Works matching IS 10614036 AND DT 2015 AND VI 47 AND IP 1

Results: 24
    1

    Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 73, doi. 10.1038/ng.3153
    By:
    • Simons, Cas;
    • Rash, Lachlan D;
    • Crawford, Joanna;
    • Ma, Linlin;
    • Cristofori-Armstrong, Ben;
    • Ru, Kelin;
    • Baillie, Gregory J;
    • King, Glenn F;
    • McGaughran, Julie;
    • Gabbett, Michael T;
    • Taft, Ryan J;
    • Miller, David;
    • Alanay, Yasemin;
    • Jacquinet, Adeline;
    • Debray, François-Guillaume;
    • Verloes, Alain;
    • Shen, Joseph;
    • Yesil, Gözde;
    • Guler, Serhat;
    • Yuksel, Adnan
    Publication type:
    Article
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    4

    Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 78, doi. 10.1038/ng.3154
    By:
    • Debette, Stéphanie;
    • Dichgans, Martin;
    • Gschwendtner, Andreas;
    • Wolf, Christiane;
    • Dittrich, Ralf;
    • Ringelstein, Erich-Bernd;
    • Touzé, Emmanuel;
    • Southerland, Andrew M;
    • Samson, Yves;
    • Abboud, Shérine;
    • Béjot, Yannick;
    • Caso, Valeria;
    • Bersano, Anna;
    • Boncoraglio, Giorgio B;
    • Kamatani, Yoichiro;
    • Sessa, Maria;
    • Cole, John;
    • Cheng, Yu-Ching;
    • Lamy, Chantal;
    • Medeiros, Elisabeth
    Publication type:
    Article
    5
    6

    Noncoding mutation in T-ALL.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 7, doi. 10.1038/ng.3184
    By:
    • Niemitz, Emily
    Publication type:
    Article
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    9

    A conditional piggyBac transposition system for genetic screening in mice identifies oncogenic networks in pancreatic cancer.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 47, doi. 10.1038/ng.3164
    By:
    • Rad, Roland;
    • ten Hoeve, Jelle;
    • Wessels, Lodewyk;
    • Bauer, Judith;
    • Heikenwälder, Mathias;
    • Knösel, Thomas;
    • Rümmele, Petra;
    • Aust, Daniela;
    • Grützmann, Robert;
    • Pilarsky, Christian;
    • Esposito, Irene;
    • Rad, Lena;
    • Wang, Wei;
    • Strong, Alexander;
    • Ponstingl, Hannes;
    • Bronner, Iraad F;
    • Mayho, Matthew;
    • Friedrich, Mathias;
    • Prosser, Haydn;
    • Metzakopian, Emmanouil
    Publication type:
    Article
    10

    Clonal evolution of B-ALL.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 7, doi. 10.1038/ng.3183
    By:
    • LaFlamme, Brooke
    Publication type:
    Article
    11
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    A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 39, doi. 10.1038/ng.3144
    By:
    • Muona, Mikko;
    • Tinuper, Paolo;
    • Licchetta, Laura;
    • Scheffer, Ingrid E;
    • Criscuolo, Chiara;
    • Filla, Alessandro;
    • Ferlazzo, Edoardo;
    • Ahmad, Jamil;
    • Ahmad, Adeel;
    • Baykan, Betul;
    • Said, Edith;
    • Topcu, Meral;
    • King, Mary D;
    • Berkovic, Samuel F;
    • Oliver, Karen L;
    • Hildebrand, Michael S;
    • Ozkara, Cigdem;
    • Andrade, Danielle M;
    • Engelsen, Bernt A;
    • Crespel, Arielle
    Publication type:
    Article
    14

    Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 13, doi. 10.1038/ng.3146
    By:
    • Durinck, Steffen;
    • Stawiski, Eric W;
    • Pedrosa, Ivan;
    • de Sauvage, Frederic J;
    • Pavía-Jiménez, Andrea;
    • Toffessi-Tcheuyap, Vanina;
    • Peña-Llopis, Samuel;
    • Holloman, Eboni;
    • Hill, Haley M;
    • Brugarolas, James;
    • Modrusan, Zora;
    • Jaiswal, Bijay S;
    • Zhang, Na;
    • Nguyen, Thong T;
    • Pahuja, Kanika Bajaj;
    • Chen, Ying-Jiun;
    • Chaudhuri, Subhra;
    • Heldens, Sherry;
    • Jackson, Marlena;
    • Guillory, Joseph
    Publication type:
    Article
    15

    Corrigendum: Identification of recurrent SMO and BRAF mutations in ameloblastomas.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 97, doi. 10.1038/ng0115-97b
    By:
    • Sweeney, Robert T;
    • McClary, Andrew C;
    • Myers, Benjamin R;
    • Biscocho, Jewison;
    • Neahring, Lila;
    • Kwei, Kevin A;
    • Qu, Kunbin;
    • Gong, Xue;
    • Ng, Tony;
    • Jones, Carol D;
    • Varma, Sushama;
    • Odegaard, Justin I;
    • Sugiyama, Toshihiro;
    • Koyota, Souichi;
    • Rubin, Brian P;
    • Troxell, Megan L;
    • Pelham, Robert J;
    • Zehnder, James L;
    • Beachy, Philip A;
    • Pollack, Jonathan R
    Publication type:
    Article
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    What are super-enhancers?

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 8, doi. 10.1038/ng.3167
    By:
    • Pott, Sebastian;
    • Lieb, Jason D
    Publication type:
    Article
    21

    The genome sequence of the orchid Phalaenopsis equestris.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 65, doi. 10.1038/ng.3149
    By:
    • Cai, Jing;
    • Liu, Ke-Wei;
    • Su, Yong-Yu;
    • Huang, Lai-Qiang;
    • Chen, Hong-Hwa;
    • Van de Peer, Yves;
    • Liu, Zhong-Jian;
    • Liu, Xin;
    • Bian, Chao;
    • Zheng, Zhijun;
    • Sun, Fengming;
    • Liu, Weiqing;
    • Xu, Xun;
    • Wang, Jun-Yi;
    • Wang, Jun;
    • Vanneste, Kevin;
    • Proost, Sebastian;
    • He, Ying;
    • Tsai, Wen-Chieh;
    • Chen, Li-Jun
    Publication type:
    Article
    22

    Anopheline mosquito genomes.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 7, doi. 10.1038/ng.3181
    By:
    • Bahcall, Orli
    Publication type:
    Article
    23

    Mutations in the deubiquitinase gene USP8 cause Cushing's disease.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 31, doi. 10.1038/ng.3166
    By:
    • Reincke, Martin;
    • Osswald, Andrea;
    • Beuschlein, Felix;
    • Allolio, Bruno;
    • Buchfelder, Michael;
    • Strom, Tim M;
    • Fassnacht, Martin;
    • Sbiera, Silviu;
    • Hayakawa, Akira;
    • Mizuno-Yamasaki, Emi;
    • Kawaguchi, Kohei;
    • Komada, Masayuki;
    • Theodoropoulou, Marily;
    • Meitinger, Thomas;
    • Saeki, Yasushi;
    • Tanaka, Keiji;
    • Wieland, Thomas;
    • Graf, Elisabeth;
    • Saeger, Wolfgang;
    • Ronchi, Cristina L
    Publication type:
    Article
    24

    BAZ2A (TIP5) is involved in epigenetic alterations in prostate cancer and its overexpression predicts disease recurrence.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 22, doi. 10.1038/ng.3165
    By:
    • Gu, Lei;
    • Provenzano, Maurizio;
    • Yaspo, Marie-Laure;
    • Korbel, Jan;
    • Schlomm, Thorsten;
    • Eils, Roland;
    • Frommel, Sandra C;
    • Oakes, Christopher C;
    • Baer, Constance;
    • Weiss, Melanie;
    • Plass, Christoph;
    • Simon, Ronald;
    • Grupp, Katharina;
    • Sauter, Guido;
    • Gerig, Cristina Y;
    • Bär, Dominik;
    • Santoro, Raffaella;
    • Robinson, Mark D;
    • Gu, Zuguang;
    • Brors, Benedikt
    Publication type:
    Article