Sfoglia per Rivista  AMERICAN JOURNAL OF HUMAN GENETICS

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Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. 1-gen-2014 Peloso, Gm; Auer, Pl; Bis, Jc; Voorman, A; Morrison, Ac; Stitziel, No; Brody, Ja; Khetarpal, Sa; Crosby, Jr; Fornage, M; Isaacs, A; Jakobsdottir, J; Feitosa, Mf; Davies, G; Huffman, Je; Manichaikul, A; Davis, B; Lohman, K; Joon, Ay; Smith, Av; Grove, Ml; Zanoni, P; Redon, V; Demissie, S; Lawson, K; Peters, U; Carlson, C; Jackson, Rd; Ryckman, Kk; Mackey, Rh; Robinson, Jg; Siscovick, Ds; Schreiner, Pj; Mychaleckyj, Jc; Pankow, Js; Hofman, A; Uitterlinden, Ag; Harris, Tb; Taylor, Kd; Stafford, Jm; Reynolds, Lm; Marioni, Re; Dehghan, A; Franco, Oh; Patel, Ap; Lu, Y; Hindy, G; Gottesman, O; Bottinger, Ep; Melander, O; Orho-Melander, M; Loos, Rj; Duga, S; Merlini, Pa; Farrall, M; Goel, A; Asselta, R; Girelli, D; Martinelli, N; Shah, Sh; Kraus, We; Li, M; Rader, Dj; Reilly, Mp; Mcpherson, R; Watkins, H; Ardissino, D; NHLBI GO Exome Sequencing, Project; Zhang, Q; Wang, J; Tsai, My; Taylor, Ha; Correa, A; Griswold, Me; Lange, La; Starr, Jm; Rudan, I; Eiriksdottir, G; Launer, Lj; Ordovas, Jm; Levy, D; Chen, Yd; Reiner, Ap; Hayward, C; Polasek, O; Deary, Ij; Borecki, Ib; Liu, Y; Gudnason, V; Wilson, Jg; van Duijn, Cm; Kooperberg, C; Rich, Ss; Psaty, Bm; Rotter, Ji; O'Donnell, Cj; Rice, K; Boerwinkle, E; Kathiresan, S; Cupples, La.
Characterization of Large Structural Genetic Mosaicism in Human Autosomes 1-gen-2015 Machiela, Mj; Zhou, Wy; Sampson, Jn; Dean, Mc; Jacobs, Kb; Black, A; Brinton, La; Chang, Is; Chen, C; Chen, C; Chen, Kx; Cook, Ls; Bou, Mc; De Vivo, I; Doherty, J; Friedenreich, Cm; Gaudet, Mm; Haiman, Ca; Hankinson, Se; Hartge, P; Henderson, Be; Hong, Yc; Hosgood, Hd; Hsiung, Ca; Hu, W; Hunter, Dj; Jessop, L; Kim, Hn; Kim, Yh; Kim, Yt; Klein, R; Kraft, P; Lan, Q; Lin, Dx; Liu, Jj; Le Marchand, L; Liang, Xl; Lissowska, J; Lu, Lg; Magliocco, Am; Matsuo, K; Olson, Sh; Orlow, I; Park, Jy; Pooler, L; Prescott, J; Rastogi, R; Risch, Ha; Schumacher, F; Seow, A; Setiawan, Vw; Shen, Hb; Sheng, X; Shin, Mh; Shu, Xo; VanDen Berg, D; Wang, Jc; Wentzensen, N; Wong, Mp; Wu, C; Wu, Tc; Wu, Yl; Xia, L; Yang, Hp; Yang, Pc; Zheng, W; Zhou, Bs; Abnet, Cc; Albanes, D; Aldrich, Mc; Amos, C; Amundadottir, Lt; Berndt, Si; Blot, Wj; Bock, Ch; Bracci, Pm; Burdett, L; Buring, Je; Butler, Ma; Carreon, T; Chatterjee, N; Chung, Cc; Cook, Mb; Cullen, M; Davis, Fg; Ding, T; Duell, Ej; Epstein, Cg; Fan, Jh; Figueroa, Jd; Fraumeni, Jf; Freedman, Nd; Fuchs, Cs; Gao, Yt; Gapstur, Sm; Patino-Garcia, A; Garcia-Closas, M; Gaziano, Jm; Giles, Gg; Gillanders, Em; Giovannucci, El; Goldin, L; Goldstein, Am; Greene, Mh; Hallmans, G; Harris, Cc; Henriksson, R; Holly, Ea; Hoover, Rn; Hu, N; Hutchinson, A; Jenab, M; Johansen, C; Khaw, Kt; Koh, Wp; Kolonel, Ln; Kooperberg, C; Krogh, V; Kurtz, Rc; Lacroix, A; Landgren, A; Landi, Mt; Li, Dh; Liao, Lm; Malats, N; Mcglynn, Ka; Mcneill, Lh; Mcwilliams, Rr; Melin, Bs; Mirabello, L; Peplonska, B; Peters, U; Petersen, Gm; Prokunina-Olsson, L; Purdue, M; Qiao, Yl; Rabe, Kg; Rajaraman, P; Real, Fx; Riboli, E; Rodriguez-Santiago, B; Rothman, N; Ruder, Am; Savage, Sa; Schwartz, Ag; Schwartz, Kl; Sesso, Hd; Severi, G; Silverman, Dt; Spitz, Mr; Stevens, Vl; Stolzenberg-Solomon, R; Stram, D; Tang, Zz; Taylor, Pr; Teras, Lr; Tobias, Gs; Viswanathan, K; Wacholder, S; Wang, Zm; Weinstein, Sj; Wheeler, W; White, E; Wiencke, Jk; Wolpin, Bm; Wu, Xf; Wunder, Js; Yu, K; Zanetti, Ka; Zeleniuch-Jacquotte, A; Ziegler, Rg; De Andrade, M; Barnes, Kc; Beaty, Th; Bierut, Lj; Desch, Kc; Doheny, Kf; Feenstra, B; Ginsburg, D; Heit, Ja; Kang, Jh; Laurie, Ca; Li, Jz; Lowe, Wl; Marazita, Ml; Melbye, M; Mirel, Db; Murray, Jc; Nelson, Sc; Pasquale, Lr; Rice, K; Wiggs, Jl; Wise, A; Tucker, M; Perez-Jurado, La; Laurie, Cc; Caporaso, Ne; Yeager, M; Chanock, Sj
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 1-gen-2009 Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R
Duplications disrupt chromatin architecture and rewire GPR101-enhancer communication in X-linked acrogigantism 1-gen-2022 Franke, Martin; Daly, Adrian F; Palmeira, Leonor; Tirosh, Amit; Stigliano, Antonio; Trifan, Eszter; Faucz, Fabio R; Abboud, Dayana; Petrossians, Patrick; Tena, Juan J; Vitali, Eleonora; Lania, Andrea G; Gómez-Skarmeta, José L; Beckers, Albert; Stratakis, Constantine A; Trivellin, Giampaolo
Family-based association analysis of the critical 3.4 Mb region on 17q24 reveals association between multiple sclerosis and the PRKCA gene 1-gen-2004 Kallio, Sp; Saarela, J; Asselta, R; Chen, Dc; Jokiaho, A; Palotie, A; Peltonen, L
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 1-gen-2009 Asselta, R; Paraboschi, E; Solda, G; Dall’Osso, C; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S
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