Found: 25

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  • A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 984, doi. 10.1038/ng2085
    By:
    • Tomlinson, Ian;
    • Webb, Emily;
    • Carvajal-Carmona, Luis;
    • Broderick, Peter;
    • Kemp, Zoe;
    • Spain, Sarah;
    • Penegar, Steven;
    • Chandler, Ian;
    • Gorman, Maggie;
    • Wood, Wendy;
    • Barclay, Ella;
    • Lubbe, Steven;
    • Martin, Lynn;
    • Sellick, Gabrielle;
    • Jaeger, Emma;
    • Hubner, Richard;
    • Wild, Ruth;
    • Rowan, Andrew;
    • Fielding, Sarah;
    • Howarth, Kimberley
    Publication type:
    Article

  • Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 989, doi. 10.1038/ng2089
    By:
    • Zanke, Brent W.;
    • Greenwood, Celia M. T.;
    • Rangrej, Jagadish;
    • Kustra, Rafal;
    • Tenesa, Albert;
    • Farrington, Susan M.;
    • Prendergast, James;
    • Olschwang, Sylviane;
    • Chiang, Theodore;
    • Crowdy, Edgar;
    • Ferretti, Vincent;
    • Laflamme, Philippe;
    • Sundararajan, Saravanan;
    • Roumy, Stéphanie;
    • Olivier, Jean-François;
    • Robidoux, Frédérick;
    • Sladek, Robert;
    • Montpetit, Alexandre;
    • Campbell, Peter;
    • Bezieau, Stephane
    Publication type:
    Article

  • Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 1000, doi. 10.1038/ng2099
    By:
    • Winkelmann, Juliane;
    • Schormair, Barbara;
    • Lichtner, Peter;
    • Ripke, Stephan;
    • Lan Xiong;
    • Jalilzadeh, Shapour;
    • Fulda, Stephany;
    • Pütz, Benno;
    • Eckstein, Gertrud;
    • Hauk, Stephanie;
    • Trenkwalder, Claudia;
    • Zimprich, Alexander;
    • Stiasny-Kolster, Karin;
    • Oertel, Wolfgang;
    • Bachmann, Cornelius G.;
    • Paulus, Walter;
    • Peglau, Ines;
    • Eisensehr, Ilonka;
    • Montplaisir, Jacques;
    • Turecki, Gustavo
    Publication type:
    Article

  • Compete, collaborate, compel.

    Published in:
    2007
    Publication type:
    Editorial

  • Splinkerette PCR for more efficient characterization of gene trap events.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 933, doi. 10.1038/ng0807-933
    By:
    • Horn, Carsten;
    • Hansen, Jens;
    • Schnütgen, Frank;
    • Seisenberger, Claudia;
    • Floss, Thomas;
    • Irgang, Markus;
    • De-Zolt, Silke;
    • Wurst, Wolfgang;
    • von Melchner, Harald;
    • Noppinger, Patricia Ruiz
    Publication type:
    Article

  • Target mimics modulate miRNAs.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 935, doi. 10.1038/ng0807-935
    By:
    • Chitwood, Daniel H.;
    • Timmermans, Marja C. P.
    Publication type:
    Article

  • Axons need glial peroxisomes.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 936, doi. 10.1038/ng0807-936
    By:
    • Aubourg, Patrick
    Publication type:
    Article

  • A step forward for restless legs syndrome.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 938, doi. 10.1038/ng0807-938
    By:
    • Mignot, Emmanuel
    Publication type:
    Article

  • Touching base.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 941, doi. 10.1038/ng0807-941
    By:
    • Bahcall, Orli;
    • Niemitz, Emily;
    • Vogan, Kyle
    Publication type:
    Article

  • Research Highlights.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 943, doi. 10.1038/ng0807-943
    By:
    • Bahcall, Orli;
    • Niemitz, Emily;
    • Vogan, Kyle
    Publication type:
    Article

  • Genetic variation in Mon1a affects protein trafficking and modifies macrophage iron loading in mice.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 1025, doi. 10.1038/ng2059
    By:
    • Wang, Fudi;
    • Paradkar, Prasad N.;
    • Custodio, Angel O.;
    • Ward, Diane McVey;
    • Fleming, Mark D.;
    • Campagna, Dean;
    • Roberts, Kristina A.;
    • Boyartchuk, Victor;
    • Dietrich, William F.;
    • Kaplan, Jerry;
    • Andrews, Nancy C.
    Publication type:
    Article

  • Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 977, doi. 10.1038/ng2062
    By:
    • Gudmundsson, Julius;
    • Sulem, Patrick;
    • Steinthorsdottir, Valgerdur;
    • Bergthorsson, Jon T.;
    • Thorleifsson, Gudmar;
    • Manolescu, Andrei;
    • Rafnar, Thorunn;
    • Gudbjartsson, Daniel;
    • Agnarsson, Bjarni A.;
    • Baker, Adam;
    • Sigurdsson, Asgeir;
    • Benediktsdottir, Kristrun R.;
    • Jakobsdottir, Margret;
    • Thorarinn Blondal1,;
    • Stacey, Simon N.;
    • Helgason, Agnar;
    • Gunnarsdottir, Steinunn;
    • Olafsdottir, Adalheidur;
    • Kristinsson, Kari T.;
    • Birgisdottir, Birgitta
    Publication type:
    Article

  • Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 957, doi. 10.1038/ng2063
    By:
    • Kantarci, Sibel;
    • Al-Gazali, Lihadh;
    • Hill, R. Sean;
    • Donnai, Dian;
    • Black, Graeme C. M.;
    • Bieth, Eric;
    • Chassaing, Nicolas;
    • Lacombe, Didier;
    • Devriendt, Koen;
    • Teebi, Ahmad;
    • Loscertales, Maria;
    • Robson, Caroline;
    • Tianming Liu;
    • MacLaughlin, David T.;
    • Noonan, Kristin M.;
    • Russell, Meaghan K.;
    • Walsh, Christopher A.;
    • Donahoe, Patricia K.;
    • Pober, Barbara R.
    Publication type:
    Article

  • Bi-orientation of achiasmatic chromosomes in meiosis I oocytes contributes to aneuploidy in mice.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 966, doi. 10.1038/ng2065
    By:
    • Kouznetsova, Anna;
    • Lister, Lisa;
    • Nordenskjöld, Magnus;
    • Herbert, Mary;
    • Höög, Christer
    Publication type:
    Article

  • Common variants in WFS1 confer risk of type 2 diabetes.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 951, doi. 10.1038/ng2067
    By:
    • Sandhu, Manjinder S.;
    • Weedon, Michael N.;
    • Fawcett, Katherine A.;
    • Wasson, Jon;
    • Debenham, Sally L.;
    • Daly, Allan;
    • Lango, Hana;
    • Frayling, Timothy M.;
    • Neumann, Rosalind J.;
    • Sherva, Richard;
    • Blech, Ilana;
    • Pharoah, Paul D.;
    • Palmer, Colin N. A.;
    • Kimber, Charlotte;
    • Tavendale, Roger;
    • Morris, Andrew D.;
    • McCarthy, Mark I.;
    • Walker, Mark;
    • Hitman, Graham;
    • Glaser, Benjamin
    Publication type:
    Article

  • Axonal loss and neuroinflammation caused by peroxisome-deficient oligodendrocytes.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 969, doi. 10.1038/ng2070
    By:
    • Kassmann, Celia M.;
    • Lappe-Siefke, Corinna;
    • Baes, Myriam;
    • Brügger, Britta;
    • Mildner, Alexander;
    • Werner, Hauke B.;
    • Natt, Oliver;
    • Michaelis, Thomas;
    • Prinz, Marco;
    • Frahm, Jens;
    • Nave, Klaus-Armin
    Publication type:
    Article

  • Evolution of chromosome organization driven by selection for reduced gene expression noise.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 945, doi. 10.1038/ng2071
    By:
    • Batada, Nizar N.;
    • Hurst, Laurence D.
    Publication type:
    Article

  • Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 1018, doi. 10.1038/ng2072
    By:
    • Attanasio, Massimo;
    • Uhlenhaut, N. Henriette;
    • Sousa, Vitor H.;
    • O'Toole, John F.;
    • Otto, Edgar;
    • Anlag, Katrin;
    • Klugmann, Claudia;
    • Treier, Anna-Corina;
    • Helou, Juliana;
    • Sayer, John A.;
    • Seelow, Dominik;
    • Nürnberg, Gudrun;
    • Becker, Christian;
    • Chudley, Albert E.;
    • Nürnberg, Peter;
    • Hildebrandt, Friedhelm;
    • Treier, Mathias
    Publication type:
    Article

  • Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 1007, doi. 10.1038/ng2073
    By:
    • Pandit, Bhaswati;
    • Sarkozy, Anna;
    • Pennacchio, Len A.;
    • Carta, Claudio;
    • Oishi, Kimihiko;
    • Martinelli, Simone;
    • Pogna, Edgar A.;
    • Schackwitz, Wendy;
    • Ustaszewska, Anna;
    • Landstrom, Andrew;
    • Bos, J. Martijn;
    • Ommen, Steve R.;
    • Esposito, Giorgia;
    • Lepri, Francesca;
    • Faul, Christian;
    • Mundel, Peter;
    • Siguero, Juan P. López;
    • Tenconi, Romano;
    • Selicorni, Angelo;
    • Rossi, Cesare
    Publication type:
    Article

  • Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 960, doi. 10.1038/ng2076
    By:
    • Sobacchi, Cristina;
    • Frattini, Annalisa;
    • Guerrini, Matteo M.;
    • Abinun, Mario;
    • Pangrazio, Alessandra;
    • Susani, Lucia;
    • Bredius, Robbert;
    • Mancini, Grazia;
    • Cant, Andrew;
    • Bishop, Nick;
    • Grabowski, Peter;
    • del Fattore, Andrea;
    • Messina, Chiara;
    • Errigo, Gabriella;
    • Coxon, Fraser P.;
    • Scott, Debbie I.;
    • Teti, Anna;
    • Rogers, Michael J.;
    • Vezzoni, Paolo;
    • Villa, Anna
    Publication type:
    Article

  • Germline gain-of-function mutations in RAF1 cause Noonan syndrome.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 1013, doi. 10.1038/ng2078
    By:
    • Razzaque, M. Abdur;
    • Nishizawa, Tsutomu;
    • Komoike, Yuta;
    • Yagi, Hisato;
    • Furutani, Michiko;
    • Amo, Ryunosuke;
    • Kamisago, Mitsuhiro;
    • Momma, Kazuo;
    • Katayama, Hiroshi;
    • Nakagawa, Masao;
    • Fujiwara, Yuko;
    • Matsushima, Masaki;
    • Mizuno, Katsumi;
    • Tokuyama, Mika;
    • Hirota, Hamao;
    • Muneuchi, Jun;
    • Higashinakagawa, Toru;
    • Matsuoka, Rumiko
    Publication type:
    Article

  • Target mimicry provides a new mechanism for regulation of microRNA activity.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 1033, doi. 10.1038/ng2079
    By:
    • Franco-Zorrilla, José Manuel;
    • Valli, Adrián;
    • Todesco, Marco;
    • Mateos, Isabel;
    • Puga, María Isabel;
    • Rubio-Somoza, Ignacio;
    • Leyva, Antonio;
    • Weigel, Detlef;
    • García, Juan Antonio;
    • Paz-Ares, Javier
    Publication type:
    Article

  • Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 963, doi. 10.1038/ng2083
    By:
    • Douglas, Jenny;
    • Cilliers, Deirdre;
    • Coleman, Kim;
    • Tatton-Brown, Katrina;
    • Barker, Karen;
    • Bernhard, Brigitte;
    • Burn, John;
    • Huson, Susan;
    • Josifova, Dragana;
    • Lacombe, Didier;
    • Malik, Mohsin;
    • Mansour, Sahar;
    • Reid, Evan;
    • Cormier-Daire, Valerie;
    • Cole, Trevor;
    • Rahman, Nazneen
    Publication type:
    Article

  • A common genetic risk factor for colorectal and prostate cancer.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 954, doi. 10.1038/ng2098
    By:
    • Haiman, Christopher A.;
    • Le Marchand, Loïc;
    • Yamamato, Jennifer;
    • Stram, Daniel O.;
    • Xin Sheng;
    • Kolonel, Laurence N.;
    • Wu, Anna H.;
    • Reich, David;
    • Henderson, Brian E.
    Publication type:
    Article

  • A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 995, doi. 10.1038/ng2101
    By:
    • Buch, Stephan;
    • Schafmayer, Clemens;
    • Völzke, Henry;
    • Becker, Christian;
    • Franke, Andre;
    • von Eller-Eberstein, Huberta;
    • Kluck, Christian;
    • Bässmann, Ingelore;
    • Brosch, Mario;
    • Lammert, Frank;
    • Miquel, Juan Francisco;
    • Nervi, Flavio;
    • Wittig, Michael;
    • Rosskopf, Dieter;
    • Timm, Birgit;
    • Höll, Christine;
    • Seeger, Marcus;
    • ElSharawy, Abdou;
    • Tim Lu;
    • Egberts, Jan
    Publication type:
    Article