Works in Journal of Human Genetics, 2010, Vol 55, Issue 9
Results: 14
Combined effect of longevity-associated mitochondrial DNA 5178 C/A polymorphism and coffee consumption on the risk of hyper-LDL cholesterolemia in middle-aged Japanese men.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 577, doi. 10.1038/jhg.2010.71
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- Article
Glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) and idiopathic male infertility: novel perspectives versus facts.
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- 2010
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- Publication type:
- Opinion
The pattern of natural selection in somatic cancer mutations of human mtDNA.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 605, doi. 10.1038/jhg.2010.76
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- Article
Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 621, doi. 10.1038/jhg.2010.81
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- Article
An association study between the dymeclin gene and schizophrenia in the Japanese population.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 631, doi. 10.1038/jhg.2010.72
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- Article
Homozygosity for constitutional chromosomal rearrangements: a systematic review with reference to origin, ascertainment and phenotype.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 559, doi. 10.1038/jhg.2010.80
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- Article
The GCKR rs780094 polymorphism is associated with susceptibility of type 2 diabetes, reduced fasting plasma glucose levels, increased triglycerides levels and lower HOMA-IR in Japanese population.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 600, doi. 10.1038/jhg.2010.75
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- Article
Worldwide allele frequency distribution of four polymorphisms associated with warfarin dose requirements.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 582, doi. 10.1038/jhg.2010.73
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- Article
Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 590, doi. 10.1038/jhg.2010.74
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- Article
Commentary on 'Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center'.
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- 2010
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- Publication type:
- Opinion
Linkage analysis and mutation screening of the rhodopsin gene in a Chinese Bai family with autosomal dominant retinitis pigmentosa.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 571, doi. 10.1038/jhg.2010.68
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- Article
A genome-wide analysis of loss of heterozygosity and chromosomal copy number variation in Proteus syndrome using high-density SNP microarrays.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 627, doi. 10.1038/jhg.2010.70
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- Article
The association of glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) with idiopathic male infertility.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 565, doi. 10.1038/jhg.2010.59
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- Article
Examination of disease-based selection, demographic history and population structure in European Y-chromosome haplogroup I.
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- Journal of Human Genetics, 2010, v. 55, n. 9, p. 613, doi. 10.1038/jhg.2010.77
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- Article