Works matching IS 10614036 AND DT 2012 AND VI 44 AND IP 1

Results: 28
    1

    Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 67, doi. 10.1038/ng.1019
    By:
    • Cho, Yoon Shin;
    • Chen, Chien-Hsiun;
    • Hu, Cheng;
    • Long, Jirong;
    • Hee Ong, Rick Twee;
    • Sim, Xueling;
    • Takeuchi, Fumihiko;
    • Wu, Ying;
    • Go, Min Jin;
    • Yamauchi, Toshimasa;
    • Chang, Yi-Cheng;
    • Kwak, Soo Heon;
    • Ma, Ronald C W;
    • Yamamoto, Ken;
    • Adair, Linda S;
    • Aung, Tin;
    • Cai, Qiuyin;
    • Chang, Li-Ching;
    • Chen, Yuan-Tsong;
    • Gao, Yutang
    Publication type:
    Article
    2

    Large-scale discovery of enhancers from human heart tissue.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 89, doi. 10.1038/ng.1006
    By:
    • May, Dalit;
    • Blow, Matthew J;
    • Kaplan, Tommy;
    • McCulley, David J;
    • Jensen, Brian C;
    • Akiyama, Jennifer A;
    • Holt, Amy;
    • Plajzer-Frick, Ingrid;
    • Shoukry, Malak;
    • Wright, Crystal;
    • Afzal, Veena;
    • Simpson, Paul C;
    • Rubin, Edward M;
    • Black, Brian L;
    • Bristow, James;
    • Pennacchio, Len A;
    • Visel, Axel
    Publication type:
    Article
    3

    Unifying antipsychotic drugs.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 15, doi. 10.1038/ng.1063
    By:
    • Feliciano, Pamela
    Publication type:
    Article
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    Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 53, doi. 10.1038/ng.1031
    By:
    • Graubert, Timothy A;
    • Shen, Dong;
    • Ding, Li;
    • Okeyo-Owuor, Theresa;
    • Lunn, Cara L;
    • Shao, Jin;
    • Krysiak, Kilannin;
    • Harris, Christopher C;
    • Koboldt, Daniel C;
    • Larson, David E;
    • McLellan, Michael D;
    • Dooling, David J;
    • Abbott, Rachel M;
    • Fulton, Robert S;
    • Schmidt, Heather;
    • Kalicki-Veizer, Joelle;
    • O'Laughlin, Michelle;
    • Grillot, Marcus;
    • Baty, Jack;
    • Heath, Sharon
    Publication type:
    Article
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    Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 58, doi. 10.1038/ng.993
    By:
    • Broderick, Peter;
    • Chubb, Daniel;
    • Johnson, David C;
    • Weinhold, Niels;
    • Försti, Asta;
    • Lloyd, Amy;
    • Olver, Bianca;
    • Ma, Yussanne P;
    • Dobbins, Sara E;
    • Walker, Brian A;
    • Davies, Faith E;
    • Gregory, Walter A;
    • Child, J Anthony;
    • Ross, Fiona M;
    • Jackson, Graham H;
    • Neben, Kai;
    • Jauch, Anna;
    • Hoffmann, Per;
    • Mühleisen, Thomas W;
    • Nöthen, Markus M
    Publication type:
    Article
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    Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 85, doi. 10.1038/ng.1016
    By:
    • Le Goff, Carine;
    • Mahaut, Clémentine;
    • Abhyankar, Avinash;
    • Le Goff, Wilfried;
    • Serre, Valérie;
    • Afenjar, Alexandra;
    • Destrée, Anne;
    • di Rocco, Maja;
    • Héron, Delphine;
    • Jacquemont, Sébastien;
    • Marlin, Sandrine;
    • Simon, Marleen;
    • Tolmie, John;
    • Verloes, Alain;
    • Casanova, Jean-Laurent;
    • Munnich, Arnold;
    • Cormier-Daire, Valérie
    Publication type:
    Article
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    Improved imputation of common and uncommon SNPs with a new reference set.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 6, doi. 10.1038/ng.1044
    By:
    • Wang, Zhaoming;
    • Jacobs, Kevin B;
    • Yeager, Meredith;
    • Hutchinson, Amy;
    • Sampson, Joshua;
    • Chatterjee, Nilanjan;
    • Albanes, Demetrius;
    • Berndt, Sonja I;
    • Chung, Charles C;
    • Diver, W Ryan;
    • Gapstur, Susan M;
    • Teras, Lauren R;
    • Haiman, Christopher A;
    • Henderson, Brian E;
    • Stram, Daniel;
    • Deng, Xiang;
    • Hsing, Ann W;
    • Virtamo, Jarmo;
    • Eberle, Michael A;
    • Stone, Jennifer L
    Publication type:
    Article
    19

    Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 78, doi. 10.1038/ng.1013
    By:
    • Elia, Josephine;
    • Glessner, Joseph T;
    • Wang, Kai;
    • Takahashi, Nagahide;
    • Shtir, Corina J;
    • Hadley, Dexter;
    • Sleiman, Patrick M A;
    • Zhang, Haitao;
    • Kim, Cecilia E;
    • Robison, Reid;
    • Lyon, Gholson J;
    • Flory, James H;
    • Bradfield, Jonathan P;
    • Imielinski, Marcin;
    • Hou, Cuiping;
    • Frackelton, Edward C;
    • Chiavacci, Rosetta M;
    • Sakurai, Takeshi;
    • Rabin, Cara;
    • Middleton, Frank A
    Publication type:
    Article
    20

    Dnmt3a is essential for hematopoietic stem cell differentiation.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 23, doi. 10.1038/ng.1009
    By:
    • Challen, Grant A;
    • Sun, Deqiang;
    • Jeong, Mira;
    • Luo, Min;
    • Jelinek, Jaroslav;
    • Berg, Jonathan S;
    • Bock, Christoph;
    • Vasanthakumar, Aparna;
    • Gu, Hongcang;
    • Xi, Yuanxin;
    • Liang, Shoudan;
    • Lu, Yue;
    • Darlington, Gretchen J;
    • Meissner, Alexander;
    • Issa, Jean-Pierre J;
    • Godley, Lucy A;
    • Li, Wei;
    • Goodell, Margaret A
    Publication type:
    Article
    21

    Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 47, doi. 10.1038/ng.1032
    By:
    • Quesada, Víctor;
    • Conde, Laura;
    • Villamor, Neus;
    • Ordóñez, Gonzalo R;
    • Jares, Pedro;
    • Bassaganyas, Laia;
    • Ramsay, Andrew J;
    • Beà, Sílvia;
    • Pinyol, Magda;
    • Martínez-Trillos, Alejandra;
    • López-Guerra, Mónica;
    • Colomer, Dolors;
    • Navarro, Alba;
    • Baumann, Tycho;
    • Aymerich, Marta;
    • Rozman, María;
    • Delgado, Julio;
    • Giné, Eva;
    • Hernández, Jesús M;
    • González-Díaz, Marcos
    Publication type:
    Article
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    GATA6 haploinsufficiency causes pancreatic agenesis in humans.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 20, doi. 10.1038/ng.1035
    By:
    • Allen, Hana Lango;
    • Flanagan, Sarah E;
    • Shaw-Smith, Charles;
    • De Franco, Elisa;
    • Akerman, Ildem;
    • Caswell, Richard;
    • Ferrer, Jorge;
    • Hattersley, Andrew T;
    • Ellard, Sian
    Publication type:
    Article
    26

    Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.

    Published in:
    2012
    By:
    • Hunt, Karen A;
    • Smyth, Deborah J;
    • Balschun, Tobias;
    • Ban, Maria;
    • Mistry, Vanisha;
    • Ahmad, Tariq;
    • Anand, Vidya;
    • Barrett, Jeffrey C;
    • Bhaw-Rosun, Leena;
    • Bockett, Nicholas A;
    • Brand, Oliver J;
    • Brouwer, Elisabeth;
    • Concannon, Patrick;
    • Cooper, Jason D;
    • Dias, Kerith-Rae M;
    • van Diemen, Cleo C;
    • Dubois, Patrick C;
    • Edkins, Sarah;
    • Fölster-Holst, Regina;
    • Fransen, Karin
    Publication type:
    Letter
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