Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies

Joshua C. Denny(National Institutes of Health), Mariza de Andrade(Mayo Clinic), Rex L. Chisholm(Northwestern University), Dana C. Crawford(Vanderbilt University), David Carrell(Kaiser Permanente Washington Health Research Institute), Jyotishman Pathak(Mayo Clinic), Andrea H. Ramirez(Vanderbilt University Medical Center), Catherine A. McCarty(University of Minnesota, Duluth), Noah Weston(Kaiser Permanente Washington Health Research Institute), M. Geoffrey Hayes(Northwestern University), Peter Kopp(Northwestern University), Gail P. Jarvik(University of Washington Medical Center), Christopher G. Chute(Johns Hopkins University), Melissa Basford(VA Office of Research and Development), Rebecca L. Zuvich, Luke V. Rasmussen(Northwestern University), Martha Matsumoto(Mayo Clinic in Florida), Marylyn D. Ritchie(Medical University of South Carolina), Katherine M. Newton(Group Health Cooperative), Peggy Peissig(Pew Research Center), Teri A. Manolio(National Institutes of Health), Xiaoming Wang(Vanderbilt University), Abel Kho(Northwestern University), Russell A. Wilke(Vanderbilt University Medical Center), Iftikhar J. Kullo(Mayo Clinic in Arizona), Lisa Bastarache(Vanderbilt University Medical Center), Rongling Li(University of Tennessee Health Science Center), Eric B. Larson(University of Washington), Daniel R. Masys(University of Washington), High Seng Chai(Mayo Clinic in Florida), Yuki Bradford(National Institutes of Health), Suzette J. Bielinski(Mayo Clinic in Florida), Dan M. Roden(Vanderbilt University), Jennifer A. Pacheco(Northwestern University)
The American Journal of Human Genetics
October 1, 2011
Cited by 256


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