Works matching IS 10614036 AND DT 2013 AND VI 45 AND IP 8

Results: 31
    1

    An atlas of over 90,000 conserved noncoding sequences provides insight into crucifer regulatory regions.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 891, doi. 10.1038/ng.2684
    By:
    • Haudry, Annabelle;
    • Platts, Adrian E;
    • Vello, Emilio;
    • Hoen, Douglas R;
    • Leclercq, Mickael;
    • Williamson, Robert J;
    • Forczek, Ewa;
    • Joly-Lopez, Zoé;
    • Steffen, Joshua G;
    • Hazzouri, Khaled M;
    • Dewar, Ken;
    • Stinchcombe, John R;
    • Schoen, Daniel J;
    • Wang, Xiaowu;
    • Schmutz, Jeremy;
    • Town, Christopher D;
    • Edger, Patrick P;
    • Pires, J Chris;
    • Schumaker, Karen S;
    • Jarvis, David E
    Publication type:
    Article
    2

    Whole-genome sequence-based analysis of high-density lipoprotein cholesterol.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 899, doi. 10.1038/ng.2671
    By:
    • Morrison, Alanna C;
    • Voorman, Arend;
    • Johnson, Andrew D;
    • Liu, Xiaoming;
    • Yu, Jin;
    • Li, Alexander;
    • Muzny, Donna;
    • Yu, Fuli;
    • Rice, Kenneth;
    • Zhu, Chengsong;
    • Bis, Joshua;
    • Heiss, Gerardo;
    • O'Donnell, Christopher J;
    • Psaty, Bruce M;
    • Cupples, L Adrienne;
    • Gibbs, Richard;
    • Boerwinkle, Eric
    Publication type:
    Article
    3

    Genome-wide meta-analysis identifies new susceptibility loci for migraine.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 912, doi. 10.1038/ng.2676
    By:
    • Anttila, Verneri;
    • Winsvold, Bendik S;
    • Gormley, Padhraig;
    • Kurth, Tobias;
    • Bettella, Francesco;
    • McMahon, George;
    • Kallela, Mikko;
    • Malik, Rainer;
    • de Vries, Boukje;
    • Terwindt, Gisela;
    • Medland, Sarah E;
    • Todt, Unda;
    • McArdle, Wendy L;
    • Quaye, Lydia;
    • Koiranen, Markku;
    • Ikram, M Arfan;
    • Lehtimäki, Terho;
    • Stam, Anine H;
    • Ligthart, Lannie;
    • Wedenoja, Juho
    Publication type:
    Article
    4

    Integrated molecular analysis of clear-cell renal cell carcinoma.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 860, doi. 10.1038/ng.2699
    By:
    • Sato, Yusuke;
    • Yoshizato, Tetsuichi;
    • Shiraishi, Yuichi;
    • Maekawa, Shigekatsu;
    • Okuno, Yusuke;
    • Kamura, Takumi;
    • Shimamura, Teppei;
    • Sato-Otsubo, Aiko;
    • Nagae, Genta;
    • Suzuki, Hiromichi;
    • Nagata, Yasunobu;
    • Yoshida, Kenichi;
    • Kon, Ayana;
    • Suzuki, Yutaka;
    • Chiba, Kenichi;
    • Tanaka, Hiroko;
    • Niida, Atsushi;
    • Fujimoto, Akihiro;
    • Tsunoda, Tatsuhiko;
    • Morikawa, Teppei
    Publication type:
    Article
    5
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    Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 868, doi. 10.1038/ng.2652
    By:
    • Berndt, Sonja I;
    • Skibola, Christine F;
    • Joseph, Vijai;
    • Camp, Nicola J;
    • Nieters, Alexandra;
    • Wang, Zhaoming;
    • Cozen, Wendy;
    • Monnereau, Alain;
    • Wang, Sophia S;
    • Kelly, Rachel S;
    • Lan, Qing;
    • Teras, Lauren R;
    • Chatterjee, Nilanjan;
    • Chung, Charles C;
    • Yeager, Meredith;
    • Brooks-Wilson, Angela R;
    • Hartge, Patricia;
    • Purdue, Mark P;
    • Birmann, Brenda M;
    • Armstrong, Bruce K
    Publication type:
    Article
    8

    Ministry of Noise.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 843, doi. 10.1038/ng.2724
    Publication type:
    Article
    9

    A new player SETs in myeloid malignancy.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 846, doi. 10.1038/ng.2709
    By:
    • Trimarchi, Thomas;
    • Ntziachristos, Panagiotis;
    • Aifantis, Iannis
    Publication type:
    Article
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    Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 923, doi. 10.1038/ng.2668
    By:
    • Tarpey, Patrick S;
    • Behjati, Sam;
    • Cooke, Susanna L;
    • Van Loo, Peter;
    • Wedge, David C;
    • Pillay, Nischalan;
    • Marshall, John;
    • O'Meara, Sarah;
    • Davies, Helen;
    • Nik-Zainal, Serena;
    • Beare, David;
    • Butler, Adam;
    • Gamble, John;
    • Hardy, Claire;
    • Hinton, Jonathon;
    • Jia, Ming Ming;
    • Jayakumar, Alagu;
    • Jones, David;
    • Latimer, Calli;
    • Maddison, Mark
    Publication type:
    Article
    14

    A genome-wide association study identifies susceptibility loci for Wilms tumor.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 962, doi. 10.1038/ng0813-962a
    By:
    • Turnbull, Clare;
    • Perdeaux, Elizabeth R;
    • Pernet, David;
    • Naranjo, Arlene;
    • Renwick, Anthony;
    • Seal, Sheila;
    • Munoz-Xicola, Rosa Maria;
    • Hanks, Sandra;
    • Slade, Ingrid;
    • Zachariou, Anna;
    • Warren-Perry, Margaret;
    • Ruark, Elise;
    • Gerrard, Mary;
    • Hale, Juliet;
    • Hewitt, Martin;
    • Kohler, Janice;
    • Lane, Sheila;
    • Levitt, Gill;
    • Madi, Mabrook;
    • Morland, Bruce
    Publication type:
    Article
    15

    Oncogenic microRNA.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 851, doi. 10.1038/ng.2722
    By:
    • Niemitz, Emily
    Publication type:
    Article
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    Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 937, doi. 10.1038/ng.2698
    By:
    • Sakaguchi, Hirotoshi;
    • Okuno, Yusuke;
    • Muramatsu, Hideki;
    • Yoshida, Kenichi;
    • Shiraishi, Yuichi;
    • Takahashi, Mariko;
    • Kon, Ayana;
    • Sanada, Masashi;
    • Chiba, Kenichi;
    • Tanaka, Hiroko;
    • Makishima, Hideki;
    • Wang, Xinan;
    • Xu, Yinyan;
    • Doisaki, Sayoko;
    • Hama, Asahito;
    • Nakanishi, Koji;
    • Takahashi, Yoshiyuki;
    • Yoshida, Nao;
    • Maciejewski, Jaroslaw P;
    • Miyano, Satoru
    Publication type:
    Article
    20
    21

    ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 951, doi. 10.1038/ng.2681
    By:
    • Hoff, Sylvia;
    • Halbritter, Jan;
    • Epting, Daniel;
    • Frank, Valeska;
    • Nguyen, Thanh-Minh T;
    • van Reeuwijk, Jeroen;
    • Boehlke, Christopher;
    • Schell, Christoph;
    • Yasunaga, Takayuki;
    • Helmstädter, Martin;
    • Mergen, Miriam;
    • Filhol, Emilie;
    • Boldt, Karsten;
    • Horn, Nicola;
    • Ueffing, Marius;
    • Otto, Edgar A;
    • Eisenberger, Tobias;
    • Elting, Mariet W;
    • van Wijk, Joanna A E;
    • Bockenhauer, Detlef
    Publication type:
    Article
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    Somatic SETBP1 mutations in myeloid malignancies.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 942, doi. 10.1038/ng.2696
    By:
    • Makishima, Hideki;
    • Yoshida, Kenichi;
    • Nguyen, Nhu;
    • Przychodzen, Bartlomiej;
    • Sanada, Masashi;
    • Okuno, Yusuke;
    • Ng, Kwok Peng;
    • Gudmundsson, Kristbjorn O;
    • Vishwakarma, Bandana A;
    • Jerez, Andres;
    • Gomez-Segui, Ines;
    • Takahashi, Mariko;
    • Shiraishi, Yuichi;
    • Nagata, Yasunobu;
    • Guinta, Kathryn;
    • Mori, Hiraku;
    • Sekeres, Mikkael A;
    • Chiba, Kenichi;
    • Tanaka, Hiroko;
    • Muramatsu, Hideki
    Publication type:
    Article
    25

    Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 927, doi. 10.1038/ng.2682
    By:
    • Jones, David T W;
    • Hutter, Barbara;
    • Jäger, Natalie;
    • Korshunov, Andrey;
    • Kool, Marcel;
    • Warnatz, Hans-Jörg;
    • Zichner, Thomas;
    • Lambert, Sally R;
    • Ryzhova, Marina;
    • Quang, Dong Anh Khuong;
    • Fontebasso, Adam M;
    • Stütz, Adrian M;
    • Hutter, Sonja;
    • Zuckermann, Marc;
    • Sturm, Dominik;
    • Gronych, Jan;
    • Lasitschka, Bärbel;
    • Schmidt, Sabine;
    • Şeker-Cin, Huriye;
    • Witt, Hendrik
    Publication type:
    Article
    26

    Massive genomic variation and strong selection in Arabidopsis thaliana lines from Sweden.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 884, doi. 10.1038/ng.2678
    By:
    • Long, Quan;
    • Rabanal, Fernando A;
    • Meng, Dazhe;
    • Huber, Christian D;
    • Farlow, Ashley;
    • Platzer, Alexander;
    • Zhang, Qingrun;
    • Vilhjálmsson, Bjarni J;
    • Korte, Arthur;
    • Nizhynska, Viktoria;
    • Voronin, Viktor;
    • Korte, Pamela;
    • Sedman, Laura;
    • Mandáková, Terezie;
    • Lysak, Martin A;
    • Seren, Ümit;
    • Hellmann, Ines;
    • Nordborg, Magnus
    Publication type:
    Article
    27

    Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 902, doi. 10.1038/ng.2694
    By:
    • Bønnelykke, Klaus;
    • Matheson, Melanie C;
    • Pers, Tune H;
    • Granell, Raquel;
    • Strachan, David P;
    • Alves, Alexessander Couto;
    • Linneberg, Allan;
    • Curtin, John A;
    • Warrington, Nicole M;
    • Standl, Marie;
    • Kerkhof, Marjan;
    • Jonsdottir, Ingileif;
    • Bukvic, Blazenka K;
    • Kaakinen, Marika;
    • Sleimann, Patrick;
    • Thorleifsson, Gudmar;
    • Thorsteinsdottir, Unnur;
    • Schramm, Katharina;
    • Baltic, Svetlana;
    • Kreiner-Møller, Eskil
    Publication type:
    Article
    28

    An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophy.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 947, doi. 10.1038/ng.2670
    By:
    • Weedon, Michael N;
    • Ellard, Sian;
    • Prindle, Marc J;
    • Caswell, Richard;
    • Allen, Hana Lango;
    • Oram, Richard;
    • Godbole, Koumudi;
    • Yajnik, Chittaranjan S;
    • Sbraccia, Paolo;
    • Novelli, Giuseppe;
    • Turnpenny, Peter;
    • McCann, Emma;
    • Goh, Kim Jee;
    • Wang, Yukai;
    • Fulford, Jonathan;
    • McCulloch, Laura J;
    • Savage, David B;
    • O'Rahilly, Stephen;
    • Kos, Katarina;
    • Loeb, Lawrence A
    Publication type:
    Article
    29
    30

    Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 962, doi. 10.1038/ng0813-962b
    By:
    • Poirier, Karine;
    • Lebrun, Nicolas;
    • Broix, Loic;
    • Tian, Guoling;
    • Saillour, Yoann;
    • Boscheron, Cécile;
    • Parrini, Elena;
    • Valence, Stephanie;
    • Pierre, Benjamin Saint;
    • Oger, Madison;
    • Lacombe, Didier;
    • Geneviève, David;
    • Fontana, Elena;
    • Darra, Franscesca;
    • Cances, Claude;
    • Barth, Magalie;
    • Bonneau, Dominique;
    • Bernadina, Bernardo Dalla;
    • N'Guyen, Sylvie;
    • Gitiaux, Cyril
    Publication type:
    Article
    31