Works matching IS 10614036 AND DT 2012 AND VI 44 AND IP 6


Results: 32
    • A genome-wide association study identifies susceptibility loci for Wilms tumor.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 681, doi. 10.1038/ng.2251
      By:
      • Turnbull, Clare;
      • Perdeaux, Elizabeth R;
      • Pernet, David;
      • Naranjo, Arlene;
      • Renwick, Anthony;
      • Seal, Sheila;
      • Munoz-Xicola, Rosa Maria;
      • Hanks, Sandra;
      • Slade, Ingrid;
      • Zachariou, Anna;
      • Warren-Perry, Margaret;
      • Ruark, Elise;
      • Gerrard, Mary;
      • Hale, Juliet;
      • Hewitt, Martin;
      • Kohler, Janice;
      • Lane, Sheila;
      • Levitt, Gill;
      • Madi, Mabrook;
      • Morland, Bruce
      Publication type:
      Article
    • A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 659, doi. 10.1038/ng.2274
      By:
      • Manning, Alisa K;
      • Hivert, Marie-France;
      • Scott, Robert A;
      • Grimsby, Jonna L;
      • Bouatia-Naji, Nabila;
      • Chen, Han;
      • Rybin, Denis;
      • Liu, Ching-Ti;
      • Bielak, Lawrence F;
      • Prokopenko, Inga;
      • Amin, Najaf;
      • Barnes, Daniel;
      • Cadby, Gemma;
      • Hottenga, Jouke-Jan;
      • Ingelsson, Erik;
      • Jackson, Anne U;
      • Johnson, Toby;
      • Kanoni, Stavroula;
      • Ladenvall, Claes;
      • Lagou, Vasiliki
      Publication type:
      Article
    • Exploring the variation within.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 614, doi. 10.1038/ng.2311
      By:
      • Macosko, Evan Z;
      • McCarroll, Steven A
      Publication type:
      Article
    • CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 714, doi. 10.1038/ng.2277
      By:
      • Panizzi, Jennifer R;
      • Becker-Heck, Anita;
      • Castleman, Victoria H;
      • Al-Mutairi, Dalal A;
      • Liu, Yan;
      • Loges, Niki T;
      • Pathak, Narendra;
      • Austin-Tse, Christina;
      • Sheridan, Eamonn;
      • Schmidts, Miriam;
      • Olbrich, Heike;
      • Werner, Claudius;
      • Häffner, Karsten;
      • Hellman, Nathan;
      • Chodhari, Rahul;
      • Gupta, Amar;
      • Kramer-Zucker, Albrecht;
      • Olale, Felix;
      • Burdine, Rebecca D;
      • Schier, Alexander F
      Publication type:
      Article
    • Epigenetic activation by long RNA.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2321
      By:
      • Niemitz, Emily
      Publication type:
      Article
    • ITGA3 and epithelial integrity.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2319
      By:
      • Vogan, Kyle
      Publication type:
      Article
    • Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 639, doi. 10.1038/ng.2262
      By:
      • Koolen, David A;
      • Kramer, Jamie M;
      • Neveling, Kornelia;
      • Nillesen, Willy M;
      • Moore-Barton, Heather L;
      • Elmslie, Frances V;
      • Toutain, Annick;
      • Amiel, Jeanne;
      • Malan, Valérie;
      • Tsai, Anne Chun-Hui;
      • Cheung, Sau Wai;
      • Gilissen, Christian;
      • Verwiel, Eugene T P;
      • Martens, Sarah;
      • Feuth, Ton;
      • Bongers, Ernie M H F;
      • de Vries, Petra;
      • Scheffer, Hans;
      • Vissers, Lisenka E L M;
      • de Brouwer, Arjan P M
      Publication type:
      Article
    • Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 699, doi. 10.1038/ng.2263
      By:
      • Jaeger, Emma;
      • Leedham, Simon;
      • Lewis, Annabelle;
      • Segditsas, Stefania;
      • Becker, Martin;
      • Cuadrado, Pedro Rodenas;
      • Davis, Hayley;
      • Kaur, Kulvinder;
      • Heinimann, Karl;
      • Howarth, Kimberley;
      • East, James;
      • Taylor, Jenny;
      • Thomas, Huw;
      • Tomlinson, Ian
      Publication type:
      Article
    • Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume.

      Published in:
      2012
      By:
      • Ikram, M Arfan;
      • Fornage, Myriam;
      • Smith, Albert V;
      • Seshadri, Sudha;
      • Schmidt, Reinhold;
      • Debette, Stéphanie;
      • Vrooman, Henri A;
      • Sigurdsson, Sigurdur;
      • Ropele, Stefan;
      • Taal, H Rob;
      • Mook-Kanamori, Dennis O;
      • Coker, Laura H;
      • Longstreth, W T;
      • Niessen, Wiro J;
      • DeStefano, Anita L;
      • Beiser, Alexa;
      • Zijdenbos, Alex P;
      • Struchalin, Maksim;
      • Jack, Clifford R;
      • Rivadeneira, Fernando
      Publication type:
      Erratum
    • Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 709, doi. 10.1038/ng.2259
      By:
      • Bonnard, Carine;
      • Strobl, Anna C;
      • Shboul, Mohammad;
      • Lee, Hane;
      • Merriman, Barry;
      • Nelson, Stanley F;
      • Ababneh, Osama H;
      • Uz, Elif;
      • Güran, Tülay;
      • Kayserili, Hülya;
      • Hamamy, Hanan;
      • Reversade, Bruno
      Publication type:
      Article
    • Detectable clonal mosaicism from birth to old age and its relationship to cancer.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 642, doi. 10.1038/ng.2271
      By:
      • Laurie, Cathy C;
      • Laurie, Cecelia A;
      • Rice, Kenneth;
      • Doheny, Kimberly F;
      • Zelnick, Leila R;
      • McHugh, Caitlin P;
      • Ling, Hua;
      • Hetrick, Kurt N;
      • Pugh, Elizabeth W;
      • Amos, Chris;
      • Wei, Qingyi;
      • Wang, Li-e;
      • Lee, Jeffrey E;
      • Barnes, Kathleen C;
      • Hansel, Nadia N;
      • Mathias, Rasika;
      • Daley, Denise;
      • Beaty, Terri H;
      • Scott, Alan F;
      • Ruczinski, Ingo
      Publication type:
      Article
    • One gene's shattering effects.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 616, doi. 10.1038/ng.2289
      By:
      • Olsen, Kenneth M
      Publication type:
      Article
    • Exome sequencing and the genetic basis of complex traits.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 623, doi. 10.1038/ng.2303
      By:
      • Kiezun, Adam;
      • Garimella, Kiran;
      • Do, Ron;
      • Stitziel, Nathan O;
      • Neale, Benjamin M;
      • McLaren, Paul J;
      • Gupta, Namrata;
      • Sklar, Pamela;
      • Sullivan, Patrick F;
      • Moran, Jennifer L;
      • Hultman, Christina M;
      • Lichtenstein, Paul;
      • Magnusson, Patrik;
      • Lehner, Thomas;
      • Shugart, Yin Yao;
      • Price, Alkes L;
      • de Bakker, Paul I W;
      • Purcell, Shaun M;
      • Sunyaev, Shamil R
      Publication type:
      Article
    • Erratum: A transposon in tb1 drove maize domestication.

      Published in:
      2012
      By:
      • Tsiantis, Miltos
      Publication type:
      Erratum
    • Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 704, doi. 10.1038/ng.2254
      By:
      • Wan, Jijun;
      • Yourshaw, Michael;
      • Mamsa, Hafsa;
      • Rudnik-Schöneborn, Sabine;
      • Menezes, Manoj P;
      • Hong, Ji Eun;
      • Leong, Derek W;
      • Senderek, Jan;
      • Salman, Michael S;
      • Chitayat, David;
      • Seeman, Pavel;
      • von Moers, Arpad;
      • Graul-Neumann, Luitgard;
      • Kornberg, Andrew J;
      • Castro-Gago, Manuel;
      • Sobrido, María-Jesús;
      • Sanefuji, Masafumi;
      • Shieh, Perry B;
      • Salamon, Noriko;
      • Kim, Ronald C
      Publication type:
      Article
    • How do you feel?

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2317
      By:
      • Feliciano, Pamela
      Publication type:
      Article
    • Traversing the genomic landscape of prostate cancer from diagnosis to death.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 613, doi. 10.1038/ng.2301
      By:
      • Hieronymus, Haley;
      • Sawyers, Charles L
      Publication type:
      Article
    • Extremely low-coverage sequencing and imputation increases power for genome-wide association studies.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 631, doi. 10.1038/ng.2283
      By:
      • Pasaniuc, Bogdan;
      • Rohland, Nadin;
      • McLaren, Paul J;
      • Garimella, Kiran;
      • Zaitlen, Noah;
      • Li, Heng;
      • Gupta, Namrata;
      • Neale, Benjamin M;
      • Daly, Mark J;
      • Sklar, Pamela;
      • Sullivan, Patrick F;
      • Bergen, Sarah;
      • Moran, Jennifer L;
      • Hultman, Christina M;
      • Lichtenstein, Paul;
      • Magnusson, Patrik;
      • Purcell, Shaun M;
      • Haas, David W;
      • Liang, Liming;
      • Sunyaev, Shamil
      Publication type:
      Article
    • piRNA, epigenetics and memory formation.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2318
      By:
      • Niemitz, Emily
      Publication type:
      Article
    • Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 694, doi. 10.1038/ng.2256
      By:
      • Guichard, Cécile;
      • Amaddeo, Giuliana;
      • Imbeaud, Sandrine;
      • Ladeiro, Yannick;
      • Pelletier, Laura;
      • Maad, Ichrafe Ben;
      • Calderaro, Julien;
      • Bioulac-Sage, Paulette;
      • Letexier, Mélanie;
      • Degos, Françoise;
      • Clément, Bruno;
      • Balabaud, Charles;
      • Chevet, Eric;
      • Laurent, Alexis;
      • Couchy, Gabrielle;
      • Letouzé, Eric;
      • Calvo, Fabien;
      • Zucman-Rossi, Jessica
      Publication type:
      Article
    • The Pediatric Cancer Genome Project.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 619, doi. 10.1038/ng.2287
      By:
      • Downing, James R;
      • Wilson, Richard K;
      • Zhang, Jinghui;
      • Mardis, Elaine R;
      • Pui, Ching-Hon;
      • Ding, Li;
      • Ley, Timothy J;
      • Evans, William E
      Publication type:
      Article
    • Corrigendum: Arabidopsis thaliana as a model for the genetics of local adaptation.

      Published in:
      2012
      By:
      • Gaut, Brandon
      Publication type:
      Erratum
    • Parallel domestication of the Shattering1 genes in cereals.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 720, doi. 10.1038/ng.2281
      By:
      • Lin, Zhongwei;
      • Li, Xianran;
      • Shannon, Laura M;
      • Yeh, Cheng-Ting;
      • Wang, Ming L;
      • Bai, Guihua;
      • Peng, Zhao;
      • Li, Jiarui;
      • Trick, Harold N;
      • Clemente, Thomas E;
      • Doebley, John;
      • Schnable, Patrick S;
      • Tuinstra, Mitchell R;
      • Tesso, Tesfaye T;
      • White, Frank;
      • Yu, Jianming
      Publication type:
      Article
    • Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 685, doi. 10.1038/ng.2279
      By:
      • Barbieri, Christopher E;
      • Baca, Sylvan C;
      • Lawrence, Michael S;
      • Demichelis, Francesca;
      • Blattner, Mirjam;
      • Theurillat, Jean-Philippe;
      • White, Thomas A;
      • Stojanov, Petar;
      • Van Allen, Eliezer;
      • Stransky, Nicolas;
      • Nickerson, Elizabeth;
      • Chae, Sung-Suk;
      • Boysen, Gunther;
      • Auclair, Daniel;
      • Onofrio, Robert C;
      • Park, Kyung;
      • Kitabayashi, Naoki;
      • MacDonald, Theresa Y;
      • Sheikh, Karen;
      • Vuong, Terry
      Publication type:
      Article
    • Genetics of blond hair.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 618, doi. 10.1038/ng.2320
      By:
      • Bahcall, Orli
      Publication type:
      Article
    • Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 636, doi. 10.1038/ng.2257
      By:
      • Zollino, Marcella;
      • Orteschi, Daniela;
      • Murdolo, Marina;
      • Lattante, Serena;
      • Battaglia, Domenica;
      • Stefanini, Chiara;
      • Mercuri, Eugenio;
      • Chiurazzi, Pietro;
      • Neri, Giovanni;
      • Marangi, Giuseppe
      Publication type:
      Article
    • The '3Is' of animal experimentation.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 611, doi. 10.1038/ng.2322
      Publication type:
      Article
    • Meta-analysis identifies six new susceptibility loci for atrial fibrillation.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 670, doi. 10.1038/ng.2261
      By:
      • Ellinor, Patrick T;
      • Lunetta, Kathryn L;
      • Albert, Christine M;
      • Glazer, Nicole L;
      • Ritchie, Marylyn D;
      • Smith, Albert V;
      • Arking, Dan E;
      • Müller-Nurasyid, Martina;
      • Krijthe, Bouwe P;
      • Lubitz, Steven A;
      • Bis, Joshua C;
      • Chung, Mina K;
      • Dörr, Marcus;
      • Ozaki, Kouichi;
      • Roberts, Jason D;
      • Smith, J Gustav;
      • Pfeufer, Arne;
      • Sinner, Moritz F;
      • Lohman, Kurt;
      • Ding, Jingzhong
      Publication type:
      Article
    • Exome sequencing of liver fluke-associated cholangiocarcinoma.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 690, doi. 10.1038/ng.2273
      By:
      • Ong, Choon Kiat;
      • Subimerb, Chutima;
      • Pairojkul, Chawalit;
      • Wongkham, Sopit;
      • Cutcutache, Ioana;
      • Yu, Willie;
      • McPherson, John R;
      • Allen, George E;
      • Ng, Cedric Chuan Young;
      • Wong, Bernice Huimin;
      • Myint, Swe Swe;
      • Rajasegaran, Vikneswari;
      • Heng, Hong Lee;
      • Gan, Anna;
      • Zang, Zhi Jiang;
      • Wu, Yingting;
      • Wu, Jeanie;
      • Lee, Ming Hui;
      • Huang, DaChuan;
      • Ong, Pauline
      Publication type:
      Article
    • A model-based approach for analysis of spatial structure in genetic data.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 725, doi. 10.1038/ng.2285
      By:
      • Yang, Wen-Yun;
      • Novembre, John;
      • Eskin, Eleazar;
      • Halperin, Eran
      Publication type:
      Article
    • Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 676, doi. 10.1038/ng.2272
      By:
      • Jin, Ying;
      • Birlea, Stanca A;
      • Fain, Pamela R;
      • Ferrara, Tracey M;
      • Ben, Songtao;
      • Riccardi, Sheri L;
      • Cole, Joanne B;
      • Gowan, Katherine;
      • Holland, Paulene J;
      • Bennett, Dorothy C;
      • Luiten, Rosalie M;
      • Wolkerstorfer, Albert;
      • van der Veen, J P Wietze;
      • Hartmann, Anke;
      • Eichner, Saskia;
      • Schuler, Gerold;
      • van Geel, Nanja;
      • Lambert, Jo;
      • Kemp, E Helen;
      • Gawkrodger, David J
      Publication type:
      Article
    • Detectable clonal mosaicism and its relationship to aging and cancer.

      Published in:
      Nature Genetics, 2012, v. 44, n. 6, p. 651, doi. 10.1038/ng.2270
      By:
      • Jacobs, Kevin B;
      • Yeager, Meredith;
      • Zhou, Weiyin;
      • Wacholder, Sholom;
      • Wang, Zhaoming;
      • Rodriguez-Santiago, Benjamin;
      • Hutchinson, Amy;
      • Deng, Xiang;
      • Liu, Chenwei;
      • Horner, Marie-Josephe;
      • Cullen, Michael;
      • Epstein, Caroline G;
      • Burdett, Laurie;
      • Dean, Michael C;
      • Chatterjee, Nilanjan;
      • Sampson, Joshua;
      • Chung, Charles C;
      • Kovaks, Joseph;
      • Gapstur, Susan M;
      • Stevens, Victoria L
      Publication type:
      Article