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Results 11-20 of 98 (Search time: 0.002 seconds).
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First PublishedTitleAuthor(s)Type
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
Feb-2012Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.Salvi, E; Kutalik, Z; Glorioso, N; Benaglio, P; Frau, F; Kuznetsova, T; Arima, H; Hoggart, C; Tichet, J; Nikitin, YP; Conti, C; Seidlerova, J; Tikhonoff, V; Stolarz-Skrzypek, K; Johnson, T; Devos, N; Zagato, L; Guarrera, S; Zaninello, R; Calabria, A; Stancanelli, B; Troffa, C; Thijs, L; Rizzi, F; Simonova, G; Lupoli, S; Argiolas, G; Braga, D; D'Alessio, MC; Ortu, MF; Ricceri, F; Mercurio, M; Descombes, P; Marconi, M; Chalmers, J; Harrap, S; Filipovsky, J; Bochud, M; Iacoviello, L; Ellis, J; Stanton, AV; Laan, M; Padmanabhan, S; Dominiczak, AF; Samani, NJ; Melander, O; Jeunemaitre, X; Manunta, P; Shabo, A; Vineis, P; Cappuccio, FP; Caulfield, MJ; Matullo, G; Rivolta, C; Munroe, PB; Barlassina, C; Staessen, JA; Beckmann, JS; Cusi, DJournal 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
1-May-2003White cell telomere length and risk of premature myocardial infarction.Brouilette, S; Singh, RK; Thompson, JR; Goodall, AH; 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
Jun-2008Common 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, 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
Mar-2009Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.Myocardial Infarction Genetics Consortium; Kathiresan, S; Voight, BF; Purcell, S; Musunuru, K; Ardissino, D; Mannucci, PM; Anand, S; Engert, JC; Samani, NJ; Schunkert, H; Erdmann, J; Reilly, MP; Rader, DJ; Morgan, T; Spertus, JA; Stoll, M; Girelli, D; McKeown, PP; Patterson, CC; Siscovick, DS; O'Donnell, CJ; Elosua, R; Peltonen, L; Salomaa, V; Schwartz, SM; Melander, O; Altshuler, D; Ardissino, D; Merlini, PA; Berzuini, C; Bernardinelli, L; Peyvandi, F; Tubaro, M; Celli, P; Ferrario, M; Fetiveau, R; Marziliano, N; Casari, G; Galli, M; Ribichini, F; Rossi, M; Bernardi, F; Zonzin, P; Piazza, A; Mannucci, PM; Schwartz, SM; Siscovick, DS; Yee, J; Friedlander, Y; Elosua, R; Marrugat, J; Lucas, G; Subirana, I; Sala, J; Ramos, R; Kathiresan, S; Meigs, JB; Williams, G; Nathan, DM; MacRae, CA; O'Donnell, CJ; Salomaa, V; Havulinna, AS; Peltonen, L; Melander, O; Berglund, G; Voight, BF; Kathiresan, S; Hirschhorn, JN; Asselta, R; Duga, S; Spreafico, M; Musunuru, K; Daly, MJ; Purcell, S; Voight, BF; Purcell, S; Nemesh, J; Korn, JM; McCarroll, SA; Schwartz, SM; Yee, J; Kathiresan, S; Lucas, G; Subirana, I; Elosua, R; Surti, A; Guiducci, C; Gianniny, L; Mirel, D; Parkin, M; Burtt, N; Gabriel, SB; Samani, NJ; Thompson, JR; Braund, PS; Wright, BJ; Balmforth, AJ; Ball, SG; Hall, AS; Wellcome Trust Case Control Consortium; Schunkert, H; Erdmann, J; Linsel-Nitschke, P; Lieb, W; Ziegler, A; König, I; Hengstenberg, C; Fischer, M; Stark, K; Grosshennig, A; Preuss, M; Wichmann, HE; Schreiber, S; Schunkert, H; Samani, NJ; Erdmann, J; Ouwehand, W; Hengstenberg, C; Deloukas, P; Scholz, M; Cambien, F; Reilly, MP; Li, M; Chen, Z; Wilensky, R; Matthai, W; Qasim, A; Hakonarson, HH; Devaney, J; Burnett, MS; Pichard, AD; Kent, KM; Satler, L; Lindsay, JM; Waksman, R; Knouff, CW; Waterworth, DM; Walker, MC; Mooser, V; Epstein, SE; Rader, DJ; Scheffold, T; Berger, K; Stoll, M; Huge, A; Girelli, D; Martinelli, N; Olivieri, O; Corrocher, R; Morgan, T; Spertus, JA; McKeown, P; Patterson, CC; Schunkert, H; Erdmann, E; Linsel-Nitschke, P; Lieb, W; Ziegler, A; König, IR; Hengstenberg, C; Fischer, M; Stark, K; Grosshennig, A; Preuss, M; Wichmann, HE; Schreiber, S; Hólm, H; Thorleifsson, G; Thorsteinsdottir, U; Stefansson, K; Engert, JC; Do, R; Xie, C; Anand, S; Kathiresan, S; Ardissino, D; Mannucci, PM; Siscovick, D; O'Donnell, CJ; Samani, NJ; Melander, O; Elosua, R; Peltonen, L; Salomaa, V; Schwartz, SM; Altshuler, DJournal Article