Josephine Hoh, PhD
Associate Professor of Epidemiology (Chronic Diseases) and of Ophthalmology and Visual ScienceCards
Appointments
Contact Info
Yale School of Public Health
PO Box 208034, 60 College Street
New Haven, CT 06520-8034
United States
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Titles
Associate Professor of Epidemiology (Chronic Diseases) and of Ophthalmology and Visual Science
Biography
Josephine Hoh, associate professor in chronic disease epidemiology and of ophthalmology and visual science, is currently involved in interdisciplinary research to elucidate disease pathophysiology, including how the genetic factors can actually lead individuals who carrying the risk variants to be ill at one point in life, what the environmental exposures are, and how they can influence an individual’s chance of contracting the disease.
Dr. Hoh was trained in mathematics in Taiwan and theoretical statistics and probability under the supervision of Professor Zhiliang Ying and the late Professor Herbert Robbins at Rutgers University.
As a research assistant professor at Rockefeller University she worked with Jurg Ott on linkage analysis for genetic factors of human disease and developed her expertise in biology. Two of the computational methods and tools they developed, SUMSTAT and p53MH, continue to be widely used. SUMSTAT can efficiently and effectively identify disease associated genetic variants, while p53MH and its extension can identify the DNA response elements of a tumor suppressor p53 as well as other transcription factors.
Now an associate professor at the Yale School of Public Health, Hoh focuses on developing new approaches to discover the genetic risks for more common diseases which usually have complex influences from both genetics and environmental exposures. Collaborating with national and international groups (Drs. Emily Chew and Rick Ferris at the National Eye Institute and Dr. Calvin Pang of Hong Kong University) her work on age-related macular degeneration (AMD), the most common cause of blindness in developed world, led to the first successful application of the genome-wide association study (GWAS) approach and was published widely. By employing GWAS, the Hoh lab has also investigated other complex traits including carcinoid cancer, scleroderma, asthma, longevity, among others.
Appointments
Chronic Disease Epidemiology
Associate Professor TenurePrimaryOphthalmology
Associate Professor TenureSecondary
Other Departments & Organizations
- Chronic Disease Epidemiology
- High Performance Computation
- Hoh Lab
- Ophthalmology
- Yale Cancer Center
- Yale School of Public Health
- Yale Ventures
Education & Training
- PhD
- Rutgers University (1998)
- BS
- National Tsing Hua University (1989)
Research
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Overview
Medical Research Interests
Public Health Interests
Research at a Glance
Yale Co-Authors
Publications Timeline
Andrew DeWan, PhD, MPH
Evan Vosburgh
Former YSMJudith Lichtman, PhD, MPH
Peter Smith, DVM, DACLAM
Zuoheng Anita Wang, PhD
Publications
2026
Whole genome analysis of breed-specific copy number variations in dogs
Wang S, Li Z, Bargmann W, Chen Z, Gruen J, Hoh J. Whole genome analysis of breed-specific copy number variations in dogs. Genomics 2026, 118: 111257. PMID: 42055148, DOI: 10.1016/j.ygeno.2026.111257.Peer-Reviewed Original Research
2024
Complement factor H in molecular regulation of angiogenesis
Li J, Wang K, Starodubtseva M, Nadyrov E, Kapron C, Hoh J, Liu J. Complement factor H in molecular regulation of angiogenesis. Medical Review 2024, 4: 452-466. PMID: 39444793, PMCID: PMC11495524, DOI: 10.1515/mr-2023-0048.Peer-Reviewed Reviews, Practice Guidelines, Standards, and Consensus StatementsCitationsAltmetric
2023
Systematically identifying genetic signatures including novel SNP-clusters, nonsense variants, frame-shift INDELs, and long STR expansions that potentially link to unknown phenotypes existing in dog breeds
Li Z, Wang Z, Chen Z, Voegeli H, Lichtman J, Smith P, Liu J, DeWan A, Hoh J. Systematically identifying genetic signatures including novel SNP-clusters, nonsense variants, frame-shift INDELs, and long STR expansions that potentially link to unknown phenotypes existing in dog breeds. BMC Genomics 2023, 24: 302. PMID: 37277710, PMCID: PMC10240460, DOI: 10.1186/s12864-023-09390-6.Peer-Reviewed Original ResearchCitationsAltmetric
2010
A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum
Walsh KM, Choi M, Oberg K, Kulke MH, Yao JC, Wu C, Jurkiewicz M, Hsu LI, Hooshmand SM, Hassan M, Janson ET, Cunningham JL, Vosburgh E, Sackler RS, Lifton RP, DeWan AT, Hoh J. A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. Endocrine Related Cancer 2010, 18: 171-180. PMID: 21139019, PMCID: PMC3221459, DOI: 10.1677/erc-10-0248.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords
2009
p53 responsive elements in human retrotransposons
Harris CR, DeWan A, Zupnick A, Normart R, Gabriel A, Prives C, Levine AJ, Hoh J. p53 responsive elements in human retrotransposons. Oncogene 2009, 28: 3857-3865. PMID: 19718052, PMCID: PMC3193277, DOI: 10.1038/onc.2009.246.Peer-Reviewed Original ResearchCitations
2007
Linkage Disequilibrium Mapping for Complex Disease Genes
DeWan A, Klein RJ, Hoh J. Linkage Disequilibrium Mapping for Complex Disease Genes. Methods In Molecular Biology 2007, 376: 85-107. PMID: 17984540, DOI: 10.1007/978-1-59745-389-9_7.ChaptersCitations
2006
HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration
DeWan A, Liu M, Hartman S, Zhang SS, Liu DT, Zhao C, Tam PO, Chan WM, Lam DS, Snyder M, Barnstable C, Pang CP, Hoh J. HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration. Science 2006, 314: 989-992. PMID: 17053108, DOI: 10.1126/science.1133807.Peer-Reviewed Original ResearchCitationsAltmetricMeSH KeywordsAgedAged, 80 and overAgingAsian PeopleChromatin ImmunoprecipitationChromosomes, Human, Pair 10FemaleGenetic Predisposition to DiseaseGenotypeHeLa CellsHigh-Temperature Requirement A Serine Peptidase 1HumansLinkage DisequilibriumMacular DegenerationMaleMiddle AgedPolymorphism, Single NucleotidePromoter Regions, GeneticRetinal NeovascularizationSerine EndopeptidasesSerum Response FactorTranscription Factor AP-2A Variant of the HTRA1 Gene Increases Susceptibility to Age-Related Macular Degeneration
Yang Z, Camp NJ, Sun H, Tong Z, Gibbs D, Cameron DJ, Chen H, Zhao Y, Pearson E, Li X, Chien J, DeWan A, Harmon J, Bernstein PS, Shridhar V, Zabriskie NA, Hoh J, Howes K, Zhang K. A Variant of the HTRA1 Gene Increases Susceptibility to Age-Related Macular Degeneration. Science 2006, 314: 992-993. PMID: 17053109, DOI: 10.1126/science.1133811.Peer-Reviewed Original ResearchCitationsAltmetricMeSH KeywordsAgedAgingAllelesCase-Control StudiesChromosomes, Human, Pair 10Cohort StudiesFemaleGenetic Predisposition to DiseaseGenotypeHigh-Temperature Requirement A Serine Peptidase 1HomozygoteHumansLymphocytesMacular DegenerationMaleMiddle AgedPigment Epithelium of EyePolymorphism, Single NucleotidePromoter Regions, GeneticRetinal DrusenReverse Transcriptase Polymerase Chain ReactionRNA, MessengerSerine EndopeptidasesWhite People
2002
Statistics in Genetics and in the Environmental Science
Hoh J. Statistics in Genetics and in the Environmental Science. Heredity 2002, 89: 80-81. DOI: 10.1038/sj.hdy.6800093.Commentaries, Editorials and Letters
2001
Two Approaches for Consolidating Results from Genome Scans of Complex Traits: Selection Methods and Scan Statistics
Gordon D, Hoh J, Finch S, Levenstien M, Edington J, EdingtonLi W, Majewski J, Ott J. Two Approaches for Consolidating Results from Genome Scans of Complex Traits: Selection Methods and Scan Statistics. Genetic Epidemiology 2001, 21: s396-s402. PMID: 11793706, DOI: 10.1002/gepi.2001.21.s1.s396.Peer-Reviewed Original ResearchCitations
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Yale School of Public Health
PO Box 208034, 60 College Street
New Haven, CT 06520-8034
United States
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New Haven, CT 06510