Works matching IS 10614036 AND DT 2009 AND VI 41 AND IP 9

Results: 21
    1

    Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.

    Published in:
    Nature Genetics, 2009, v. 41, n. 9, p. 986, doi. 10.1038/ng.429
    By:
    • Amundadottir, Laufey;
    • Kraft, Peter;
    • Stolzenberg-Solomon, Rachael Z.;
    • Fuchs, Charles S.;
    • Petersen, Gloria M.;
    • Arslan, Alan A.;
    • Bueno-de-Mesquita, H. Bas;
    • Gross, Myron;
    • Helzlsouer, Kathy;
    • Jacobs, Eric J.;
    • LaCroix, Andrea;
    • Wei Zheng;
    • Albanes, Demetrius;
    • Bamlet, William;
    • Berg, Christine D.;
    • Berrino, Franco;
    • Bingham, Sheila;
    • Buring, Julie E.;
    • Bracci, Paige M.;
    • Canzian, Federico
    Publication type:
    Article
    2
    3
    4
    5

    Mutations in PYCR1 cause cutis laxa with progeroid features.

    Published in:
    Nature Genetics, 2009, v. 41, n. 9, p. 1016, doi. 10.1038/ng.413
    By:
    • Reversade, Bruno;
    • Escande-Beillard, Nathalie;
    • Dimopoulou, Aikaterini;
    • Fischer, Björn;
    • Chng, Serene C;
    • Yun Li;
    • Shboul, Mohammad;
    • Tham, Puay-Yoke;
    • Kayserili, Hülya;
    • Al-Gazali, Lihadh;
    • Shahwan, Monzer;
    • Brancati, Francesco;
    • Lee, Hane;
    • O'Connor, Brian D;
    • Kegler, Mareen Schmidt-von;
    • Merriman, Barry;
    • Nelson, Stanley F.;
    • Masri, Amira;
    • Alkazaleh, Fawaz;
    • Guerra, Deanna
    Publication type:
    Article
    6

    A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.

    Published in:
    Nature Genetics, 2009, v. 41, n. 9, p. 996, doi. 10.1038/ng.424
    By:
    • Song, Honglin;
    • Ramus, Susan J.;
    • Tyrer, Jonathan;
    • Bolton, Kelly L.;
    • Gentry-Maharaj, Aleksandra;
    • Wozniak, Eva;
    • Anton-Culver, Hoda;
    • Chang-Claude, Jenny;
    • Cramer, Daniel W;
    • DiCioccio, Richard;
    • Dörk, Thilo;
    • Goode, Ellen L.;
    • Goodman, Marc T.;
    • Schildkraut, Joellen M.;
    • Sellers, Thomas;
    • Baglietto, Laura;
    • Beckmann, Matthias W.;
    • Beesley, Jonathan;
    • Blaakaer, Jan;
    • Carney, Michael E.
    Publication type:
    Article
    7

    Germline genomic variants associated with childhood acute lymphoblastic leukemia.

    Published in:
    Nature Genetics, 2009, v. 41, n. 9, p. 1001, doi. 10.1038/ng.432
    By:
    • Treviño, Lisa R.;
    • Wenjian Yang;
    • French, Deborah;
    • Hunger, Stephen P.;
    • Carroll, William L.;
    • Devidas, Meenakshi;
    • Willman, Cheryl;
    • Neale, Geoffrey;
    • Downing, James;
    • Raimondi, Susana C.;
    • Pui, Ching-Hon;
    • Evans, William E.;
    • Relling, Mary V.
    Publication type:
    Article
    8
    9

    Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource.

    Published in:
    Nature Genetics, 2009, v. 41, n. 9, p. 1011, doi. 10.1038/ng.434
    By:
    • Dendrou, Calliope A.;
    • Plagnol, Vincent;
    • Fung, Erik;
    • Yang, Jennie H. M.;
    • Downes, Kate;
    • Cooper, Jason D.;
    • Nutland, Sarah;
    • Coleman, Gillian;
    • Himsworth, Matthew;
    • Hardy, Matthew;
    • Burren, Oliver;
    • Healy, Barry;
    • Walker, Neil M.;
    • Koch, Kerstin;
    • Ouwehand, Willem H.;
    • Bradley, John R.;
    • Wareham, Nicholas J.;
    • Todd, John A.;
    • Wicker, Linda S.
    Publication type:
    Article
    10

    Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer.

    Published in:
    Nature Genetics, 2009, v. 41, n. 9, p. 991, doi. 10.1038/ng.421
    By:
    • Xifeng Wu;
    • Yuanqing Ye;
    • Kiemeney, Lambertus A.;
    • Sulem, Patrick;
    • Rafnar, Thorunn;
    • Matullo, Giuseppe;
    • Seminara, Daniela;
    • Yoshida, Teruhiko;
    • Saeki, Norihisa;
    • Andrew, Angeline S.;
    • Dinney, Colin P.;
    • Czerniak, Bogdan;
    • Zuo-feng Zhang;
    • Kiltie, Anne E.;
    • Bishop, D. Timothy;
    • Vineis, Paolo;
    • Porru, Stefano;
    • Buntinx, Frank;
    • Kellen, Eliane;
    • Zeegers, Maurice P.
    Publication type:
    Article
    11

    Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair.

    Published in:
    Nature Genetics, 2009, v. 41, n. 9, p. 1022, doi. 10.1038/ng.425
    By:
    • Cordeddu, Viviana;
    • Di Schiavi, Elia;
    • Pennacchio, Len A.;
    • Ma'ayan, Avi;
    • Sarkozy, Anna;
    • Fodale, Valentina;
    • Cecchetti, Serena;
    • Cardinale, Alessio;
    • Martin, Joel;
    • Schackwitz, Wendy;
    • Lipzen, Anna;
    • Zampino, Giuseppe;
    • Mazzanti, Laura;
    • Digilio, Maria C.;
    • Martinelli, Simone;
    • Flex, Elisabetta;
    • Lepri, Francesca;
    • Bartholdi, Deborah;
    • Kutsche, Kerstin;
    • Ferrero, Giovanni B
    Publication type:
    Article
    12
    13

    Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies.

    Published in:
    Nature Genetics, 2009, v. 41, n. 9, p. 1032, doi. 10.1038/ng.423
    By:
    • Bielas, Stephanie L.;
    • Silhavy, Jennifer L.;
    • Brancati, Francesco;
    • Kisseleva, Marina V.;
    • Al-Gazali, Lihadh;
    • Sztriha, Laszlo;
    • Bayoumi, Riad A.;
    • Zaki, Maha S;
    • Abdel-Aleem, Alice;
    • Rosti, Rasim Ozgur;
    • Kayserili, Hulya;
    • Swistun, Dominika;
    • Scott, Lesley C.;
    • Bertini, Enrico;
    • Boltshauser, Eugen;
    • Fazzi, Elisa;
    • Travaglini, Lorena;
    • Field, Seth J.;
    • Gayral, Stephanie;
    • Jacoby, Monique
    Publication type:
    Article
    14
    15

    Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.

    Published in:
    2009
    By:
    • Haug, Karsten;
    • Warnstedt, Maike;
    • Alekov, Alexi K;
    • Sander, Thomas;
    • Ramírez, Alfredo;
    • Poser, Barbara;
    • Maljevic, Snezana;
    • Hebeisen, Simon;
    • Kubisch, Christian;
    • Rebstock, Johannes;
    • Horvath, Steve;
    • Hallmann, Kerstin;
    • Dullinger, Joern S;
    • Rau, Birgit;
    • Haverkamp, Fritz;
    • Beyenburg, Stefan;
    • Schulz, Herbert;
    • Janz, Dieter;
    • Giese, Bernd;
    • Müller-Newen, Gerhard
    Publication type:
    Correction Notice
    16
    17

    CLCN2 variants in idiopathic generalized epilepsy.

    Published in:
    2009
    By:
    • Kleefuß-Lie, Ailing;
    • Friedl, Waltraut;
    • Cichon, Sven;
    • Haug, Karsten;
    • Warnstedt, Maike;
    • Alekov, Alexi;
    • Sander, Thomas;
    • Ramirez, Alfredo;
    • Poser, Barbara;
    • Maljevic, Snezana;
    • Hebeisen, Simon;
    • Kubisch, Christian;
    • Rebstock, Johannes;
    • Horvath, Steve;
    • Hallmann, Kerstin;
    • Dullinger, Jörn S.;
    • Rau, Birgit;
    • Haverkamp, Fritz;
    • Beyenburg, Stefan;
    • Schulz, Herbert
    Publication type:
    Letter
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    Research Highlights.

    Published in:
    Nature Genetics, 2009, v. 41, n. 9, p. 962, doi. 10.1038/ng0909-962
    Publication type:
    Article