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Paper Details

Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.
Am J Hum Genet
16
2021
BCL2, FBN1, TAA, TAA disease, TCF7L2, Thoracic aortic aneurysm, aortic eQTL, heritable disease, single genes, third intron, thoracic aortic aneurysm, type 2 diabetes, vascular smooth, vascular smooth muscle cell
Author NameAffiliation
Wei ZhouUniversity of Michigan, Massachusetts General Hospital, USA Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT
Ida SurakkaUniversity of Michigan ann arbor
Chad M BrummettUniversity of Michigan ann arbor
Santhi K GaneshUniversity of Michigan ann arbor
Anne Heidi SkogholtK.G. Jebsen Center for Genetic Epidemiology, Norwegian University of Science and Technology
Kristian HveemK.G. Jebsen Center for Genetic Epidemiology, Norwegian University of Science and Technology, Norway HUNT Research Center
Derek KlarinMalcolm Randall VA Medical Center, University of Florida College of Medicine, Broad Institute of MIT and Harvard
Scott M DamrauerCorporal Michael Crescenz VA Medical Center, Perelman School of Medicine, University of Pennsylvania
Scott M DamrauerCorporal Michael Crescenz VA Medical Center, Perelman School of Medicine, University of Pennsylvania
Suzanne M LealCenter for Statistical Genetics, Columbia University Medical Center, USA Taub Institute for Alzheimer disease and the Aging Brain, Columbia University
Yuqing E ChenUniversity of Michigan ann arbor
Cristen J WillerUniversity of Michigan ann arbor
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