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Results 1-10 of 23 (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
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
May-2008Genome-wide association analysis identifies 20 loci that influence adult height.Weedon, MN; Lango, H; Lindgren, CM; Wallace, C; Evans, DM; Mangino, M; Freathy, RM; Perry, JR; Stevens, S; Hall, AS; Samani, NJ; Shields, B; Prokopenko, I; Farrall, M; Dominiczak, A; Diabetes Genetics Initiative; Wellcome Trust Case Control Consortium; Johnson, T; Bergmann, S; Beckmann, JS; Vollenweider, P; Waterworth, DM; Mooser, V; Palmer, CN; Morris, AD; Ouwehand, WH; Cambridge GEM Consortium; Zhao, JH; Li, S; Loos, RJ; Barroso, I; Deloukas, P; Sandhu, MS; Wheeler, E; Soranzo, N; Inouye, M; Wareham, NJ; Caulfield, M; Munroe, PB; Hattersley, AT; McCarthy, MI; Frayling, TMJournal 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
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
May-2010Meta-analysis and imputation refines the association of 15q25 with smoking quantity.Liu, JZ; Tozzi, F; Waterworth, DM; Pillai, SG; Muglia, P; Middleton, L; Berrettini, W; Knouff, CW; Yuan, X; Waeber, G; Vollenweider, P; Preisig, M; Wareham, NJ; Zhao, JH; Loos, RJ; Barroso, I; Khaw, KT; Grundy, S; Barter, P; Mahley, R; Kesaniemi, A; McPherson, R; Vincent, JB; Strauss, J; Kennedy, JL; Farmer, A; McGuffin, P; Day, R; Matthews, K; Bakke, P; Gulsvik, A; Lucae, S; Ising, M; Brueckl, T; Horstmann, S; Wichmann, HE; Rawal, R; Dahmen, N; Lamina, C; Polasek, O; Zgaga, L; Huffman, J; Campbell, S; Kooner, J; Chambers, JC; Burnett, MS; Devaney, JM; Pichard, AD; Kent, KM; Satler, L; Lindsay, JM; Waksman, R; Epstein, S; Wilson, JF; Wild, SH; Campbell, H; Vitart, V; Reilly, MP; Li, M; Qu, L; Wilensky, R; Matthai, W; Hakonarson, HH; Rader, DJ; Franke, A; Wittig, M; Schäfer, A; Uda, M; Terracciano, A; Xiao, X; Busonero, F; Scheet, P; Schlessinger, D; St Clair D; Rujescu, D; Abecasis, GR; Grabe, HJ; Teumer, A; Völzke, H; Petersmann, A; John, U; Rudan, I; Hayward, C; Wright, AF; Kolcic, I; Wright, BJ; Thompson, JR; Balmforth, AJ; Hall, AS; Samani, NJ; Anderson, CA; Ahmad, T; Mathew, CG; Parkes, M; Satsangi, J; Caulfield, M; Munroe, PB; Farrall, M; Dominiczak, A; Worthington, J; Thomson, W; Eyre, S; Barton, A; Wellcome Trust Case Control Consortium; Mooser, V; Francks, C; Marchini, JJournal Article
16-Apr-2009A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function.Soranzo, N; Rendon, A; Gieger, C; Jones, CI; Watkins, NA; Menzel, S; Döring, A; Stephens, J; Prokisch, H; Erber, W; Potter, SC; Bray, SL; Burns, P; Jolley, J; Falchi, M; Kühnel, B; Erdmann, J; Schunkert, H; Samani, NJ; Illig, T; Garner, SF; Rankin, A; Meisinger, C; Bradley, JR; Thein, SL; Goodall, AH; Spector, TD; Deloukas, P; Ouwehand, WHJournal Article