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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
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
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
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
2-Nov-2010Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.Assimes, TL; Hólm, H; Kathiresan, S; Reilly, MP; Thorleifsson, G; Voight, BF; Erdmann, J; Willenborg, C; Vaidya, D; Xie, C; Patterson, CC; Morgan, TM; Burnett, MS; Li, M; Hlatky, MA; Knowles, JW; Thompson, JR; Absher, D; Iribarren, C; Go, A; Fortmann, SP; Sidney, S; Risch, N; Tang, H; Myers, RM; Berger, K; Stoll, M; Shah, SH; Thorgeirsson, G; Andersen, K; Havulinna, AS; Herrera, JE; Faraday, N; Kim, Y; Kral, BG; Mathias, RA; Ruczinski, I; Suktitipat, B; Wilson, AF; Yanek, LR; Becker, LC; Linsel-Nitschke, P; Lieb, W; König, IR; Hengstenberg, C; Fischer, M; Stark, K; Reinhard, W; Winogradow, J; Grassl, M; Grosshennig, A; Preuss, M; Schreiber, S; Wichmann, HE; Meisinger, C; Yee, J; Friedlander, Y; Do, R; Meigs, JB; Williams, G; Nathan, DM; MacRae, CA; Qu, L; Wilensky, RL; Matthai, WH; Qasim, AN; Hakonarson, H; Pichard, AD; Kent, KM; Satler, L; Lindsay, JM; Waksman, R; Knouff, CW; Waterworth, DM; Walker, MC; Mooser, VE; Marrugat, J; Lucas, G; Subirana, I; Sala, J; Ramos, R; Martinelli, N; Olivieri, O; Trabetti, E; Malerba, G; Pignatti, PF; Guiducci, C; Mirel, D; Parkin, M; Hirschhorn, JN; Asselta, R; Duga, S; Musunuru, K; Daly, MJ; Purcell, S; Eifert, S; Braund, PS; Wright, BJ; Balmforth, AJ; Ball, SG; Myocardial Infarction Genetics Consortium; Wellcome Trust Case Control Consortium; Cardiogenics; Ouwehand, WH; Deloukas, P; Scholz, M; Cambien, F; Huge, A; Scheffold, T; Salomaa, V; Girelli, D; Granger, CB; Peltonen, L; McKeown, PP; Altshuler, D; Melander, O; Devaney, JM; Epstein, SE; Rader, DJ; Elosua, R; Engert, JC; Anand, SS; Hall, AS; Ziegler, A; O'Donnell, CJ; Spertus, JA; Siscovick, D; Schwartz, SM; Becker, D; Thorsteinsdottir, U; Stefansson, K; Schunkert, H; Samani, NJ; Quertermous, TJournal Article
Oct-2007The interleukin-10-1082 'A' allele and abdominal aortic aneurysms.Bown, MJ; Lloyd, GM; Sandford, RM; Thompson, JR; London, NJ; Samani, NJ; Sayers, RDJournal 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
11-Aug-2001Telomere shortening in atherosclerosis.Samani, NJ; Boultby, R; Butler, R; Thompson, JR; Goodall, AHJournal 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
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