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

Denny JC, Crawford DC, Ritchie MD, Bielinski SJ, Basford MA, Bradford Y, Chai HS, Bastarache L, Zuvich R, Peissig P, Carrell D, Ramirez AH, Pathak J, Wilke RA, Rasmussen L, Wang X, Pacheco JA, Kho AN, Hayes MG, Weston N, Matsumoto M, Kopp PA, Newton KM, Jarvik GP, Li R, Manolio TA, Kullo IJ, Chute CG, Chisholm RL, Larson EB, McCarty CA, Masys DR, Roden DM, de Andrade M
Am J Hum Genet. 2011 89 (4): 529-42

PMID: 21981779 · PMCID: PMC3188836 · DOI:10.1016/j.ajhg.2011.09.008

MeSH Terms (16)

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

Connections (3)

This publication is referenced by other Labnodes entities: