Works matching IS 10614036 AND DT 2010 AND VI 42 AND IP 3

Results: 21
    1
    2

    A map of open chromatin in human pancreatic islets.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 255, doi. 10.1038/ng.530
    By:
    • Gaulton, Kyle J.;
    • Nammo, Takao;
    • Pasquali, Lorenzo;
    • Simon, Jeremy M.;
    • Giresi, Paul G.;
    • Fogarty, Marie P.;
    • Panhuis, Tami M.;
    • Mieczkowski, Piotr;
    • Secchi, Antonio;
    • Bosco, Domenico;
    • Berney, Thierry;
    • Montanya, Eduard;
    • Mohlke, Karen L.;
    • Lieb, Jason D.;
    • Ferrer, Jorge
    Publication type:
    Article
    3
    4

    Plasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugs.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 268, doi. 10.1038/ng.528
    By:
    • Jianbing Mu;
    • Myers, Rachel A.;
    • Hongying Jiang;
    • Shengfa Liu;
    • Ricklefs, Stacy;
    • Waisberg, Michael;
    • Chotivanich, Kesinee;
    • Wilairatana, Polrat;
    • Krudsood, Srivicha;
    • White, Nicholas J.;
    • Udomsangpetch, Rachanee;
    • Liwang Cui;
    • May Ho;
    • Fengzhen Ou;
    • Haibo Li;
    • Jianping Song;
    • Guoqiao Li;
    • Xinhua Wang;
    • Seila, Suon;
    • Sokunthea, Sreng
    Publication type:
    Article
    5
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    Common variants near TERC are associated with mean telomere length.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 197, doi. 10.1038/ng.532
    By:
    • Codd, Veryan;
    • Mangino, Massimo;
    • van der Harst, Pim;
    • Braund, Peter S.;
    • Kaiser, Michael;
    • Beveridge, Alan J.;
    • Rafelt, Suzanne;
    • Moore, Jasbir;
    • Nelson, Chris;
    • Soranzo, Nicole;
    • Guangju Zhai;
    • Valdes, Ana M.;
    • Blackburn, Hannah;
    • Leach, Irene Mateo;
    • de Boer, Rudolf A.;
    • Goodall, Alison H.;
    • Ouwehand, Willem;
    • van Veldhuisen, Dirk J.;
    • van Gilst, Wiek H.;
    • Navis, Gerjan
    Publication type:
    Article
    7

    Variants in FAM13A are associated with chronic obstructive pulmonary disease.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 200, doi. 10.1038/ng.535
    By:
    • Cho, Michael H.;
    • Boutaoui, Nadia;
    • Klanderman, Barbara J.;
    • Sylvia, Jody S.;
    • Ziniti, John P.;
    • Hersh, Craig P.;
    • DeMeo, Dawn L.;
    • Hunninghake, Gary M.;
    • Litonjua, Augusto A.;
    • Sparrow, David;
    • Lange, Christoph;
    • Sungho Won;
    • Murphy, James R.;
    • Beaty, Terri H.;
    • Regan, Elizabeth A.;
    • Make, Barry J.;
    • Hokanson, John E.;
    • Crapo, James D.;
    • Xiangyang Kong;
    • Anderson, Wayne H.
    Publication type:
    Article
    8

    A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 203, doi. 10.1038/ng.534
    By:
    • Girirajan, Santhosh;
    • Rosenfeld, Jill A.;
    • Cooper, Gregory M.;
    • Antonacci, Francesca;
    • Siswara, Priscillia;
    • Itsara, Andy;
    • Vives, Laura;
    • Walsh, Tom;
    • McCarthy, Shane E.;
    • Baker, Carl;
    • Mefford, Heather C.;
    • Kidd, Jeffrey M.;
    • Browning, Sharon R.;
    • Browning, Brian L.;
    • Dickel, Diane E.;
    • Levy, Deborah L.;
    • Ballif, Blake C.;
    • Platky, Kathryn;
    • Farber, Darren M.;
    • Gowans, Gordon C.
    Publication type:
    Article
    9
    10

    Identification of DOK genes as lung tumor suppressors.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 216, doi. 10.1038/ng.527
    By:
    • Berger, Alice H.;
    • Niki, Masaru;
    • Morotti, Alessandro;
    • Taylor, Barry S.;
    • Socci, Nicholas D.;
    • Viale, Agnes;
    • Brennan, Cameron;
    • Szoke, Janos;
    • Motoi, Noriko;
    • Rothman, Paul B.;
    • Teruya-Feldstein, Julie;
    • Gerald, William L.;
    • Ladanyi, Marc;
    • Pandolfi, Pier Paolo
    Publication type:
    Article
    11

    A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 224, doi. 10.1038/ng.522
    By:
    • Petersen, Gloria M.;
    • Amundadottir, Laufey;
    • Fuchs, Charles S.;
    • Kraft, Peter;
    • Stolzenberg-Solomon, Rachael Z.;
    • Jacobs, Kevin B.;
    • Arslan, Alan A.;
    • Bueno-de-Mesquita, H. Bas;
    • Gallinger, Steven;
    • Gross, Myron;
    • Helzlsouer, Kathy;
    • Holly, Elizabeth A.;
    • Jacobs, Eric J.;
    • Klein, Alison P.;
    • LaCroix, Andrea;
    • Donghui Li;
    • Mandelson, Margaret T.;
    • Olson, Sara H.;
    • Risch, Harvey A.;
    • Wei Zheng
    Publication type:
    Article
    12

    Germline mutations in TMEM127 confer susceptibility to pheochromocytoma.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 229, doi. 10.1038/ng.533
    By:
    • Yuejuan Qin;
    • Li Yao;
    • King, Elizabeth E.;
    • Buddavarapu, Kalyan;
    • Lenci, Romina E.;
    • Chocron, E Sandra;
    • Lechleiter, James D.;
    • Sass, Meghan;
    • Aronin, Neil;
    • Schiavi, Francesca;
    • Boaretto, Francesca;
    • Opocher, Giuseppe;
    • Toledo, Rodrigo A.;
    • Toledo, Sergio P. A.;
    • Stiles, Charles;
    • Aguiar, Ricardo C. T.;
    • Dahia, Patricia L. M.
    Publication type:
    Article
    13

    Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 234, doi. 10.1038/ng.536
    By:
    • Van Deerlin, Vivianna M.;
    • Sleiman, Patrick M. A.;
    • Martinez-Lage, Maria;
    • Chen-Plotkin, Alice;
    • Li-San Wang;
    • Graff-Radford, Neill R.;
    • Dickson, Dennis W.;
    • Rademakers, Rosa;
    • Boeve, Bradley F.;
    • Grossman, Murray;
    • Arnold, Steven E.;
    • Mann, David M. A.;
    • Pickering-Brown, Stuart M.;
    • Seelaar, Harro;
    • Heutink, Peter;
    • van Swieten, John C.;
    • Murrell, Jill R.;
    • Ghetti, Bernardino;
    • Spina, Salvatore;
    • Grafman, Jordan
    Publication type:
    Article
    14

    Common variants in KCNN3 are associated with lone atrial fibrillation.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 240, doi. 10.1038/ng.537
    By:
    • Ellinor, Patrick T.;
    • Lunetta, Kathryn L.;
    • Glazer, Nicole L.;
    • Pfeufer, Arne;
    • Alonso, Alvaro;
    • Chung, Mina K.;
    • Sinner, Moritz F.;
    • de Bakker, Paul I. W.;
    • Mueller, Martina;
    • Lubitz, Steven A.;
    • Fox, Ervin;
    • Darbar, Dawood;
    • Smith, Nicholas L.;
    • Smith, Jonathan D.;
    • Schnabel, Renate B.;
    • Soliman, Elsayed Z.;
    • Rice, Kenneth M.;
    • Van Wagoner, David R.;
    • Beckmann, Britt-M.;
    • van Noord, Charlotte
    Publication type:
    Article
    15

    Mutations in PNKP cause microcephaly, seizures and defects in DNA repair.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 245, doi. 10.1038/ng.526
    By:
    • Jun Shen;
    • Gilmore, Edward C.;
    • Marshall, Christine A.;
    • Haddadin, Mary;
    • Reynolds, John J.;
    • Eyaid, Wafaa;
    • Bodell, Adria;
    • Barry, Brenda;
    • Gleason, Danielle;
    • Allen, Kathryn;
    • Ganesh, Vijay S.;
    • Chang, Bernard S.;
    • Grix, Arthur;
    • Hill, R. Sean;
    • Topcu, Meral;
    • Caldecott, Keith W.;
    • Barkovich, A. James;
    • Walsh, Christopher A.
    Publication type:
    Article
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    Research highlights.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 195, doi. 10.1038/ng0310-195
    By:
    • Bahcall, Orli;
    • Colosimo, Pamela;
    • Niemitz, Emily;
    • Vogan, Kyle
    Publication type:
    Article