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Results 31-40 of 211 (Search time: 0.002 seconds).
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First PublishedTitleAuthor(s)Type
Oct-2010Is there an association between angiotensin converting enzyme (ACE) genotypes and abdominal aortic aneurysm?Obukofe, B; Sayers, RD; Sandford, RM; London, NJM; Samani, NJ; Bown, MJ; Thompson, JJournal Article
Apr-2012A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complexDavies, RW; Wells, GA; Chen, L; Stewart, AFR; Dandona, S; Roberts, R; McPherson, R; Erdmann, J; Nahrstaedt, J; Loley, C; Schunkert, H; Shah, SH; Kraus, WE; Granger, CB; Ferguson, JF; Reilly, MP; Hall, AS; Anand, SS; Burnett, MS; Epstein, SE; Nahrstaedt, J; Loley, C; König, IR; Engert, JC; Hengstenberg, C; Wichmann, H-E; Schreiber, S; Tang, WHW; Ellis, SG; Hazen, SL; Rader, DJ; Samani, NJ; McPherson, RJournal Article
15-Jan-2007Complementary intron sequence motifs associated with human exon repetition: a role for intragenic, inter-transcript interactions in gene expression.Dixon, RJ; Eperon, IC; 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
Jun-2009Genome-wide association study identifies eight loci associated with blood pressure.Newton-Cheh, C; Johnson, T; Gateva, V; Tobin, MD; Bochud, M; Coin, L; Najjar, SS; Zhao, JH; Heath, SC; Eyheramendy, S; Papadakis, K; Voight, BF; Scott, LJ; Zhang, F; Farrall, M; Tanaka, T; Wallace, C; Chambers, JC; Khaw, KT; Nilsson, P; van der Harst P; Polidoro, S; Grobbee, DE; Onland-Moret, NC; Bots, ML; Wain, LV; Elliott, KS; Teumer, A; Luan, J; Lucas, G; Kuusisto, J; Burton, PR; Hadley, D; McArdle, WL; Wellcome Trust Case Control Consortium; Brown, M; Dominiczak, A; Newhouse, SJ; Samani, NJ; Webster, J; Zeggini, E; Beckmann, JS; Bergmann, S; Lim, N; Song, K; Vollenweider, P; Waeber, G; Waterworth, DM; Yuan, X; Groop, L; Orho-Melander, M; Allione, A; Di Gregorio A; Guarrera, S; Panico, S; Ricceri, F; Romanazzi, V; Sacerdote, C; Vineis, P; Barroso, I; Sandhu, MS; Luben, RN; Crawford, GJ; Jousilahti, P; Perola, M; Boehnke, M; Bonnycastle, LL; Collins, FS; Jackson, AU; Mohlke, KL; Stringham, HM; Valle, TT; Willer, CJ; Bergman, RN; Morken, MA; Döring, A; Gieger, C; Illig, T; Meitinger, T; Org, E; Pfeufer, A; Wichmann, HE; Kathiresan, S; Marrugat, J; O'Donnell, CJ; Schwartz, SM; Siscovick, DS; Subirana, I; Freimer, NB; Hartikainen, AL; McCarthy, MI; O'Reilly, PF; Peltonen, L; Pouta, A; de Jong PE; Snieder, H; van Gilst WH; Clarke, R; Goel, A; Hamsten, A; Peden, JF; Seedorf, U; Syvänen, AC; Tognoni, G; Lakatta, EG; Sanna, S; Scheet, P; Schlessinger, D; Scuteri, A; Dörr, M; Ernst, F; Felix, SB; Homuth, G; Lorbeer, R; Reffelmann, T; Rettig, R; Völker, U; Galan, P; Gut, IG; Hercberg, S; Lathrop, GM; Zelenika, D; Deloukas, P; Soranzo, N; Williams, FM; Zhai, G; Salomaa, V; Laakso, M; Elosua, R; Forouhi, NG; Völzke, H; Uiterwaal, CS; van der Schouw YT; Numans, ME; Matullo, G; Navis, G; Berglund, G; Bingham, SA; Kooner, JS; Connell, JM; Bandinelli, S; Ferrucci, L; Watkins, H; Spector, TD; Tuomilehto, J; Altshuler, D; Strachan, DP; Laan, M; Meneton, P; Wareham, NJ; Uda, M; Jarvelin, MR; Mooser, V; Melander, O; Loos, RJ; Elliott, P; Abecasis, GR; Caulfield, M; Munroe, PBJournal 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
Nov-2009A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.Soranzo, N; Spector, TD; Mangino, M; Kühnel, B; Rendon, A; Teumer, A; Willenborg, C; Wright, B; Chen, L; Li, M; Salo, P; Voight, BF; Burns, P; Laskowski, RA; Xue, Y; Menzel, S; Altshuler, D; Bradley, JR; Bumpstead, S; Burnett, MS; Devaney, J; Döring, A; Elosua, R; Epstein, SE; Erber, W; Falchi, M; Garner, SF; Ghori, MJ; Goodall, AH; Gwilliam, R; Hakonarson, HH; Hall, AS; Hammond, N; Hengstenberg, C; Illig, T; König, IR; Knouff, CW; McPherson, R; Melander, O; Mooser, V; Nauck, M; Nieminen, MS; O'Donnell, CJ; Peltonen, L; Potter, SC; Prokisch, H; Rader, DJ; Rice, CM; Roberts, R; Salomaa, V; Sambrook, J; Schreiber, S; Schunkert, H; Schwartz, SM; Serbanovic-Canic, J; Sinisalo, J; Siscovick, DS; Stark, K; Surakka, I; Stephens, J; Thompson, JR; Völker, U; Völzke, H; Watkins, NA; Wells, GA; Wichmann, HE; Van Heel DA; Tyler-Smith, C; Thein, SL; Kathiresan, S; Perola, M; Reilly, MP; Stewart, AF; Erdmann, J; Samani, NJ; Meisinger, C; Greinacher, A; Deloukas, P; Ouwehand, WH; Gieger, CJournal Article
Mar-2009New susceptibility locus for coronary artery disease on chromosome 3q22.3.Erdmann, J; Grosshennig, A; Braund, PS; König, IR; Hengstenberg, C; Hall, AS; Linsel-Nitschke, P; Kathiresan, S; Wright, B; Trégouët, DA; Cambien, F; Bruse, P; Aherrahrou, Z; Wagner, AK; Stark, K; Schwartz, SM; Salomaa, V; Elosua, R; Melander, O; Voight, BF; O'Donnell, CJ; Peltonen, L; Siscovick, DS; Altshuler, D; Merlini, PA; Peyvandi, F; Bernardinelli, L; Ardissino, D; Schillert, A; Blankenberg, S; Zeller, T; Wild, P; Schwarz, DF; Tiret, L; Perret, C; Schreiber, S; El Mokhtari NE; Schäfer, A; März, W; Renner, W; Bugert, P; Klüter, H; Schrezenmeir, J; Rubin, D; Ball, SG; Balmforth, AJ; Wichmann, HE; Meitinger, T; Fischer, M; Meisinger, C; Baumert, J; Peters, A; Ouwehand, WH; Italian, Atherosclerosis; Thrombosis; and Vascular Biology Working Group; Myocardial Infarction Genetics Consortium; Wellcome Trust Case Control Consortium; Cardiogenics, Consortium; Deloukas, P; Thompson, JR; Ziegler, A; Samani, NJ; Schunkert, HJournal Article
Mar-2009Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.Trégouët, DA; König, IR; Erdmann, J; Munteanu, A; Braund, PS; Hall, AS; Grosshennig, A; Linsel-Nitschke, P; Perret, C; DeSuremain, M; Meitinger, T; Wright, BJ; Preuss, M; Balmforth, AJ; Ball, SG; Meisinger, C; Germain, C; Evans, A; Arveiler, D; Luc, G; Ruidavets, JB; Morrison, C; van der Harst P; Schreiber, S; Neureuther, K; Schäfer, A; Bugert, P; El Mokhtari NE; Schrezenmeir, J; Stark, K; Rubin, D; Wichmann, HE; Hengstenberg, C; Ouwehand, W; Wellcome Trust Case Control Consortium; Cardiogenics, Consortium; Ziegler, A; Tiret, L; Thompson, JR; Cambien, F; Schunkert, H; Samani, NJJournal Article
Mar-2010Common variants near TERC are associated with mean telomere length.Codd, V; Mangino, M; van der Harst P; Braund, PS; Kaiser, M; Beveridge, AJ; Rafelt, S; Moore, J; Nelson, C; Soranzo, N; Zhai, G; Valdes, AM; Blackburn, H; Mateo Leach I; de Boer RA; Kimura, M; Aviv, A; Wellcome Trust Case Control Consortium; Goodall, AH; Ouwehand, W; van Veldhuisen DJ; van Gilst WH; Navis, G; Burton, PR; Tobin, MD; Hall, AS; Thompson, JR; Spector, T; Samani, NJJournal Article