Works matching IS 10614036 AND DT 2009 AND VI 41 AND IP 8

Results: 22
    1

    Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 936, doi. 10.1038/ng.405
    By:
    • Schwarz, Klaus;
    • Iolascon, Achille;
    • Verissimo, Fatima;
    • Trede, Nikolaus S.;
    • Horsley, Wyatt;
    • Wen Chen;
    • Paw, Barry H.;
    • Hopfner, Karl-Peter;
    • Holzmann, Karlheinz;
    • Russo, Roberta;
    • Esposito, Maria Rosaria;
    • Spano, Daniela;
    • De Falco, Luigia;
    • Heinrich, Katja;
    • Joggerst, Brigitte;
    • Rojewski, Markus T.;
    • Perrotta, Silverio;
    • Denecke, Jonas;
    • Pannicke, Ulrich;
    • Delaunay, Jean
    Publication type:
    Article
    2
    3

    Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 926, doi. 10.1038/ng.404
    By:
    • Thorleifsson, Gudmar;
    • Holm, Hilma;
    • Edvardsson, Vidar;
    • Walters, G. Bragi;
    • Styrkarsdottir, Unnur;
    • Gudbjartsson, Daniel F.;
    • Sulem, Patrick;
    • Halldorsson, Bjarni V.;
    • de Vegt, Femmie;
    • d'Ancona, Frank C. H.;
    • den Heijer, Martin;
    • Franzson, Leifur;
    • Christiansen, Claus;
    • Alexandersen, Peter;
    • Rafnar, Thorunn;
    • Kristjansson, Kristleifur;
    • Sigurdsson, Gunnar;
    • Kiemeney, Lambertus A.;
    • Bodvarsson, Magnus;
    • Indridason, Olafur S.
    Publication type:
    Article
    4

    De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 931, doi. 10.1038/ng.415
    By:
    • Greenway, Steven C.;
    • Pereira, Alexandre C.;
    • Lin, Jennifer C.;
    • DePalma, Steven R.;
    • Israel, Samuel J.;
    • Mesquita, Sonia M.;
    • Ergul, Emel;
    • Conta, Jessie H.;
    • Korn, Joshua M.;
    • McCarroll, Steven A.;
    • Gorham, Joshua M.;
    • Gabriel, Stacey;
    • Altshuler, David M.;
    • Quintanilla-Dieck, Maria de Lourdes;
    • Artunduaga, Maria Alexandra;
    • Eavey, Roland D.;
    • Plenge, Robert M.;
    • Shadick, Nancy A.;
    • Weinblatt, Michael E.;
    • De Jager, Philip L.
    Publication type:
    Article
    5

    Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 915, doi. 10.1038/ng.410
    By:
    • Falchi, Mario;
    • Bataille, Veronique;
    • Hayward, Nicholas K.;
    • Duffy, David L.;
    • Bishop, Julia A. Newton;
    • Pastinen, Tomi;
    • Cervino, Alessandra;
    • Zhao, Zhen Z.;
    • Deloukas, Panos;
    • Soranzo, Nicole;
    • Elder, David E.;
    • Barrett, Jennifer H.;
    • Martin, Nicholas G.;
    • Bishop, D. Timothy;
    • Montgomery, Grant W.;
    • Spector, Timothy D.
    Publication type:
    Article
    6

    Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 873, doi. 10.1038/ng.419
    By:
    • Skibola, Christine F.;
    • Bracci, Paige M.;
    • Halperin, Eran;
    • Conde, Lucia;
    • Craig, David W.;
    • Agana, Luz;
    • Iyadurai, Kelly;
    • Becker, Nikolaus;
    • Brooks-Wilson, Angela;
    • Curry, John D.;
    • Spinelli, John J.;
    • Holly, Elizabeth A.;
    • Riby, Jacques;
    • Luoping Zhang;
    • Nieters, Alexandra;
    • Smith, Martyn T.;
    • Brown, Kevin M.
    Publication type:
    Article
    7

    A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 876, doi. 10.1038/ng.417
    By:
    • Gudbjartsson, Daniel F.;
    • Holm, Hilma;
    • Gretarsdottir, Solveig;
    • Thorleifsson, Gudmar;
    • Walters, G. Bragi;
    • Thorgeirsson, Gudmundur;
    • Gulcher, Jeffrey;
    • Mathiesen, Ellisiv B.;
    • Njølstad, Inger;
    • Nyrnes, Audhild;
    • Wilsgaard, Tom;
    • Hald, Erin M.;
    • Hveem, Kristian;
    • Stoltenberg, Camilla;
    • Kucera, Gayle;
    • Stubblefield, Tanya;
    • Carter, Shannon;
    • Roden, Dan;
    • Ng, Maggie C. Y.;
    • Baum, Larry
    Publication type:
    Article
    8

    Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 879, doi. 10.1038/ng.416
    By:
    • Benjamin, Emelia J.;
    • Rice, Kenneth M.;
    • Arking, Dan E.;
    • Pfeufer, Arne;
    • van Noord, Charlotte;
    • Smith, Albert V.;
    • Schnabel, Renate B.;
    • Bis, Joshua C.;
    • Boerwinkle, Eric;
    • Sinner, Moritz F.;
    • Dehghan, Abbas;
    • Lubitz, Steven A.;
    • D'Agostino Sr, Ralph B.;
    • Lumley, Thomas;
    • Ehret, Georg B.;
    • Heeringa, Jan;
    • Aspelund, Thor;
    • Newton-Cheh, Christopher;
    • Larson, Martin G.;
    • Marciante, Kristin D.
    Publication type:
    Article
    9

    The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 882, doi. 10.1038/ng.403
    By:
    • Pomerantz, Mark M.;
    • Ahmadiyeh, Nasim;
    • Jia, Li;
    • Herman, Paula;
    • Verzi, Michael P.;
    • Doddapaneni, Harshavardhan;
    • Beckwith, Christine A.;
    • Chan, Jennifer A.;
    • Hills, Adam;
    • Davis, Matt;
    • Yao, Keluo;
    • Kehoe, Sarah M.;
    • Lenz, Heinz-Josef;
    • Haiman, Christopher A.;
    • Chunli Yan;
    • Henderson, Brian E.;
    • Frenkel, Baruch;
    • Barretina, Jordi;
    • Bass, Adam;
    • Tabernero, Josep
    Publication type:
    Article
    10

    The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 885, doi. 10.1038/ng.406
    By:
    • Tuupanen, Sari;
    • Turunen, Mikko;
    • Lehtonen, Rainer;
    • Hallikas, Outi;
    • Vanharanta, Sakari;
    • Kivioja, Teemu;
    • Björklund, Mikael;
    • Gonghong Wei;
    • Jian Yan;
    • Niittymäki, Iina;
    • Mecklin, Jukka-Pekka;
    • Järvinen, Heikki;
    • Ristimäki, Ari;
    • Di-Bernardo, Mariachiara;
    • East, Phil;
    • Carvajal-Carmona, Luis;
    • Houlston, Richard S.;
    • Tomlinson, Ian;
    • Palin, Kimmo;
    • Ukkonen, Esko
    Publication type:
    Article
    11
    12

    Genome-wide association study identifies five susceptibility loci for glioma.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 899, doi. 10.1038/ng.407
    By:
    • Shete, Sanjay;
    • Hosking, Fay J.;
    • Robertson, Lindsay B.;
    • Dobbins, Sara E.;
    • Sanson, Marc;
    • Malmer, Beatrice;
    • Simon, Matthias;
    • Marie, Yannick;
    • Boisselier, Blandine;
    • Delattre, Jean-Yves;
    • Khe Hoang-Xuan;
    • El Hallani, Soufiane;
    • Idbaih, Ahmed;
    • Zelenika, Diana;
    • Andersson, Ulrika;
    • Henriksson, Roger;
    • Bergenheim, A. Tommy;
    • Feychting, Maria;
    • Lönn, Stefan;
    • Ahlbom, Anders
    Publication type:
    Article
    13

    Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 905, doi. 10.1038/ng.408
    By:
    • Wrensch, Margaret;
    • Jenkins, Robert B.;
    • Chang, Jeffrey S.;
    • Ru-Fang Yeh;
    • Yuanyuan Xiao;
    • Decker, Paul A.;
    • Ballman, Karla V.;
    • Berger, Mitchel;
    • Buckner, Jan C.;
    • Chang, Susan;
    • Giannini, Caterina;
    • Halder, Chandralekha;
    • Kollmeyer, Thomas M.;
    • Kosel, Matthew L.;
    • LaChance, Daniel H.;
    • McCoy, Lucie;
    • O'Neill, Brian P.;
    • Patoka, Joe;
    • Pico, Alexander R.;
    • Prados, Michael
    Publication type:
    Article
    14

    New common variants affecting susceptibility to basal cell carcinoma.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 909, doi. 10.1038/ng.412
    By:
    • Stacey, Simon N.;
    • Sulem, Patrick;
    • Masson, Gisli;
    • Gudjonsson, Sigurjon A.;
    • Thorleifsson, Gudmar;
    • Jakobsdottir, Margret;
    • Sigurdsson, Asgeir;
    • Gudbjartsson, Daniel F.;
    • Sigurgeirsson, Bardur;
    • Benediktsdottir, Kristrun R.;
    • Thorisdottir, Kristin;
    • Ragnarsson, Rafn;
    • Scherer, Dominique;
    • Hemminki, Kari;
    • Rudnai, Peter;
    • Gurzau, Eugene;
    • Koppova, Kvetoslava;
    • Botella-Estrada, Rafael;
    • Soriano, Virtudes;
    • Juberias, Pablo
    Publication type:
    Article
    15
    16

    Genome-wide association study identifies three loci associated with melanoma risk.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 920, doi. 10.1038/ng.411
    By:
    • Bishop, D. Timothy;
    • Demenais, Florence;
    • Iles, Mark M.;
    • Harland, Mark;
    • Taylor, John C.;
    • Corda, Eve;
    • Randerson-Moor, Juliette;
    • Aitken, Joanne F.;
    • Avril, Marie-Francoise;
    • Azizi, Esther;
    • Bakker, Bert;
    • Bianchi-Scarrà, Giovanna;
    • Paillerets, Brigitte Bressac-de;
    • Calista, Donato;
    • Cannon-Albright, Lisa A.;
    • Chin-A-Woeng, Thomas;
    • Dębniak, Tadeusz;
    • Galore-Haskel, Gilli;
    • Ghiorzo, Paola;
    • Gut, Ivo
    Publication type:
    Article
    17
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    22

    Research highlights.

    Published in:
    2009
    By:
    • Bahcall, Orli;
    • Colosimo, Pamela;
    • Niemitz, Emily;
    • Vogan, Kyle
    Publication type:
    Abstract