Works matching IS 10614036 AND DT 2010 AND VI 42 AND IP 8

Results: 22
    1

    Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 703, doi. 10.1038/ng.624
    By:
    • Mizuki, Nobuhisa;
    • Meguro, Akira;
    • Ota, Masao;
    • Ohno, Shigeaki;
    • Shiota, Tomoko;
    • Kawagoe, Tatsukata;
    • Ito, Norihiko;
    • Kera, Jiro;
    • Okada, Eiichi;
    • Yatsu, Keisuke;
    • Yeong-Wook Song;
    • Eun-Bong Lee;
    • Kitaichi, Nobuyoshi;
    • Namba, Kenichi;
    • Horie, Yukihiro;
    • Takeno, Mitsuhiro;
    • Sugita, Sunao;
    • Mochizuki, Manabu;
    • Bahram, Seiamak;
    • Ishigatsubo, Yoshiaki
    Publication type:
    Article
    2

    Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 684, doi. 10.1038/ng.628
    By:
    • Johansen, Christopher T.;
    • Jian Wang;
    • Lanktree, Matthew B.;
    • Henian Cao;
    • McIntyre, Adam D.;
    • Ban, Matthew R.;
    • Martins, Rebecca A.;
    • Kennedy, Brooke A.;
    • Hassell, Reina G.;
    • Visser, Maartje E.;
    • Schwartz, Stephen M.;
    • Voight, Benjamin F.;
    • Elosua, Roberto;
    • Salomaa, Veikko;
    • O'Donnell, Christopher J.;
    • Dallinga-Thie, Geesje M.;
    • Anand, Sonia S.;
    • Yusuf, Salim;
    • Huff, Murray W.;
    • Kathiresan, Sekar
    Publication type:
    Article
    3

    Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 688, doi. 10.1038/ng.623
    By:
    • Bezzina, Connie R.;
    • Pazoki, Raha;
    • Bardai, Abdennasser;
    • Marsman, Roos F.;
    • de Jong, Jonas S. S. G.;
    • Blom, Marieke T.;
    • Scicluna, Brendon P.;
    • Jukema, J. Wouter;
    • Bindraban, Navin R.;
    • Lichtner, Peter;
    • Pfeufer, Arne;
    • Bishopric, Nanette H.;
    • Roden, Dan M.;
    • Meitinger, Thomas;
    • Chugh, Sumeet S.;
    • Myerburg, Robert J.;
    • Jouven, Xavier;
    • Kääb, Stefan;
    • Dekker, Lukas R. C.;
    • Tan, Hanno L.
    Publication type:
    Article
    4

    Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 692, doi. 10.1038/ng.622
    By:
    • Gretarsdottir, Solveig;
    • Baas, Annette F.;
    • Thorleifsson, Gudmar;
    • Holm, Hilma;
    • den Heijer, Martin;
    • de Vries, Jean-Paul P. M.;
    • Kranendonk, Steef E.;
    • Zeebregts, Clark J. A. M.;
    • van Sterkenburg, Steven M.;
    • Geelkerken, Robert H.;
    • van Rij, Andre M.;
    • Williams, Michael J. A.;
    • Boll, Albert P. M.;
    • Kostic, Jelena P.;
    • Jonasdottir, Adalbjorg;
    • Jonasdottir, Aslaug;
    • Walters, G. Bragi;
    • Masson, Gisli;
    • Sulem, Patrick;
    • Saemundsdottir, Jona
    Publication type:
    Article
    5

    Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 698, doi. 10.1038/ng.625
    By:
    • Remmers, Elaine F.;
    • Cosan, Fulya;
    • Kirino, Yohei;
    • Ombrello, Michael J.;
    • Abaci, Neslihan;
    • Satorius, Colleen;
    • Le, Julie M.;
    • Yang, Barbara;
    • Korman, Benjamin D.;
    • Cakiris, Aris;
    • Aglar, Oznur;
    • Emrence, Zeliha;
    • Azakli, Hulya;
    • Ustek, Duran;
    • Tugal-Tutkun, Ilknur;
    • Akman-Demir, Gulsen;
    • Wei Chen;
    • Amos, Christopher I.;
    • Dizon, Michael B.;
    • Kose, Afet Akdag
    Publication type:
    Article
    6

    Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 655, doi. 10.1038/ng.631
    By:
    • Hirschfield, Gideon M.;
    • Xiangdong Liu;
    • Younghun Han;
    • Gorlov, Ivan P.;
    • Yan Lu;
    • Chun Xu;
    • Yue Lu;
    • Wei Chen;
    • Juran, Brian D.;
    • Coltescu, Catalina;
    • Mason, Andrew L.;
    • Milkiewicz, Piotr;
    • Myers, Robert P.;
    • Odin, Joseph A.;
    • Luketic, Velimir A.;
    • Speiciene, Danute;
    • Vincent, Catherine;
    • Levy, Cynthia;
    • Gregersen, Peter K.;
    • Jinyi Zhang
    Publication type:
    Article
    7

    Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 658, doi. 10.1038/ng.627
    By:
    • Xiangdong Liu;
    • Invernizzi, Pietro;
    • Yue Lu;
    • Kosoy, Roman;
    • Yan Lu;
    • Bianchi, Ilaria;
    • Podda, Mauro;
    • Chun Xu;
    • Gang Xie;
    • Macciardi, Fabio;
    • Selmi, Carlo;
    • Lupoli, Sara;
    • Shigeta, Russell;
    • Ransom, Michael;
    • Lleo, Ana;
    • Lee, Annette T.;
    • Mason, Andrew L.;
    • Myers, Robert P.;
    • Peltekian, Kevork M.;
    • Ghent, Cameron N.
    Publication type:
    Article
    8

    Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 661, doi. 10.1038/ng.626
    By:
    • Conde, Lucia;
    • Halperin, Eran;
    • Akers, Nicholas K.;
    • Brown, Kevin M.;
    • Smedby, Karin E.;
    • Rothman, Nathaniel;
    • Nieters, Alexandra;
    • Slager, Susan L.;
    • Brooks-Wilson, Angela;
    • Agana, Luz;
    • Riby, Jacques;
    • Jianjun Liu;
    • Adami, Hans-Olov;
    • Darabi, Hatef;
    • Hjalgrim, Henrik;
    • Hui-Qi Low;
    • Humphreys, Keith;
    • Melbye, Mads;
    • Chang, Ellen T.;
    • Glimelius, Bengt
    Publication type:
    Article
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    Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 715, doi. 10.1038/ng.619
    By:
    • Barretina, Jordi;
    • Taylor, Barry S.;
    • Banerji, Shantanu;
    • Ramos, Alexis H.;
    • Lagos-Quintana, Mariana;
    • DeCarolis, Penelope L.;
    • Shah, Kinjal;
    • Socci, Nicholas D.;
    • Weir, Barbara A.;
    • Ho, Alan;
    • Chiang, Derek Y.;
    • Reva, Boris;
    • Mermel, Craig H.;
    • Getz, Gad;
    • Antipin, Yevgenyi;
    • Beroukhim, Rameen;
    • Major, John E.;
    • Hatton, Charles;
    • Nicoletti, Richard;
    • Hanna, Megan
    Publication type:
    Article
    19

    Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders.

    Published in:
    Nature Genetics, 2010, v. 42, n. 8, p. 722, doi. 10.1038/ng.621
    By:
    • Ernst, Thomas;
    • Chase, Andrew J.;
    • Score, Joannah;
    • Hidalgo-Curtis, Claire E.;
    • Bryant, Catherine;
    • Jones, Amy V.;
    • Waghorn, Katherine;
    • Zoi, Katerina;
    • Ross, Fiona M;
    • Reiter, Andreas;
    • Hochhaus, Andreas;
    • Drexler, Hans G.;
    • Duncombe, Andrew;
    • Cervantes, Francisco;
    • Oscier, David;
    • Boultwood, Jacqueline;
    • Grand, Francis H.;
    • Cross, Nicholas C. P.
    Publication type:
    Article
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    Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.

    Published in:
    2010
    By:
    • Beaty, Terri H;
    • Murray, Jeffrey C;
    • Marazita, Mary L;
    • Munger, Ronald G;
    • Hetmanski, Ingo Ruczinski Jacqueline B;
    • Liang, Kung Yee;
    • Wu, Tao;
    • Murray, Tanda;
    • Fallin, M Daniele;
    • Redett, Richard A;
    • Raymond, Gerald;
    • Schwender, Holger;
    • Jin, Shin C;
    • Cooper, Margaret E;
    • Dunnwald, Martine;
    • Mansilla, Maria A;
    • Leslie, Elizabeth;
    • Bullard, Stephen;
    • Lidral, Andrew C;
    • Moreno, Lina M
    Publication type:
    Correction Notice