Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Hypertension and NOS1AP[original query] |
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Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study. Human molecular genetics 2009 Nov 18 (21): 4213-8. Eijgelsheim Mark, Newton-Cheh Christopher, Aarnoudse Adrianus L H J, van Noord Charlotte, Witteman Jacqueline C M, Hofman Albert, Uitterlinden André G, Stricker Bruno H |
NOS1AP variant associated with incidence of type 2 diabetes in calcium channel blocker users in the Atherosclerosis Risk in Communities (ARIC) study. Diabetologia 2010 Mar 53 (3): 510-6. Chu A Y, Coresh J, Arking D E, Pankow J S, Tomaselli G F, Chakravarti A, Post W S, Spooner P H, Boerwinkle E, Kao W H |
Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia. Journal of the American College of Cardiology 2012 Aug 60 (9): 841-50. Jamshidi Yalda, Nolte Ilja M, Dalageorgou Chrysoula, Zheng Dongling, Johnson Toby, Bastiaenen Rachel, Ruddy Suzanne, Talbott Daniel, Norris Kris J, Snieder Harold, George Alfred L, Marshall Vanessa, Shakir Saad, Kannankeril Prince J, Munroe Patricia B, Camm A John, Jeffery Steve, Roden Dan M, Behr Elijah |
Pharmacogenetic effects of 'candidate gene complexes' on stroke in the GenHAT study. Pharmacogenetics and genomics 2014 Nov 24 (11): 556-63. Sørensen Izel F, Vazquez Ana I, Irvin Marguerite R, Sørensen Peter, Davis Barry R, Ford Charles E, Boerwinkle Eric, Eckfeldt John H, Arnett Donna |
Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort.
BMC medical genomics 2018 Jan 11 (1): 2. Hendry Liesl M, Sahibdeen Venesa, Choudhury Ananyo, Norris Shane A, Ramsay Michèle, Lombard Zané, |
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- Page last updated:Apr 22, 2024
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