Works matching IS 10614036 AND DT 2011 AND VI 43 AND IP 10

Results: 31
    1

    Germline mutations in BAP1 predispose to melanocytic tumors.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 1018, doi. 10.1038/ng.910
    By:
    • Wiesner, Thomas;
    • Obenauf, Anna C;
    • Murali, Rajmohan;
    • Fried, Isabella;
    • Griewank, Klaus G;
    • Ulz, Peter;
    • Windpassinger, Christian;
    • Wackernagel, Werner;
    • Loy, Shea;
    • Wolf, Ingrid;
    • Viale, Agnes;
    • Lash, Alex E;
    • Pirun, Mono;
    • Socci, Nicholas D;
    • Rütten, Arno;
    • Palmedo, Gabriele;
    • Abramson, David;
    • Offit, Kenneth;
    • Ott, Arthur;
    • Becker, Jürgen C
    Publication type:
    Article
    2

    Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 1012, doi. 10.1038/ng.913
    By:
    • Hahn, Christopher N;
    • Chong, Chan-Eng;
    • Carmichael, Catherine L;
    • Wilkins, Ella J;
    • Brautigan, Peter J;
    • Li, Xiao-Chun;
    • Babic, Milena;
    • Lin, Ming;
    • Carmagnac, Amandine;
    • Lee, Young K;
    • Kok, Chung H;
    • Gagliardi, Lucia;
    • Friend, Kathryn L;
    • Ekert, Paul G;
    • Butcher, Carolyn M;
    • Brown, Anna L;
    • Lewis, Ian D;
    • To, L Bik;
    • Timms, Andrew E;
    • Storek, Jan
    Publication type:
    Article
    3

    Sexually dimorphic digits.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 928, doi. 10.1038/ng.965
    By:
    • Feliciano, Pamela
    Publication type:
    Article
    4

    Erratum: Common variants in P2RY11 are associated with narcolepsy.

    Published in:
    2011
    By:
    • Kornum, Birgitte R;
    • Kawashima, Minae;
    • Faraco, Juliette;
    • Lin, Ling;
    • Rico, Thomas J;
    • Hesselson, Stephanie;
    • Axtell, Robert C;
    • Kuipers, Hedwich;
    • Weiner, Karin;
    • Hamacher, Alexandra;
    • Kassack, Matthias U;
    • Han, Fang;
    • Knudsen, Stine;
    • Li, Jing;
    • Dong, Xiaosong;
    • Winkelmann, Juliane;
    • Plazzi, Giuseppe;
    • Nevsimalova, Sona;
    • Hong, Seung-Chul;
    • Honda, Yutaka
    Publication type:
    Correction Notice
    5
    6
    7
    8

    A surprising role for FOXO.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 928, doi. 10.1038/ng.968
    By:
    • Niemitz, Emily
    Publication type:
    Article
    9

    Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 1005, doi. 10.1038/ng.922
    By:
    • Wain, Louise V;
    • Verwoert, Germaine C;
    • O'Reilly, Paul F;
    • Shi, Gang;
    • Johnson, Toby;
    • Johnson, Andrew D;
    • Bochud, Murielle;
    • Rice, Kenneth M;
    • Henneman, Peter;
    • Smith, Albert V;
    • Ehret, Georg B;
    • Amin, Najaf;
    • Larson, Martin G;
    • Mooser, Vincent;
    • Hadley, David;
    • Dörr, Marcus;
    • Bis, Joshua C;
    • Aspelund, Thor;
    • Esko, Tõnu;
    • Janssens, A Cecile J W
    Publication type:
    Article
    10

    Genome-wide association study identifies five new schizophrenia loci.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 969, doi. 10.1038/ng.940
    By:
    • Ripke, Stephan;
    • Sanders, Alan R;
    • Kendler, Kenneth S;
    • Levinson, Douglas F;
    • Sklar, Pamela;
    • Holmans, Peter A;
    • Lin, Dan-Yu;
    • Duan, Jubao;
    • Ophoff, Roel A;
    • Andreassen, Ole A;
    • Scolnick, Edward;
    • Cichon, Sven;
    • St. Clair, David;
    • Corvin, Aiden;
    • Gurling, Hugh;
    • Werge, Thomas;
    • Rujescu, Dan;
    • Blackwood, Douglas H R;
    • Pato, Carlos N;
    • Malhotra, Anil K
    Publication type:
    Article
    11
    12

    Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 984, doi. 10.1038/ng.921
    By:
    • Kooner, Jaspal S;
    • Saleheen, Danish;
    • Sim, Xueling;
    • Sehmi, Joban;
    • Zhang, Weihua;
    • Frossard, Philippe;
    • Been, Latonya F;
    • Chia, Kee-Seng;
    • Dimas, Antigone S;
    • Hassanali, Neelam;
    • Jafar, Tazeen;
    • Jowett, Jeremy B M;
    • Li, Xinzhong;
    • Radha, Venkatesan;
    • Rees, Simon D;
    • Takeuchi, Fumihiko;
    • Young, Robin;
    • Aung, Tin;
    • Basit, Abdul;
    • Chidambaram, Manickam
    Publication type:
    Article
    13

    Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 964, doi. 10.1038/ng.936
    By:
    • Bass, Adam J;
    • Lawrence, Michael S;
    • Brace, Lear E;
    • Ramos, Alex H;
    • Drier, Yotam;
    • Cibulskis, Kristian;
    • Sougnez, Carrie;
    • Voet, Douglas;
    • Saksena, Gordon;
    • Sivachenko, Andrey;
    • Jing, Rui;
    • Parkin, Melissa;
    • Pugh, Trevor;
    • Verhaak, Roel G;
    • Stransky, Nicolas;
    • Boutin, Adam T;
    • Barretina, Jordi;
    • Solit, David B;
    • Vakiani, Evi;
    • Shao, Wenlin
    Publication type:
    Article
    14
    15
    16

    Germline deletion of the miR-17?92 cluster causes skeletal and growth defects in humans.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 1026, doi. 10.1038/ng.915
    By:
    • de Pontual, Loïc;
    • Yao, Evelyn;
    • Callier, Patrick;
    • Faivre, Laurence;
    • Drouin, Valérie;
    • Cariou, Sandra;
    • Van Haeringen, Arie;
    • Geneviève, David;
    • Goldenberg, Alice;
    • Oufadem, Myriam;
    • Manouvrier, Sylvie;
    • Munnich, Arnold;
    • Vidigal, Joana Alves;
    • Vekemans, Michel;
    • Lyonnet, Stanislas;
    • Henrion-Caude, Alexandra;
    • Ventura, Andrea;
    • Amiel, Jeanne
    Publication type:
    Article
    17

    Whole-genome sequencing of multiple Arabidopsis thaliana populations.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 956, doi. 10.1038/ng.911
    By:
    • Cao, Jun;
    • Schneeberger, Korbinian;
    • Ossowski, Stephan;
    • Günther, Torsten;
    • Bender, Sebastian;
    • Fitz, Joffrey;
    • Koenig, Daniel;
    • Lanz, Christa;
    • Stegle, Oliver;
    • Lippert, Christoph;
    • Wang, Xi;
    • Ott, Felix;
    • Müller, Jonas;
    • Alonso-Blanco, Carlos;
    • Borgwardt, Karsten;
    • Schmid, Karl J;
    • Weigel, Detlef
    Publication type:
    Article
    18

    Oncogenic IL7R gain-of-function mutations in childhood T-cell acute lymphoblastic leukemia.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 932, doi. 10.1038/ng.924
    By:
    • Zenatti, Priscila P;
    • Ribeiro, Daniel;
    • Li, Wenqing;
    • Zuurbier, Linda;
    • Silva, Milene C;
    • Paganin, Maddalena;
    • Tritapoe, Julia;
    • Hixon, Julie A;
    • Silveira, André B;
    • Cardoso, Bruno A;
    • Sarmento, Leonor M;
    • Correia, Nádia;
    • Toribio, Maria L;
    • Kobarg, Jörg;
    • Horstmann, Martin;
    • Pieters, Rob;
    • Brandalise, Silvia R;
    • Ferrando, Adolfo A;
    • Meijerink, Jules P;
    • Durum, Scott K
    Publication type:
    Article
    19
    20
    21

    Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 929, doi. 10.1038/ng.923
    By:
    • Ostergaard, Pia;
    • Simpson, Michael A;
    • Connell, Fiona C;
    • Steward, Colin G;
    • Brice, Glen;
    • Woollard, Wesley J;
    • Dafou, Dimitra;
    • Kilo, Tatjana;
    • Smithson, Sarah;
    • Lunt, Peter;
    • Murday, Victoria A;
    • Hodgson, Shirley;
    • Keenan, Russell;
    • Pilz, Daniela T;
    • Martinez-Corral, Ines;
    • Makinen, Taija;
    • Mortimer, Peter S;
    • Jeffery, Steve;
    • Trembath, Richard C;
    • Mansour, Sahar
    Publication type:
    Article
    22
    23

    Maternal imprinting defect.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 928, doi. 10.1038/ng.967
    By:
    • Vogan, Kyle
    Publication type:
    Article
    24

    Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 940, doi. 10.1038/ng.920
    By:
    • Bis, Joshua C;
    • Kavousi, Maryam;
    • Franceschini, Nora;
    • Isaacs, Aaron;
    • Abecasis, Gonçalo R;
    • Schminke, Ulf;
    • Post, Wendy S;
    • Smith, Albert V;
    • Cupples, L Adrienne;
    • Markus, Hugh S;
    • Schmidt, Reinhold;
    • Huffman, Jennifer E;
    • Lehtimäki, Terho;
    • Baumert, Jens;
    • Münzel, Thomas;
    • Heckbert, Susan R;
    • Dehghan, Abbas;
    • North, Kari;
    • Oostra, Ben;
    • Bevan, Steve
    Publication type:
    Article
    25

    Germline BAP1 mutations predispose to malignant mesothelioma.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 1022, doi. 10.1038/ng.912
    By:
    • Testa, Joseph R;
    • Cheung, Mitchell;
    • Pei, Jianming;
    • Below, Jennifer E;
    • Tan, Yinfei;
    • Sementino, Eleonora;
    • Cox, Nancy J;
    • Dogan, A Umran;
    • Pass, Harvey I;
    • Trusa, Sandra;
    • Hesdorffer, Mary;
    • Nasu, Masaki;
    • Powers, Amy;
    • Rivera, Zeyana;
    • Comertpay, Sabahattin;
    • Tanji, Mika;
    • Gaudino, Giovanni;
    • Yang, Haining;
    • Carbone, Michele
    Publication type:
    Article
    26

    Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 977, doi. 10.1038/ng.943
    By:
    • Sklar, Pamela;
    • Ripke, Stephan;
    • Scott, Laura J;
    • Andreassen, Ole A;
    • Cichon, Sven;
    • Craddock, Nick;
    • Edenberg, Howard J;
    • Nurnberger, John I;
    • Rietschel, Marcella;
    • Blackwood, Douglas;
    • Corvin, Aiden;
    • Flickinger, Matthew;
    • Guan, Weihua;
    • Mattingsdal, Morten;
    • McQuillin, Andrew;
    • Kwan, Phoenix;
    • Wienker, Thomas F;
    • Daly, Mark;
    • Dudbridge, Frank;
    • Holmans, Peter A
    Publication type:
    Article
    27
    28

    Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 996, doi. 10.1038/ng.934
    By:
    • LeMaire, Scott A;
    • McDonald, Merry-Lynn N;
    • Guo, Dong-chuan;
    • Russell, Ludivine;
    • Miller, Charles C;
    • Johnson, Ralph J;
    • Bekheirnia, Mir Reza;
    • Franco, Luis M;
    • Nguyen, Mary;
    • Pyeritz, Reed E;
    • Bavaria, Joseph E;
    • Devereux, Richard;
    • Maslen, Cheryl;
    • Holmes, Kathryn W;
    • Eagle, Kim;
    • Body, Simon C;
    • Seidman, Christine;
    • Seidman, J G;
    • Isselbacher, Eric M;
    • Bray, Molly
    Publication type:
    Article
    29
    30

    The genome of the mesopolyploid crop species Brassica rapa.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 1035, doi. 10.1038/ng.919
    By:
    • Wang, Xiaowu;
    • Wang, Hanzhong;
    • Wang, Jun;
    • Sun, Rifei;
    • Wu, Jian;
    • Liu, Shengyi;
    • Bai, Yinqi;
    • Mun, Jeong-Hwan;
    • Bancroft, Ian;
    • Cheng, Feng;
    • Huang, Sanwen;
    • Li, Xixiang;
    • Hua, Wei;
    • Wang, Junyi;
    • Wang, Xiyin;
    • Freeling, Michael;
    • Pires, J Chris;
    • Paterson, Andrew H;
    • Chalhoub, Boulos;
    • Wang, Bo
    Publication type:
    Article
    31

    Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 1001, doi. 10.1038/ng.938
    By:
    • Arakawa, Satoshi;
    • Takahashi, Atsushi;
    • Ashikawa, Kyota;
    • Hosono, Naoya;
    • Aoi, Tomomi;
    • Yasuda, Miho;
    • Oshima, Yuji;
    • Yoshida, Shigeo;
    • Enaida, Hiroshi;
    • Tsuchihashi, Takashi;
    • Mori, Keisuke;
    • Honda, Shigeru;
    • Negi, Akira;
    • Arakawa, Akira;
    • Kadonosono, Kazuaki;
    • Kiyohara, Yutaka;
    • Kamatani, Naoyuki;
    • Nakamura, Yusuke;
    • Ishibashi, Tatsuro;
    • Kubo, Michiaki
    Publication type:
    Article