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Results 1-10 of 27 (Search time: 0.001 seconds).
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First PublishedTitleAuthor(s)Type
Dec-2010Coronary artery disease-related genetic variant on chromosome 10q11 is associated with carotid intima-media thickness and atherosclerosis.Kiechl, S; Laxton, RC; Xiao, Q; Hernesniemi, JA; Raitakari, OT; Kähönen, M; Mayosi, BM; Jula, A; Moilanen, L; Willeit, J; Watkins, H; Samani, NJ; Lehtimäki, TJ; Keavney, B; Xu, Q; Ye, SJournal Article
Oct-2010Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls.Preuss, M; König, IR; Thompson, JR; Erdmann, J; Absher, D; Assimes, TL; Blankenberg, S; Boerwinkle, E; Chen, L; Cupples, LA; Hall, AS; Halperin, E; Hengstenberg, C; Holm, H; Laaksonen, R; Li, M; März, W; McPherson, R; Musunuru, K; Nelson, CP; Burnett, MS; Epstein, SE; O'Donnell, CJ; Quertermous, T; Rader, DJ; Roberts, R; Schillert, A; Stefansson, K; Stewart, AF; Thorleifsson, G; Voight, BF; Wells, GA; Ziegler, A; Kathiresan, S; Reilly, MP; Samani, NJ; Schunkert, H; CARDIoGRAM, ConsortiumJournal Article
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
Aug-2010Genetic regulation of serum phytosterol levels and risk of coronary artery disease.Teupser, D; Baber, R; Ceglarek, U; Scholz, M; Illig, T; Gieger, C; Holdt, LM; Leichtle, A; Greiser, KH; Huster, D; Linsel-Nitschke, P; Schäfer, A; Braund, PS; Tiret, L; Stark, K; Raaz-Schrauder, D; Fiedler, GM; Wilfert, W; Beutner, F; Gielen, S; Grosshennig, A; König, IR; Lichtner, P; Heid, IM; Kluttig, A; El Mokhtari NE; Rubin, D; Ekici, AB; Reis, A; Garlichs, CD; Hall, AS; Matthes, G; Wittekind, C; Hengstenberg, C; Cambien, F; Schreiber, S; Werdan, K; Meitinger, T; Loeffler, M; Samani, NJ; Erdmann, J; Wichmann, HE; Schunkert, H; Thiery, JJournal 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
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
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
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
Oct-2008Association between the coronary artery disease risk locus on chromosome 9p21.3 and abdominal aortic aneurysm.Bown, MJ; Braund, PS; Thompson, J; London, NJ; Samani, NJ; Sayers, RDJournal Article