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Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on cardiac repolarization in 3761 individuals from two independent populations.
Int J Epidemiol. 2008 Oct;37(5):1132-41. doi: 10.1093/ije/dyn091. Epub 2008 May 29.
Int J Epidemiol. 2008.
PMID: 18511491
Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population.
Tobin MD, Tomaszewski M, Braund PS, Hajat C, Raleigh SM, Palmer TM, Caulfield M, Burton PR, Samani NJ.
Tobin MD, et al.
Hypertension. 2008 Jun;51(6):1658-64. doi: 10.1161/HYPERTENSIONAHA.108.112664. Epub 2008 Apr 28.
Hypertension. 2008.
PMID: 18443236
Free article.
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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
Wallace C, Newhouse SJ, Braund P, Zhang F, Tobin M, Falchi M, Ahmadi K, Dobson RJ, Marçano AC, Hajat C, Burton P, Deloukas P, Brown M, Connell JM, Dominiczak A, Lathrop GM, Webster J, Farrall M, Spector T, Samani NJ, Caulfield MJ, Munroe PB.
Wallace C, et al.
Am J Hum Genet. 2008 Jan;82(1):139-49. doi: 10.1016/j.ajhg.2007.11.001.
Am J Hum Genet. 2008.
PMID: 18179892
Free PMC article.
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The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol.
Samani NJ, Braund PS, Erdmann J, Götz A, Tomaszewski M, Linsel-Nitschke P, Hajat C, Mangino M, Hengstenberg C, Stark K, Ziegler A, Caulfield M, Burton PR, Schunkert H, Tobin MD.
Samani NJ, et al.
J Mol Med (Berl). 2008 Nov;86(11):1233-41. doi: 10.1007/s00109-008-0387-2. Epub 2008 Jul 23.
J Mol Med (Berl). 2008.
PMID: 18649068
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