Works matching IS 10614036 AND DT 2012 AND VI 44 AND IP 9

Results: 30
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    3

    African genomics.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 967, doi. 10.1038/ng.2401
    By:
    • Bahcall, Orli
    Publication type:
    Article
    4

    Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 981, doi. 10.1038/ng.2383
    By:
    • Morris, Andrew P;
    • Voight, Benjamin F;
    • Teslovich, Tanya M;
    • Ferreira, Teresa;
    • Segrè, Ayellet V;
    • Steinthorsdottir, Valgerdur;
    • Strawbridge, Rona J;
    • Khan, Hassan;
    • Grallert, Harald;
    • Mahajan, Anubha;
    • Prokopenko, Inga;
    • Kang, Hyun Min;
    • Dina, Christian;
    • Esko, Tonu;
    • Fraser, Ross M;
    • Kanoni, Stavroula;
    • Kumar, Ashish;
    • Lagou, Vasiliki;
    • Langenberg, Claudia;
    • Luan, Jian'an
    Publication type:
    Article
    5

    Chromatin and stress.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 967, doi. 10.1038/ng.2403
    By:
    • Feliciano, Pamela
    Publication type:
    Article
    6

    Lifestyle transitions in plant pathogenic Colletotrichum fungi deciphered by genome and transcriptome analyses.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 1060, doi. 10.1038/ng.2372
    By:
    • O'Connell, Richard J;
    • Thon, Michael R;
    • Hacquard, Stéphane;
    • Amyotte, Stefan G;
    • Kleemann, Jochen;
    • Torres, Maria F;
    • Damm, Ulrike;
    • Buiate, Ester A;
    • Epstein, Lynn;
    • Alkan, Noam;
    • Altmüller, Janine;
    • Alvarado-Balderrama, Lucia;
    • Bauser, Christopher A;
    • Becker, Christian;
    • Birren, Bruce W;
    • Chen, Zehua;
    • Choi, Jaeyoung;
    • Crouch, Jo Anne;
    • Duvick, Jonathan P;
    • Farman, Mark A
    Publication type:
    Article
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    NMNAT1 mutations cause Leber congenital amaurosis.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 1040, doi. 10.1038/ng.2361
    By:
    • Falk, Marni J;
    • Zhang, Qi;
    • Nakamaru-Ogiso, Eiko;
    • Kannabiran, Chitra;
    • Fonseca-Kelly, Zoe;
    • Chakarova, Christina;
    • Audo, Isabelle;
    • Mackay, Donna S;
    • Zeitz, Christina;
    • Borman, Arundhati Dev;
    • Staniszewska, Magdalena;
    • Shukla, Rachna;
    • Palavalli, Lakshmi;
    • Mohand-Said, Saddek;
    • Waseem, Naushin H;
    • Jalali, Subhadra;
    • Perin, Juan C;
    • Place, Emily;
    • Ostrovsky, Julian;
    • Xiao, Rui
    Publication type:
    Article
    10

    Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 991, doi. 10.1038/ng.2385
    By:
    • Scott, Robert A;
    • Lagou, Vasiliki;
    • Welch, Ryan P;
    • Wheeler, Eleanor;
    • Montasser, May E;
    • Luan, Jian'an;
    • Mägi, Reedik;
    • Strawbridge, Rona J;
    • Rehnberg, Emil;
    • Gustafsson, Stefan;
    • Kanoni, Stavroula;
    • Rasmussen-Torvik, Laura J;
    • Yengo, Loïc;
    • Lecoeur, Cecile;
    • Shungin, Dmitry;
    • Sanna, Serena;
    • Sidore, Carlo;
    • Johnson, Paul C D;
    • Jukema, J Wouter;
    • Johnson, Toby
    Publication type:
    Article
    11

    Shigella sonnei genome sequencing and phylogenetic analysis indicate recent global dissemination from Europe.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 1056, doi. 10.1038/ng.2369
    By:
    • Holt, Kathryn E;
    • Baker, Stephen;
    • Weill, François-Xavier;
    • Holmes, Edward C;
    • Kitchen, Andrew;
    • Yu, Jun;
    • Sangal, Vartul;
    • Brown, Derek J;
    • Coia, John E;
    • Kim, Dong Wook;
    • Choi, Seon Young;
    • Kim, Su Hee;
    • da Silveira, Wanderley D;
    • Pickard, Derek J;
    • Farrar, Jeremy J;
    • Parkhill, Julian;
    • Dougan, Gordon;
    • Thomson, Nicholas R
    Publication type:
    Article
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    Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 1006, doi. 10.1038/ng.2359
    By:
    • Krauthammer, Michael;
    • Kong, Yong;
    • Ha, Byung Hak;
    • Evans, Perry;
    • Bacchiocchi, Antonella;
    • McCusker, James P;
    • Cheng, Elaine;
    • Davis, Matthew J;
    • Goh, Gerald;
    • Choi, Murim;
    • Ariyan, Stephan;
    • Narayan, Deepak;
    • Dutton-Regester, Ken;
    • Capatana, Ana;
    • Holman, Edna C;
    • Bosenberg, Marcus;
    • Sznol, Mario;
    • Kluger, Harriet M;
    • Brash, Douglas E;
    • Stern, David F
    Publication type:
    Article
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    The malaria parasite Plasmodium vivax exhibits greater genetic diversity than Plasmodium falciparum.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 1046, doi. 10.1038/ng.2373
    By:
    • Neafsey, Daniel E;
    • Galinsky, Kevin;
    • Jiang, Rays H Y;
    • Young, Lauren;
    • Sykes, Sean M;
    • Saif, Sakina;
    • Gujja, Sharvari;
    • Goldberg, Jonathan M;
    • Young, Sarah;
    • Zeng, Qiandong;
    • Chapman, Sinéad B;
    • Dash, Aditya P;
    • Anvikar, Anupkumar R;
    • Sutton, Patrick L;
    • Birren, Bruce W;
    • Escalante, Ananias A;
    • Barnwell, John W;
    • Carlton, Jane M
    Publication type:
    Article
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    Erratum: BAP1 loss defines a new class of renal cell carcinoma.

    Published in:
    2012
    By:
    • Peña-Llopis, Samuel;
    • Vega-Rubín-de-Celis, Silvia;
    • Liao, Arnold;
    • Leng, Nan;
    • Pavía-Jiménez, Andrea;
    • Wang, Shanshan;
    • Yamasaki, Toshinari;
    • Zhrebker, Leah;
    • Sivanand, Sharanya;
    • Spence, Patrick;
    • Kinch, Lisa;
    • Hambuch, Tina;
    • Jain, Suneer;
    • Lotan, Yair;
    • Margulis, Vitaly;
    • Sagalowsky, Arthur I;
    • Summerour, Pia Banerji;
    • Kabbani, Wareef;
    • Wong, S W Wendy;
    • Grishin, Nick
    Publication type:
    Erratum
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    Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 975, doi. 10.1038/ng.2357
    By:
    • Perrault, Isabelle;
    • Hanein, Sylvain;
    • Zanlonghi, Xavier;
    • Serre, Valérie;
    • Nicouleau, Michael;
    • Defoort-Delhemmes, Sabine;
    • Delphin, Nathalie;
    • Fares-Taie, Lucas;
    • Gerber, Sylvie;
    • Xerri, Olivia;
    • Edelson, Catherine;
    • Goldenberg, Alice;
    • Duncombe, Alice;
    • Le Meur, Gylène;
    • Hamel, Christian;
    • Silva, Eduardo;
    • Nitschke, Patrick;
    • Calvas, Patrick;
    • Munnich, Arnold;
    • Roche, Olivier
    Publication type:
    Article
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    Plasmodium cynomolgi genome sequences provide insight into Plasmodium vivax and the monkey malaria clade.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 1051, doi. 10.1038/ng.2375
    By:
    • Tachibana, Shin-Ichiro;
    • Sullivan, Steven A;
    • Kawai, Satoru;
    • Nakamura, Shota;
    • Kim, Hyunjae R;
    • Goto, Naohisa;
    • Arisue, Nobuko;
    • Palacpac, Nirianne M Q;
    • Honma, Hajime;
    • Yagi, Masanori;
    • Tougan, Takahiro;
    • Katakai, Yuko;
    • Kaneko, Osamu;
    • Mita, Toshihiro;
    • Kita, Kiyoshi;
    • Yasutomi, Yasuhiro;
    • Sutton, Patrick L;
    • Shakhbatyan, Rimma;
    • Horii, Toshihiro;
    • Yasunaga, Teruo
    Publication type:
    Article
    25

    Disease-specific iPS cells.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 967, doi. 10.1038/ng.2402
    By:
    • Niemitz, Emily
    Publication type:
    Article
    26

    De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 1030, doi. 10.1038/ng.2358
    By:
    • Heinzen, Erin L;
    • Swoboda, Kathryn J;
    • Hitomi, Yuki;
    • Gurrieri, Fiorella;
    • Nicole, Sophie;
    • de Vries, Boukje;
    • Tiziano, F Danilo;
    • Fontaine, Bertrand;
    • Walley, Nicole M;
    • Heavin, Sinéad;
    • Panagiotakaki, Eleni;
    • Neri, Giovanni;
    • Koelewijn, Stephany;
    • Kamphorst, Jessica;
    • Geilenkirchen, Marije;
    • Pelzer, Nadine;
    • Laan, Laura;
    • Haan, Joost;
    • Ferrari, Michel;
    • van den Maagdenberg, Arn
    Publication type:
    Article
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    Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 968, doi. 10.1038/ng.2360
    By:
    • Ludwig, Kerstin U;
    • Mangold, Elisabeth;
    • Herms, Stefan;
    • Nowak, Stefanie;
    • Reutter, Heiko;
    • Paul, Anna;
    • Becker, Jessica;
    • Herberz, Ruth;
    • AlChawa, Taofik;
    • Nasser, Entessar;
    • Böhmer, Anne C;
    • Mattheisen, Manuel;
    • Alblas, Margrieta A;
    • Barth, Sandra;
    • Kluck, Nadine;
    • Lauster, Carola;
    • Braumann, Bert;
    • Reich, Rudolf H;
    • Hemprich, Alexander;
    • Pötzsch, Simone
    Publication type:
    Article
    29

    Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 1035, doi. 10.1038/ng.2356
    By:
    • Koenekoop, Robert K;
    • Wang, Hui;
    • Majewski, Jacek;
    • Wang, Xia;
    • Lopez, Irma;
    • Ren, Huanan;
    • Chen, Yiyun;
    • Li, Yumei;
    • Fishman, Gerald A;
    • Genead, Mohammed;
    • Schwartzentruber, Jeremy;
    • Solanki, Naimesh;
    • Traboulsi, Elias I;
    • Cheng, Jingliang;
    • Logan, Clare V;
    • McKibbin, Martin;
    • Hayward, Bruce E;
    • Parry, David A;
    • Johnson, Colin A;
    • Nageeb, Mohammed
    Publication type:
    Article
    30

    Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 972, doi. 10.1038/ng.2370
    By:
    • Chiang, Pei-Wen;
    • Wang, Juan;
    • Chen, Yang;
    • Fu, Quan;
    • Zhong, Jing;
    • Chen, Yanhua;
    • Yi, Xin;
    • Wu, Renhua;
    • Gan, Haixue;
    • Shi, Yong;
    • Chen, Yanling;
    • Barnett, Christopher;
    • Wheaton, Dianna;
    • Day, Megan;
    • Sutherland, Joanne;
    • Heon, Elise;
    • Weleber, Richard G;
    • Gabriel, Luis Alexandre Rassi;
    • Cong, Peikuan;
    • Chuang, KuangHsiang
    Publication type:
    Article