Works matching IS 10614036 AND DT 2009 AND VI 41 AND IP 1

Results: 25
    1

    New sequence variants associated with bone mineral density.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 15, doi. 10.1038/ng.284
    By:
    • Styrkarsdottir, Unnur;
    • Halldorsson, Bjarni V.;
    • Gretarsdottir, Solveig;
    • Gudbjartsson, Daniel F.;
    • Walters, G. Bragi;
    • Ingvarsson, Thorvaldur;
    • Jonsdottir, Thorbjorg;
    • Saemundsdottir, Jona;
    • Snorradóttir, Steinunn;
    • Center, Jacqueline R.;
    • Nguyen, Tuan V.;
    • Alexandersen, Peter;
    • Gulcher, Jeffrey R.;
    • Eisman, John A.;
    • Christiansen, Claus;
    • Sigurdsson, Gunnar;
    • Kong, Augustine;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari
    Publication type:
    Article
    2

    Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 25, doi. 10.1038/ng.287
    By:
    • Willer, Cristen J.;
    • Speliotes, Elizabeth K.;
    • Loos, Ruth J. F.;
    • Shengxu Li;
    • Lindgren, Cecilia M.;
    • Heid, Iris M.;
    • Berndt, Sonja I.;
    • Elliott, Amanda L.;
    • Jackson, Anne U.;
    • Lamina, Claudia;
    • Lettre, Guillaume;
    • Lim, Noha;
    • Lyon, Helen N.;
    • McCarroll, Steven A.;
    • Papadakis, Konstantinos;
    • Lu Qi;
    • Randall, Joshua C.;
    • Roccasecca, Rosa Maria;
    • Sanna, Serena;
    • Scheet, Paul
    Publication type:
    Article
    3

    Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 18, doi. 10.1038/ng.274
    By:
    • Thorleifsson, Gudmar;
    • Walters, G. Bragi;
    • Gudbjartsson, Daniel F.;
    • Steinthorsdottir, Valgerdur;
    • Sulem, Patrick;
    • Helgadottir, Anna;
    • Styrkarsdottir, Unnur;
    • Gretarsdottir, Solveig;
    • Thorlacius, Steinunn;
    • Jonsdottir, Ingileif;
    • Jonsdottir, Thorbjorg;
    • Olafsdottir, Elinborg J.;
    • Olafsdottir, Gudridur H.;
    • Jonsson, Thorvaldur;
    • Jonsson, Frosti;
    • Borch-Johnsen, Knut;
    • Hansen, Torben;
    • Andersen, Gitte;
    • Jorgensen, Torben;
    • Lauritzen, Torsten
    Publication type:
    Article
    4
    5

    Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 106, doi. 10.1038/ng.278
    By:
    • Lagresle-Peyrou, Chantal;
    • Six, Emmanuelle M.;
    • Picard, Capucine;
    • Rieux-Laucat, Frédéric;
    • Michel, Vincent;
    • Ditadi, Andrea;
    • Chappedelaine, Corinne Demerens-de;
    • Morillon, Estelle;
    • Valensi, Françoise;
    • Simon-Stoos, Karen L;
    • Mullikin, James C;
    • Noroski, Lenora M;
    • Besse, Céline;
    • Wulffraat, Nicolas M.;
    • Ferster, Alina;
    • Abecasis, Manuel M.;
    • Calvo, Fabien;
    • Petit, Christine;
    • Candotti, Fabio;
    • Abel, Laurent
    Publication type:
    Article
    6

    Teamwork.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 1, doi. 10.1038/ng0109-1
    Publication type:
    Article
    7
    8

    Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 47, doi. 10.1038/ng.269
    By:
    • Aulchenko, Yurii S.;
    • Ripatti, Samuli;
    • Lindqvist, Ida;
    • Boomsma, Dorret;
    • Heid, Iris M.;
    • Pramstaller, Peter P.;
    • Penninx, Brenda W. J. H.;
    • Janssens, A. Cecile J. W.;
    • Wilson, James F.;
    • Spector, Tim;
    • Martin, Nicholas G.;
    • Pedersen, Nancy L.;
    • Kyvik, Kirsten Ohm;
    • Kaprio, Jaakko;
    • Hofman, Albert;
    • Freimer, Nelson B.;
    • Jarvelin, Marjo-Riitta;
    • Gyllensten, Ulf;
    • Campbell, Harry;
    • Rudan, Igor
    Publication type:
    Article
    9

    Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 35, doi. 10.1038/ng.271
    By:
    • Sabatti, Chiara;
    • Service, Susan K.;
    • Hartikainen, Anna-Liisa;
    • Pouta, Anneli;
    • Ripatti, Samuli;
    • Brodsky, Jae;
    • Jones, Chris G.;
    • Zaitlen, Noah A.;
    • Varilo, Teppo;
    • Kaakinen, Marika;
    • Sovio, Ulla;
    • Ruokonen, Aimo;
    • Laitinen, Jaana;
    • Jakkula, Eveliina;
    • Coin, Lachlan;
    • Hoggart, Clive;
    • Collins, Andrew;
    • Turunen, Hannu;
    • Gabriel, Stacey;
    • Elliot, Paul
    Publication type:
    Article
    10

    Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 112, doi. 10.1038/ng.283
    By:
    • Ligtenberg, Marjolijn J. L.;
    • Kuiper, Roland P.;
    • Tsun Leung Chan;
    • Goossens, Monique;
    • Hebeda, Konnie M.;
    • Voorendt, Marsha;
    • Lee, Tracy Y. H.;
    • Bodmer, Danielle;
    • Hoenselaar, Eveline;
    • Hendriks-Cornelissen, Sandra J. B.;
    • Wai Yin Tsui;
    • Chi Kwan Kong;
    • Brunner, Han G.;
    • van Kessel, Ad Geurts;
    • Siu Tsan Yuen;
    • van Krieken, J Han J. M.;
    • Leung, Suet Yi;
    • Hoogerbrugge, Nicoline
    Publication type:
    Article
    11

    Common variants at 30 loci contribute to polygenic dyslipidemia.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 56, doi. 10.1038/ng.291
    By:
    • Kathiresan, Sekar;
    • Willer, Cristen J.;
    • Peloso, Gina M;
    • Demissie, Serkalem;
    • Musunuru, Kiran;
    • Schadt, Eric E.;
    • Kaplan, Lee;
    • Bennett, Derrick;
    • Li, Yun;
    • Tanaka, Toshiko;
    • Voight, Benjamin F.;
    • Bonnycastle, Lori L.;
    • Jackson, Anne U.;
    • Crawford, Gabriel;
    • Surti, Aarti;
    • Guiducci, Candace;
    • Burtt, Noel P.;
    • Parish, Sarah;
    • Clarke, Robert;
    • Zelenika, Diana
    Publication type:
    Article
    12
    13

    Common variants in the NLRP3 region contribute to Crohn's disease susceptibility.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 71, doi. 10.1038/ng.285
    By:
    • Villani, Alexandra-Chloé;
    • Lemire, Mathieu;
    • Fortin, Geneviève;
    • Louis, Edouard;
    • Silverberg, Mark S.;
    • Collette, Catherine;
    • Baba, Nobuyasu;
    • Libioulle, Cécile;
    • Belaiche, Jacques;
    • Bitton, Alain;
    • Gaudet, Daniel;
    • Cohen, Albert;
    • Langelier, Diane;
    • Fortin, Paul R.;
    • Wither, Joan E.;
    • Sarfati, Marika;
    • Rutgeerts, Paul;
    • Rioux, John D.;
    • Vermeire, Severine;
    • Hudson, Thomas J.
    Publication type:
    Article
    14

    Variants in MTNR1B influence fasting glucose levels.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 77, doi. 10.1038/ng.290
    By:
    • Prokopenko, Inga;
    • Langenberg, Claudia;
    • Florez, Jose C.;
    • Saxena, Richa;
    • Soranzo, Nicole;
    • Thorleifsson, Gudmar;
    • Loos, Ruth J. F.;
    • Manning, Alisa K.;
    • Jackson, Anne U.;
    • Aulchenko, Yurii;
    • Potter, Simon C.;
    • Erdos, Michael R.;
    • Sanna, Serena;
    • Hottenga, Jouke-Jan;
    • Wheeler, Eleanor;
    • Kaakinen, Marika;
    • Lyssenko, Valeriya;
    • Chen, Wei-Min;
    • Ahmadi, Kourosh;
    • Beckmann, Jacques S.
    Publication type:
    Article
    15

    Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 82, doi. 10.1038/ng.288
    By:
    • Lyssenko, Valeriya;
    • Nagorny, Cecilia L. F.;
    • Erdos, Michael R.;
    • Wierup, Nils;
    • Jonsson, Anna;
    • Spégel, Peter;
    • Bugliani, Marco;
    • Saxena, Richa;
    • Fex, Malin;
    • Pulizzi, Nicolo;
    • Isomaa, Bo;
    • Tuomi, Tiinamaija;
    • Nilsson, Peter;
    • Kuusisto, Johanna;
    • Tuomilehto, Jaakko;
    • Boehnke, Michael;
    • Altshuler, David;
    • Sundler, Frank;
    • Eriksson, Johan G.;
    • Jackson, Anne U.
    Publication type:
    Article
    16

    A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 89, doi. 10.1038/ng.277
    By:
    • Bouatia-Naji, Nabila;
    • Bonnefond, Amélie;
    • Cavalcanti-Proença, Christine;
    • Sparsø, Thomas;
    • Holmkvist, Johan;
    • Marchand, Marion;
    • Delplanque, Jérôme;
    • Lobbens, Stéphane;
    • Rocheleau, Ghislain;
    • Durand, Emmanuelle;
    • De Graeve, Franck;
    • Chèvre, Jean-Claude;
    • Borch-Johnsen, Knut;
    • Hartikainen, Anna-Liisa;
    • Ruokonen, Aimo;
    • Tichet, Jean;
    • Marre, Michel;
    • Weill, Jacques;
    • Heude, Barbara;
    • Tauber, Maithé
    Publication type:
    Article
    17

    Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 95, doi. 10.1038/ng.270
    By:
    • Jenkins, Zandra A.;
    • van Kogelenberg, Margriet;
    • Morgan, Tim;
    • Jeffs, Aaron;
    • Fukuzawa, Ryuji;
    • Pearl, Esther;
    • Thaller, Christina;
    • Hing, Anne V.;
    • Porteous, Mary E.;
    • Garcia-Miñaur, Sixto;
    • Bohring, Axel;
    • Lacombe, Didier;
    • Stewart, Fiona;
    • Fiskerstrand, Torunn;
    • Bindoff, Laurence;
    • Berland, Siren;
    • Adès, Lesley C.;
    • Tchan, Michel;
    • David, Albert;
    • Wilson, Louise C.
    Publication type:
    Article
    18
    19

    Research Highlights.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 13, doi. 10.1038/ng0109-13
    By:
    • Bachall, Orli;
    • Khidr, Lily;
    • Packer, Alan;
    • Vogan, Kyle
    Publication type:
    Article
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