Found: 26

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  • miRNAs and malaria resistance.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1079, doi. 10.1038/ng.2428
    By:
    • Feliciano, Pamela
    Publication type:
    Article

  • Bringing the genomic landscape of small-cell lung cancer into focus.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1074, doi. 10.1038/ng.2415
    By:
    • Pietanza, M Catherine;
    • Ladanyi, Marc
    Publication type:
    Article

  • Mutations in ABCD4 cause a new inborn error of vitamin B<sub>12</sub> metabolism.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1152, doi. 10.1038/ng.2386
    By:
    • Coelho, David;
    • Kim, Jaeseung C;
    • Miousse, Isabelle R;
    • Fung, Stephen;
    • du Moulin, Marcel;
    • Buers, Insa;
    • Suormala, Terttu;
    • Burda, Patricie;
    • Frapolli, Michele;
    • Stucki, Martin;
    • Nürnberg, Peter;
    • Thiele, Holger;
    • Robenek, Horst;
    • Höhne, Wolfgang;
    • Longo, Nicola;
    • Pasquali, Marzia;
    • Mengel, Eugen;
    • Watkins, David;
    • Shoubridge, Eric A;
    • Majewski, Jacek
    Publication type:
    Article

  • Exome sequencing of hepatitis B virus-associated hepatocellular carcinoma.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1117, doi. 10.1038/ng.2391
    By:
    • Huang, Jian;
    • Deng, Qing;
    • Wang, Qun;
    • Li, Kun-Yu;
    • Dai, Ji-Hong;
    • Li, Niu;
    • Zhu, Zhi-Dong;
    • Zhou, Bo;
    • Liu, Xiao-Yan;
    • Liu, Rui-Fang;
    • Fei, Qian-Lan;
    • Chen, Hui;
    • Cai, Bing;
    • Zhou, Boping;
    • Xiao, Hua-Sheng;
    • Qin, Lun-Xiu;
    • Han, Ze-Guang
    Publication type:
    Article

  • Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1104, doi. 10.1038/ng.2396
    By:
    • Peifer, Martin;
    • Fernández-Cuesta, Lynnette;
    • Sos, Martin L;
    • George, Julie;
    • Seidel, Danila;
    • Kasper, Lawryn H;
    • Plenker, Dennis;
    • Leenders, Frauke;
    • Sun, Ruping;
    • Zander, Thomas;
    • Menon, Roopika;
    • Koker, Mirjam;
    • Dahmen, Ilona;
    • Müller, Christian;
    • Di Cerbo, Vincenzo;
    • Schildhaus, Hans-Ulrich;
    • Altmüller, Janine;
    • Baessmann, Ingelore;
    • Becker, Christian;
    • de Wilde, Bram
    Publication type:
    Article

  • Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1090, doi. 10.1038/ng.2411
    By:
    • Wu, Chen;
    • Kraft, Peter;
    • Zhai, Kan;
    • Chang, Jiang;
    • Wang, Zhaoming;
    • Li, Yun;
    • Hu, Zhibin;
    • He, Zhonghu;
    • Jia, Weihua;
    • Abnet, Christian C;
    • Liang, Liming;
    • Hu, Nan;
    • Miao, Xiaoping;
    • Zhou, Yifeng;
    • Liu, Zhihua;
    • Zhan, Qimin;
    • Liu, Yu;
    • Qiao, Yan;
    • Zhou, Yuling;
    • Jin, Guangfu
    Publication type:
    Article

  • Single-stranded siRNA therapeutics.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1079, doi. 10.1038/ng.2429
    By:
    • Feliciano, Pamela
    Publication type:
    Article

  • Comprehensive genomic analysis identifies SOX2 as a frequently amplified gene in small-cell lung cancer.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1111, doi. 10.1038/ng.2405
    By:
    • Rudin, Charles M;
    • Durinck, Steffen;
    • Stawiski, Eric W;
    • Poirier, John T;
    • Modrusan, Zora;
    • Shames, David S;
    • Bergbower, Emily A;
    • Guan, Yinghui;
    • Shin, James;
    • Guillory, Joseph;
    • Rivers, Celina Sanchez;
    • Foo, Catherine K;
    • Bhatt, Deepali;
    • Stinson, Jeremy;
    • Gnad, Florian;
    • Haverty, Peter M;
    • Gentleman, Robert;
    • Chaudhuri, Subhra;
    • Janakiraman, Vasantharajan;
    • Jaiswal, Bijay S
    Publication type:
    Article

  • A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1122, doi. 10.1038/ng.2388
    By:
    • Jenkins, Robert B;
    • Xiao, Yuanyuan;
    • Sicotte, Hugues;
    • Decker, Paul A;
    • Kollmeyer, Thomas M;
    • Hansen, Helen M;
    • Kosel, Matthew L;
    • Zheng, Shichun;
    • Walsh, Kyle M;
    • Rice, Terri;
    • Bracci, Paige;
    • McCoy, Lucie S;
    • Smirnov, Ivan;
    • Patoka, Joseph S;
    • Hsuang, George;
    • Wiemels, Joe L;
    • Tihan, Tarik;
    • Pico, Alexander R;
    • Prados, Michael D;
    • Chang, Susan M
    Publication type:
    Article

  • Regulatory regions.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1079, doi. 10.1038/ng.2432
    By:
    • Bahcall, Orli
    Publication type:
    Article

  • A direct characterization of human mutation based on microsatellites.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1161, doi. 10.1038/ng.2398
    By:
    • Sun, James X;
    • Helgason, Agnar;
    • Masson, Gisli;
    • Ebenesersdóttir, Sigríður Sunna;
    • Li, Heng;
    • Mallick, Swapan;
    • Gnerre, Sante;
    • Patterson, Nick;
    • Kong, Augustine;
    • Reich, David;
    • Stefansson, Kari
    Publication type:
    Article

  • Respectful re-use.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1073, doi. 10.1038/ng.2433
    Publication type:
    Article

  • Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1147, doi. 10.1038/ng.2397
    By:
    • Holliday, Elizabeth G;
    • Maguire, Jane M;
    • Evans, Tiffany-Jane;
    • Koblar, Simon A;
    • Jannes, Jim;
    • Sturm, Jonathan W;
    • Hankey, Graeme J;
    • Baker, Ross;
    • Golledge, Jonathan;
    • Parsons, Mark W;
    • Malik, Rainer;
    • McEvoy, Mark;
    • Biros, Erik;
    • Lewis, Martin D;
    • Lincz, Lisa F;
    • Peel, Roseanne;
    • Oldmeadow, Christopher;
    • Smith, Wayne;
    • Moscato, Pablo;
    • Barlera, Simona
    Publication type:
    Article

  • Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1126, doi. 10.1038/ng.2387
    By:
    • Diskin, Sharon J;
    • Capasso, Mario;
    • Schnepp, Robert W;
    • Cole, Kristina A;
    • Attiyeh, Edward F;
    • Hou, Cuiping;
    • Diamond, Maura;
    • Carpenter, Erica L;
    • Winter, Cynthia;
    • Lee, Hanna;
    • Jagannathan, Jayanti;
    • Latorre, Valeria;
    • Iolascon, Achille;
    • Hakonarson, Hakon;
    • Devoto, Marcella;
    • Maris, John M
    Publication type:
    Article

  • Mapping cis- and trans-regulatory effects across multiple tissues in twins.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1084, doi. 10.1038/ng.2394
    By:
    • Grundberg, Elin;
    • Small, Kerrin S;
    • Hedman, Åsa K;
    • Nica, Alexandra C;
    • Buil, Alfonso;
    • Keildson, Sarah;
    • Bell, Jordana T;
    • Yang, Tsun-Po;
    • Meduri, Eshwar;
    • Barrett, Amy;
    • Nisbett, James;
    • Sekowska, Magdalena;
    • Wilk, Alicja;
    • Shin, So-Youn;
    • Glass, Daniel;
    • Travers, Mary;
    • Min, Josine L;
    • Ring, Sue;
    • Ho, Karen;
    • Thorleifsson, Gudmar
    Publication type:
    Article

  • Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1131, doi. 10.1038/ng.2408
    By:
    • Su, Zhan;
    • Gay, Laura J;
    • Strange, Amy;
    • Palles, Claire;
    • Band, Gavin;
    • Whiteman, David C;
    • Lescai, Francesco;
    • Langford, Cordelia;
    • Nanji, Manoj;
    • Edkins, Sarah;
    • van der Winkel, Anouk;
    • Levine, David;
    • Sasieni, Peter;
    • Bellenguez, Céline;
    • Howarth, Kimberley;
    • Freeman, Colin;
    • Trudgill, Nigel;
    • Tucker, Art T;
    • Pirinen, Matti;
    • Peppelenbosch, Maikel P
    Publication type:
    Article

  • Rapid variance components-based method for whole-genome association analysis.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1166, doi. 10.1038/ng.2410
    By:
    • Svishcheva, Gulnara R;
    • Axenovich, Tatiana I;
    • Belonogova, Nadezhda M;
    • van Duijn, Cornelia M;
    • Aulchenko, Yurii S
    Publication type:
    Article

  • Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1137, doi. 10.1038/ng.2395
    By:
    • Liu, Jimmy Z;
    • Almarri, Mohamed A;
    • Gaffney, Daniel J;
    • Mells, George F;
    • Jostins, Luke;
    • Cordell, Heather J;
    • Ducker, Samantha J;
    • Day, Darren B;
    • Heneghan, Michael A;
    • Neuberger, James M;
    • Donaldson, Peter T;
    • Bathgate, Andrew J;
    • Burroughs, Andrew;
    • Davies, Mervyn H;
    • Jones, David E;
    • Alexander, Graeme J;
    • Barrett, Jeffrey C;
    • Sandford, Richard N;
    • Anderson, Carl A
    Publication type:
    Article

  • Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1142, doi. 10.1038/ng.2390
    By:
    • Vithana, Eranga N;
    • Khor, Chiea-Chuen;
    • Qiao, Chunyan;
    • Nongpiur, Monisha E;
    • George, Ronnie;
    • Chen, Li-Jia;
    • Do, Tan;
    • Abu-Amero, Khaled;
    • Huang, Chor Kai;
    • Low, Sancy;
    • Tajudin, Liza-Sharmini A;
    • Perera, Shamira A;
    • Cheng, Ching-Yu;
    • Xu, Liang;
    • Jia, Hongyan;
    • Ho, Ching-Lin;
    • Sim, Kar Seng;
    • Wu, Ren-Yi;
    • Tham, Clement C Y;
    • Chew, Paul T K
    Publication type:
    Article

  • Transcription programs and cell division.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1079, doi. 10.1038/ng.2431
    By:
    • Niemitz, Emily
    Publication type:
    Article

  • Genomic landscape of liver cancer.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1075, doi. 10.1038/ng.2412
    By:
    • Zhang, Zemin
    Publication type:
    Article

  • New recessive autism syndrome.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1079, doi. 10.1038/ng.2430
    By:
    • Vogan, Kyle
    Publication type:
    Article

  • The draft genome of a diploid cotton Gossypium raimondii.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1098, doi. 10.1038/ng.2371
    By:
    • Wang, Kunbo;
    • Wang, Zhiwen;
    • Li, Fuguang;
    • Ye, Wuwei;
    • Wang, Junyi;
    • Song, Guoli;
    • Yue, Zhen;
    • Cong, Lin;
    • Shang, Haihong;
    • Zhu, Shilin;
    • Zou, Changsong;
    • Li, Qin;
    • Yuan, Youlu;
    • Lu, Cairui;
    • Wei, Hengling;
    • Gou, Caiyun;
    • Zheng, Zequn;
    • Yin, Ye;
    • Zhang, Xueyan;
    • Liu, Kun
    Publication type:
    Article

  • Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1156, doi. 10.1038/ng.2409
    By:
    • Zhang, Sheng-Quan;
    • Jiang, Tao;
    • Li, Min;
    • Zhang, Xin;
    • Ren, Yun-Qing;
    • Wei, Sheng-Cai;
    • Sun, Liang-Dan;
    • Cheng, Hui;
    • Li, Yang;
    • Yin, Xian-Yong;
    • Hu, Zheng-Mao;
    • Wang, Zhen-Ying;
    • Liu, Yuan;
    • Guo, Bi-Rong;
    • Tang, Hua-Yang;
    • Tang, Xian-Fa;
    • Ding, Yan-Tao;
    • Wang, Jian-Bo;
    • Li, Ping;
    • Wu, Bao-Yu
    Publication type:
    Article

  • Tissue specificity of genetic regulation of gene expression.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1077, doi. 10.1038/ng.2420
    By:
    • Göring, Harald H H
    Publication type:
    Article

  • Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.

    Published in:
    Nature Genetics, 2012, v. 44, n. 10, p. 1080, doi. 10.1038/ng.2406
    By:
    • Zimo?, Magdalena;
    • Baets, Jonathan;
    • Almeida-Souza, Leonardo;
    • De Vriendt, Els;
    • Nikodinovic, Jelena;
    • Parman, Yesim;
    • gcaron, Esra;
    • Matur, Zeliha;
    • Guergueltcheva, Velina;
    • Tournev, Ivailo;
    • Auer-Grumbach, Michaela;
    • De Rijk, Peter;
    • Petersen, Britt-Sabina;
    • Müller, Thomas;
    • Fransen, Erik;
    • Van Damme, Philip;
    • Löscher, Wolfgang N;
    • Bariši?, Nina;
    • Mitrovic, Zoran;
    • Previtali, Stefano C
    Publication type:
    Article