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Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants 1-gen-2009 Kathiresan, S.; Voight, B. F.; Purcell, S.; Musunuru, K.; Ardissino, D.; Mannucci, P. M.; Anand, S.; Engert, J. C.; Samani, N. J.; Schunkert, H.; Erdmann, J.; Reilly, M. P.; Rader, D. J.; Morgan, T.; Spertus, J. A.; Stoll, M.; Girelli, D.; Mckeown, P. P.; Patterson, C. C.; Siscovick, D. S.; O'Donnell, C. J.; Elosua, R.; Peltonen, L.; Salomaa, V.; Schwartz, S. M.; Melander, O.; Altshuler, D.; Ardissino, D.; Merlini, P. A.; 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, P. M.; Schwartz, S. M.; Siscovick, D. S.; Yee, J.; Friedlander, Y.; Elosua, R.; Marrugat, J.; Lucas, G.; Subirana, I.; Sala, J.; Ramos, R.; Kathiresan, S.; Meigs, J. B.; Williams, G.; Nathan, D. M.; Macrae, C. A.; O'Donnell, C. J.; Salomaa, V.; Havulinna, A. S.; Peltonen, L.; Melander, O.; Berglund, G.; Voight, B. F.; Kathiresan, S.; Hirschhorn, J. N.; Asselta, R.; Duga, S.; Spreafico, M.; Musunuru, K.; Daly, M. J.; Purcell, S.; Voight, B. F.; Purcell, S.; Nemesh, J.; Korn, J. M.; Mccarroll, S. A.; Schwartz, S. M.; Yee, J.; Kathiresan, S.; Lucas, G.; Subirana, I.; Elosua, R.; Surti, A.; Guiducci, C.; Gianniny, L.; Mirel, D.; Parkin, M.; Burtt, N.; Gabriel, S. B.; Samani, N. J.; Thompson, J. R.; Braund, P. S.; Wright, B. J.; Balmforth, A. J.; Ball, S. G.; Hall, A. S.; Trust Case Control Consortium, Wellcome; Schunkert, H.; Erdmann, J.; Linsel Nitschke, P.; Lieb, W.; Ziegler, A.; König, I.; Hengstenberg, C.; Fischer, M.; Stark, K.; Grosshennig, A.; Preuss, M.; Wichmann, H. E.; Schreiber, S.; Schunkert, H.; Samani, N. J.; Erdmann, J.; Ouwehand, W.; Hengstenberg, C.; Deloukas, P.; Scholz, M.; Cambien, F.; Reilly, M. P.; Li, M.; Chen, Z.; Wilensky, R.; Matthai, W.; Qasim, A.; Hakonarson, H. H.; Devaney, J.; Burnett, M. S.; Pichard, A. D.; Kent, K. M.; Satler, L.; Lindsay, J. M.; Waksman, W. R.; Knouff, C. W.; Waterworth, D. M.; Walker, M. C.; Mooser, V.; Epstein, S. E.; Rader, D. J.; Scheffold, T.; Berger, K.; Stoll, M.; Huge, A.; Girelli, D.; Martinelli, N.; Olivieri, O.; Corrocher, R.; Morgan, T.; Spertus, J. A.; Mckeown, P.; Patterson, C. C.; Schunkert, H.; Erdmann, E.; Linsel Nitschke, P.; Lieb, W.; Ziegler, A.; König, I. R.; Hengstenberg, C.; Fischer, M.; Stark, K.; Grosshennig, A.; Preuss, M.; Wichmann, H. E.; Schreiber, S.; Hólm, H.; Thorleifsson, G.; Thorsteinsdottir, U.; Stefansson, K.; Engert, J. C.; Do, R.; Xie, C.; Anand, S.; Kathiresan, S.; Ardissino, D.; Mannucci, P. M.; Siscovick, D.; O'Donnell, C. J.; Samani, N. J.; Melander, O.; Elosua, R.; Peltonen, L.; Salomaa, V.; Schwartz, S. M.; Altshuler, D.
Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3 1-gen-2011 Purdue, Mp; Johansson, M; Zelenika, D; Toro, Jr; Scelo, G; Moore, Le; Prokhortchouk, E; Wu, Xf; Kiemeney, La; Gaborieau, V; Jacobs, Kb; Chow, Wh; Zaridze, D; Matveev, V; Lubinski, J; Trubicka, J; Szeszenia-Dabrowska, N; Lissowska, J; Rudnai, P; Fabianova, E; Bucur, A; Bencko, V; Foretova, L; Janout, V; Boffetta, P; Colt, Js; Davis, Fg; Schwartz, Kl; Banks, Re; Selby, Pj; Harnden, P; Berg, Cd; Hsing, Aw; Grubb, Rl; Boeing, H; Vineis, P; Clavel-Chapelon, F; Palli, D; Tumino, R; Krogh, V; Panico, S; Duell, Ej; Quiros, Jr; Sanchez, Mj; Navarro, C; Ardanaz, E; Dorronsoro, M; Khaw, Kt; Allen, Ne; Bueno-De-Mesquita, Hb; Peeters, Phm; Trichopoulos, D; Linseisen, J; Ljungberg, B; Overvad, K; Tjonneland, A; Romieu, I; Riboli, E; Mukeria, A; Shangina, O; Stevens, Vl; Thun, Mj; Diver, Wr; Gapstur, Sm; Pharoah, Pd; Easton, Df; Albanes, D; Weinstein, Sj; Virtamo, J; Vatten, L; Hveem, K; Njolstad, I; Tell, Gs; Stoltenberg, C; Kumar, R; Koppova, K; Cussenot, O; Benhamou, S; Oosterwijk, E; Vermeulen, Sh; Aben, Kkh; van der Marel, Sl; Ye, Yq; Wood, Cg; Pu, X; Mazur, Am; Boulygina, Es; Chekanov, Nn; Foglio, M; Lechner, D; Gut, I; Heath, S; Blanche, H; Hutchinson, A; Thomas, G; Wang, Zm; Yeager, M; Fraumeni, Jf; Skryabin, Kg; Mckay, Jd; Rothman, N; Chanock, Sj; Lathrop, M; Brennan, P
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis 1-gen-2010 Liu, X; Invernizzi, P; Lu, Yue; Kosoy, R; Lu, Yan; Bianchi, I; Podda, M; Xu, C; Xie, G; Macciardi, F; Selmi, C; Lupoli, S; Shigeta, R; Ransom, M; LLEO De Nalda, A; Lee, At; Mason, Al; Myers, Rp; Peltekian, Km; Ghent, Cn; Bernuzzi, F; Zuin, M; Icpbcg, ; Gregersen, Pk; Heathcote, Ej; Hirschfield, Gm; Siminovitch, Ka; Amos, Ci; Gershwin, Me; Seldin, Mf
Identification of a new prostate cancer susceptibility locus on chromosome 8q24 1-gen-2009 Yeager, M; Chatterjee, N; Ciampa, J; Jacobs, Kb; Gonzalez-Bosquet, J; Hayes, Rb; Kraft, P; Wacholder, S; Orr, N; Berndt, S; Yu, K; Hutchinson, A; Wang, Zm; Amundadottir, L; Feigelson, Hs; Thun, Mj; Diver, Wr; Albanes, D; Virtamo, J; Weinstein, S; Schumacher, Fr; Cancel-Tassin, G; Cussenot, O; Valeri, A; Andriole, Gl; Crawford, Ed; Haiman, Ca; Henderson, B; Kolonel, L; Le Marchand, L; Siddiq, A; Riboli, E; Key, Tj; Kaaks, R; Isaacs, W; Isaacs, S; Wiley, Ke; Gronberg, H; Wiklund, F; Stattin, P; Xu, Jf; Zheng, Sl; Sun, Jl; Vatten, Lj; Hveem, K; Kumle, M; Tucker, M; Gerhard, Ds; Hoover, Rn; Fraumeni, Jf; Hunter, Dj; Thomas, G; Chanock, Sj
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 1-gen-2022 Marasca, Federica; Sinha, Shruti; Vadalà, Rebecca; Polimeni, Benedetto; Ranzani, Valeria; Paraboschi, Elvezia Maria; Burattin, Filippo Vittorio; Ghilotti, Marco; Crosti, Mariacristina; Negri, Maria Luce; Campagnoli, Susanna; Notarbartolo, Samuele; Sartore-Bianchi, Andrea; Siena, Salvatore; Prati, Daniele; Montini, Giovanni; Viale, Giuseppe; Torre, Olga; Harari, Sergio; Grifantini, Renata; Soldà, Giulia; Biffo, Stefano; Abrignani, Sergio; Bodega, Beatrice
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (vol 46, pg 736, 2014) 1-gen-2017 Wang, Y; Mckay, Jd; Rafnar, T; Wang, Zm; Timofeeva, Mn; Broderick, P; Zong, Xc; Laplana, M; Wei, Y; Han, Y; Lloyd, A; Delahaye-Sourdeix, M; Chubb, D; Gaborieau, V; Wheeler, W; Chatterjee, N; Thorleifsson, G; Sulem, P; Liu, G; Kaaks, R; Henrion, M; Kinnersley, B; Vallee, M; Calvez-Kelm, Fl; Stevens, Vl; Gapstur, Sm; Chen, Wv; Zaridze, D; Szeszenia-Dabrowska, N; Lissowska, J; Rudnai, P; Fabianova, E; Mates, D; Bencko, V; Foretova, L; Janout, V; Krokan, He; Gabrielsen, Me; Skorpen, F; Vatten, L; Njolstad, I; Chen, C; Goodman, G; Benhamou, S; Vooder, T; Valk, K; Nelis, M; Metspalu, A; Lener, M; Lubinski, J; Johansson, M; Vineis, P; Agudo, A; Clavel-Chapelon, F; Bueno-De-Mesquita, Hb; Trichopoulos, D; Khaw, Kt; Johansson, M; Weiderpass, E; Tjonneland, A; Riboli, E; Lathrop, M; Scelo, G; Albanes, D; Caporaso, Ne; Ye, Yq; Gu, J; Wu, Xf; Spitz, Mr; Dienemann, H; Rosenberger, A; Su, L; Matakidou, A; Eisen, T; Stefansson, K; Risch, A; Chanock, Sj; Christiani, Dc; Hung, Rj; Brennan, P; Landi, Mt; Houlston, Rs; Amos, Ci
Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study 1-gen-2011 Kote-Jarai, Z; Al Olama, Aa; Giles, Gg; Severi, G; Schleutker, J; Weischer, M; Campa, D; Riboli, E; Key, T; Gronberg, H; Hunter, Dj; Kraft, P; Thun, Mj; Ingles, S; Chanock, S; Albanes, D; Hayes, Rb; Neal, De; Hamdy, Fc; Donovan, Jl; Pharoah, P; Schumacher, F; Henderson, Be; Stanford, Jl; Ostrander, Ea; Sorensen, Kd; Dork, T; Andriole, G; Dickinson, Jl; Cybulski, C; Lubinski, J; Spurdle, A; Clements, Ja; Chambers, S; Aitken, J; Gardiner, Raf; Thibodeau, Sn; Schaid, D; John, Em; Maier, C; Vogel, W; Cooney, Ka; Park, Jy; Cannon-Albright, L; Brenner, H; Habuchi, T; Zhang, Hw; Lu, Yj; Kaneva, R; Muir, K; Benlloch, S; Leongamornlert, Da; Saunders, Ej; Tymrakiewicz, M; Mahmud, N; Guy, M; O'Brien, Lt; Wilkinson, Ra; Hall, Al; Sawyer, Ej; Dadaev, T; Morrison, J; Dearnaley, Dp; Horwich, A; Huddart, Ra; Khoo, Vs; Parker, Cc; Van As, N; Woodhouse, Cj; Thompson, A; Christmas, T; Ogden, C; Cooper, Cs; Lophatonanon, A; Southey, Mc; Hopper, Jl; English, Dr; Wahlfors, T; Tammela, Tlj; Klarskov, P; Nordestgaard, Bg; Roder, Ma; Tybjaerg-Hansen, A; Bojesen, Se; Travis, R; Canzian, F; Kaaks, R; Wiklund, F; Aly, M; Lindstrom, S; Diver, Wr; Gapstur, S; Stern, Mc; Corral, R; Virtamo, J; Cox, A; Haiman, Ca; Le Marchand, L; Fitzgerald, L; Kolb, S; Kwon, Em; Karyadi, Dm; Orntoft, Tf; Borre, M; Meyer, A; Serth, J; Yeager, M; Berndt, Si; Marthick, Jr; Patterson, B; Wokolorczyk, D; Batra, J; Lose, F; Mcdonnell, Sk; Joshi, Ad; Shahabi, A; Rinckleb, Ae; Ray, A; Sellers, Ta; Lin, Hy; Stephenson, Ra; Farnham, J; Muller, H; Rothenbacher, D; Tsuchiya, N; Narita, S; Cao, Gw; Slavov, C; Mitev, V; Easton, Df; Eeles, Ra
A specific missense mutation in GTF2I occurs at high frequency in thymic epithelial tumors 1-gen-2014 Petrini, Iacopo; Meltzer, Paul S; Kim, In-Kyu; Lucchi, Marco; Park, Kang-Seo; Fontanini, Gabriella; Gao, James; Zucali, Paolo A; Calabrese, Fiorella; Favaretto, Adolfo; Rea, Federico; Rodriguez-Canales, Jaime; Walker, Robert L; Pineda, Marbin; Zhu, Yuelin J; Lau, Christopher; Killian, Keith J; Bilke, Sven; Voeller, Donna; Dakshanamurthy, Sivanesan; Wang, Yisong; Giaccone, Giuseppe
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