Works matching IS 10614036 AND DT 2010 AND VI 42 AND IP 2

Results: 19
    1

    New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 105, doi. 10.1038/ng.520
    By:
    • Dupuis, Josée;
    • Langenberg, Claudia;
    • Prokopenko, Inga;
    • Saxena, Richa;
    • Soranzo, Nicole;
    • Jackson, Anne U.;
    • Wheeler, Eleanor;
    • Glazer, Nicole L.;
    • Bouatia-Naji, Nabila;
    • Gloyn, Anna L.;
    • Lindgren, Cecilia M.;
    • Mägi, Reedik;
    • Morris, Andrew P.;
    • Randall, Joshua;
    • Johnson, Toby;
    • Elliott, Paul;
    • Rybin, Denis;
    • Thorleifsson, Gudmar;
    • Steinthorsdottir, Valgerdur;
    • Henneman, Peter
    Publication type:
    Article
    2

    Several common variants modulate heart rate, PR interval and QRS duration.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 117, doi. 10.1038/ng.511
    By:
    • Holm, Hilma;
    • Gudbjartsson, Daniel F.;
    • Arnar, David O.;
    • Thorleifsson, Gudmar;
    • Thorgeirsson, Gudmundur;
    • Stefansdottir, Hrafnhildur;
    • Gudjonsson, Sigurjon A.;
    • Jonasdottir, Aslaug;
    • Mathiesen, Ellisiv B.;
    • Njølstad, Inger;
    • Nyrnes, Audhild;
    • Wilsgaard, Tom;
    • Hald, Erin M.;
    • Hveem, Kristian;
    • Stoltenberg, Camilla;
    • Løchen, Maja-Lisa;
    • Kong, Augustine;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari
    Publication type:
    Article
    3

    Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 123, doi. 10.1038/ng.513
    By:
    • Reveille, John D.;
    • Sims, Anne-Marie;
    • Danoy, Patrick;
    • Evans, David M.;
    • Leo, Paul;
    • Pointon, Jennifer J.;
    • Rui Jin;
    • Xiaodong Zhou;
    • Bradbury, Linda A.;
    • Appleton, Louise H.;
    • Davis, John C.;
    • Diekman, Laura;
    • Doan, Tracey;
    • Dowling, Alison;
    • Duan, Ran;
    • Duncan, Emma L.;
    • Farrar, Claire;
    • Hadler, Johanna;
    • Harvey, David;
    • Karaderi, Tugce
    Publication type:
    Article
    4

    Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 128, doi. 10.1038/ng.523
    By:
    • McMahon, Francis J.;
    • Akula, Nirmala;
    • Schulze, Thomas G.;
    • Muglia, Pierandrea;
    • Tozzi, Federica;
    • Detera-Wadleigh, Sevilla D.;
    • Steele, C. J. M.;
    • Breuer, René;
    • Strohmaier, Jana;
    • Wendland, Jens R.;
    • Mattheisen, Manuel;
    • Mühleisen, Thomas W.;
    • Maier, Wolfgang;
    • Nöthen, Markus M.;
    • Cichon, Sven;
    • Farmer, Anne;
    • Vincent, John B.;
    • Holsboer, Florian;
    • Preisig, Martin;
    • Rietschel, Marcella
    Publication type:
    Article
    5

    Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 132, doi. 10.1038/ng.510
    By:
    • Crowther-Swanepoel, Dalemari;
    • Broderick, Peter;
    • Di Bernardo, Maria Chiara;
    • Dobbins, Sara E.;
    • Torres, María;
    • Mansouri, Mahmoud;
    • Ruiz-Ponte, Clara;
    • Enjuanes, Anna;
    • Rosenquist, Richard;
    • Carracedo, Angel;
    • Jurlander, Jesper;
    • Campo, Elias;
    • Juliusson, Gunnar;
    • Montserrat, Emilio;
    • Smedby, Karin E.;
    • Dyer, Martin J. S.;
    • Matutes, Estella;
    • Dearden, Claire;
    • Sunter, Nicola J.;
    • Hall, Andrew G.
    Publication type:
    Article
    6

    A genome-wide perspective of genetic variation in human metabolism.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 137, doi. 10.1038/ng.507
    By:
    • Illig, Thomas;
    • Gieger, Christian;
    • Guangju Zhai;
    • Römisch-Margl, Werner;
    • Wang-Sattler, Rui;
    • Prehn, Cornelia;
    • Altmaier, Elisabeth;
    • Kastenmüller, Gabi;
    • Kato, Bernet S.;
    • Mewes, Hans-Werner;
    • Meitinger, Thomas;
    • de Angelis, Martin Hrabé;
    • Kronenberg, Florian;
    • Soranzo, Nicole;
    • Wichmann, H-Erich;
    • Spector, Tim D.;
    • Adamski, Jerzy;
    • Suhre, Karsten
    Publication type:
    Article
    7

    Mutations in TRPV4 cause Charcot-Marie-Tooth disease type 2C.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 170, doi. 10.1038/ng.512
    By:
    • Landouré, Guida;
    • Zdebik, Anselm A.;
    • Martinez, Tara L.;
    • Burnett, Barrington G.;
    • Stanescu, Horia C.;
    • Inada, Hitoshi;
    • Yijun Shi;
    • Taye, Addis A.;
    • Lingling Kong;
    • Munns, Clare H.;
    • Choo, Shelly S.;
    • Phelps, Christopher B.;
    • Paudel, Reema;
    • Houlden, Henry;
    • Ludlow, Christy L.;
    • Caterina, Michael J.;
    • Gaudet, Rachelle;
    • Kleta, Robert;
    • Fischbeck, Kenneth H.;
    • Sumner, Charlotte J.
    Publication type:
    Article
    8

    Genetic variation in SCN10A influences cardiac conduction.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 149, doi. 10.1038/ng.516
    By:
    • John C. Chambers;
    • Jing Zhao;
    • Terracciano, Cesare M. N.;
    • Bezzina, Connie R.;
    • Weihua Zhang;
    • Kaba, Riyaz;
    • Navaratnarajah, Manoraj;
    • Lotlikar, Amol;
    • Sehmi, Joban S.;
    • Kooner, Manraj K.;
    • Guohong Deng;
    • Siedlecka, Urszula;
    • Parasramka, Saurabh;
    • El-Hamamsy, Ismail;
    • Wass, Mark N.;
    • Dekker, Lukas R. C.;
    • de Jong, Jonas S. S. G.;
    • Sternberg, Michael J. E.;
    • McKenna, William;
    • Severs, Nicholas J.
    Publication type:
    Article
    9

    Genome-wide association study of PR interval.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 153, doi. 10.1038/ng.517
    By:
    • Pfeufer, Arne;
    • van Noord, Charlotte;
    • Marciante, Kristin D.;
    • Arking, Dan E.;
    • Larson, Martin G.;
    • Smith, Albert Vernon;
    • Tarasov, Kirill V.;
    • Müller, Martina;
    • Sotoodehnia, Nona;
    • Sinner, Moritz F.;
    • Verwoert, Germaine C.;
    • Man Li1;
    • Kao, W. H. Linda;
    • Köttgen, Anna;
    • Coresh, Josef;
    • Bis, Joshua C.;
    • Psaty, Bruce M.;
    • Rice, Kenneth;
    • Rotter, Jerome I.;
    • Rivadeneira, Fernando
    Publication type:
    Article
    10

    Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 160, doi. 10.1038/ng.508
    By:
    • Auer-Grumbach, Michaela;
    • Olschewski, Andrea;
    • Papić, Lea;
    • Kremer, Hannie;
    • McEntagart, Meriel E.;
    • Uhrig, Sabine;
    • Fischer, Carina;
    • Fröhlich, Eleonore;
    • Bálint, Zoltán;
    • Bi Tang;
    • Strohmaier, Heimo;
    • Lochmüller, Hanns;
    • Schlotter-Weigel, Beate;
    • Senderek, Jan;
    • Krebs, Angelika;
    • Dick, Katherine J.;
    • Petty, Richard;
    • Longman, Cheryl;
    • Anderson, Neil E.;
    • Padberg, George W.
    Publication type:
    Article
    11
    12

    Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 142, doi. 10.1038/ng.521
    By:
    • Saxena, Richa;
    • Hivert, Marie-France;
    • Langenberg, Claudia;
    • Tanaka, Toshiko;
    • Pankow, James S.;
    • Vollenweider, Peter;
    • Lyssenko, Valeriya;
    • Bouatia-Naji, Nabila;
    • Dupuis, Josée;
    • Jackson, Anne U.;
    • Linda Kao, W. H.;
    • Man Li;
    • Glazer, Nicole L.;
    • Manning, Alisa K.;
    • Jian'an Luan;
    • Stringham, Heather M.;
    • Prokopenko, Inga;
    • Johnson, Toby;
    • Grarup, Niels;
    • Boesgaard, Trine W.
    Publication type:
    Article
    13

    AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 175, doi. 10.1038/ng.519
    By:
    • Louie, Carrie M.;
    • Caridi, Gianluca;
    • Lopes, Vanda S.;
    • Brancati, Francesco;
    • Kispert, Andreas;
    • Lancaster, Madeline A.;
    • Schlossman, Andrew M.;
    • Otto, Edgar A.;
    • Leitges, Michael;
    • Gröne, Hermann-Josef;
    • Lopez, Irma;
    • Gudiseva, Harini V.;
    • O'Toole, John F.;
    • Vallespin, Elena;
    • Ayyagari, Radha;
    • Ayuso, Carmen;
    • Cremers, Frans P. M.;
    • den Hollander, Anneke I.;
    • Koenekoop, Robert K.;
    • Dallapiccola, Bruno
    Publication type:
    Article
    14

    Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 181, doi. 10.1038/ng.518
    By:
    • Morin, Ryan D.;
    • Johnson, Nathalie A.;
    • Severson, Tesa M.;
    • Mungall, Andrew J.;
    • Jianghong An;
    • Goya, Rodrigo;
    • Paul, Jessica E.;
    • Boyle, Merrill;
    • Woolcock, Bruce W.;
    • Kuchenbauer, Florian;
    • Yap, Damian;
    • Humphries, R. Keith;
    • Griffith, Obi L.;
    • Shah, Sohrab;
    • Zhu, Henry;
    • Kimbara, Michelle;
    • Shashkin, Pavel;
    • Charlot, Jean F.;
    • Tcherpakov, Marianna;
    • Corbett, Richard
    Publication type:
    Article
    15
    16

    Research highlights.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 103, doi. 10.1038/ng0210-103
    By:
    • Bahcall, Orli;
    • Colosimo, Pamela;
    • Niemitz, Emily;
    • Vogan, Kyle
    Publication type:
    Article
    17
    18

    Inborn variation in metabolism.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 97, doi. 10.1038/ng0210-97
    By:
    • Mootha, Vamsi K.;
    • Hirschhorn, Joel N.
    Publication type:
    Article
    19

    Channelopathies converge on TRPV4.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 98, doi. 10.1038/ng0210-98
    By:
    • Nilius, Bernd;
    • Owsianik, Grzegorz
    Publication type:
    Article