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First PublishedTitleAuthor(s)Type
Nov-2010Genetic variants influencing circulating lipid levels and risk of coronary artery disease.Waterworth, DM; Ricketts, SL; Song, K; Chen, L; Zhao, JH; Ripatti, S; Aulchenko, YS; Zhang, W; Yuan, X; Lim, N; Luan, J; Ashford, S; Wheeler, E; Young, EH; Hadley, D; Thompson, JR; Braund, PS; Johnson, T; Struchalin, M; Surakka, I; Luben, R; Khaw, KT; Rodwell, SA; Loos, RJ; Boekholdt, SM; Inouye, M; Deloukas, P; Elliott, P; Schlessinger, D; Sanna, S; Scuteri, A; Jackson, A; Mohlke, KL; Tuomilehto, J; Roberts, R; Stewart, A; Kesäniemi, YA; Mahley, RW; Grundy, SM; Wellcome Trust Case Control Consortium; McArdle, W; Cardon, L; Waeber, G; Vollenweider, P; Chambers, JC; Boehnke, M; Abecasis, GR; Salomaa, V; Järvelin, MR; Ruokonen, A; Barroso, I; Epstein, SE; Hakonarson, HH; Rader, DJ; Reilly, MP; Witteman, JC; Hall, AS; Samani, NJ; Strachan, DP; Barter, P; van Duijn CM; Kooner, JS; Peltonen, L; Wareham, NJ; McPherson, R; Mooser, V; Sandhu, MSJournal 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
1-Apr-2010Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.Wellcome Trust Case Control Consortium; Craddock, N; Hurles, ME; Cardin, N; Pearson, RD; Plagnol, V; Robson, S; Vukcevic, D; Barnes, C; Conrad, DF; Giannoulatou, E; Holmes, C; Marchini, JL; Stirrups, K; Tobin, MD; Wain, LV; Yau, C; Aerts, J; Ahmad, T; Andrews, TD; Arbury, H; Attwood, A; Auton, A; Ball, SG; Balmforth, AJ; Barrett, JC; Barroso, I; Barton, A; Bennett, AJ; Bhaskar, S; Blaszczyk, K; Bowes, J; Brand, OJ; Braund, PS; Bredin, F; Breen, G; Brown, MJ; Bruce, IN; Bull, J; Burren, OS; Burton, J; Byrnes, J; Caesar, S; Clee, CM; Coffey, AJ; Connell, JM; Cooper, JD; Dominiczak, AF; Downes, K; Drummond, HE; Dudakia, D; Dunham, A; Ebbs, B; Eccles, D; Edkins, S; Edwards, C; Elliot, A; Emery, P; Evans, DM; Evans, G; Eyre, S; Farmer, A; Ferrier, IN; Feuk, L; Fitzgerald, T; Flynn, E; Forbes, A; Forty, L; Franklyn, JA; Freathy, RM; Gibbs, P; Gilbert, P; Gokumen, O; Gordon-Smith, K; Gray, E; Green, E; Groves, CJ; Grozeva, D; Gwilliam, R; Hall, A; Hammond, N; Hardy, M; Harrison, P; Hassanali, N; Hebaishi, H; Hines, S; Hinks, A; Hitman, GA; Hocking, L; Howard, E; Howard, P; Howson, JM; Hughes, D; Hunt, S; Isaacs, JD; Jain, M; Jewell, DP; Johnson, T; Jolley, JD; Jones, IR; Jones, LA; Kirov, G; Langford, CF; Lango-Allen, H; Lathrop, GM; Lee, J; Lee, KL; Lees, C; Lewis, K; Lindgren, CM; Maisuria-Armer, M; Maller, J; Mansfield, J; Martin, P; Massey, DC; McArdle, WL; McGuffin, P; McLay, KE; Mentzer, A; Mimmack, ML; Morgan, AE; Morris, AP; Mowat, C; Myers, S; Newman, W; Nimmo, ER; O'Donovan, MC; Onipinla, A; Onyiah, I; Ovington, NR; Owen, MJ; Palin, K; Parnell, K; Pernet, D; Perry, JR; Phillips, A; Pinto, D; Prescott, NJ; Prokopenko, I; Quail, MA; Rafelt, S; Rayner, NW; Redon, R; Reid, DM; Renwick; Ring, SM; Robertson, N; Russell, E; St Clair D; Sambrook, JG; Sanderson, JD; Schuilenburg, H; Scott, CE; Scott, R; Seal, S; Shaw-Hawkins, S; Shields, BM; Simmonds, MJ; Smyth, DJ; Somaskantharajah, E; Spanova, K; Steer, S; Stephens, J; Stevens, HE; Stone, MA; Su, Z; Symmons, DP; Thompson, JR; Thomson, W; Travers, ME; Turnbull, C; Valsesia, A; Walker, M; Walker, NM; Wallace, C; Warren-Perry, M; Watkins, NA; Webster, J; Weedon, MN; Wilson, AG; Woodburn, M; Wordsworth, BP; Young, AH; Zeggini, E; Carter, NP; Frayling, TM; Lee, C; McVean, G; Munroe, PB; Palotie, A; Sawcer, SJ; Scherer, SW; Strachan, DP; Tyler-Smith, C; Brown, MA; Burton, PR; Caulfield, MJ; Compston, A; Farrall, M; Gough, SC; Hall, AS; Hattersley, AT; Hill, AV; Mathew, CG; Pembrey, M; Satsangi, J; Stratton, MR; Worthington, J; Deloukas, P; Duncanson, A; Kwiatkowski, DP; McCarthy, MI; Ouwehand, W; Parkes, M; Rahman, N; Todd, JA; Samani, NJ; Donnelly, PJournal 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
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
6-Oct-2011Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.International Consortium for Blood Pressure Genome-Wide Association Studies; Ehret, GB; Munroe, PB; Rice, KM; Bochud, M; Johnson, AD; Chasman, DI; Smith, AV; Tobin, MD; Verwoert, GC; Hwang, SJ; Pihur, V; Vollenweider, P; O'Reilly, PF; Amin, N; Bragg-Gresham, JL; Teumer, A; Glazer, NL; Launer, L; Zhao, JH; Aulchenko, Y; Heath, S; Sõber, S; Parsa, A; Luan, J; Arora, P; Dehghan, A; Zhang, F; Lucas, G; Hicks, AA; Jackson, AU; Peden, JF; Tanaka, T; Wild, SH; Rudan, I; Igl, W; Milaneschi, Y; Parker, AN; Fava, C; Chambers, JC; Fox, ER; Kumari, M; Go, MJ; van der Harst P; Kao, WH; Sjögren, M; Vinay, DG; Alexander, M; Tabara, Y; Shaw-Hawkins, S; Whincup, PH; Liu, Y; Shi, G; Kuusisto, J; Tayo, B; Seielstad, M; Sim, X; Nguyen, KD; Lehtimäki, T; Matullo, G; Wu, Y; Gaunt, TR; Onland-Moret, NC; Cooper, MN; Platou, CG; Org, E; Hardy, R; Dahgam, S; Palmen, J; Vitart, V; Braund, PS; Kuznetsova, T; Uiterwaal, CS; Adeyemo, A; Palmas, W; Campbell, H; Ludwig, B; Tomaszewski, M; Tzoulaki, I; Palmer, ND; CARDIoGRAM, consortium; CKDGen, Consortium; KidneyGen, Consortium; EchoGen, consortium; CHARGE-HF, consortium; Aspelund, T; Garcia, M; Chang, YP; O'Connell, JR; Steinle, NI; Grobbee, DE; Arking, DE; Kardia, SL; Morrison, AC; Hernandez, D; Najjar, S; McArdle, WL; Hadley, D; Brown, MJ; Connell, JM; Hingorani, AD; Day, IN; Lawlor, DA; Beilby, JP; Lawrence, RW; Clarke, R; Hopewell, JC; Ongen, H; Dreisbach, AW; Li, Y; Young, JH; Bis, JC; Kähönen, M; Viikari, J; Adair, LS; Lee, NR; Chen, MH; Olden, M; Pattaro, C; Bolton, JA; Köttgen, A; Bergmann, S; Mooser, V; Chaturvedi, N; Frayling, TM; Islam, M; Jafar, TH; Erdmann, J; Kulkarni, SR; Bornstein, SR; Grässler, J; Groop, L; Voight, BF; Kettunen, J; Howard, P; Taylor, A; Guarrera, S; Ricceri, F; Emilsson, V; Plump, A; Barroso, I; Khaw, KT; Weder, AB; Hunt, SC; Sun, YV; Bergman, RN; Collins, FS; Bonnycastle, LL; Scott, LJ; Stringham, HM; Peltonen, L; Perola, M; Vartiainen, E; Brand, SM; Staessen, JA; Wang, TJ; Burton, PR; Soler Artigas M; Dong, Y; Snieder, H; Wang, X; Zhu, H; Lohman, KK; Rudock, ME; Heckbert, SR; Smith, NL; Wiggins, KL; Doumatey, A; Shriner, D; Veldre, G; Viigimaa, M; Kinra, S; Prabhakaran, D; Tripathy, V; Langefeld, CD; Rosengren, A; Thelle, DS; Corsi, AM; Singleton, A; Forrester, T; Hilton, G; McKenzie, CA; Salako, T; Iwai, N; Kita, Y; Ogihara, T; Ohkubo, T; Okamura, T; Ueshima, H; Umemura, S; Eyheramendy, S; Meitinger, T; Wichmann, HE; Cho, YS; Kim, HL; Lee, JY; Scott, J; Sehmi, JS; Zhang, W; Hedblad, B; Nilsson, P; Smith, GD; Wong, A; Narisu, N; Stančáková, A; Raffel, LJ; Yao, J; Kathiresan, S; O'Donnell, CJ; Schwartz, SM; Ikram, MA; Longstreth, WT; Mosley, TH; Seshadri, S; Shrine, NR; Wain, LV; Morken, MA; Swift, AJ; Laitinen, J; Prokopenko, I; Zitting, P; Cooper, JA; Humphries, SE; Danesh, J; Rasheed, A; Goel, A; Hamsten, A; Watkins, H; Bakker, SJ; van Gilst WH; Janipalli, CS; Mani, KR; Yajnik, CS; Hofman, A; Mattace-Raso, FU; Oostra, BA; Demirkan, A; Isaacs, A; Rivadeneira, F; Lakatta, EG; Orru, M; Scuteri, A; Ala-Korpela, M; Kangas, AJ; Lyytikäinen, LP; Soininen, P; Tukiainen, T; Würtz, P; Ong, RT; Dörr, M; Kroemer, HK; Völker, U; Völzke, H; Galan, P; Hercberg, S; Lathrop, M; Zelenika, D; Deloukas, P; Mangino, M; Spector, TD; Zhai, G; Meschia, JF; Nalls, MA; Sharma, P; Terzic, J; Kumar, MV; Denniff, M; Zukowska-Szczechowska, E; Wagenknecht, LE; Fowkes, FG; Charchar, FJ; Schwarz, PE; Hayward, C; Guo, X; Rotimi, C; Bots, ML; Brand, E; Samani, NJ; Polasek, O; Talmud, PJ; Nyberg, F; Kuh, D; Laan, M; Hveem, K; Palmer, LJ; van der Schouw YT; Casas, JP; Mohlke, KL; Vineis, P; Raitakari, O; Ganesh, SK; Wong, TY; Tai, ES; Cooper, RS; Laakso, M; Rao, DC; Harris, TB; Morris, RW; Dominiczak, AF; Kivimaki, M; Marmot, MG; Miki, T; Saleheen, D; Chandak, GR; Coresh, J; Navis, G; Salomaa, V; Han, BG; Zhu, X; Kooner, JS; Melander, O; Ridker, PM; Bandinelli, S; Gyllensten, UB; Wright, AF; Wilson, JF; Ferrucci, L; Farrall, M; Tuomilehto, J; Pramstaller, PP; Elosua, R; Soranzo, N; Sijbrands, EJ; Altshuler, D; Loos, RJ; Shuldiner, AR; Gieger, C; Meneton, P; Uitterlinden, AG; Wareham, NJ; Gudnason, V; Rotter, JI; Rettig, R; Uda, M; Strachan, DP; Witteman, JC; Hartikainen, AL; Beckmann, JS; Boerwinkle, E; Vasan, RS; Boehnke, M; Larson, MG; Järvelin, MR; Psaty, BM; Abecasis, GR; Chakravarti, A; Elliott, P; van Duijn CM; Newton-Cheh, C; Levy, D; Caulfield, MJ; Johnson, TJournal Article
Apr-2011Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.Schunkert, H; König, IR; Kathiresan, S; Reilly, MP; Assimes, TL; Holm, H; Preuss, M; Stewart, AF; Barbalic, M; Gieger, C; Absher, D; Aherrahrou, Z; Allayee, H; Altshuler, D; Anand, SS; Andersen, K; Anderson, JL; Ardissino, D; Ball, SG; Balmforth, AJ; Barnes, TA; Becker, DM; Becker, LC; Berger, K; Bis, JC; Boekholdt, SM; Boerwinkle, E; Braund, PS; Brown, MJ; Burnett, MS; Buysschaert, I; Cardiogenics; Carlquist, JF; Chen, L; Cichon, S; Codd, V; Davies, RW; Dedoussis, G; Dehghan, A; Demissie, S; Devaney, JM; Diemert, P; Do, R; Doering, A; Eifert, S; Mokhtari, NE; Ellis, SG; Elosua, R; Engert, JC; Epstein, SE; de Faire U; Fischer, M; Folsom, AR; Freyer, J; Gigante, B; Girelli, D; Gretarsdottir, S; Gudnason, V; Gulcher, JR; Halperin, E; Hammond, N; Hazen, SL; Hofman, A; Horne, BD; Illig, T; Iribarren, C; Jones, GT; Jukema, JW; Kaiser, MA; Kaplan, LM; Kastelein, JJ; Khaw, KT; Knowles, JW; Kolovou, G; Kong, A; Laaksonen, R; Lambrechts, D; Leander, K; Lettre, G; Li, M; Lieb, W; Loley, C; Lotery, AJ; Mannucci, PM; Maouche, S; Martinelli, N; McKeown, PP; Meisinger, C; Meitinger, T; Melander, O; Merlini, PA; Mooser, V; Morgan, T; Mühleisen, TW; Muhlestein, JB; Münzel, T; Musunuru, K; Nahrstaedt, J; Nelson, CP; Nöthen, MM; Olivieri, O; Patel, RS; Patterson, CC; Peters, A; Peyvandi, F; Qu, L; Quyyumi, AA; Rader, DJ; Rallidis, LS; Rice, C; Rosendaal, FR; Rubin, D; Salomaa, V; Sampietro, ML; Sandhu, MS; Schadt, E; Schäfer, A; Schillert, A; Schreiber, S; Schrezenmeir, J; Schwartz, SM; Siscovick, DS; Sivananthan, M; Sivapalaratnam, S; Smith, A; Smith, TB; Snoep, JD; Soranzo, N; Spertus, JA; Stark, K; Stirrups, K; Stoll, M; Tang, WH; Tennstedt, S; Thorgeirsson, G; Thorleifsson, G; Tomaszewski, M; Uitterlinden, AG; van Rij AM; Voight, BF; Wareham, NJ; Wells, GA; Wichmann, HE; Wild, PS; Willenborg, C; Witteman, JC; Wright, BJ; Ye, S; Zeller, T; Ziegler, A; Cambien, F; Goodall, AH; Cupples, LA; Quertermous, T; März, W; Hengstenberg, C; Blankenberg, S; Ouwehand, WH; Hall, AS; Deloukas, P; Thompson, JR; Stefansson, K; Roberts, R; Thorsteinsdottir, U; O'Donnell, CJ; McPherson, R; Erdmann, J; CARDIoGRAM, Consortium; Samani, NJJournal Article
24-Mar-2016Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary DiseaseMyocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators; Stitziel, NO; Stirrups, KE; Masca, NGD; Erdmann, J; Ferrario, PG; König, IR; Weeke, PE; Webb, TR; Auer, PL; Schick, UM; Lu, Y; Zhang, H; Dube, M-P; Goel, A; Farrall, M; Peloso, GM; Won, H-H; Do, R; van Iperen, E; Kanoni, S; Kruppa, J; Mahajan, A; Scott, RA; Willenberg, C; Braund, PS; van Capelleveen, JC; Doney, ASF; Donnelly, LA; Asselta, R; Merlini, PA; Duga, S; Marziliano, N; Denny, JC; Shaffer, CM; El-Mokhtari, NE; Franke, A; Gottesman, O; Heilmann, S; Hengstenberg, C; Hoffman, P; Holmen, OL; Hveem, K; Jansson, J-H; Jöckel, K-H; Kessler, T; Kriebel, J; Laugwitz, KL; Marouli, E; Martinelli, N; McCarthy, MI; Van Zuydam, NR; Meisinger, C; Esko, T; Mihailov, E; Escher, SA; Alver, M; Moebus, S; Morris, AD; Müller-Nurasyid, M; Nikpay, M; Olivieri, O; Lemieux Perreault, L-P; AlQarawi, A; Robertson, NR; Akinsanya, KO; Reilly, DF; Vogt, TF; Yin, W; Asselbergs, FW; Kooperberg, C; Jackson, RD; Stahl, E; Strauch, K; Varga, TV; Waldenberger, M; Zeng, L; Kraja, AT; Liu, C; Ehret, GB; Newton-Cheh, C; Chasman, DI; Chowdhury, R; Ferrario, M; Ford, I; Jukema, JW; Kee, F; Kuulasmaa, K; Nordestgaard, BG; Perola, M; Saleheen, D; Sattar, N; Surendran, P; Tregouet, D; Young, R; Howson, JMM; Butterworth, AS; Danesh, J; Ardissino, D; Bottinger, EP; Erbel, R; Franks, PW; Girelli, D; Hall, AS; Hovingh, GK; Kastrati, A; Lieb, W; Meitinger, T; Kraus, WE; Shah, SH; McPherson, R; Orho-Melander, M; Melander, O; Metspalu, A; Palmer, CNA; Peters, A; Rader, D; Reilly, MP; Loos, RJF; Reiner, AP; Roden, DM; Tardif, J-C; Thompson, JR; Wareham, NJ; Watkins, H; Willer, CJ; Kathiresan, S; Deloukas, P; Samani, NJ; Schunkert, HJournal Article
27-Jul-2016Analysis with the exome array identifies multiple new independent variants in lipid loci.Kanoni, S; Masca, NGD; Stirrups, KE; Varga, TV; Warren, HR; Scott, RA; Southam, L; Zhang, W; Yaghootkar, H; Müller-Nurasyid, M; Couto Alves, A; Strawbridge, RJ; Lataniotis, L; An Hashim, N; Besse, C; Boland, A; Braund, PS; Connell, JM; Dominiczak, A; Farmaki, A-E; Franks, S; Grallert, H; Jansson, J-H; Karaleftheri, M; Keinänen-Kiukaanniemi, S; Matchan, A; Pasko, D; Peters, A; Poulter, N; Rayner, NW; Renström, F; Rolandsson, O; Sabater-Lleal, M; Sennblad, B; Sever, P; Shields, D; Silveira, A; Stanton, AV; Strauch, K; Tomaszewski, M; Tsafantakis, E; Waldenberger, M; Blakemore, AIF; Dedoussis, G; Escher, SA; Kooner, JS; McCarthy, MI; Palmer, CNA; Wellcome Trust Case Control Consortium; Hamsten, A; Caulfield, MJ; Frayling, TM; Tobin, MD; Jarvelin, M-R; Zeggini, E; Gieger, C; Chambers, JC; Wareham, NJ; Munroe, PB; Franks, PW; Samani, NJ; Deloukas, PJournal Article