Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: Using electronic medical records for genome- and phenome-wide studies

American Journal of Human Genetics

Volumn 89, Issue 4, 2011, Pages 529-542

  Denny, Joshua C ^a,b   Crawford, Dana C ^a,c   Ritchie, Marylyn D ^a,c   Bielinski, Suzette J ^d   Basford, Melissa A ^b   Bradford, Yuki ^a   Chai, High Seng ^d   Bastarache, Lisa ^a   Zuvich, Rebecca ^a,c   Peissig, Peggy ^e   Carrell, David ^f   Ramirez, Andrea H ^b   Pathak, Jyotishman ^d   Wilke, Russell A ^b   Rasmussen, Luke ^e   Wang, Xiaoming ^b   Pacheco, Jennifer A ^j   Kho, Abel N ^g   Hayes, M Geoffrey ^g   Weston, Noah ^f   Matsumoto, Martha ^d   Kopp, Peter A ^g,j   Newton, Katherine M ^e   Jarvik, Gail P ^h   Li, Rongling ⁱ   Manolio, Teri A ⁱ   Kullo, Iftikhar J ^d   Chute, Christopher G ^d   Chisholm, Rex L ^j   Larson, Eric B ^f   McCarty, Catherine A ^e   Masys, Daniel R ^a   Roden, Dan M ^b   De Andrade, Mariza ^d   more..

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b VANDERBILT UNIVERSITY   (United States)

^c VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d MAYO CLINIC   (United States)

^e MARSHFIELD CLINIC   (United States)

^f GROUP HEALTH RESEARCH INSTITUTE   (United States)

^g NORTHWESTERN UNIVERSITY   (United States)

^h UNIVERSITY OF WASHINGTON MEDICAL CENTER   (United States)

ⁱ NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^j NORTHWESTERN UNIVERSITY   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

THYROID TRANSCRIPTION FACTOR 2;

AGED; ARTICLE; CONTROLLED STUDY; ELECTRONIC MEDICAL RECORD; FEMALE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME ANALYSIS; GENOMICS; GENOTYPE; HASHIMOTO DISEASE; HUMAN; HYPOTHYROIDISM; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; THYROID DISEASE; THYROID DYSGENESIS;

AGED; ALGORITHMS; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENETIC MARKERS; GENETIC VARIATION; GENOME; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; HYPOTHYROIDISM; MALE; MEDICAL RECORDS SYSTEMS, COMPUTERIZED; MIDDLE AGED; PHENOTYPE; PREDICTIVE VALUE OF TESTS;

EID: 80053896220     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2011.09.008     Document Type: Article

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