Works matching IS 10614036 AND DT 2011 AND VI 43 AND IP 12

Results: 32
    1

    Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1256, doi. 10.1038/ng.1004
    By:
    • Pansuriya, Twinkal C;
    • van Eijk, Ronald;
    • d'Adamo, Pio;
    • van Ruler, Maayke A J H;
    • Kuijjer, Marieke L;
    • Oosting, Jan;
    • Cleton-Jansen, Anne-Marie;
    • van Oosterwijk, Jolieke G;
    • Verbeke, Sofie L J;
    • Meijer, Daniëlle;
    • van Wezel, Tom;
    • Nord, Karolin H;
    • Sangiorgi, Luca;
    • Toker, Berkin;
    • Liegl-Atzwanger, Bernadette;
    • San-Julian, Mikel;
    • Sciot, Raf;
    • Limaye, Nisha;
    • Kindblom, Lars-Gunnar;
    • Daugaard, Soeren
    Publication type:
    Article
    2

    He et al. reply.

    Published in:
    2011
    By:
    • He, Xionglei;
    • Chen, Xiaoshu;
    • Xiong, Yuanyan;
    • Chen, Zhidong;
    • Wang, Xunzhang;
    • Shi, Suhua;
    • Wang, Xueqin;
    • Zhang, Jianzhi
    Publication type:
    Letter
    3
    4

    PTEN ceRNAs in melanoma.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1178, doi. 10.1038/ng.1022
    By:
    • Feliciano, Pamela
    Publication type:
    Article
    5
    6

    Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1193, doi. 10.1038/ng.998
    By:
    • Trynka, Gosia;
    • Hunt, Karen A;
    • Bockett, Nicholas A;
    • Romanos, Jihane;
    • Mistry, Vanisha;
    • Szperl, Agata;
    • Bakker, Sjoerd F;
    • Bardella, Maria Teresa;
    • Bhaw-Rosun, Leena;
    • Castillejo, Gemma;
    • de la Concha, Emilio G;
    • de Almeida, Rodrigo Coutinho;
    • Dias, Kerith-Rae M;
    • van Diemen, Cleo C;
    • Dubois, Patrick C A;
    • Duerr, Richard H;
    • Edkins, Sarah;
    • Franke, Lude;
    • Fransen, Karin;
    • Gutierrez, Javier
    Publication type:
    Article
    7
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    12

    A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1210, doi. 10.1038/ng.985
    By:
    • Haiman, Christopher A;
    • Chen, Gary K;
    • Vachon, Celine M;
    • Canzian, Federico;
    • Dunning, Alison;
    • Millikan, Robert C;
    • Wang, Xianshu;
    • Ademuyiwa, Foluso;
    • Ahmed, Shahana;
    • Ambrosone, Christine B;
    • Baglietto, Laura;
    • Balleine, Rosemary;
    • Bandera, Elisa V;
    • Beckmann, Matthias W;
    • Berg, Christine D;
    • Bernstein, Leslie;
    • Blomqvist, Carl;
    • Blot, William J;
    • Brauch, Hiltrud;
    • Buring, Julie E
    Publication type:
    Article
    13

    A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1237, doi. 10.1038/ng.974
    By:
    • Takahashi, Yohei;
    • Kou, Ikuyo;
    • Takahashi, Atsushi;
    • Johnson, Todd A;
    • Kono, Katsuki;
    • Kawakami, Noriaki;
    • Uno, Koki;
    • Ito, Manabu;
    • Minami, Shohei;
    • Yanagida, Haruhisa;
    • Taneichi, Hiroshi;
    • Tsuji, Taichi;
    • Suzuki, Teppei;
    • Sudo, Hideki;
    • Kotani, Toshiaki;
    • Watanabe, Kota;
    • Chiba, Kazuhiro;
    • Hosono, Naoya;
    • Kamatani, Naoyuki;
    • Tsunoda, Tatsuhiko
    Publication type:
    Article
    14
    15

    Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1262, doi. 10.1038/ng.994
    By:
    • Amary, M Fernanda;
    • Damato, Stephen;
    • Halai, Dina;
    • Eskandarpour, Malihe;
    • Berisha, Fitim;
    • Bonar, Fiona;
    • McCarthy, Stan;
    • Fantin, Valeria R;
    • Straley, Kimberly S;
    • Lobo, Samira;
    • Aston, Will;
    • Green, Claire L;
    • Gale, Rosemary E;
    • Tirabosco, Roberto;
    • Futreal, Andrew;
    • Campbell, Peter;
    • Presneau, Nadège;
    • Flanagan, Adrienne M
    Publication type:
    Article
    16
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    18

    Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1186, doi. 10.1038/ng.975
    By:
    • Al-Mayouf, Sulaiman M;
    • Sunker, Asma;
    • Abdwani, Reem;
    • Abrawi, Safiya Al;
    • Almurshedi, Fathiya;
    • Alhashmi, Nadia;
    • Al Sonbul, Abdullah;
    • Sewairi, Wafaa;
    • Qari, Aliya;
    • Abdallah, Eiman;
    • Al-Owain, Mohammed;
    • Al Motywee, Saleh;
    • Al-Rayes, Hanan;
    • Hashem, Mais;
    • Khalak, Hanif;
    • Al-Jebali, Latifa;
    • Alkuraya, Fowzan S
    Publication type:
    Article
    19

    Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1241, doi. 10.1038/ng.981
    By:
    • Khor, Chiea Chuen;
    • Davila, Sonia;
    • Breunis, Willemijn B;
    • Lee, Yi-Ching;
    • Shimizu, Chisato;
    • Wright, Victoria J;
    • Yeung, Rae S M;
    • Tan, Dennis E K;
    • Sim, Kar Seng;
    • Wang, Jie Jin;
    • Wong, Tien Yin;
    • Pang, Junxiong;
    • Mitchell, Paul;
    • Cimaz, Rolando;
    • Dahdah, Nagib;
    • Cheung, Yiu-Fai;
    • Huang, Guo-Ying;
    • Yang, Wanling;
    • Park, In-Sook;
    • Lee, Jong-Keuk
    Publication type:
    Article
    20
    21

    Personalized asthma control.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1178, doi. 10.1038/ng.1023
    By:
    • Peng, Wayne
    Publication type:
    Article
    22
    23

    Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1219, doi. 10.1038/ng.982
    By:
    • Wang, Kai;
    • Kan, Junsuo;
    • Yuen, Siu Tsan;
    • Shi, Stephanie T;
    • Chu, Kent Man;
    • Law, Simon;
    • Chan, Tsun Leung;
    • Kan, Zhengyan;
    • Chan, Annie S Y;
    • Tsui, Wai Yin;
    • Lee, Siu Po;
    • Ho, Siu Lun;
    • Chan, Anthony K W;
    • Cheng, Grace H W;
    • Roberts, Peter C;
    • Rejto, Paul A;
    • Gibson, Neil W;
    • Pocalyko, David J;
    • Mao, Mao;
    • Xu, Jiangchun
    Publication type:
    Article
    24

    Priming for chemotherapy.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1178, doi. 10.1038/ng.1021
    By:
    • Feliciano, Pamela
    Publication type:
    Article
    25

    Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1189, doi. 10.1038/ng.995
    By:
    • Logan, Clare V;
    • Lucke, Barbara;
    • Pottinger, Caroline;
    • Abdelhamed, Zakia A;
    • Parry, David A;
    • Szymanska, Katarzyna;
    • Diggle, Christine P;
    • Riesen, Anne van;
    • Morgan, Joanne E;
    • Markham, Grace;
    • Ellis, Ian;
    • Manzur, Adnan Y;
    • Markham, Alexander F;
    • Shires, Mike;
    • Helliwell, Tim;
    • Scoto, Mariacristina;
    • Hübner, Christoph;
    • Bonthron, David T;
    • Taylor, Graham R;
    • Sheridan, Eamonn
    Publication type:
    Article
    26

    Leishmaniasis genomes.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1178, doi. 10.1038/ng.1025
    By:
    • Bahcall, Orli
    Publication type:
    Article
    27
    28

    Common variants on 8p12 and 1q24.2 confer risk of schizophrenia.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1224, doi. 10.1038/ng.980
    By:
    • Shi, Yongyong;
    • Li, Zhiqiang;
    • Xu, Qi;
    • Wang, Ti;
    • Li, Tao;
    • Shen, Jiawei;
    • Zhang, Fengyu;
    • Chen, Jianhua;
    • Zhou, Guoquan;
    • Ji, Weidong;
    • Li, Baojie;
    • Xu, Yifeng;
    • Liu, Dengtang;
    • Wang, Peng;
    • Yang, Ping;
    • Liu, Benxiu;
    • Sun, Wensheng;
    • Wan, Chunling;
    • Qin, Shengying;
    • He, Guang
    Publication type:
    Article
    29
    30

    A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1232, doi. 10.1038/ng.976
    By:
    • Raychaudhuri, Soumya;
    • Iartchouk, Oleg;
    • Chin, Kimberly;
    • Tan, Perciliz L;
    • Tai, Albert K;
    • Ripke, Stephan;
    • Gowrisankar, Sivakumar;
    • Vemuri, Soumya;
    • Montgomery, Kate;
    • Yu, Yi;
    • Reynolds, Robyn;
    • Zack, Donald J;
    • Campochiaro, Betsy;
    • Campochiaro, Peter;
    • Katsanis, Nicholas;
    • Daly, Mark J;
    • Seddon, Johanna M
    Publication type:
    Article
    31
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