria on the estimates of linkage: An example using manic‐depressive illness and color blindness Biodemography And Social Biology 1980, 27: 1-10. PMID: 6974894, DOI: 10.1080/19485565.1980.9988398.
- Probable linkage between the human galactose-1-P uridyl transferase locus and 9qh.Sparkes R, Epstein P, Kidd K, Klisak I, Sparkes M, Crist M, Morton L. Probable linkage between the human galactose-1-P uridyl transferase locus and 9qh. American Journal Of Human Genetics 1980, 32: 188-93. PMID: 6247907, PMCID: PMC1686012.
- Penetrance estimates and recurrence risks for fibromuscular dysplasiaGladstien K, Rushton A, Kidd K. Penetrance estimates and recurrence risks for fibromuscular dysplasia Clinical Genetics 1980, 17: 115-116. PMID: 7363496, DOI: 10.1111/j.1399-0004.1980.tb00117.x.
- Alternative genetic models for the analysis of complex traits.Kidd K, Gladstien K. Alternative genetic models for the analysis of complex traits. Progress In Clinical And Biological Research 1980, 46: 407-35. PMID: 7022462.
- Recurrence risks in schizophrenia: Are they model dependent?Morton L, Kidd K, Matthysse S, Richards R. Recurrence risks in schizophrenia: Are they model dependent? Behavior Genetics 1979, 9: 389-406. PMID: 539966, DOI: 10.1007/bf01066977.
- Genetic Linkage and HemochromatosisKidd K. Genetic Linkage and Hemochromatosis New England Journal Of Medicine 1979, 301: 209-210. PMID: 449978, DOI: 10.1056/nejm197907263010409.
- Importance of Studying Gene-Environment Interactions Psychiatric Disorders-ReplyKidd K, Matthysse S. Importance of Studying Gene-Environment Interactions Psychiatric Disorders-Reply JAMA Psychiatry 1979, 36: 720-721. DOI: 10.1001/archpsyc.1979.01780060110015.
- The Genetics of Sex and Its ConsequencesKidd K. The Genetics of Sex and Its Consequences 1979, 401-426. DOI: 10.1007/978-1-4684-3560-3_16.
- Research Designs for the Study of Gene-Environment Interactions in Psychiatric Disorders: Report of a Foundations Fund for Research in Psychiatry PanelKidd K, Matthysee S. Research Designs for the Study of Gene-Environment Interactions in Psychiatric Disorders: Report of a Foundations Fund for Research in Psychiatry Panel JAMA Psychiatry 1978, 35: 925-932. PMID: 678045, DOI: 10.1001/archpsyc.1978.01770320019001.
- The value of dual mating data in estimating genetic parametersMATTHYSSE S, KIDD K. The value of dual mating data in estimating genetic parameters Annals Of Human Genetics 1978, 41: 477-480. PMID: 655637, DOI: 10.1111/j.1469-1809.1978.tb00919.x.
- The possible causes of the sex ratio in stuttering and its implicationsKidd K, Kidd J, Records M. The possible causes of the sex ratio in stuttering and its implications Journal Of Fluency Disorders 1978, 3: 13-23. DOI: 10.1016/0094-730x(78)90003-7.
- Why We Do Not Yet Understand the Genetics of Affective DisordersKidd K, Weissman M. Why We Do Not Yet Understand the Genetics of Affective Disorders 1978, 107-121. DOI: 10.1007/978-1-4684-2397-6_6.
- Handedness and stuttering: A dead horse?Records M, Heimbuch R, Kidd K. Handedness and stuttering: A dead horse? Journal Of Fluency Disorders 1977, 2: 271-282. DOI: 10.1016/0094-730x(77)90031-6.
- A genetic perspective on stutteringKidd K. A genetic perspective on stuttering Journal Of Fluency Disorders 1977, 2: 259-269. DOI: 10.1016/0094-730x(77)90030-4.
- Did They Ignore Genetics?Hsia Y, Kidd K. Did They Ignore Genetics? Pediatrics 1977, 60: 938-938. DOI: 10.1542/peds.60.6.938.
- Increased frequency of heterozygotes for α1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21FINEMAN R, KIDD K, JOHNSON A, BREG W. Increased frequency of heterozygotes for α1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21 Nature 1976, 260: 320-321. PMID: 1082990, DOI: 10.1038/260320a0.
- THE ROLE OF GENETIC DRIFT IN THE DIFFERENTIATION OF ICELANDIC AND NORWEGIAN CATTLEKidd K, Cavalli-Sforza L. THE ROLE OF GENETIC DRIFT IN THE DIFFERENTIATION OF ICELANDIC AND NORWEGIAN CATTLE Evolution 1974, 28: 381-395. PMID: 28564858, DOI: 10.1111/j.1558-5646.1974.tb00759.x.
- Book reviewsCombs J, Bingle G, Kidd K, Williams P, Bennett K, Bailar J. Book reviews Biodemography And Social Biology 1974, 21: 209-217. DOI: 10.1080/19485565.1974.9988112.
- Error in The Reconstruction of Evolutionary TreesKidd K, Astolfi P, Cavalli-Sforza L. Error in The Reconstruction of Evolutionary Trees 1974, 121-136. DOI: 10.1007/978-1-4684-2139-2_11.
- An analysis of the genetics of schizophreniaKidd K, Cavalli‐Sforza L. An analysis of the genetics of schizophrenia Biodemography And Social Biology 1973, 20: 254-264. PMID: 4763753, DOI: 10.1080/19485565.1973.9988051.
- Genetic Structure of the HL‐A System in a Nahua Indian Population in MexicoCann H, Kidd K, Lisker R, Radvany R, Payne R. Genetic Structure of the HL‐A System in a Nahua Indian Population in Mexico HLA 1973, 3: 364-372. PMID: 4771177, DOI: 10.1111/j.1399-0039.1973.tb00505.x.
- Genetic Relationships Among Cattle BreedsKidd K, Sgaramella-Zonta L. Genetic Relationships Among Cattle Breeds 1972, 241-244. DOI: 10.1007/978-94-017-5456-9_42.
- Biological divergences in south-central Bougainville: an analysis of blood polymorphism gene frequencies and anthropometric measurements utilizing tree models, and a comparison of these variables with linguistic, geographic, and migrational "distances".Friedlaender J, Sgaramella-Zonta L, Kidd K, Lai L, Clark P, Walsh R. Biological divergences in south-central Bougainville: an analysis of blood polymorphism gene frequencies and anthropometric measurements utilizing tree models, and a comparison of these variables with linguistic, geographic, and migrational "distances". American Journal Of Human Genetics 1971, 23: 253-70. PMID: 4996844, PMCID: PMC1706734.
- Phylogenetic analysis: concepts and methods.Kidd K, Sgaramella-Zonta L. Phylogenetic analysis: concepts and methods. American Journal Of Human Genetics 1971, 23: 235-52. PMID: 5089842, PMCID: PMC1706731.