Pathogenic variants for mendelian and complex traits in exomes of 6,517 european and african americans: Implications for the return of incidental results

American Journal of Human Genetics

Volumn 95, Issue 2, 2014, Pages 183-193

  Tabor, Holly K ^a,b   Auer, Paul L ^c,d   Jamal, Seema M ^b   Chong, Jessica X ^b   Yu, Joon Ho ^b   Gordon, Adam S ^e   Graubert, Timothy A ^f   O'Donnell, Christopher J ^g   Rich, Stephen S ^h   Nickerson, Deborah A ^e   Bamshad, Michael J ^b,e  

^a SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^c Fred Hutchinson Cancer Research Center   (United States)

^d UNIVERSITY OF WISCONSIN MILWAUKEE   (United States)

^e UNIVERSITY OF WASHINGTON   (United States)

^f HARVARD UNIVERSITY   (United States)

^g NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

^h UNIVERSITY OF VIRGINIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AFRICAN AMERICAN; ARTICLE; CONTROLLED STUDY; DATA BASE; EUROPEAN AMERICAN; EXOME; GENE FREQUENCY; GENE IDENTIFICATION; GENE LOCUS; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; HUMAN; NATIONAL HEALTH ORGANIZATION; NEWBORN SCREENING; PATHOGENICITY; PHENOTYPE; PRACTICE GUIDELINE; PRIORITY JOURNAL; RETINA MACULA AGE RELATED DEGENERATION;

AFRICAN AMERICANS; ALLELES; BASE SEQUENCE; CHROMOSOME MAPPING; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXOME; GENETIC VARIATION; GENOME, HUMAN; HUMANS; MACULAR DEGENERATION; MODELS, GENETIC; MULTIFACTORIAL INHERITANCE; SEQUENCE ANALYSIS, DNA;

EID: 84905912748     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2014.07.006     Document Type: Article

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