Works matching IS 10614036 AND DT 2008 AND VI 40 AND IP 2

Results: 32
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    Positively disruptive.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 119, doi. 10.1038/ng0208-119
    Publication type:
    Article
    3

    The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 217, doi. 10.1038/ng.72
    By:
    • Helgadottir, Anna;
    • Thorleifsson, Gudmar;
    • Magnusson, Kristinn P.;
    • Grétarsdottir, Solveig;
    • Steinthorsdottir, Valgerdur;
    • Manolescu, Andrei;
    • Jones, Gregory T.;
    • Rinkel, Gabriel J. E.;
    • Blankensteijn, Jan D.;
    • Ronkainen, Antti;
    • Jääskeläinen, Juha E.;
    • Kyo, Yoshiki;
    • Lenk, Guy M.;
    • Sakalihasan, Natzi;
    • Kostulas, Konstantinos;
    • Gottsäter, Anders;
    • Flex, Andrea;
    • Stefansson, Hreinn;
    • Hansen, Torben;
    • Andersen, Gitte
    Publication type:
    Article
    4

    Common variants in the GDF5-UQCC region are associated with variation in human height.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 198, doi. 10.1038/ng.74
    By:
    • Sanna, Serena;
    • Jackson, Anne U.;
    • Nagaraja, Ramaiah;
    • Willer, Cristen J.;
    • Wei-Min Chen;
    • Bonnycastle, Lori L.;
    • Haiqing Shen;
    • Timpson, Nicholas;
    • Lettre, Guillaume;
    • Usala, Gianluca;
    • Chines, Peter S.;
    • Stringham, Heather M.;
    • Scott, Laura J.;
    • Dei, Mariano;
    • Lai, Sandra;
    • Albai, Giuseppe;
    • Crisponi, Laura;
    • Naitza, Silvia;
    • Doheny, Kimberly F.;
    • Pugh, Elizabeth W.
    Publication type:
    Article
    5

    Newly identified loci that influence lipid concentrations and risk of coronary artery disease.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 161, doi. 10.1038/ng.76
    By:
    • Willer, Cristen J.;
    • Sanna, Serena;
    • Jackson, Anne U.;
    • Scuteri, Angelo;
    • Bonnycastle, Lori L.;
    • Clarke, Robert;
    • Heath, Simon C.;
    • Timpson, Nicholas J.;
    • Najjar, Samer S.;
    • Stringham, Heather M.;
    • Strait, James;
    • Duren, William L.;
    • Maschio, Andrea;
    • Busonero, Fabio;
    • Mulas, Antonella;
    • Albai, Giuseppe;
    • Swift, Amy J.;
    • Morken, Mario A.;
    • Narisu, Narisu;
    • Bennett, Derrick
    Publication type:
    Article
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    Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 237, doi. 10.1038/ng.2007.56
    By:
    • Kagami, Masayo;
    • Sekita, Yoichi;
    • Nishimura, Gen;
    • Irie, Masahito;
    • Kato, Fumiko;
    • Okada, Michiyo;
    • Yamamori, Shunji;
    • Kishimoto, Hiroshi;
    • Nakayama, Masahiro;
    • Tanaka, Yukichi;
    • Matsuoka, Kentarou;
    • Takahashi, Tsutomu;
    • Noguchi, Mika;
    • Tanaka, Yoko;
    • Masumoto, Kouji;
    • Utsunomiya, Takeshi;
    • Kouzan, Hiroko;
    • Komatsu, Yumiko;
    • Ohashi, Hirofumi;
    • Kurosawa, Kenji
    Publication type:
    Article
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    Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 149, doi. 10.1038/ng.2007.61
    By:
    • Kooner, Jaspal S.;
    • Chambers, John C.;
    • Aguilar-Salinas, Carlos A.;
    • Hinds, David A.;
    • Hyde, Craig L.;
    • Warnes, Gregory R.;
    • Gómez Pérez, Francisco J.;
    • Frazer, Kelly A.;
    • Elliott, Paul;
    • Scott, James;
    • Milos, Patrice M.;
    • Cox, David R.;
    • Thompson, John F.
    Publication type:
    Article
    12

    Deficiency or inhibition of oxygen sensor Phd1 induces hypoxia tolerance by reprogramming basal metabolism.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 170, doi. 10.1038/ng.2007.62
    By:
    • Aragonés, Julián;
    • Schneider, Martin;
    • Van Geyte, Katie;
    • Fraisl, Peter;
    • Dresselaers, Tom;
    • Mazzone, Massimiliano;
    • Dirkx, Ruud;
    • Zacchigna, Serena;
    • Lemieux, Hélène;
    • Nam Ho Jeoung;
    • Lambrechts, Diether;
    • Bishop, Tammie;
    • Lafuste, Peggy;
    • Diez-Juan, Antonio;
    • Harten, Sarah K.;
    • Van Noten, Pieter;
    • De Bock, Katrien;
    • Willam, Carsten;
    • Tjwa, Marc;
    • Grosfeld, Alexandra
    Publication type:
    Article
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    A nonsynonymous functional variant in integrin-α<sub>M</sub> (encoded by ITGAM) is associated with systemic lupus erythematosus.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 152, doi. 10.1038/ng.71
    By:
    • Nath, Swapan K.;
    • Shizhong Han;
    • Kim-Howard, Xana;
    • Kelly, Jennifer A.;
    • Viswanathan, Parvathi;
    • Gilkeson, Gary S.;
    • Wei Chen;
    • Cheng Zhu;
    • McEver, Rodger P.;
    • Kimberly, Robert P.;
    • Alarcón-Riquelme, Marta E.;
    • Vyse, Timothy J.;
    • Quan-Zhen Li;
    • Wakeland, Edward K.;
    • Merrill, Joan T.;
    • James, Judith A.;
    • Kaufman, Kenneth M.;
    • Guthridge, Joel M.;
    • Harley, John B.
    Publication type:
    Article
    18

    Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 204, doi. 10.1038/ng.81
    By:
    • Harley, John B.;
    • Alarcón-Riquelme, Marta E.;
    • Criswell, Lindsey A.;
    • Jacob, Chaim O.;
    • Kimberly, Robert P.;
    • Moser, Kathy L.;
    • Tsao, Betty P.;
    • Vyse, Timothy J.;
    • Langefeld, Carl D.;
    • Nath, Swapan K.;
    • Guthridge, Joel M.;
    • Cobb, Beth L.;
    • Mirel, Daniel B.;
    • Marion, Miranda C.;
    • Williams, Adrienne H.;
    • Divers, Jasmin;
    • Wei Wang;
    • Frank, Summer G.;
    • Namjou, Bahram;
    • Gabriel, Stacey B.
    Publication type:
    Article
    19

    Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 189, doi. 10.1038/ng.75
    By:
    • Kathiresan, Sekar;
    • Melander, Olle;
    • Guiducci, Candace;
    • Surti, Aarti;
    • Burtt, Noël P.;
    • Rieder, Mark J.;
    • Cooper, Gregory M.;
    • Roos, Charlotta;
    • Voight, Benjamin F.;
    • Havulinna, Aki S.;
    • Wahlstrand, Björn;
    • Hedner, Thomas;
    • Corella, Dolores;
    • Tai, E. Shyong;
    • Ordovas, Jose M.;
    • Berglund, Göran;
    • Vartiainen, Erkki;
    • Jousilahti, Pekka;
    • Hedblad, Bo;
    • Taskinen, Marja-Riitta
    Publication type:
    Article
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    Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 211, doi. 10.1038/ng.79
    By:
    • Kozyrev, Sergey V.;
    • Abelson, Anna-Karin;
    • Wojcik, Jerome;
    • Zaghlool, Ammar;
    • Linga Reddy, M. V. Prasad;
    • Sanchez, Elena;
    • Gunnarsson, Iva;
    • Svenungsson, Elisabet;
    • Sturfelt, Gunnar;
    • Jönsen, Andreas;
    • Truedsson, Lennart;
    • Pons-Estel, Bernardo A.;
    • Witte, Torsten;
    • D'Alfonso, Sandra;
    • Barrizzone, Nadia;
    • Danieli, Maria Giovanna;
    • Gutierrez, Carmen;
    • Suarez, Ana;
    • Junker, Peter;
    • Laustrup, Helle
    Publication type:
    Article
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    Touching base.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 137, doi. 10.1038/ng0208-137
    By:
    • E. N.
    Publication type:
    Article
    25

    Research highlights.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 139, doi. 10.1038/ng0208-139
    By:
    • Bahcall, Orli;
    • Niemitz, Emily;
    • Packer, Alan;
    • Vogan, Kyle
    Publication type:
    Article
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    Hypoxic reprogramming.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 132, doi. 10.1038/ng0208-132
    By:
    • Kelly, Daniel P.
    Publication type:
    Article
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