Works matching IS 10614036 AND DT 2010 AND VI 42 AND IP 6

Results: 24
    1

    Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 508, doi. 10.1038/ng.582
    By:
    • Stahl, Eli A.;
    • Raychaudhuri, Soumya;
    • Remmers, Elaine F.;
    • Gang Xie;
    • Eyre, Stephen;
    • Thomson, Brian P.;
    • Yonghong Li;
    • Kurreeman, Fina A. S.;
    • Zhernakova, Alexandra;
    • Hinks, Anne;
    • Guiducci, Candace;
    • Chen, Robert;
    • Alfredsson, Lars;
    • Amos, Christopher I.;
    • Ardlie, Kristin G.;
    • Barton, Anne;
    • Bowes, John;
    • Brouwer, Elisabeth;
    • Burtt, Noel P.;
    • Catanese, Joseph J.
    Publication type:
    Article
    2

    Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 495, doi. 10.1038/ng.584
    By:
    • Sanna, Serena;
    • Pitzalis, Maristella;
    • Zoledziewska, Magdalena;
    • Zara, Ilenia;
    • Sidore, Carlo;
    • Murru, Raffaele;
    • Whalen, Michael B.;
    • Busonero, Fabio;
    • Maschio, Andrea;
    • Costa, Gianna;
    • Melis, Maria Cristina;
    • Deidda, Francesca;
    • Poddie, Fausto;
    • Morelli, Laura;
    • Farina, Gabriele;
    • Yun Li;
    • Dei, Mariano;
    • Lai, Sandra;
    • Mulas, Antonella;
    • Cuccuru, Gianmauro
    Publication type:
    Article
    3

    Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 492, doi. 10.1038/ng.585
    By:
    • Sherborne, Amy L.;
    • Hosking, Fay J.;
    • Prasad, Rashmi B.;
    • Kumar, Rajiv;
    • Koehler, Rolf;
    • Vijayakrishnan, Jayaram;
    • Papaemmanuil, Elli;
    • Bartram, Claus R.;
    • Stanulla, Martin;
    • Schrappe, Martin;
    • Gast, Andreas;
    • Dobbins, Sara E.;
    • Ma, Yussanne;
    • Sheridan, Eamonn;
    • Taylor, Malcolm;
    • Kinsey, Sally E.;
    • Lightfoot, Tracey;
    • Roman, Eve;
    • Irving, Julie A. E.;
    • Allan, James M.
    Publication type:
    Article
    4
    5

    De novo mutations of SETBP1 cause Schinzel-Giedion syndrome.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 483, doi. 10.1038/ng.581
    By:
    • Hoischen, Alexander;
    • van Bon, Bregje W. M.;
    • Gilissen, Christian;
    • Arts, Peer;
    • van Lier, Bart;
    • Steehouwer, Marloes;
    • de Vries, Petra;
    • de Reuver, Rick;
    • Wieskamp, Nienke;
    • Mortier, Geert;
    • Devriendt, Koen;
    • Amorim, Marta Z.;
    • Revencu, Nicole;
    • Kidd, Alexa;
    • Barbosa, Mafalda;
    • Turner, Anne;
    • Smith, Janine;
    • Oley, Christina;
    • Henderson, Alex;
    • Hayes, Ian M.
    Publication type:
    Article
    6

    Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 486, doi. 10.1038/ng.588
    By:
    • Shoubridge, Cheryl;
    • Tarpey, Patrick S.;
    • Abidi, Fatima;
    • Ramsden, Sarah L.;
    • Rujirabanjerd, Sinitdhorn;
    • Murphy, Jessica A.;
    • Boyle, Jackie;
    • Shaw, Marie;
    • Gardner, Alison;
    • Proos, Anne;
    • Puusepp, Helen;
    • Raymond, F. Lucy;
    • Schwartz, Charles E.;
    • Stevenson, Roger E.;
    • Turner, Gill;
    • Field, Michael;
    • Walikonis, Randall S.;
    • Harvey, Robert J.;
    • Hackett, Anna;
    • Futreal, P. Andrew
    Publication type:
    Article
    7
    8

    Genome-wide association study identifies five new breast cancer susceptibility loci.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 504, doi. 10.1038/ng.586
    By:
    • Turnbull, Clare;
    • Ahmed, Shahana;
    • Morrison, Jonathan;
    • Pernet, David;
    • Renwick, Anthony;
    • Maranian, Mel;
    • Seal, Sheila;
    • Ghoussaini, Maya;
    • Hines, Sarah;
    • Healey, Catherine S.;
    • Hughes, Deborah;
    • Warren-Perry, Margaret;
    • Tapper, William;
    • Eccles, Diana;
    • Evans, D. Gareth;
    • Hooning, Maartje;
    • Schutte, Mieke;
    • van den Ouweland, Ans;
    • Houlston, Richard;
    • Ross, Gillian
    Publication type:
    Article
    9

    A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 515, doi. 10.1038/ng.583
    By:
    • Kochi, Yuta;
    • Okada, Yukinori;
    • Suzuki, Akari;
    • Ikari, Katsunori;
    • Terao, Chikashi;
    • Takahashi, Atsushi;
    • Yamazaki, Keiko;
    • Hosono, Naoya;
    • Myouzen, Keiko;
    • Tsunoda, Tatsuhiko;
    • Kamatani, Naoyuki;
    • Furuichi, Tatsuya;
    • Ikegawa, Shiro;
    • Ohmura, Koichiro;
    • Mimori, Tsuneyo;
    • Matsuda, Fumihiko;
    • Iwamoto, Takuji;
    • Momohara, Shigeki;
    • Yamanaka, Hisashi;
    • Yamada, Ryo
    Publication type:
    Article
    10

    Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 520, doi. 10.1038/ng.562
    By:
    • Albagha, Omar M. E.;
    • Visconti, Micaela R.;
    • Alonso, Nerea;
    • Langston, Anne L.;
    • Cundy, Tim;
    • Dargie, Rosemary;
    • Dunlop, Malcolm G.;
    • Fraser, William D.;
    • Hooper, Michael J.;
    • Isaia, Gianluca;
    • Nicholson, Geoff C.;
    • del Pino Montes, Javier;
    • Gonzalez-Sarmiento, Rogelio;
    • di Stefano, Marco;
    • Tenesa, Albert;
    • Walsh, John P.;
    • Ralston, Stuart H.
    Publication type:
    Article
    11

    A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 525, doi. 10.1038/ng.580
    By:
    • Beaty, Terri H.;
    • Murray, Jeffrey C.;
    • Marazita, Mary L.;
    • Munger, Ronald G.;
    • Ruczinski, Ingo;
    • Hetmanski, Jacqueline B.;
    • Kung Yee Liang;
    • Wu, Tao;
    • Murray, Tanda;
    • Fallin, M. Daniele;
    • Redett, Richard A.;
    • Raymond, Gerald;
    • Schwender, Holger;
    • Jin, Sheng Chih;
    • Cooper, Margaret E.;
    • Dunnwald, Martine;
    • Mansilla, Maria A.;
    • Leslie, Elizabeth;
    • Bullard, Stephen;
    • Lidral, Andrew C.
    Publication type:
    Article
    12

    Deletion of the protein tyrosine phosphatase gene PTPN2 in T-cell acute lymphoblastic leukemia.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 530, doi. 10.1038/ng.587
    By:
    • Kleppe, Maria;
    • Lahortiga, Idoya;
    • El Chaar, Tiama;
    • De Keersmaecker, Kim;
    • Mentens, Nicole;
    • Graux, Carlos;
    • Van Roosbroeck, Katrien;
    • Ferrando, Adolfo A;
    • Langerak, Anton W;
    • Meijerink, Jules P P;
    • Sigaux, François;
    • Haferlach, Torsten;
    • Wlodarska, Iwona;
    • Vandenberghe, Peter;
    • Soulier, Jean;
    • Cools, Jan
    Publication type:
    Article
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    Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis.

    Published in:
    2010
    By:
    • Booth, David R.;
    • Heard, Robert N.;
    • Stewart, Graeme J.;
    • Cox, Mathew;
    • Scott, Rodney J.;
    • Lechner-Scott, Jeannette;
    • Goris, An;
    • Dobosi, Rita;
    • Dubois, Bénédicte;
    • Saarela, Janna;
    • Leppä, Virpi;
    • Peltonen, Leena;
    • Pirttila, Tuula;
    • Cournu-Rebeix, Isabelle;
    • Fontaine, Bertrand;
    • Bergamaschi, Laura;
    • D'Alfonso, Sandra;
    • Leone, Maurizio;
    • Lorentzen, Åslaug R;
    • Harbo, Hanne F.
    Publication type:
    Letter
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    Shaping a better rice plant.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 475, doi. 10.1038/ng0610-475
    By:
    • Springer, Nathan
    Publication type:
    Article
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    Research highlights.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 481, doi. 10.1038/ng0610-481
    By:
    • Bahcall, Orli;
    • Colosimo, Pamela;
    • Niemitz, Emily;
    • Vogan, Kyle
    Publication type:
    Article