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Results 1-10 of 13 (Search time: 0.001 seconds).
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First PublishedTitleAuthor(s)Type
Mar-2004Genotypes and haplotypes predisposing to myocardial infarction: a multilocus case-control study.Tobin, MD; Braund, PS; Burton, PR; Thompson, JR; Steeds, R; Channer, K; Cheng, S; Lindpaintner, K; Samani, NJJournal Article
Mar-2007Enhanced 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 GroupJournal Article
Jan-2008Genome-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, PBJournal Article
Jan-2005Mapping of a major locus that determines telomere length in humans.Vasa-Nicotera, M; Brouilette, S; Mangino, M; Thompson, JR; Braund, P; Clemitson, JR; Mason, A; Bodycote, CL; Raleigh, SM; Louis, E; Samani, NJJournal Article
15-Aug-2008A regulatory SNP of the BICD1 gene contributes to telomere length variation in humans.Mangino, M; Brouilette, S; Braund, P; Tirmizi, N; Vasa-Nicotera, M; Thompson, JR; Samani, NJJournal Article
Oct-2008Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on cardiac repolarization in 3761 individuals from two independent populations.Tobin, MD; Kähönen, M; Braund, P; Nieminen, T; Hajat, C; Tomaszewski, M; Viik, J; Lehtinen, R; Ng, GA; Macfarlane, PW; Burton, PR; Lehtimäki, T; Samani, NJJournal Article
Nov-2008The 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, MDJournal Article
Dec-2007Beyond "misunderstanding": written information and decisions about taking part in a genetic epidemiology study.Dixon-Woods, M; Ashcroft, RE; Jackson, CJ; Tobin, MD; Kivits, J; Burton, PR; Samani, NJJournal Article
13-Jan-2007Telomere length, risk of coronary heart disease, and statin treatment in the West of Scotland Primary Prevention Study: a nested case-control study.Brouilette, SW; Moore, JS; McMahon, AD; Thompson, JR; Ford, I; Shepherd, J; Packard, CJ; Samani, NJ; West of Scotland Coronary Prevention Study GroupJournal Article
1-Apr-2008Repeated 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, ConsortiumJournal Article