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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
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
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
Nov-2007Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.Wellcome Trust Case Control Consortium; Australo-Anglo-American Spondylitis Consortium (TASC); Burton, PR; Clayton, DG; Cardon, LR; Craddock, N; Deloukas, P; Duncanson, A; Kwiatkowski, DP; McCarthy, MI; Ouwehand, WH; Samani, NJ; Todd, JA; Donnelly, P; Barrett, JC; Davison, D; Easton, D; Evans, DM; Leung, HT; Marchini, JL; Morris, AP; Spencer, CC; Tobin, MD; Attwood, AP; Boorman, JP; Cant, B; Everson, U; Hussey, JM; Jolley, JD; Knight, AS; Koch, K; Meech, E; Nutland, S; Prowse, CV; Stevens, HE; Taylor, NC; Walters, GR; Walker, NM; Watkins, NA; Winzer, T; Jones, RW; McArdle, WL; Ring, SM; Strachan, DP; Pembrey, M; Breen, G; St Clair D; Caesar, S; Gordon-Smith, K; Jones, L; Fraser, C; Green, EK; Grozeva, D; Hamshere, ML; Holmans, PA; Jones, IR; Kirov, G; Moskivina, V; Nikolov, I; O'Donovan, MC; Owen, MJ; Collier, DA; Elkin, A; Farmer, A; Williamson, R; McGuffin, P; Young, AH; Ferrier, IN; Ball, SG; Balmforth, AJ; Barrett, JH; Bishop, TD; Iles, MM; Maqbool, A; Yuldasheva, N; Hall, AS; Braund, PS; Dixon, RJ; Mangino, M; Stevens, S; Thompson, JR; Bredin, F; Tremelling, M; Parkes, M; Drummond, H; Lees, CW; Nimmo, ER; Satsangi, J; Fisher, SA; Forbes, A; Lewis, CM; Onnie, CM; Prescott, NJ; Sanderson, J; Matthew, CG; Barbour, J; Mohiuddin, MK; Todhunter, CE; Mansfield, JC; Ahmad, T; Cummings, FR; Jewell, DP; Webster, J; Brown, MJ; Lathrop, MG; Connell, J; Dominiczak, A; Marcano, CA; Burke, B; Dobson, R; Gungadoo, J; Lee, KL; Munroe, PB; Newhouse, SJ; Onipinla, A; Wallace, C; Xue, M; Caulfield, M; Farrall, M; Barton, A; Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steering Committee; Bruce, IN; Donovan, H; Eyre, S; Gilbert, PD; Hilder, SL; Hinks, AM; John, SL; Potter, C; Silman, AJ; Symmons, DP; Thomson, W; Worthington, J; Dunger, DB; Widmer, B; Frayling, TM; Freathy, RM; Lango, H; Perry, JR; Shields, BM; Weedon, MN; Hattersley, AT; Hitman, GA; Walker, M; Elliott, KS; Groves, CJ; Lindgren, CM; Rayner, NW; Timpson, NJ; Zeggini, E; Newport, M; Sirugo, G; Lyons, E; Vannberg, F; Hill, AV; Bradbury, LA; Farrar, C; Pointon, JJ; Wordsworth, P; Brown, MA; Franklyn, JA; Heward, JM; Simmonds, MJ; Gough, SC; Seal, S; Breast Cancer Susceptibility Collaboration (UK); Stratton, MR; Rahman, N; Ban, M; Goris, A; Sawcer, SJ; Compston, A; Conway, D; Jallow, M; Newport, M; Sirugo, G; Rockett, KA; Bumpstead, SJ; Chaney, A; Downes, K; Ghori, MJ; Gwilliam, R; Hunt, SE; Inouye, M; Keniry, A; King, E; McGinnis, R; Potter, S; Ravindrarajah, R; Whittaker, P; Widden, C; Withers, D; Cardin, NJ; Davison, D; Ferreira, T; Pereira-Gale, J; Hallgrimsdo'ttir, IB; Howie, BN; Su, Z; Teo, YY; Vukcevic, D; Bentley, D; Brown, MA; Compston, A; Farrall, M; Hall, AS; Hattersley, AT; Hill, AV; Parkes, M; Pembrey, M; Stratton, MR; Mitchell, SL; Newby, PR; Brand, OJ; Carr-Smith, J; Pearce, SH; McGinnis, R; Keniry, A; Deloukas, P; Reveille, JD; Zhou, X; Sims, AM; Dowling, A; Taylor, J; Doan, T; Davis, JC; Savage, L; Ward, MM; Learch, TL; Weisman, MH; Brown, MJournal 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
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
Aug-2008Physiological interaction between alpha-adducin and WNK1-NEDD4L pathways on sodium-related blood pressure regulation.Manunta, P; Lavery, G; Lanzani, C; Braund, PS; Simonini, M; Bodycote, C; Zagato, L; Delli Carpini S; Tantardini, C; Brioni, E; Bianchi, G; Samani, NJJournal Article