Works matching IS 14345161 AND DT 2013 AND VI 58 AND IP 6
Results: 14
Combined linkage analysis and exome sequencing identifies novel genes for familial goiter.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 366, doi. 10.1038/jhg.2013.20
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Use of pharmacogenetics for predicting cancer prognosis and treatment exposure, response and toxicity.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 346, doi. 10.1038/jhg.2013.42
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Pharmacogenomics of severe cutaneous adverse reactions and drug-induced liver injury.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 317, doi. 10.1038/jhg.2013.37
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Special Section on Pharmacogenomics: recent advances and future directions.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 305, doi. 10.1038/jhg.2013.53
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Important and critical scientific aspects in pharmacogenomics analysis: lessons from controversial results of tamoxifen and CYP2D6 studies.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 327, doi. 10.1038/jhg.2013.39
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Pharmacogenetics of warfarin: challenges and opportunities.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 334, doi. 10.1038/jhg.2013.40
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Characteristics of pharmacogenomics/biomarker-guided clinical trials for regulatory approval of anti-cancer drugs in Japan.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 313, doi. 10.1038/jhg.2013.36
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Pharmacogenomics of anti-platelet therapy: how much evidence is enough for clinical implementation?
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 339, doi. 10.1038/jhg.2013.41
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New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 362, doi. 10.1038/jhg.2013.14
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Impact of polymorphisms in drug pathway genes on disease-free survival in adults with acute myeloid leukemia.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 353, doi. 10.1038/jhg.2013.38
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Pharmacogenomics of endocrine therapy in breast cancer.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 306, doi. 10.1038/jhg.2013.35
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Five linkage regions each harbor multiple type 2 diabetes genes in the African American subset of the GENNID Study.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 378, doi. 10.1038/jhg.2013.21
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Powerful tests for association on quantitative trait loci incorporating imprinting effects.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 384, doi. 10.1038/jhg.2013.22
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Exome sequencing identifies a novel INPPL1 mutation in opsismodysplasia.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 391, doi. 10.1038/jhg.2013.25
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- Article