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A conserved sorting-associated protein is mutant in chorea-acanthocytosis RID C-2505-2009 RID A-4495-2010 1-gen-2001 Rampoldi, L; Dobson-Stone, C; Rubio, Jp; Danek, A; Chalmers, Rm; Wood, Nw; Verellen, C; Ferrer, X; Malandrini, A; Fabrizi, Gm; Brown, R; Vance, J; Pericak-Vance, M; Rudolf, G; Carre, S; Alonso, E; Manfredi, M; Nemeth, Ah; Monaco, Ap
A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis 1-gen-2006 Witt, H; SAHIN TOTH, M; Landt, O; Chen, Jm; Kahne, T; Drenth, Jp; Kukor, Z; Szepessy, E; Halangk, W; Dahm, S; Rohde, K; Schulz, Hu; LE MARECHAL, C; Akar, N; Ammann, Rw; Truninger, K; Bargetzi, M; Bhatia, E; Castellani, C; Cavestro, GIULIA MARTINA; Cerny, M; DESTRO BISOL, G; Spedini, G; Eiberg, H; Jansen, Jb; Koudova, M; Rausova, E; MACEK M., Jr; Malats, N; Real, Fx; Menzel, Hj; Moral, P; Galavotti, R; Pignatti, Pf; Rickards, O; Spicak, J; Zarnescu, No; Bock, W; Gress, Tm; Friess, H; Ockenga, J; Schmidt, H; Pfutzer, R; Lohr, M; Simon, P; Weiss, Fu; Lerch, Mm; Teich, N; Keim, V; Berg, T; Wiedenmann, B; Luck, W; Groneberg, Da; Becker, M; Keil, T; Kage, A; Bernardova, J; Braun, M; Guldner, C; Halangk, J; Rosendahl, J; Witt, U; Treiber, M; Nickel, R; Ferec, C.
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 1-gen-2013 International Multiple Sclerosis Genetics, Consortium; Beecham, Ah; Patsopoulos, Na; Xifara, Dk; Davis, Mf; Kemppinen, A; Cotsapas, C; Shah, Ts; Spencer, C; Booth, D; Goris, A; Oturai, A; Saarela, J; Fontaine, B; Hemmer, B; Martin, C; Zipp, F; D'Alfonso, S; Martinelli Boneschi, F; Taylor, B; Harbo, Hf; Kockum, I; Hillert, J; Olsson, T; Ban, M; Oksenberg, Jr; Hintzen, R; Barcellos, Lf; Wellcome Trust Case Control Consortium, 2; International IBD Genetics, Consortium; Agliardi, C; Alfredsson, L; Alizadeh, M; Anderson, C; Andrews, R; Søndergaard, Hb; Baker, A; Band, G; Baranzini, Se; Barizzone, N; Barrett, J; Bellenguez, C; Bergamaschi, L; Bernardinelli, L; Berthele, A; Biberacher, V; Binder, Tm; Blackburn, H; Bomfim, Il; Brambilla, P; Broadley, S; Brochet, B; Brundin, L; Buck, D; Butzkueven, H; Caillier, Sj; Camu, W; Carpentier, W; Cavalla, P; Celius, Eg; Coman, I; Comi, Giancarlo; Corrado, L; Cosemans, L; Cournu Rebeix, I; Cree, Ba; Cusi, D; Damotte, V; Defer, G; Delgado, Sr; Deloukas, P; di Sapio, A; Dilthey, At; Donnelly, P; Dubois, B; Duddy, M; Edkins, S; Elovaara, I; Esposito, F; Evangelou, N; Fiddes, B; Field, J; Franke, A; Freeman, C; Frohlich, Iy; Galimberti, D; Gieger, C; Gourraud, Pa; Graetz, C; Graham, A; Grummel, V; Guaschino, C; Hadjixenofontos, A; Hakonarson, H; Halfpenny, C; Hall, G; Hall, P; Hamsten, A; Harley, J; Harrower, T; Hawkins, C; Hellenthal, G; Hillier, C; Hobart, J; Hoshi, M; Hunt, Se; Jagodic, M; Jelčić, I; Jochim, A; Kendall, B; Kermode, A; Kilpatrick, T; Koivisto, K; Konidari, I; Korn, T; Kronsbein, H; Langford, C; Larsson, M; Lathrop, M; Lebrun Frenay, C; Lechner Scott, J; Lee, Mh; Leone, Ma; Leppä, V; Liberatore, G; Lie, Ba; Lill, Cm; Lindén, M; Link, J; Luessi, F; Lycke, J; Macciardi, F; Männistö, S; Manrique, Cp; Martin, R; Martinelli, V; Mason, D; Mazibrada, G; Mccabe, C; Mero, Il; Mescheriakova, J; Moutsianas, L; Myhr, Km; Nagels, G; Nicholas, R; Nilsson, P; Piehl, F; Pirinen, M; Price, Se; Quach, H; Reunanen, M; Robberecht, W; Robertson, Np; Rodegher, M; Rog, D; Salvetti, M; Schnetz Boutaud, Nc; Sellebjerg, F; Selter, Rc; Schaefer, C; Shaunak, S; Shen, L; Shields, S; Siffrin, V; Slee, M; Sorensen, Ps; Sorosina, M; Sospedra, M; Spurkland, A; Strange, A; Sundqvist, E; Thijs, V; Thorpe, J; Ticca, A; Tienari, P; van Duijn, C; Visser, Em; Vucic, S; Westerlind, H; Wiley, Js; Wilkins, A; Wilson, Jf; Winkelmann, J; Zajicek, J; Zindler, E; Haines, Jl; Pericak Vance, Ma; Ivinson, Aj; Stewart, G; Hafler, D; Hauser, Sl; Compston, A; Mcvean, G; De Jager, P; Sawcer, Sj; Mccauley, J. L.
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis 1-gen-2012 Stahl, ; Ea, Wegmann; D, Trynka; G, Gutierrez achury; J, Do; R, Voight; Bf, Kraft; P, Che; R, Kallberg; H, ; Kurreeman, F; Diabetes Genetics Replication And Meta analysis Consortium: Myocardial Infarction Genetics, Consortium; Casari, GIORGIO NEVIO; Kathiresan, ; S, ; Wijmenga, C; Gregersen, Pk; Alfredsson, L; Siminovitch, Ka; Worthington, J; De Bakker, Pi; Raychaudhuri, S; Plenge, Rm
BMP6 orchestrates iron metabolism 1-gen-2009 Camaschella, Clara
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 1-gen-2000 Bolino, A; Muglia, M; Conforti, Fl; Leguern, E; Salih, Mam; Georgiou, Dm; Christodoulou, K; Hausmanowa-Petrusewicz, I; Mandich, P; Schenone, A; Gambardella, A; Bono, F; Quattrone, A; Devoto, M; Monaco, Ap
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. 1-gen-2015 Childs, Ej; Mocci, E; Campa, D; Bracci, Pm; Gallinger, S; Goggins, M; Li, D; Neale, Re; Olson, Sh; Scelo, G; Amundadottir, Lt; Bamlet, Wr; Bijlsma, Mf; Blackford, A; Borges, M; Brennan, P; Brenner, H; Bueno de Mesquita, Hb; Canzian, F; Capurso, G; Cavestro, GIULIA MARTINA; Chaffee, Kg; Chanock, Sj; Cleary, Sp; Cotterchio, M; Foretova, L; Fuchs, C; Funel, N; Gazouli, M; Hassan, M; Herman, Jm; Holcatova, I; Holly, Ea; Hoover, Rn; Hung, Rj; Janout, V; Key, Tj; Kupcinskas, J; Kurtz, Rc; Landi, S; Lu, L; Malecka Panas, E; Mambrini, A; Mohelnikova Duchonova, B; Neoptolemos, Jp; Oberg, Al; Orlow, I; Pasquali, C; Pezzilli, R; Rizzato, C; Saldia, A; Scarpa, A; Stolzenberg Solomon, Rz; Strobel, O; Tavano, F; Vashist, Yk; Vodicka, P; Wolpin, Bm; Yu, H; Petersen, Gm; Risch, Ha; Klein, A. P.
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood 1-gen-2012 Heinzen, El; Swoboda, Kj; Hitomi, Y; Gurrieri, F; Nicole, S; de Vries, B; Tiziano, Fd; Fontaine, B; Walley, Nm; Heavin, S; Panagiotakaki, E; European Alternating Hemiplegia of Childhood Genetics, Consortium; Nicole, S; Gurrieri, F; Neri, G; de Vries, B; Koelewijn, S; Kamphorst, J; Geilenkirchen, M; Pelzer, N; Laan, L; Haan, J; Ferrari, M; van den Maagdenberg, A; Biobanca e., Registro Clinico per l'Emiplegia Alternante Consortium; Zucca, C; Bassi, Mt; Franchini, F; Vavassori, R; Giannotta, M; Gobbi, G; Granata, T; Nardocci, N; De Grandis, E; Veneselli, E; Stagnaro, M; Gurrieri, F; Neri, G; Vigevano, F; European Network for Research on Alternating Hemiplegia for, Small; Medium sized Enterpriese, Consortium; Panagiotakaki, E; Oechsler, C; Arzimanoglou, A; Nicole, S; Giannotta, M; Gobbi, G; Ninan, M; Neville, B; Ebinger, F; Fons, C; Campistol, J; Kemlink, D; Nevsimalova, S; Laan, L; Peeters Scholte, C; van den Maagdenberg, A; Casaer, P; Casari, GIORGIO NEVIO; Sange, G; Spiel, G; Martinelli Boneschi, F; Zucca, C; Bassi, Mt; Schyns, T; Crawley, F; Poncelin, D; Vavassori, R; Fiori, S; Abiusi, E; Di Pietro, L; Sweney, Mt; Newcomb, Tm; Viollet, L; Huff, C; Jorde, Lb; Reyna, Sp; Murphy, Kj; Shianna, Kv; Gumbs, Ce; Little, L; Silver, K; Ptáček, Lj; Haan, J; Ferrari, Md; Bye, Am; Herkes, Gk; Whitelaw, Cm; Webb, D; Lynch, Bj; Uldall, P; King, Md; Scheffer, Ie; Neri, G; Arzimanoglou, A; van den Maagdenberg, Am; Sisodiya, Sm; Mikati, Ma; Goldstein, D. B.
Defining the role of common variation in the genomic and biological architecture of adult human height 1-gen-2014 Wood, Ar; Esko, T; Yang, J; Vedantam, S; Pers, Th; Gustafsson, S; Chu, Ay; Estrada, K; Luan, J; Kutalik, Z; Amin, N; Buchkovich, Ml; CROTEAU CHONKA, Dc; Day, Fr; Duan, Y; Fall, T; Fehrmann, R; Ferreira, T; Jackson, Au; Karjalainen, J; Lo, Ks; Locke, Ae; Mägi, R; Mihailov, E; Porcu, E; Randall, Jc; Scherag, A; Vinkhuyzen, Aa; Westra, Hj; Winkler, Tw; Workalemahu, T; Zhao, Jh; Absher, D; Albrecht, E; Anderson, D; Baron, J; Beekman, M; Demirkan, A; Ehret, Gb; Feenstra, B; Feitosa, Mf; Fischer, K; Fraser, Rm; Goel, A; Gong, J; Justice, Ae; Kanoni, S; Kleber, Me; Kristiansson, K; Lim, U; Lotay, V; Lui, Jc; Mangino, M; MATEO LEACH, I; MEDINA GOMEZ, C; Nalls, Ma; Nyholt, Dr; Palmer, Cd; Pasko, D; Pechlivanis, S; Prokopenko, I; Ried, Js; Ripke, S; Shungin, D; Stancáková, A; Strawbridge, Rj; Sung, Yj; Tanaka, T; Teumer, A; Trompet, S; VAN DER LAAN, Sw; VAN SETTEN, J; VAN VLIET OSTAPTCHOUK, Jv; Wang, Z; Yengo, L; Zhang, W; Afzal, U; Arnlöv, J; Arscott, Gm; Bandinelli, S; Barrett, A; Bellis, C; Bennett, Aj; Berne, C; Blüher, M; Bolton, Jl; Böttcher, Y; Boyd, Ha; Bruinenberg, M; Buckley, Bm; Buyske, S; Caspersen, Ih; Chines, Ps; Clarke, R; CLAUDI BOEHM, S; Cooper, M; Daw, Ew; DE JONG, Pa; Deelen, J; Delgado, G; Denny, Jc; DHONUKSHE RUTTEN, R; Dimitriou, M; Doney, As; Dörr, M; Eklund, N; Eury, E; Folkersen, L; Garcia, Me; Geller, F; Giedraitis, V; Go, As; Grallert, H; Grammer, Tb; Gräßler, J; Grönberg, H; DE GROOT, Lc; Groves, Cj; Haessler, J; Hall, P; Haller, T; Hallmans, G; Hannemann, A; Hartman, Ca; Hassinen, M; Hayward, C; HEARD COSTA, Nl; Helmer, Q; Hemani, G; Henders, Ak; Hillege, Hl; Hlatky, Ma; Hoffmann, W; Hoffmann, P; Holmen, O; HOUWING DUISTERMAAT, Jj; Illig, T; Isaacs, A; James, Al; Jeff, J; Johansen, B; Johansson, A; Jolley, J; Juliusdottir, T; Junttila, J; Kho, An; Kinnunen, L; Klopp, N; Kocher, T; Kratzer, W; Lichtner, P; Lind, L; Lindström, J; Lobbens, S; Lorentzon, M; Lu, Y; Lyssenko, V; Magnusson, Pk; Mahajan, A; Maillard, M; Mcardle, Wl; Mckenzie, Ca; Mclachlan, S; Mclaren, Pj; Menni, C; Merger, S; Milani, L; Moayyeri, A; Monda, Kl; Morken, Ma; Müller, G; MÜLLER NURASYID, M; Musk, Aw; Narisu, N; Nauck, M; Nolte, Im; Nöthen, Mm; Oozageer, L; Pilz, S; Rayner, Nw; Renstrom, F; Robertson, Nr; Rose, Lm; Roussel, R; Sanna, S; Scharnagl, H; Scholtens, S; Schumacher, Fr; Schunkert, H; Scott, Ra; Sehmi, J; Seufferlein, T; Shi, J; Silventoinen, K; Smit, Jh; Smith, Av; Smolonska, J; Stanton, Av; Stirrups, K; Stott, Dj; Stringham, Hm; Sundström, J; Swertz, Ma; Syvänen, Ac; Tayo, Bo; Thorleifsson, G; Tyrer, Jp; VAN DIJK, S; VAN SCHOOR, Nm; VAN DER VELDE, N; VAN HEEMST, D; VAN OORT, Fv; Vermeulen, Sh; Verweij, N; Vonk, Jm; Waite, Ll; Waldenberger, M; Wennauer, R; Wilkens, Lr; Willenborg, C; Wilsgaard, T; Wojczynski, Mk; Wong, A; Wright, Af; Zhang, Q; Arveiler, D; Bakker, Sj; Beilby, J; Bergman, Rn; Bergmann, S; Biffar, R; Blangero, J; Boomsma, Di; Bornstein, Sr; Bovet, P; Brambilla, P; Brown, Mj; Campbell, H; Caulfield, Mj; Chakravarti, A; Collins, R; Collins, Fs; Crawford, Dc; Cupples, La; Danesh, J; DE FAIRE, U; DEN RUIJTER, Hm; Erbel, R; Erdmann, J; Eriksson, Jg; Farrall, M; Ferrannini, E; Ferrières, J; Ford, I; Forouhi, Ng; Forrester, T; Gansevoort, Rt; Gejman, Pv; Gieger, C; Golay, A; Gottesman, O; Gudnason, V; Gyllensten, U; Haas, Dw; Hall, As; Harris, Tb; Hattersley, At; Heath, Ac; Hengstenberg, C; Hicks, Aa; Hindorff, La; Hingorani, Ad; Hofman, A; Hovingh, Gk; Humphries, Se; Hunt, Sc; Hypponen, E; Jacobs, Kb; Jarvelin, Mr; Jousilahti, P; Jula, Am; Kaprio, J; Kastelein, Jj; Kayser, M; Kee, F; KEINANEN KIUKAANNIEMI, Sm; Kiemeney, La; Kooner, Js; Kooperberg, C; Koskinen, S; Kovacs, P; Kraja, At; Kumari, M; Kuusisto, J; Lakka, Ta; Langenberg, C; LE MARCHAND, L; Lehtimäki, T; Lupoli, S; Madden, Pa; Männistö, S; Manunta, Paolo; Marette, A; Matise, Tc; Mcknight, B; Meitinger, T; Moll, Fl; Montgomery, Gw; Morris, Ad; Morris, Ap; Murray, Jc; Nelis, M; Ohlsson, C; Oldehinkel, Aj; Ong, Kk; Ouwehand, Wh; Pasterkamp, G; Peters, A; Pramstaller, Pp; Price, Jf; Qi, L; Raitakari, Ot; Rankinen, T; Rao, Dc; Rice, Tk; Ritchie, M; Rudan, I; Salomaa, V; Samani, Nj; Saramies, J; Sarzynski, Ma; Schwarz, Pe; Sebert, S; Sever, P; Shuldiner, Ar; Sinisalo, J; Steinthorsdottir, V; Stolk, Rp; Tardif, Jc; Tönjes, A; Tremblay, A; Tremoli, E; Virtamo, J; Vohl, Mc; ELECTRONIC MEDICAL RECORDS AND GENOMICS, Consortium; Migen, Consortium; Page, Consortium; LIFELINES COHORT, Study; Amouyel, P; Asselbergs, Fw; Assimes, Tl; Bochud, M; Boehm, Bo; Boerwinkle, E; Bottinger, Ep; Bouchard, C; Cauchi, S; Chambers, Jc; Chanock, Sj; Cooper, Rs; DE BAKKER, Pi; Dedoussis, G; Ferrucci, L; Franks, Pw; Froguel, P; Groop, Lc; Haiman, Ca; Hamsten, A; Hayes, Mg; Hui, J; Hunter, Dj; Hveem, K; Jukema, Jw; Kaplan, Rc; Kivimaki, M; Kuh, D; Laakso, M; Liu, Y; Martin, Ng; März, W; Melbye, M; Moebus, S; Munroe, Pb; Njølstad, I; Oostra, Ba; Palmer, Cn; Pedersen, Nl; Perola, M; Pérusse, L; Peters, U; Powell, Je; Power, C; Quertermous, T; Rauramaa, R; Reinmaa, E; Ridker, Pm; Rivadeneira, F; Rotter, Ji; Saaristo, Te; Saleheen, D; Schlessinger, D; Slagboom, Pe; Snieder, H; Spector, Td; Strauch, K; Stumvoll, M; Tuomilehto, J; Uusitupa, M; VAN DER HARST, P; Völzke, H; Walker, M; Wareham, Nj; Watkins, H; Wichmann, He; Wilson, Jf; Zanen, P; Deloukas, P; Heid, Im; Lindgren, Cm; Mohlke, Kl; Speliotes, Ek; Thorsteinsdottir, U; Barroso, I; Fox, Cs; North, Ke; Strachan, Dp; Beckmann, Js; Berndt, Si; Boehnke, M; Borecki, Ib; Mccarthy, Mi; Metspalu, A; Stefansson, K; Uitterlinden, Ag; VAN DUIJN, Cm; Franke, L; Willer, Cj; Price, Al; Lettre, G; Loos, Rj; Weedon, Mn; Ingelsson, E; O'Connell, Jr; Abecasis, Gr; Chasman, Di; Goddard, Me; Visscher, Pm; Hirschhorn, Jn; Frayling, Tm
EFFICIENT LENTIVIRAL TRANSDUCTION OF LIVER REQUIRES CELL CYCLING IN VIVO 1-gen-2000 Park, F; Ohashi, K; Chiu, W; Naldini, Luigi; Kay, Ma
Erratum: Mutations in GDI1 are responsible for X-linked non-specific mental retardation (Nature Genetics (1998) 19 (134-139)) 1-gen-1998 D'Adamo, P.; Menegon, A.; Nigro, C. L.; Grasso, M.; Gulisano, M.; Tamanini, F.; Bienvenu, T.; Gedeon, A. K.; Oostra, B.; Wu, S. -K.; Tandon, A.; Valtorta, F.; Batch, W. E.; Chelly, J.; Toniolo, D.
A GENE FOR HIRSCHSPRUNG DISEASE MAPS TO THE PROXIMAL LONG ARM OF CHROMOSOME-10 1-gen-1993 Lyonnet, S; Bolino, A; Pelet, A; Abel, L; Nihoulfekete, C; Briard, Ml; Moksiu, V; Kaariainen, H; Martucciello, G; Lerone, M; Puliti, A; Luo, Y; Weissenbach, J; Devoto, M; Munnich, A; Romeo, G
GENE TRANSDUCTION BY LENTIVIRAL VECTORS IS LIMITED BY NUCLEAR TRANSLOCATION OF THE GENOME AND IS RESCUED BY INCORPORATION OF CIS-ACTING SEQUENCES FOR THE HIV-1 POL GENE 1-gen-2000 Follenzi, A.; Ailles, L. E.; Bakovic, S.; Geuna, M.; Naldini, Luigi
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci 1-gen-2017 Aung, Tin; Ozaki, Mineo; Lee, Mei Chin; Schlötzer Schrehardt, Ursula; Thorleifsson, Gudmar; Mizoguchi, Takanori; Igo, Robert P; Haripriya, Aravind; Williams, Susan E; Astakhov, Yury S; Orr, Andrew C; Burdon, Kathryn P; Nakano, Satoko; Mori, Kazuhiko; Abu Amero, Khaled; Hauser, Michael; Li, Zheng; Prakadeeswari, Gopalakrishnan; Bailey, Jessica N. Cooke; Cherecheanu, Alina Popa; Kang, Jae H; Nelson, Sarah; Hayashi, Ken; Manabe, Shin Ichi; Kazama, Shigeyasu; Zarnowski, Tomasz; Inoue, Kenji; Irkec, Murat; Coca Prados, Miguel; Sugiyama, Kazuhisa; Järvelä, Irma; Schlottmann, Patricio; Lerner, S. Fabian; Lamari, Hasnaa; Nilgün, Yildirim; Bikbov, Mukharram; Park, Ki Ho; Cha, Soon Cheol; Yamashiro, Kenji; Zenteno, Juan C; Jonas, Jost B; Kumar, Rajesh S; Perera, Shamira A; Chan, Anita S. Y; Kobakhidze, Nino; George, Ronnie; Vijaya, Lingam; Do, Tan; Edward, Deepak P; de Juan Marcos, Lourdes; Pakravan, Mohammad; Moghimi, Sasan; Ideta, Ryuichi; Bach Holm, Daniella; Kappelgaard, Per; Wirostko, Barbara; Thomas, Samuel; Gaston, Daniel; Bedard, Karen; Greer, Wenda L; Yang, Zhenglin; Chen, Xueyi; Huang, Lulin; Sang, Jinghong; Jia, Hongyan; Jia, Liyun; Qiao, Chunyan; Zhang, Hui; Liu, Xuyang; Zhao, Bowen; Wang, Ya Xing; Xu, Liang; Leruez, Stéphanie; Reynier, Pascal; Chichua, George; Tabagari, Sergo; Uebe, Steffen; Zenkel, Matthias; Berner, Daniel; Mossböck, Georg; Weisschuh, Nicole; Hoja, Ursula; Welge Luessen, Ulrich Christoph; Mardin, Christian; Founti, Panayiota; Chatzikyriakidou, Anthi; Pappas, Theofanis; Anastasopoulos, Eleftherios; Lambropoulos, Alexandros; Ghosh, Arkasubhra; Shetty, Rohit; Porporato, Natalia; Saravanan, Vijayan; Venkatesh, Rengaraj; Shivkumar, Chandrashekaran; Kalpana, Narendran; Sarangapani, Sripriya; Kanavi, Mozhgan R; Beni, Afsaneh Naderi; Yazdani, Shahin; Lashay, Alireza; Naderifar, Homa; Khatibi, Nassim; Fea, Antonio; Lavia, Carlo; Dallorto, Laura; Rolle, Teresa; Frezzotti, Paolo; Paoli, Daniela; Salvi, Erika; Manunta, Paolo; Mori, Yosai; Miyata, Kazunori; Higashide, Tomomi; Chihara, Etsuo; Ishiko, Satoshi; Yoshida, Akitoshi; Yanagi, Masahide; Kiuchi, Yoshiaki; Ohashi, Tsutomu; Sakurai, Toshiya; Sugimoto, Takako; Chuman, Hideki; Aihara, Makoto; Inatani, Masaru; Miyake, Masahiro; Gotoh, Norimoto; Matsuda, Fumihiko; Yoshimura, Nagahisa; Ikeda, Yoko; Ueno, Morio; Sotozono, Chie; Jeoung, Jin Wook; Sagong, Min; Park, Kyu Hyung; Ahn, Jeeyun; Cruz Aguilar, Marisa; Ezzouhairi, Sidi M; Rafei, Abderrahman; Chong, Yaan Fun; Ng, Xiao Yu; Goh, Shuang Ru; Chen, Yueming; Yong, Victor H. K; Khan, Muhammad Imran; Olawoye, Olusola O; Ashaye, Adeyinka O; Ugbede, Idakwo; Onakoya, Adeola; Kizor Akaraiwe, Nkiru; Teekhasaenee, Chaiwat; Suwan, Yanin; Supakontanasan, Wasu; Okeke, Suhanya; Uche, Nkechi J; Asimadu, Ifeoma; Ayub, Humaira; Akhtar, Farah; Kosior Jarecka, Ewa; Lukasik, Urszula; Lischinsky, Ignacio; Castro, Vania; Grossmann, Rodolfo Perez; Megevand, Gordana Sunaric; Roy, Sylvain; Dervan, Edward; Silke, Eoin; Rao, Aparna; Sahay, Priti; Fornero, Pablo; Cuello, Osvaldo; Sivori, Delia; Zompa, Tamara; Mills, Richard A; Souzeau, Emmanuelle; Mitchell, Paul; Wang, Jie Jin; Hewitt, Alex W; Coote, Michael; Crowston, Jonathan G; Astakhov, Sergei Y; Akopov, Eugeny L; Emelyanov, Anton; Vysochinskaya, Vera; Kazakbaeva, Gyulli; Fayzrakhmanov, Rinat; Al Obeidan, Saleh A; Owaidhah, Ohoud; Aljasim, Leyla Ali; Chowbay, Balram; Foo, Jia Nee; Soh, Raphael Q; Sim, Kar Seng; Xie, Zhicheng; Cheong, Augustine W. O; Mok, Shi Qi; Soo, Hui Meng; Chen, Xiao Yin; Peh, Su Qin; Heng, Khai Koon; Husain, Rahat; Ho, Su Ling; Hillmer, Axel M; Cheng, Ching Yu; Escudero Domínguez, Francisco A; González Sarmiento, Rogelio; Martinon Torres, Frederico; Salas, Antonio; Pathanapitoon, Kessara; Hansapinyo, Linda; Wanichwecharugruang, Boonsong; Kitnarong, Naris; Sakuntabhai, Anavaj; Nguyn, Hip X; Nguyn, Giang T. T; Nguyn, Trình V; Zenz, Werner; Binder, Alexander; Klobassa, Daniela S; Hibberd, Martin L; Davila, Sonia; Herms, Stefan; Nöthen, Markus M; Moebus, Susanne; Rautenbach, Robyn M; Ziskind, Ari; Carmichael, Trevor R; Ramsay, Michele; Álvarez, Lydia; García, Montserrat; González Iglesias, Héctor; Rodríguez Calvo, Pedro P; Cueto, Luis Fernández Vega; Oguz, Çilingir; Tamcelik, Nevbahar; Atalay, Eray; Batu, Bilge; Aktas, Dilek; Kasım, Burcu; Wilson, M. Roy; Coleman, Anne L; Liu, Yutao; Challa, Pratap; Herndon, Leon; Kuchtey, Rachel W; Kuchtey, John; Curtin, Karen; Chaya, Craig J; Crandall, Alan; Zangwill, Linda M; Wong, Tien Yin; Nakano, Masakazu; Kinoshita, Shigeru; den Hollander, Anneke I; Vesti, Eija; Fingert, John H; Lee, Richard K; Sit, Arthur J; Shingleton, Bradford J; Wang, Ningli; Cusi, Daniele; Qamar, Raheel; Kraft, Peter; Pericak Vance, Margaret A; Raychaudhuri, Soumya; Heegaard, Steffen; Kivelä, Tero; Reis, André; Kruse, Friedrich E; Weinreb, Robert N; Pasquale, Louis R; Haines, Jonathan L; Thorsteinsdottir, Unnur; Jonasson, Fridbert; Allingham, R. Rand; Milea, Dan; Ritch, Robert; Kubota, Toshiaki; Tashiro, Kei; Vithana, Eranga N; Micheal, Shazia; Topouzis, Fotis; Craig, Jamie E; Dubina, Michael; Sundaresan, Periasamy; Stefansson, Kari; Wiggs, Janey L; Pasutto, Francesca; Khor, Chiea Chuen
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants 1-gen-2009 Kathiresan, S; Altschuler, D; Anand, S; Ardissino, D; Asselta, R; Ball, Sg; Balmforth, Aj; Berger, K; Berglund, G; Bernardi, F; Bernardinelli, L; Berzuini, C; Braund, Ps; Burnett, Ms; Burtt, N; Cambien, F; Casari, GIORGIO NEVIO; Celli, P; Chen, Z; Corrocher, R; Daly, Mj; Deloukas, P; Devaney, J; Do, R; Duga, S; Elosua, R; Engert, Jc; Epstein, Se; Erdmann, J; Ferrario, M; Fetiveau, R; Fischer, M; Friedlander, Y; Gabriel, Sb; Galli, M; Gianniny, L; Girelli, D; Grosshennig, A; Guiducci, C; Hakonarson, Hh; Hall, As; Havulinna, As; Hengstenberg, C; Hirschhorn, Jn; Holm, H; Huge, A; Kent, Km; Konig, Ir; Korn, Jm; Li, M; Lieb, W; Lindsay, Jm; Linsel Nitschke, P; Lucas, G; Macrae, Ca; Mannucci, Pm; Marrugat, J; Martinelli, N; Marziliano, N; Matthai, W; Mccarroll, Sa; Mckeown, Pp; Meigs, Jb; Melander, O; Merlini, Pa; Mirel, D; Morgan, T; Musunuru, K; Nathan, Dm; Nemesh, J; O'Donnell, Cj; Olivieri, O; Ouwehand, W; Parkin, M; Patterson, Cc; Peltonen, L; Peyvandi, F; Piazza, A; Pichard, Ad; Preuss, M; Purcell, S; Qasim, A; Rader, Dj; Ramos, R; Reilly, Mp; Ribichini, F; Rossi, M; Sala, J; Salomaa, V; Samani, Nj; Satler, L; Scheffold, T; Scholz, M; Schreiber, S; Schunkert, H; Schwartz, Sm; Siscovick, Ds; Spertus, Ja; Spreafico, M; Stark, K; Stefansson, K; Stoll, M; Subirana, I; Surti, A; Thompson, Jr; Thorleifsson, G; Thorsteinsdottir, U; Tubaro, M; Voight, Bf; Waksman, R; Wichmann, He; Wilensky, R; Williams, G; Wright, Bj; Xie, C; Yee, J; Ziegler, A; Zonzin, P.
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer 1-gen-2014 Wolpin, Bm; Rizzato, C; Kraft, P; Kooperberg, C; Petersen, Gm; Wang, Zm; Arslan, Aa; Beane-Freeman, L; Bracci, Pm; Buring, J; Canzian, F; Duell, Ej; Gallinger, S; Giles, Gg; Goodman, Ge; Goodman, Pj; Jacobs, Ej; Kamineni, A; Klein, Ap; Kolonel, Ln; Kulke, Mh; Li, Dh; Malats, N; Olson, Sh; Risch, Ha; Sesso, Hd; Visvanathan, K; White, E; Zheng, W; Abnet, Cc; Albanes, D; Andreotti, G; Austin, Ma; Barfield, R; Basso, D; Berndt, Si; Boutron-Ruault, Mc; Brotzman, M; Buchler, Mw; Bueno-de-Mesquita, Hb; Bugert, P; Burdette, L; Campa, D; Caporaso, Ne; Capurso, G; Chung, C; Cotterchio, M; Costello, E; Elena, J; Funel, N; Gaziano, Jm; Giese, Na; Giovannucci, El; Gorman, Mj; Gross, M; Haiman, Ca; Hassan, M; Helzlsouer, Kj; Henderson, Be; Holly, Ea; Hu, N; Hunter, Dj; Innocenti, F; Jenab, M; Kaaks, R; Key, Tj; Khaw, Kt; Klein, Ea; Kogevinas, M; Krogh, V; Kupcinskas, J; Kurtz, Rc; Lacroix, A; Landi, Mt; Landi, S; Le Marchand, L; Mambrini, A; Mannisto, S; Milne, Rl; Nakamura, Y; Oberg, Al; Owzar, K; Patel, Av; Peeters, Phm; Peters, U; Pezzilli, R; Piepoli, A; Porta, M; Real, Fx; Riboli, E; Rothman, N; Scarpa, A; Shu, Xo; Silverman, Dt; Soucek, P; Sund, M; Talar-Wojnarowska, R; Taylor, Pr; Theodoropoulos, Ge; Thornquist, M; Tjonneland, A; Tobias, Gs; Trichopoulos, D; Vodicka, P; Wactawski-Wende, J; Wentzensen, N; Wu, C; Yu, H; Yu, K; Zeleniuch-Jacquotte, A; Hoover, R; Hartge, P; Fuchs, C; Chanock, Sj; Stolzenberg-Solomon, Rs; Amundadottir, Lt
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture 1-gen-2013 Berndt, Si; Gustafsson, S; Mägi, R; Ganna, A; Wheeler, E; Feitosa, Mf; Justice, Ae; Monda, Kl; CROTEAU CHONKA, Dc; Day, Fr; Esko, T; Fall, T; Ferreira, T; Gentilini, D; Jackson, Au; Luan, J; Randall, Jc; Vedantam, S; Willer, Cj; Winkler, Tw; Wood, Ar; Workalemahu, T; Hu, Yj; Lee, Sh; Liang, L; Lin, Dy; Min, Jl; Neale, Bm; Thorleifsson, G; Yang, J; Albrecht, E; Amin, N; BRAGG GRESHAM, Jl; Cadby, G; DEN HEIJER, M; Eklund, N; Fischer, K; Goel, A; Hottenga, Jj; Huffman, Je; Jarick, I; Johansson, A; Johnson, T; Kanoni, S; Kleber, Me; König, Ir; Kristiansson, K; Kutalik, Z; Lamina, C; Lecoeur, C; Li, G; Mangino, M; Mcardle, Wl; MEDINA GOMEZ, C; MÜLLER NURASYID, M; Ngwa, Js; Nolte, Im; Paternoster, L; Pechlivanis, S; Perola, M; Peters, Mj; Preuss, M; Rose, Lm; Shi, J; Shungin, D; Smith, Av; Strawbridge, Rj; Surakka, I; Teumer, A; Trip, Md; Tyrer, J; VAN VLIET OSTAPTCHOUK, Jv; Vandenput, L; Waite, Ll; Zhao, Jh; Absher, D; Asselbergs, Fw; Atalay, M; Attwood, Ap; Balmforth, Aj; Basart, H; Beilby, J; Bonnycastle, Ll; Brambilla, P; Bruinenberg, M; Campbell, H; Chasman, Di; Chines, Ps; Collins, Fs; Connell, Jm; Cookson, Wo; DE FAIRE, U; DE VEGT, F; Dei, M; Dimitriou, M; Edkins, S; Estrada, K; Evans, Dm; Farrall, M; Ferrario, Mm; Ferrières, J; Franke, L; Frau, F; Gejman, Pv; Grallert, H; Grönberg, H; Gudnason, V; Hall, As; Hall, P; Hartikainen, Al; Hayward, C; HEARD COSTA, Nl; Heath, Ac; Hebebrand, J; Homuth, G; Hu, Fb; Hunt, Se; Hyppönen, E; Iribarren, C; Jacobs, Kb; Jansson, Jo; Jula, A; Kähönen, M; Kathiresan, S; Kee, F; Khaw, Kt; Kivimäki, M; Koenig, W; Kraja, At; Kumari, M; Kuulasmaa, K; Kuusisto, J; Laitinen, Jh; Lakka, Ta; Langenberg, C; Launer, Lj; Lind, L; Lindström, J; Liu, J; Liuzzi, A; Lokki, Ml; Lorentzon, M; Madden, Pa; Magnusson, Pk; Manunta, Paolo; Marek, D; März, W; MATEO LEACH, I; Mcknight, B; Medland, Se; Mihailov, E; Milani, L; Montgomery, Gw; Mooser, V; Mühleisen, Tw; Munroe, Pb; Musk, Aw; Narisu, N; Navis, G; Nicholson, G; Nohr, Ea; Ong, Kk; Oostra, Ba; Palmer, Cn; Palotie, A; Peden, Jf; Pedersen, N; Peters, A; Polasek, O; Pouta, A; Pramstaller, Pp; Prokopenko, I; Pütter, C; Radhakrishnan, A; Raitakari, O; Rendon, A; Rivadeneira, F; Rudan, I; Saaristo, Te; Sambrook, Jg; Sanders, Ar; Sanna, S; Saramies, J; Schipf, S; Schreiber, S; Schunkert, H; Shin, Sy; Signorini, S; Sinisalo, J; Skrobek, B; Soranzo, N; Stančáková, A; Stark, K; Stephens, Jc; Stirrups, K; Stolk, Rp; Stumvoll, M; Swift, Aj; Theodoraki, Ev; Thorand, B; Tregouet, Da; Tremoli, E; VAN DER KLAUW, Mm; VAN MEURS, Jb; Vermeulen, Sh; Viikari, J; Virtamo, J; Vitart, V; Waeber, G; Wang, Z; Widén, E; Wild, Sh; Willemsen, G; Winkelmann, Br; Witteman, Jc; Wolffenbuttel, Bh; Wong, A; Wright, Af; Zillikens, Mc; Amouyel, P; Boehm, Bo; Boerwinkle, E; Boomsma, Di; Caulfield, Mj; Chanock, Sj; Cupples, La; Cusi, D; Dedoussis, Gv; Erdmann, J; Eriksson, Jg; Franks, Pw; Froguel, P; Gieger, C; Gyllensten, U; Hamsten, A; Harris, Tb; Hengstenberg, C; Hicks, Aa; Hingorani, A; Hinney, A; Hofman, A; Hovingh, Kg; Hveem, K; Illig, T; Jarvelin, Mr; Jöckel, Kh; KEINANEN KIUKAANNIEMI, Sm; Kiemeney, La; Kuh, D; Laakso, M; Lehtimäki, T; Levinson, Df; Martin, Ng; Metspalu, A; Morris, Ad; Nieminen, Ms; Njølstad, I; Ohlsson, C; Oldehinkel, Aj; Ouwehand, Wh; Palmer, Lj; Penninx, B; Power, C; Province, Ma; Psaty, Bm; Qi, L; Rauramaa, R; Ridker, Pm; Ripatti, S; Salomaa, V; Samani, Nj; Snieder, H; Sørensen, Ti; Spector, Td; Stefansson, K; Tönjes, A; Tuomilehto, J; Uitterlinden, Ag; Uusitupa, M; VAN DER HARST, P; Vollenweider, P; Wallaschofski, H; Wareham, Nj; Watkins, H; Wichmann, He; Wilson, Jf; Abecasis, Gr; Assimes, Tl; Barroso, I; Boehnke, M; Borecki, Ib; Deloukas, P; Fox, Cs; Frayling, T; Groop, Lc; Haritunian, T; Heid, Im; Hunter, D; Kaplan, Rc; Karpe, F; Moffatt, Mf; Mohlke, Kl; O'Connell, Jr; Pawitan, Y; Schadt, Ee; Schlessinger, D; Steinthorsdottir, V; Strachan, Dp; Thorsteinsdottir, U; VAN DUIJN, Cm; Visscher, Pm; DI BLASIO, Am; Hirschhorn, Jn; Lindgren, Cm; Morris, Ap; Meyre, D; Scherag, A; Mccarthy, Mi; Speliotes, Ek; North, Ke; Loos, Rj; Ingelsson, E.
Germline NPM1 mutations lead to altered rRNA 2′-O-methylation and cause dyskeratosis congenita 1-gen-2019 Nachmani, D.; Bothmer, A. H.; Grisendi, S.; Mele, A.; Bothmer, D.; Lee, J. D.; Monteleone, E.; Cheng, K.; Zhang, Y.; Bester, A. C.; Guzzetti, A.; Mitchell, C. A.; Mendez, L. M.; Pozdnyakova, O.; Sportoletti, P.; Martelli, M. -P.; Vulliamy, T. J.; Safra, M.; Schwartz, S.; Luzzatto, L.; Bluteau, O.; Soulier, J.; Darnell, R. B.; Falini, B.; Dokal, I.; Ito, K.; Clohessy, J. G.; Pandolfi, P. P.
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha 2 subunit associated with familial hemiplegic migraine type 2 1-gen-2003 De Fusco, M; Marconi, R; Silvestri, L; Atorino, L; Rampoldi, L; Morgante, L; Ballabio, A; Aridon, P; Casari, GIORGIO NEVIO
Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene 1-gen-1998 Coffey, Aj; Brooksbank, Ra; Brandau, O; Oohashi, T; Howell, Gr; Bye, Jm; Cahn, Ap; Durham, J; Heath, P; Wray, P; Pavitt, R; Wilkinson, J; Leversha, M; Huckle, E; Shaw-Smith, Cj; Dunham, A; Rhodes, S; Schuster, V; Porta, G; Yin, L; Serafini, P; Sylla, B; Zollo, M; Franco, B; Bolino, A; Seri, M; Lanyi, A; Davis, Jr; Webster, D; Harris, A; Lenoir, G; St Basile, Gd; Jones, A; Behloradsky, Bh; Achatz, H; Murken, J; Fassler, R; Sumegi, J; Romeo, G; Vaudin, M; Ross, Mt; Meindl, A; Bentley, Dr
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