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

Results: 19

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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

    • Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4.

      Published in:
      Nature Genetics, 2010, v. 42, n. 2, p. 165, doi. 10.1038/ng.509
      By:
      • Han-Xiang Deng;
      • Klein, Christopher J.;
      • Jianhua Yan;
      • Yong Shi;
      • Yanhong Wu;
      • Fecto, Faisal;
      • Hau-Jie Yau;
      • Yi Yang;
      • Hong Zhai;
      • Siddique, Nailah;
      • Hedley-Whyte, E Tessa;
      • DeLong, Robert;
      • Martina, Marco;
      • Dyck, Peter J.;
      • Siddique, Teepu
      Publication type:
      Article

    • 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

    • 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

    • 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

    • Deregulation of H3K27 methylation in cancer.

      Published in:
      Nature Genetics, 2010, v. 42, n. 2, p. 100, doi. 10.1038/ng0210-100
      By:
      • Martinez-Garcia, Eva;
      • Licht, Jonathan D.
      Publication type:
      Article

    • 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

    • 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

    • Conclusion by exclusion.

      Published in:
      2010
      Publication type:
      Editorial

    • 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