Works matching IS 10614036 AND DT 2013 AND VI 45 AND IP 11

Results: 32
    1

    The long noncoding RNA SChLAP1 promotes aggressive prostate cancer and antagonizes the SWI/SNF complex.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1392, doi. 10.1038/ng.2771
    By:
    • Prensner, John R;
    • Iyer, Matthew K;
    • Sahu, Anirban;
    • Asangani, Irfan A;
    • Cao, Qi;
    • Patel, Lalit;
    • Vergara, Ismael A;
    • Davicioni, Elai;
    • Erho, Nicholas;
    • Ghadessi, Mercedeh;
    • Jenkins, Robert B;
    • Triche, Timothy J;
    • Malik, Rohit;
    • Bedenis, Rachel;
    • McGregor, Natalie;
    • Ma, Teng;
    • Chen, Wei;
    • Han, Sumin;
    • Jing, Xiaojun;
    • Cao, Xuhong
    Publication type:
    Article
    2

    No pain, more gain.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1271, doi. 10.1038/ng.2810
    By:
    • Cox, James J;
    • Wood, John N
    Publication type:
    Article
    3

    Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1375, doi. 10.1038/ng.2758
    By:
    • Zhan, Xiaowei;
    • Larson, David E;
    • Wang, Chaolong;
    • Koboldt, Daniel C;
    • Sergeev, Yuri V;
    • Fulton, Robert S;
    • Fulton, Lucinda L;
    • Fronick, Catrina C;
    • Branham, Kari E;
    • Bragg-Gresham, Jennifer;
    • Jun, Goo;
    • Hu, Youna;
    • Kang, Hyun Min;
    • Liu, Dajiang;
    • Othman, Mohammad;
    • Brooks, Matthew;
    • Ratnapriya, Rinki;
    • Boleda, Alexis;
    • Grassmann, Felix;
    • von Strachwitz, Claudia
    Publication type:
    Article
    4

    BMP signaling controls muscle mass.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1309, doi. 10.1038/ng.2772
    By:
    • Sartori, Roberta;
    • Schirwis, Elija;
    • Blaauw, Bert;
    • Bortolanza, Sergia;
    • Zhao, Jinghui;
    • Enzo, Elena;
    • Stantzou, Amalia;
    • Mouisel, Etienne;
    • Toniolo, Luana;
    • Ferry, Arnaud;
    • Stricker, Sigmar;
    • Goldberg, Alfred L;
    • Dupont, Sirio;
    • Piccolo, Stefano;
    • Amthor, Helge;
    • Sandri, Marco
    Publication type:
    Article
    5
    6

    Common variants associated with plasma triglycerides and risk for coronary artery disease.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1345, doi. 10.1038/ng.2795
    By:
    • Do, Ron;
    • Willer, Cristen J;
    • Schmidt, Ellen M;
    • Sengupta, Sebanti;
    • Gao, Chi;
    • Peloso, Gina M;
    • Gustafsson, Stefan;
    • Kanoni, Stavroula;
    • Ganna, Andrea;
    • Chen, Jin;
    • Buchkovich, Martin L;
    • Mora, Samia;
    • Beckmann, Jacques S;
    • Bragg-Gresham, Jennifer L;
    • Chang, Hsing-Yi;
    • Demirkan, Ayşe;
    • Den Hertog, Heleen M;
    • Donnelly, Louise A;
    • Ehret, Georg B;
    • Esko, Tõnu
    Publication type:
    Article
    7

    Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1409, doi. 10.1038/ng1113-1409b
    By:
    • Bezzina, Connie R;
    • Barc, Julien;
    • Mizusawa, Yuka;
    • Remme, Carol Ann;
    • Gourraud, Jean-Baptiste;
    • Simonet, Floriane;
    • Verkerk, Arie O;
    • Schwartz, Peter J;
    • Crotti, Lia;
    • Dagradi, Federica;
    • Guicheney, Pascale;
    • Fressart, Véronique;
    • Leenhardt, Antoine;
    • Antzelevitch, Charles;
    • Bartkowiak, Susan;
    • Schulze-Bahr, Eric;
    • Zumhagen, Sven;
    • Behr, Elijah R;
    • Bastiaenen, Rachel;
    • Tfelt-Hansen, Jacob
    Publication type:
    Article
    8

    Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1353, doi. 10.1038/ng.2770
    By:
    • Beecham, Ashley H;
    • Patsopoulos, Nikolaos A;
    • Xifara, Dionysia K;
    • Davis, Mary F;
    • Kemppinen, Anu;
    • Cotsapas, Chris;
    • Shah, Tejas S;
    • Spencer, Chris;
    • Booth, David;
    • Goris, An;
    • Oturai, Annette;
    • Saarela, Janna;
    • Fontaine, Bertrand;
    • Hemmer, Bernhard;
    • Martin, Claes;
    • Zipp, Frauke;
    • D'Alfonso, Sandra;
    • Martinelli-Boneschi, Filippo;
    • Taylor, Bruce;
    • Harbo, Hanne F
    Publication type:
    Article
    9

    FunSeq for cancer genomics.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1273, doi. 10.1038/ng.2819
    By:
    • Bahcall, Orli
    Publication type:
    Article
    10
    11

    Replicative mechanisms for CNV formation are error prone.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1319, doi. 10.1038/ng.2768
    By:
    • Carvalho, Claudia M B;
    • Pehlivan, Davut;
    • Ramocki, Melissa B;
    • Fang, Ping;
    • Alleva, Benjamin;
    • Franco, Luis M;
    • Belmont, John W;
    • Hastings, P J;
    • Lupski, James R
    Publication type:
    Article
    12

    Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1409, doi. 10.1038/ng1113-1409a
    By:
    • Fingerlin, Tasha E;
    • Murphy, Elissa;
    • Zhang, Weiming;
    • Peljto, Anna L;
    • Brown, Kevin K;
    • Steele, Mark P;
    • Loyd, James E;
    • Cosgrove, Gregory P;
    • Lynch, David;
    • Groshong, Steve;
    • Collard, Harold R;
    • Wolters, Paul J;
    • Bradford, Williamson Z;
    • Kossen, Karl;
    • Seiwert, Scott D;
    • du Bois, Roland M;
    • Garcia, Christine Kim;
    • Devine, Megan S;
    • Gudmundsson, Gunnar;
    • Isaksson, Helgi J
    Publication type:
    Article
    13

    Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1380, doi. 10.1038/ng.2794
    By:
    • Flannick, Jason;
    • Beer, Nicola L;
    • Bick, Alexander G;
    • Agarwala, Vineeta;
    • Molnes, Janne;
    • Gupta, Namrata;
    • Burtt, Noël P;
    • Florez, Jose C;
    • Meigs, James B;
    • Taylor, Herman;
    • Lyssenko, Valeriya;
    • Irgens, Henrik;
    • Fox, Ervin;
    • Burslem, Frank;
    • Johansson, Stefan;
    • Brosnan, M Julia;
    • Trimmer, Jeff K;
    • Newton-Cheh, Christopher;
    • Tuomi, Tiinamaija;
    • Molven, Anders
    Publication type:
    Article
    14
    15
    16
    17

    A de novo gain-of-function mutation in SCN11A causes loss of pain perception.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1399, doi. 10.1038/ng.2767
    By:
    • Leipold, Enrico;
    • Liebmann, Lutz;
    • Korenke, G Christoph;
    • Heinrich, Theresa;
    • Gießelmann, Sebastian;
    • Baets, Jonathan;
    • Ebbinghaus, Matthias;
    • Goral, R Oliver;
    • Stödberg, Tommy;
    • Hennings, J Christopher;
    • Bergmann, Markus;
    • Altmüller, Janine;
    • Thiele, Holger;
    • Wetzel, Andrea;
    • Nürnberg, Peter;
    • Timmerman, Vincent;
    • De Jonghe, Peter;
    • Blum, Robert;
    • Schaible, Hans-Georg;
    • Weis, Joachim
    Publication type:
    Article
    18

    Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1284, doi. 10.1038/ng.2792
    By:
    • Lessard, Christopher J;
    • Li, He;
    • Adrianto, Indra;
    • Ice, John A;
    • Rasmussen, Astrid;
    • Grundahl, Kiely M;
    • Kelly, Jennifer A;
    • Dozmorov, Mikhail G;
    • Miceli-Richard, Corinne;
    • Bowman, Simon;
    • Lester, Sue;
    • Eriksson, Per;
    • Eloranta, Maija-Leena;
    • Brun, Johan G;
    • Gøransson, Lasse G;
    • Harboe, Erna;
    • Guthridge, Joel M;
    • Kaufman, Kenneth M;
    • Kvarnström, Marika;
    • Jazebi, Helmi
    Publication type:
    Article
    19
    20

    Discovery and refinement of loci associated with lipid levels.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1274, doi. 10.1038/ng.2797
    By:
    • Willer, Cristen J;
    • Schmidt, Ellen M;
    • Sengupta, Sebanti;
    • Peloso, Gina M;
    • Gustafsson, Stefan;
    • Kanoni, Stavroula;
    • Ganna, Andrea;
    • Chen, Jin;
    • Buchkovich, Martin L;
    • Mora, Samia;
    • Beckmann, Jacques S;
    • Bragg-Gresham, Jennifer L;
    • Chang, Hsing-Yi;
    • Demirkan, Ayşe;
    • Den Hertog, Heleen M;
    • Do, Ron;
    • Donnelly, Louise A;
    • Ehret, Georg B;
    • Esko, Tõnu;
    • Feitosa, Mary F
    Publication type:
    Article
    21

    A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1371, doi. 10.1038/ng.2740
    By:
    • Helgason, Hannes;
    • Sulem, Patrick;
    • Duvvari, Maheswara R;
    • Luo, Hongrong;
    • Thorleifsson, Gudmar;
    • Stefansson, Hreinn;
    • Jonsdottir, Ingileif;
    • Masson, Gisli;
    • Gudbjartsson, Daniel F;
    • Walters, G Bragi;
    • Magnusson, Olafur Th;
    • Kong, Augustine;
    • Rafnar, Thorunn;
    • Kiemeney, Lambertus A;
    • Schoenmaker-Koller, Frederieke E;
    • Zhao, Ling;
    • Boon, Camiel J F;
    • Song, Yaojun;
    • Fauser, Sascha;
    • Pei, Michelle
    Publication type:
    Article
    22
    23
    24

    Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1300, doi. 10.1038/ng.2765
    By:
    • Cappello, Silvia;
    • Gray, Mary J;
    • Badouel, Caroline;
    • Lange, Simona;
    • Einsiedler, Melanie;
    • Srour, Myriam;
    • Chitayat, David;
    • Hamdan, Fadi F;
    • Jenkins, Zandra A;
    • Morgan, Tim;
    • Preitner, Nadia;
    • Uster, Tami;
    • Thomas, Jackie;
    • Shannon, Patrick;
    • Morrison, Victoria;
    • Di Donato, Nataliya;
    • Van Maldergem, Lionel;
    • Neuhann, Teresa;
    • Newbury-Ecob, Ruth;
    • Swinkells, Marielle
    Publication type:
    Article
    25
    26
    27
    28
    29

    Global chromatin profiling reveals NSD2 mutations in pediatric acute lymphoblastic leukemia.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1386, doi. 10.1038/ng.2777
    By:
    • Jaffe, Jacob D;
    • Wang, Yan;
    • Chan, Ho Man;
    • Zhang, Jinghui;
    • Huether, Robert;
    • Kryukov, Gregory V;
    • Bhang, Hyo-eun C;
    • Taylor, Jordan E;
    • Hu, Min;
    • Englund, Nathan P;
    • Yan, Feng;
    • Wang, Zhaofu;
    • Robert McDonald, E;
    • Wei, Lei;
    • Ma, Jing;
    • Easton, John;
    • Yu, Zhengtian;
    • deBeaumount, Rosalie;
    • Gibaja, Veronica;
    • Venkatesan, Kavitha
    Publication type:
    Article
    30

    The landscape of somatic mutations in Down syndrome-related myeloid disorders.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1293, doi. 10.1038/ng.2759
    By:
    • Yoshida, Kenichi;
    • Toki, Tsutomu;
    • Okuno, Yusuke;
    • Kanezaki, Rika;
    • Shiraishi, Yuichi;
    • Sato-Otsubo, Aiko;
    • Sanada, Masashi;
    • Park, Myoung-ja;
    • Terui, Kiminori;
    • Suzuki, Hiromichi;
    • Kon, Ayana;
    • Nagata, Yasunobu;
    • Sato, Yusuke;
    • Wang, RuNan;
    • Shiba, Norio;
    • Chiba, Kenichi;
    • Tanaka, Hiroko;
    • Hama, Asahito;
    • Muramatsu, Hideki;
    • Hasegawa, Daisuke
    Publication type:
    Article
    31
    32

    Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1405, doi. 10.1038/ng.2776
    By:
    • Schaaf, Christian P;
    • Gonzalez-Garay, Manuel L;
    • Xia, Fan;
    • Potocki, Lorraine;
    • Gripp, Karen W;
    • Zhang, Baili;
    • Peters, Brock A;
    • McElwain, Mark A;
    • Drmanac, Radoje;
    • Beaudet, Arthur L;
    • Caskey, C Thomas;
    • Yang, Yaping
    Publication type:
    Article