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Influence of CYP3A5 and drug transporter polymorphisms on imatinib trough concentration and clinical response among patients with chronic phase chronic myeloid leukemia

Journal of human genetics, 2010-11, Vol.55 (11), p.731-737

2010

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Association of the oxytocin receptor ( ) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population

Journal of human genetics, 2010-03, Vol.55 (3), p.137-141

2010

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Comprehensive DNA methylation analysis of peripheral blood cells derived from patients with first-episode schizophrenia

Journal of human genetics, 2013-02, Vol.58 (2), p.91-97

2013

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Common genetic variants in pre-microRNAs and risk of gallbladder cancer in North Indian population

Journal of human genetics, 2010-08, Vol.55 (8), p.495-499

2010

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Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population

Journal of human genetics, 2010-12, Vol.55 (12), p.816-821

2010

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Hypermethylation of OPRM1 promoter region in European Americans with alcohol dependence

Journal of human genetics, 2012-10, Vol.57 (10), p.670-675

2012

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Functional polymorphism ( ) in the serotonin transporter gene is associated with subjective well-being: evidence from a US nationally representative sample

Journal of human genetics, 2011-06, Vol.56 (6), p.456-459

De Neve, Jan-Emmanuel

2011

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Genome-wide association study identifies GYS2 as a novel genetic factor for polycystic ovary syndrome through obesity-related condition

Journal of human genetics, 2012-10, Vol.57 (10), p.660-664

2012

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Association of variations in the FTO, SCG3 and MTMR9 genes with metabolic syndrome in a Japanese population

Journal of human genetics, 2011-09, Vol.56 (9), p.647-651

2011

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Identification of 15 loci influencing height in a Korean population

Journal of human genetics, 2010-01, Vol.55 (1), p.27-31

2010

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Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan

Journal of human genetics, 2011-05, Vol.56 (5), p.364-368

2011

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Common variants of FTO and the risk of obesity and type 2 diabetes in Indians

Journal of human genetics, 2011-10, Vol.56 (10), p.720-726

2011

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Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients

Journal of human genetics, 2012-04, Vol.57 (4), p.238-243

2012

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Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features

Journal of human genetics, 2012-03, Vol.57 (3), p.207-211

2012

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Recapitulation of two genomewide association studies on blood pressure and essential hypertension in the Korean population

Journal of human genetics, 2010-06, Vol.55 (6), p.336-341

2010

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The association of glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) with idiopathic male infertility

Journal of human genetics, 2010-09, Vol.55 (9), p.565-570

2010

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The Amerindian mtDNA haplogroup B2 enhances the risk of HPV for cervical cancer: de-regulation of mitochondrial genes may be involved

Journal of human genetics, 2012-04, Vol.57 (4), p.269-276

2012

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Gene-gene interactions contribute to eye colour variation in humans

Journal of human genetics, 2011-06, Vol.56 (6), p.447-455

2011

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Mutational analysis of ATP7B in north Chinese patients with Wilson disease

Journal of human genetics, 2013-02, Vol.58 (2), p.67-72

2013

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Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia: extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect

Journal of human genetics, 2011-09, Vol.56 (9), p.631-639

2011

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A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma

Journal of human genetics, 2009-07, Vol.54 (7), p.392-397

2009

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Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients

Journal of human genetics, 2012-05, Vol.57 (5), p.286-293

2012

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Genotype instability during long-term subculture of lymphoblastoid cell lines

Journal of human genetics, 2013-01, Vol.58 (1), p.16-20

2013

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A genome-wide association study of a coronary artery disease risk variant

Influence of CYP3A5 and drug transporter polymorphisms on imatinib trough concentration and clinical response among patients with chronic phase chronic myeloid leukemia

Association of the oxytocin receptor ( ) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population

Comprehensive DNA methylation analysis of peripheral blood cells derived from patients with first-episode schizophrenia

Common genetic variants in pre-microRNAs and risk of gallbladder cancer in North Indian population

Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population

Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a Japanese population

Hypermethylation of OPRM1 promoter region in European Americans with alcohol dependence

Functional polymorphism ( ) in the serotonin transporter gene is associated with subjective well-being: evidence from a US nationally representative sample

Genome-wide association study identifies GYS2 as a novel genetic factor for polycystic ovary syndrome through obesity-related condition

Association of variations in the FTO, SCG3 and MTMR9 genes with metabolic syndrome in a Japanese population

Identification of 15 loci influencing height in a Korean population

Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan

Common variants of FTO and the risk of obesity and type 2 diabetes in Indians

Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients

Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features

Recapitulation of two genomewide association studies on blood pressure and essential hypertension in the Korean population

The association of glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) with idiopathic male infertility

The Amerindian mtDNA haplogroup B2 enhances the risk of HPV for cervical cancer: de-regulation of mitochondrial genes may be involved

Gene-gene interactions contribute to eye colour variation in humans

Mutational analysis of ATP7B in north Chinese patients with Wilson disease

Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia: extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect

A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma

Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients

Genotype instability during long-term subculture of lymphoblastoid cell lines

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