Works matching IS 10614036 AND DT 2015 AND VI 47 AND IP 6

Results: 32
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    A Sleeping Beauty forward genetic screen identifies new genes and pathways driving osteosarcoma development and metastasis.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 615, doi. 10.1038/ng.3293
    By:
    • Moriarity, Branden S;
    • Forster, Colleen L;
    • Modiano, Jaime F;
    • Khanna, Chand;
    • Hewitt, Stephen M;
    • Yang, Yi;
    • Gorlick, Richard;
    • Dyer, Michael A;
    • Otto, George M;
    • Rahrmann, Eric P;
    • Largaespada, David A;
    • Rathe, Susan K;
    • Temiz, Nuri A;
    • Sarver, Aaron L;
    • Wolf, Natalie K;
    • Weg, Madison T;
    • Manlove, Luke A;
    • Holly, Kevin J;
    • LaRue, Rebecca S;
    • Molyneux, Sam D
    Publication type:
    Article
    3

    A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 668, doi. 10.1038/ng.3287
    By:
    • Weren, Robbert D A;
    • Kets, C Marleen;
    • de Voer, Richarda M;
    • Verwiel, Eugène T P;
    • Spruijt, Liesbeth;
    • van Zelst-Stams, Wendy A G;
    • Jongmans, Marjolijn C;
    • Gilissen, Christian;
    • Hehir-Kwa, Jayne Y;
    • Hoischen, Alexander;
    • Kamping, Eveline J;
    • Geurts van Kessel, Ad;
    • Kuiper, Roland P;
    • Hoogerbrugge, Nicoline;
    • Ligtenberg, Marjolijn J L;
    • Shendure, Jay;
    • Boyle, Evan A;
    • Nagtegaal, Iris D;
    • Tops, Bastiaan B J;
    • van Krieken, J Han J M
    Publication type:
    Article
    4

    Mapping long-range promoter contacts in human cells with high-resolution capture Hi-C.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 598, doi. 10.1038/ng.3286
    By:
    • Mifsud, Borbala;
    • Tavares-Cadete, Filipe;
    • Sugar, Robert;
    • Young, Alice N;
    • Schoenfelder, Stefan;
    • Ferreira, Lauren;
    • Ewels, Philip A;
    • Fraser, Peter;
    • Wingett, Steven W;
    • Andrews, Simon;
    • Grey, William;
    • Herman, Bram;
    • Happe, Scott;
    • Higgs, Andy;
    • LeProust, Emily;
    • Follows, George A;
    • Luscombe, Nicholas M;
    • Osborne, Cameron S
    Publication type:
    Article
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    6

    Corrigendum: Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 689, doi. 10.1038/ng0615-689b
    By:
    • Cooper, Colin S;
    • Eeles, Rosalind;
    • Wedge, David C;
    • Van Loo, Peter;
    • Gundem, Gunes;
    • Alexandrov, Ludmil B;
    • Kremeyer, Barbara;
    • Butler, Adam;
    • Lynch, Andrew G;
    • Camacho, Niedzica;
    • Massie, Charlie E;
    • Kay, Jonathan;
    • Luxton, Hayley J;
    • Edwards, Sandra;
    • Kote-Jarai, Zsofia;
    • Dennis, Nening;
    • Merson, Sue;
    • Leongamornlert, Daniel;
    • Zamora, Jorge;
    • Corbishley, Cathy
    Publication type:
    Article
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    Corrigendum: Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 690, doi. 10.1038/ng0615-690a
    By:
    • Crowley, James J;
    • Zhabotynsky, Vasyl;
    • Sun, Wei;
    • Huang, Shunping;
    • Pakatci, Isa Kemal;
    • Kim, Yunjung;
    • Wang, Jeremy R;
    • Morgan, Andrew P;
    • Calaway, John D;
    • Aylor, David L;
    • Yun, Zaining;
    • Bell, Timothy A;
    • Buus, Ryan J;
    • Calaway, Mark E;
    • Didion, John P;
    • Gooch, Terry J;
    • Hansen, Stephanie D;
    • Robinson, Nashiya N;
    • Shaw, Ginger D;
    • Spence, Jason S
    Publication type:
    Article
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    12

    Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 579, doi. 10.1038/ng.3289
    By:
    • Legati, Andrea;
    • Sears, Renee L;
    • Ramos, Eliana Marisa;
    • Lang, Anthony E;
    • Miedzybrodzka, Zosia;
    • Simpson, Sheila A;
    • Paucar, Martin;
    • Svenningsson, Per;
    • Paulson, Henry;
    • Pariente, Jérémie;
    • Richard, Anne-Claire;
    • Salins, Naomi S;
    • Striano, Pasquale;
    • Unni, Vivek K;
    • Vanakker, Olivier;
    • Giovannini, Donatella;
    • López-Sánchez, Uriel;
    • Sitbon, Marc;
    • Battini, Jean-Luc;
    • Wessels, Marja W
    Publication type:
    Article
    13

    Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 689, doi. 10.1038/ng0615-689c
    By:
    • Aung, Tin;
    • Ozaki, Mineo;
    • Mizoguchi, Takanori;
    • Allingham, R Rand;
    • Li, Zheng;
    • Haripriya, Aravind;
    • Nakano, Satoko;
    • Uebe, Steffen;
    • Harder, Jeffrey M;
    • Chan, Anita S Y;
    • Lee, Mei Chin;
    • Burdon, Kathryn P;
    • Astakhov, Yury S;
    • Abu-Amero, Khaled K;
    • Zenteno, Juan C;
    • Nilgün, Yildirim;
    • Zarnowski, Tomasz;
    • Pakravan, Mohammad;
    • Safieh, Leen Abu;
    • Jia, Liyun
    Publication type:
    Article
    14

    Phylogeographical analysis of the dominant multidrug-resistant H58 clade of Salmonella Typhi identifies inter- and intracontinental transmission events.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 632, doi. 10.1038/ng.3281
    By:
    • Wong, Vanessa K;
    • Hart, Peter J;
    • Thieu, Nga Tran Vu;
    • Thanh, Duy Pham;
    • Breiman, Robert F;
    • Watson, Conall H;
    • Edmunds, W John;
    • Kariuki, Samuel;
    • Gordon, Melita A;
    • Heyderman, Robert S;
    • Jacobs, Jan;
    • Lunguya, Octavie;
    • Msefula, Chisomo;
    • Baker, Stephen;
    • Chabalgoity, Jose A;
    • Kama, Mike;
    • Jenkins, Kylie;
    • Dutta, Shanta;
    • Marks, Florian;
    • Campos, Josefina
    Publication type:
    Article
    15

    PDE3A mutations cause autosomal dominant hypertension with brachydactyly.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 647, doi. 10.1038/ng.3302
    By:
    • Maass, Philipp G;
    • Aydin, Atakan;
    • Qadri, Fatimunnisa;
    • Gong, Maolian;
    • Bähring, Sylvia;
    • Krawitz, Peter M;
    • Parkhomchuk, Dmitri;
    • Mundlos, Stefan;
    • Hecht, Jochen;
    • Kann, Martin;
    • Schuster, Herbert;
    • Chitayat, David;
    • Bialer, Martin G;
    • Wienker, Thomas F;
    • Ott, Jürg;
    • Jordan, Jens;
    • Tank, Jens;
    • Plessis, Ghislaine;
    • Luft, Friedrich C;
    • Mai, Knut
    Publication type:
    Article
    16

    Understanding multicellular function and disease with human tissue-specific networks.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 569, doi. 10.1038/ng.3259
    By:
    • Greene, Casey S;
    • Troyanskaya, Olga G;
    • Krishnan, Arjun;
    • Dolinski, Kara;
    • Wong, Aaron K;
    • Ricciotti, Emanuela;
    • FitzGerald, Garret A;
    • Grosser, Tilo;
    • Zelaya, Rene A;
    • Himmelstein, Daniel S;
    • Zhang, Ran;
    • Hartmann, Boris M;
    • Zaslavsky, Elena;
    • Sealfon, Stuart C;
    • Chasman, Daniel I
    Publication type:
    Article
    17

    Germline RECQL mutations are associated with breast cancer susceptibility.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 643, doi. 10.1038/ng.3284
    By:
    • Cybulski, Cezary;
    • Kluźniak, Wojciech;
    • Kashyap, Aniruddh;
    • Wokołorczyk, Dominika;
    • Huzarski, Tomasz;
    • Gronwald, Jacek;
    • Byrski, Tomasz;
    • Jakubowska, Anna;
    • Rudnicka, Helena;
    • Lener, Marcin;
    • Masojć, Bartłomiej;
    • Górski, Bohdan;
    • Dębniak, Tadeusz;
    • Lubiński, Jan;
    • Foulkes, William D;
    • Narod, Steven A;
    • Akbari, Mohammad R;
    • Carrot-Zhang, Jian;
    • Majewski, Jacek;
    • Rivera, Barbara
    Publication type:
    Article
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    COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 654, doi. 10.1038/ng.3279
    By:
    • Watkin, Levi B;
    • Forbes, Lisa R;
    • Mace, Emily M;
    • Liu, Dongfang;
    • Nicholas, Sarah K;
    • Nahmod, Karen;
    • Makedonas, George;
    • Canter, Debra L;
    • Orange, Jordan S;
    • Hicks, John;
    • Jones, Kirk D;
    • Jhangiani, Shalini N;
    • Muzny, Donna M;
    • Rosenblum, Michael D;
    • Dell, Sharon D;
    • Waterfield, Michael R;
    • Boerwinkle, Eric;
    • Gibbs, Richard A;
    • Lupski, James R;
    • Shum, Anthony K
    Publication type:
    Article
    21

    The impact of low-frequency and rare variants on lipid levels.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 589, doi. 10.1038/ng.3300
    By:
    • Surakka, Ida;
    • Sarin, Antti-Pekka;
    • Kettunen, Johannes;
    • Hottenga, Jouke-Jan;
    • de Geus, Eco J;
    • Willemsen, Gonneke;
    • Boomsma, Dorret I;
    • Isaacs, Aaron;
    • van Duijn, Cornelia M;
    • Ladenvall, Claes;
    • Beekman, Marian;
    • Deelen, Joris;
    • Slagboom, P Eline;
    • Esko, Tõnu;
    • Ried, Janina S;
    • Nelson, Christopher P;
    • Samani, Nilesh J;
    • Willenborg, Christina;
    • Erdmann, Jeanette;
    • Blades, Matthew
    Publication type:
    Article
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    Regulatory rewiring.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 568, doi. 10.1038/ng.3329
    By:
    • LaFlamme, Brooke
    Publication type:
    Article
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    NALP3 inflammasome upregulation and CASP1 cleavage of the glucocorticoid receptor cause glucocorticoid resistance in leukemia cells.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 607, doi. 10.1038/ng.3283
    By:
    • Paugh, Steven W;
    • Bonten, Erik J;
    • Ramsey, Laura B;
    • Thierfelder, William E;
    • Laudermilk, Lucas T;
    • McCorkle, J Robert;
    • Crews, Kristine R;
    • Stocco, Gabriele;
    • Wilkinson, Mark R;
    • Yang, Wenjian;
    • Fernandez, Christian A;
    • Diouf, Barthelemy;
    • Smith, Colton;
    • Hicks, J Kevin;
    • Zanut, Alessandra;
    • Giordanengo, Audrey;
    • Crona, Daniel;
    • Bianchi, Joy J;
    • Relling, Mary V;
    • Evans, William E
    Publication type:
    Article
    27

    Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 661, doi. 10.1038/ng.3282
    By:
    • Kortüm, Fanny;
    • Kutsche, Kerstin;
    • Korenke, Georg Christoph;
    • Leuzzi, Vincenzo;
    • Mowat, David;
    • Nair, Lal D V;
    • Nguyen, Thi Tuyet Mai;
    • Thierry, Patrick;
    • White, Susan M;
    • Campeau, Philippe M;
    • Tartaglia, Marco;
    • Caputo, Viviana;
    • Pizzuti, Antonio;
    • Bauer, Christiane K;
    • Stella, Lorenzo;
    • Bocchinfuso, Gianfranco;
    • Ciolfi, Andrea;
    • Flex, Elisabetta;
    • Alawi, Malik;
    • Paolacci, Stefano
    Publication type:
    Article
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    Excess of rare, inherited truncating mutations in autism.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 582, doi. 10.1038/ng.3303
    By:
    • Krumm, Niklas;
    • Turner, Tychele N;
    • Baker, Carl;
    • Vives, Laura;
    • Mohajeri, Kiana;
    • Witherspoon, Kali;
    • Coe, Bradley P;
    • Stessman, Holly A;
    • Raja, Archana;
    • Eichler, Evan E;
    • He, Zong-Xiao;
    • Leal, Suzanne M;
    • Bernier, Raphael
    Publication type:
    Article
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