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Page 1
Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk Factors.
LeBlanc M, Zuber V, Andreassen BK, Witoelar A, Zeng L, Bettella F, Wang Y, McEvoy LK, Thompson WK, Schork AJ, Reppe S, Barrett-Connor E, Ligthart S, Dehghan A, Gautvik KM, Nelson CP, Schunkert H, Samani NJ; CARDIoGRAM Consortium; Ridker PM, Chasman DI, Aukrust P, Djurovic S, Frigessi A, Desikan RS, Dale AM, Andreassen OA. LeBlanc M, et al. Among authors: samani nj. Circ Res. 2016 Jan 8;118(1):83-94. doi: 10.1161/CIRCRESAHA.115.306629. Epub 2015 Oct 20. Circ Res. 2016. PMID: 26487741 Free PMC article.
Association of WNK1 gene polymorphisms and haplotypes with ambulatory blood pressure in the general population.
Tobin MD, Raleigh SM, Newhouse S, Braund P, Bodycote C, Ogleby J, Cross D, Gracey J, Hayes S, Smith T, Ridge C, Caulfield M, Sheehan NA, Munroe PB, Burton PR, Samani NJ. Tobin MD, et al. Among authors: samani nj. Circulation. 2005 Nov 29;112(22):3423-9. doi: 10.1161/CIRCULATIONAHA.105.555474. Epub 2005 Nov 21. Circulation. 2005. PMID: 16301342
Enhanced linkage of a locus on chromosome 2 to premature coronary artery disease in the absence of hypercholesterolemia.
Nsengimana J, Samani NJ, Hall AS, Balmforth AJ, Mangino M, Yuldasheva N, Maqbool A, Braund P, Burton P, Bishop DT, Ball SG, Barrett JH; British Heart Foundation Family Heart Study Research Group. Nsengimana J, et al. Among authors: samani nj. Eur J Hum Genet. 2007 Mar;15(3):313-9. doi: 10.1038/sj.ejhg.5201752. Epub 2006 Dec 6. Eur J Hum Genet. 2007. PMID: 17149386
Genomewide association analysis of coronary artery disease.
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, König IR, Stevens SE, Szymczak S, Tregouet DA, Iles MM, Pahlke F, Pollard H, Lieb W, Cambien F, Fischer M, Ouwehand W, Blankenberg S, Balmforth AJ, Baessler A, Ball SG, Strom TM, Braenne I, Gieger C, Deloukas P, Tobin MD, Ziegler A, Thompson JR, Schunkert H; WTCCC and the Cardiogenics Consortium. Samani NJ, et al. N Engl J Med. 2007 Aug 2;357(5):443-53. doi: 10.1056/NEJMoa072366. Epub 2007 Jul 18. N Engl J Med. 2007. PMID: 17634449 Free PMC article.
Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.
Schunkert H, Götz A, Braund P, McGinnis R, Tregouet DA, Mangino M, Linsel-Nitschke P, Cambien F, Hengstenberg C, Stark K, Blankenberg S, Tiret L, Ducimetiere P, Keniry A, Ghori MJ, Schreiber S, El Mokhtari NE, Hall AS, Dixon RJ, Goodall AH, Liptau H, Pollard H, Schwarz DF, Hothorn LA, Wichmann HE, König IR, Fischer M, Meisinger C, Ouwehand W, Deloukas P, Thompson JR, Erdmann J, Ziegler A, Samani NJ; Cardiogenics Consortium. Schunkert H, et al. Among authors: samani nj. Circulation. 2008 Apr 1;117(13):1675-84. doi: 10.1161/CIRCULATIONAHA.107.730614. Epub 2008 Mar 24. Circulation. 2008. PMID: 18362232 Free PMC article.
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.
Lieb W, Zeller T, Mangino M, Götz A, Braund P, Wenzel JJ, Horn C, Proust C, Linsel-Nitschke P, Amouyel P, Bruse P, Arveiler D, König IR, Ferrières J, Ziegler A, Balmforth AJ, Evans A, Ducimetière P, Cambien F, Hengstenberg C, Stark K, Hall AS, Schunkert H, Blankenberg S, Samani NJ, Erdmann J, Tiret L. Lieb W, et al. Among authors: samani nj. J Mol Med (Berl). 2008 Oct;86(10):1163-70. doi: 10.1007/s00109-008-0376-5. Epub 2008 Jul 1. J Mol Med (Berl). 2008. PMID: 18592168
Coronary artery disease-associated locus on chromosome 9p21 and early markers of atherosclerosis.
Samani NJ, Raitakari OT, Sipilä K, Tobin MD, Schunkert H, Juonala M, Braund PS, Erdmann J, Viikari J, Moilanen L, Taittonen L, Jula A, Jokinen E, Laitinen T, Hutri-Kähönen N, Nieminen MS, Kesäniemi YA, Hall AS, Hulkkonen J, Kähönen M, Lehtimäki T. Samani NJ, et al. Arterioscler Thromb Vasc Biol. 2008 Sep;28(9):1679-83. doi: 10.1161/ATVBAHA.108.170332. Epub 2008 Jul 3. Arterioscler Thromb Vasc Biol. 2008. PMID: 18599798 Free article.
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
Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study.
Linsel-Nitschke P, Götz A, Erdmann J, Braenne I, Braund P, Hengstenberg C, Stark K, Fischer M, Schreiber S, El Mokhtari NE, Schaefer A, Schrezenmeir J, Rubin D, Hinney A, Reinehr T, Roth C, Ortlepp J, Hanrath P, Hall AS, Mangino M, Lieb W, Lamina C, Heid IM, Doering A, Gieger C, Peters A, Meitinger T, Wichmann HE, König IR, Ziegler A, Kronenberg F, Samani NJ, Schunkert H; Wellcome Trust Case Control Consortium (WTCCC); Cardiogenics Consortium. Linsel-Nitschke P, et al. Among authors: samani nj. PLoS One. 2008 Aug 20;3(8):e2986. doi: 10.1371/journal.pone.0002986. PLoS One. 2008. PMID: 18714375 Free PMC article.
779 results