Works matching IS 03406717 AND DT 2015 AND VI 134 AND IP 3
Results: 9
Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C.
- Published in:
- Human Genetics, 2015, v. 134, n. 3, p. 279, doi. 10.1007/s00439-014-1520-7
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- Publication type:
- Article
CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs.
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- Human Genetics, 2015, v. 134, n. 3, p. 291, doi. 10.1007/s00439-014-1521-6
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- Publication type:
- Article
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.
- Published in:
- Human Genetics, 2015, v. 134, n. 3, p. 305, doi. 10.1007/s00439-014-1522-5
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- Publication type:
- Article
Is there a male-specific effect on hypertension?
- Published in:
- 2015
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- Publication type:
- Letter
A systematic heritability analysis of the human whole blood transcriptome.
- Published in:
- Human Genetics, 2015, v. 134, n. 3, p. 343, doi. 10.1007/s00439-014-1524-3
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- Publication type:
- Article
Genome-wide methylation analysis in Silver-Russell syndrome patients.
- Published in:
- Human Genetics, 2015, v. 134, n. 3, p. 317, doi. 10.1007/s00439-014-1526-1
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- Publication type:
- Article
Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA).
- Published in:
- Human Genetics, 2015, v. 134, n. 3, p. 333, doi. 10.1007/s00439-014-1528-z
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- Publication type:
- Article
Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.
- Published in:
- 2015
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- Publication type:
- Erratum
Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition.
- Published in:
- Human Genetics, 2015, v. 134, n. 3, p. 269, doi. 10.1007/s00439-014-1507-4
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- Publication type:
- Article