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Results 1-10 of 12 (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
Nov-2009Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.Talmud, PJ; Drenos, F; Shah, S; Shah, T; Palmen, J; Verzilli, C; Gaunt, TR; Pallas, J; Lovering, R; Li, K; Casas, JP; Sofat, R; Kumari, M; Rodriguez, S; Johnson, T; Newhouse, SJ; Dominiczak, A; Samani, NJ; Caulfield, M; Sever, P; Stanton, A; Shields, DC; Padmanabhan, S; Melander, O; Hastie, C; Delles, C; Ebrahim, S; Marmot, MG; Smith, GD; Lawlor, DA; Munroe, PB; Day, IN; Kivimaki, M; Whittaker, J; Humphries, SE; Hingorani, AD; ASCOT, investigators; NORDIL, investigators; BRIGHT, ConsortiumJournal Article
1-Jul-2009Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease.Elliott, P; Chambers, JC; Zhang, W; Clarke, R; Hopewell, JC; Peden, JF; Erdmann, J; Braund, P; Engert, JC; Bennett, D; Coin, L; Ashby, D; Tzoulaki, I; Brown, IJ; Mt-Isa, S; McCarthy, MI; Peltonen, L; Freimer, NB; Farrall, M; Ruokonen, A; Hamsten, A; Lim, N; Froguel, P; Waterworth, DM; Vollenweider, P; Waeber, G; Jarvelin, MR; Mooser, V; Scott, J; Hall, AS; Schunkert, H; Anand, SS; Collins, R; Samani, NJ; Watkins, H; Kooner, JSJournal Article
1-May-2003White cell telomere length and risk of premature myocardial infarction.Brouilette, S; Singh, RK; Thompson, JR; Goodall, AH; 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
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
Sep-2008Coronary 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, TJournal Article
Sep-2007LGALS2 functional variant rs7291467 is not associated with susceptibility to myocardial infarction in Caucasians.Mangino, M; Braund, P; Singh, R; Steeds, R; Thompson, JR; Channer, K; Samani, NJJournal Article
May-2010Leukocyte telomere length and coronary artery calcification.Mainous, AG; Codd, V; Diaz, VA; Schoepf, UJ; Everett, CJ; Player, MS; Samani, NJJournal Article
15-Jul-2008Possible association between telomere length and renal dysfunction in patients with chronic heart failure.van der Harst P; Wong, LS; de Boer RA; Brouilette, SW; van der Steege G; Voors, AA; Hall, AS; Samani, NJ; Wikstrand, J; van Gilst WH; van Veldhuisen DJ; MERIT-HF Study GroupJournal Article