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Epigenomics comes of age with expanding roles in biological understanding and clinical application.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 395, doi. 10.1038/jhg.2013.70
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Epigenomic strategies at the interface of genetic and environmental risk factors for autism.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 396, doi. 10.1038/jhg.2013.49
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Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 402, doi. 10.1038/jhg.2013.51
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Metabolism-epigenome crosstalk in physiology and diseases.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 410, doi. 10.1038/jhg.2013.57
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Effects of embryonic manipulation and epigenetics.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 416, doi. 10.1038/jhg.2013.61
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Tet family of 5-methylcytosine dioxygenases in mammalian development.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 421, doi. 10.1038/jhg.2013.63
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Clinical application of the CpG island methylator phenotype to prognostic diagnosis in neuroblastomas.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 428, doi. 10.1038/jhg.2013.64
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- Article
DNA methylation of the BDNF gene and its relevance to psychiatric disorders.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 434, doi. 10.1038/jhg.2013.65
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- Article
Histone modifications for human epigenome analysis.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 439, doi. 10.1038/jhg.2013.66
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- Article
Regional DNA methylation differences between humans and chimpanzees are associated with genetic changes, transcriptional divergence and disease genes.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 446, doi. 10.1038/jhg.2013.55
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Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 455, doi. 10.1038/jhg.2013.56
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Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 461, doi. 10.1038/jhg.2013.23
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Extracellular matrix remodeling genes polymorphisms and risk of chronic bronchitis and recurrent pneumonia in children.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 467, doi. 10.1038/jhg.2013.24
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Association studies of TNFSF4, TNFAIP3 and FAM167A-BLK polymorphisms with primary Sjogren's syndrome in Han Chinese.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 475, doi. 10.1038/jhg.2013.26
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A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 480, doi. 10.1038/jhg.2013.27
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Replication study for the association of a single-nucleotide polymorphism, rs3746876, within KCNJ15, with susceptibility to type 2 diabetes in a Japanese population.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 490, doi. 10.1038/jhg.2013.28
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Genetic variation in phosphodiesterase (PDE) 7B in chronic lymphocytic leukemia: overview of genetic variants of cyclic nucleotide PDEs in human disease.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 494, doi. 10.1038/jhg.2013.54
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- Article