Works matching IS 10614036 AND DT 2015 AND VI 47 AND IP 9
Results: 23
Corrigendum: Transcriptional activation of retrotransposons alters the expression of adjacent genes in wheat.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1099, doi. 10.1038/ng0915-1099b
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Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinoma.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1038, doi. 10.1038/ng.3357
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Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1073, doi. 10.1038/ng.3363
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Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
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- Nature Genetics, 2015, v. 47, n. 9, p. 987, doi. 10.1038/ng.3373
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Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas.
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- Nature Genetics, 2015, v. 47, n. 9, p. 996, doi. 10.1038/ng.3361
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Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.
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- Nature Genetics, 2015, v. 47, n. 9, p. 969, doi. 10.1038/ng.3360
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Genomic landscape of cutaneous T cell lymphoma.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1011, doi. 10.1038/ng.3356
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Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1085, doi. 10.1038/ng.3379
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Linking germline and somatic variation in Ewing sarcoma.
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- Nature Genetics, 2015, v. 47, n. 9, p. 964, doi. 10.1038/ng.3387
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Whole genome?
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- Nature Genetics, 2015, v. 47, n. 9, p. 963, doi. 10.1038/ng.3397
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- Article
Corrigendum: Exploring population size changes using SNP frequency spectra.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1099, doi. 10.1038/ng0915-1099a
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Paired exome analysis of Barrett's esophagus and adenocarcinoma.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1047, doi. 10.1038/ng.3343
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Building a staircase to precision medicine for biliary tract cancer.
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- Nature Genetics, 2015, v. 47, n. 9, p. 967, doi. 10.1038/ng.3386
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Genomic spectra of biliary tract cancer.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1003, doi. 10.1038/ng.3375
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A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1079, doi. 10.1038/ng.3374
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Exome sequencing identifies somatic mutations of DDX3X in natural killer/T-cell lymphoma.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1061, doi. 10.1038/ng.3358
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Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
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- Nature Genetics, 2015, v. 47, n. 9, p. 979, doi. 10.1038/ng.3359
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The transcriptomic landscape and directed chemical interrogation of MLL-rearranged acute myeloid leukemias.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1030, doi. 10.1038/ng.3371
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Genomics and drug profiling of fatal TCF3-HLF−positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1020, doi. 10.1038/ng.3362
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Genomic analysis of mycosis fungoides and Sézary syndrome identifies recurrent alterations in TNFR2.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1056, doi. 10.1038/ng.3370
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Genetic differential calculus.
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- Nature Genetics, 2015, v. 47, n. 9, p. 965, doi. 10.1038/ng.3384
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A gene-based association method for mapping traits using reference transcriptome data.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1091, doi. 10.1038/ng.3367
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An APOBEC3A hypermutation signature is distinguishable from the signature of background mutagenesis by APOBEC3B in human cancers.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1067, doi. 10.1038/ng.3378
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