Works matching IS 10614036 AND DT 2014 AND VI 46 AND IP 8
Results: 30
Developmental origins of coronary vessels.
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- Nature Genetics, 2014, v. 46, n. 8, p. 811, doi. 10.1038/ng.3057
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Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease.
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- Nature Genetics, 2014, v. 46, n. 8, p. 812, doi. 10.1038/ng.3040
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The common marmoset genome provides insight into primate biology and evolution.
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- Nature Genetics, 2014, v. 46, n. 8, p. 850, doi. 10.1038/ng.3042
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- Article
Whole-genome sequencing of 234 bulls facilitates mapping of monogenic and complex traits in cattle.
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- Nature Genetics, 2014, v. 46, n. 8, p. 858, doi. 10.1038/ng.3034
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miR-212 and miR-132 are dispensable for mouse mammary gland development.
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- Nature Genetics, 2014, v. 46, n. 8, p. 802, doi. 10.1038/ng.2990
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Fingerprints of Epstein-Barr virus in nasopharyngeal carcinoma.
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- Nature Genetics, 2014, v. 46, n. 8, p. 809, doi. 10.1038/ng.3038
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Whole-exome and targeted gene sequencing of gallbladder carcinoma identifies recurrent mutations in the ErbB pathway.
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- Nature Genetics, 2014, v. 46, n. 8, p. 872, doi. 10.1038/ng.3030
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Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia.
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- Nature Genetics, 2014, v. 46, n. 8, p. 901, doi. 10.1038/ng.3029
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A specific missense mutation in GTF2I occurs at high frequency in thymic epithelial tumors.
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- Nature Genetics, 2014, v. 46, n. 8, p. 844, doi. 10.1038/ng.3016
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Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma.
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- Nature Genetics, 2014, v. 46, n. 8, p. 877, doi. 10.1038/ng.3037
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Host microbiome signature of Crohn's disease.
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- Nature Genetics, 2014, v. 46, n. 8, p. 811, doi. 10.1038/ng.3055
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iPSC models of retinitis pigmentosa.
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- Nature Genetics, 2014, v. 46, n. 8, p. 811, doi. 10.1038/ng.3056
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Global epistasis.
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- Nature Genetics, 2014, v. 46, n. 8, p. 811, doi. 10.1038/ng.3053
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A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1.
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- Nature Genetics, 2014, v. 46, n. 8, p. 891, doi. 10.1038/ng.3020
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Mutations in ZBTB20 cause Primrose syndrome.
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- Nature Genetics, 2014, v. 46, n. 8, p. 815, doi. 10.1038/ng.3035
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Towards sequence-based genomic selection of cattle.
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- Nature Genetics, 2014, v. 46, n. 8, p. 807, doi. 10.1038/ng.3048
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- Article
Most genetic risk for autism resides with common variation.
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- Nature Genetics, 2014, v. 46, n. 8, p. 881, doi. 10.1038/ng.3039
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Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.
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- Nature Genetics, 2014, v. 46, n. 8, p. 895, doi. 10.1038/ng.3033
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Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications.
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- Nature Genetics, 2014, v. 46, n. 8, p. 912, doi. 10.1038/ng.3036
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Ordering of mutations in preinvasive disease stages of esophageal carcinogenesis.
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- Nature Genetics, 2014, v. 46, n. 8, p. 837, doi. 10.1038/ng.3013
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Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1.
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- Nature Genetics, 2014, v. 46, n. 8, p. 886, doi. 10.1038/ng.3041
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From genomics to diagnostics of esophageal adenocarcinoma.
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- Nature Genetics, 2014, v. 46, n. 8, p. 806, doi. 10.1038/ng.3047
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miR-212 and miR-132 are dispensable for mouse mammary gland development.
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- Nature Genetics, 2014, v. 46, n. 8, p. 804, doi. 10.1038/ng.3032
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The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation.
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- Nature Genetics, 2014, v. 46, n. 8, p. 905, doi. 10.1038/ng.3031
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Intergenerational epigenetic inheritance.
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- Nature Genetics, 2014, v. 46, n. 8, p. 811, doi. 10.1038/ng.3054
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Whole-genome sequence variation, population structure and demographic history of the Dutch population.
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- Nature Genetics, 2014, v. 46, n. 8, p. 818, doi. 10.1038/ng.3021
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- Article
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
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- Nature Genetics, 2014, v. 46, n. 8, p. 826, doi. 10.1038/ng.3014
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The genomic landscape of nasopharyngeal carcinoma.
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- Nature Genetics, 2014, v. 46, n. 8, p. 866, doi. 10.1038/ng.3006
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Regulatory codewords.
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- Nature Genetics, 2014, v. 46, n. 8, p. 801, doi. 10.1038/ng.3059
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Inferring human population size and separation history from multiple genome sequences.
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- Nature Genetics, 2014, v. 46, n. 8, p. 919, doi. 10.1038/ng.3015
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