2012
DCDC2 genetic variants and susceptibility to developmental dyslexia
Marino C, Meng H, Mascheretti S, Rusconi M, Cope N, Giorda R, Molteni M, Gruen JR. DCDC2 genetic variants and susceptibility to developmental dyslexia. Psychiatric Genetics 2012, 22: 25-30. PMID: 21881542, PMCID: PMC3232293, DOI: 10.1097/ypg.0b013e32834acdb2.Peer-Reviewed Original ResearchConceptsDevelopmental dyslexiaQuantitative transmission disequilibrium test analysesNonword readingNonword spellingOrthographic choiceMarker-trait associationsQuantitative trait lociDyslexiaMemory impairmentRelated readingsTrait lociQuantitative traitsQuantitative transmission disequilibrium testTransmission disequilibrium test analysisPhenotypic complexityAssociation evidenceGenetic linkageMemoryAssociation analysisDCDC2WordsGenetic variantsTransmission disequilibrium testReadingPerformance tests
2000
Identification of polymorphisms in the GABAB receptor gene and linkage study of attention‐deficit hyperactivity disorder
Barr C, Feng Y, Wigg K, Roberts W, Malone M, Schachar R, Tannock R, Gruen J, Goei V, Kennedy J. Identification of polymorphisms in the GABAB receptor gene and linkage study of attention‐deficit hyperactivity disorder. International Journal Of Genomics 2000, 1: 194-201. DOI: 10.1002/1438-826x(200012)1:5/6<194::aid-gnfd194>3.0.co;2-2.Peer-Reviewed Original ResearchDNA sequence variantsReceptor geneInteresting candidate genesIdentification of polymorphismsChromosome locationDNA sequencesCandidate genesReceptor 1 geneGenetic linkageGenetic relationshipsLinkage analysisSequence variantsGenesGABAB receptor geneChromosome 6pCommon variantsHuman leukocyte antigen (HLA) regionLinkage studiesComorbid reading disabilitiesAntigen regionPhenotypeGenetic linkNumber of neurotransmittersReceptorsRole