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The prevalence of CYP2D6 and CYP2C19 genotypes in a population of healthy Dutch volunteers

European journal of clinical pharmacology, 2001-12, Vol.57 (10), p.717-722

2001

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CYP2D6 and CYP2C19 activity in a large population of Dutch healthy volunteers : indications for oral contraceptive-related gender differences

European journal of clinical pharmacology, 1999-05, Vol.55 (3), p.177-184

1999

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Ambulatory accelerometry to quantify involuntary movements and tics in the syndrome of Gilles de la Tourette

Behavior research methods, instruments, & computers, 2001-08, Vol.33 (3), p.357-363

2001

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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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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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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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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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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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Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors

Journal of human genetics, 2011-08, Vol.56 (8), p.566-571

2011

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Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree

Journal of human genetics, 2011-10, Vol.56 (10), p.742-747

2011

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hOGG1 Ser326Cys polymorphism and risk of lung cancer by histological type

Journal of human genetics, 2009-12, Vol.54 (12), p.739-745

2009

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The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea

Journal of human genetics, 2013-03, Vol.58 (3), p.150-154

2013

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Genome-wide association study of copy number variation identified gremlin1 as a candidate gene for lean body mass

Journal of human genetics, 2012-01, Vol.57 (1), p.33-37

2012

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Gene expression analysis in lymphoblastoid cells as a potential biomarker of bipolar disorder

Journal of human genetics, 2011-11, Vol.56 (11), p.779-783

2011

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A genome-wide CNV association study on panic disorder in a Japanese population

Journal of human genetics, 2011-12, Vol.56 (12), p.852-856

2011

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HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome

Journal of human genetics, 2011-10, Vol.56 (10), p.707-715

2011

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Estimation of carrier frequencies of six autosomal-recessive Mendelian disorders in the Korean population

Journal of human genetics, 2012-02, Vol.57 (2), p.139-144

2012

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Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome

Journal of human genetics, 2012-05, Vol.57 (5), p.335-337

2012

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High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis

Journal of human genetics, 2009-07, Vol.54 (7), p.426-429

2009

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Gender-specific association of TSNAX/DISC1 locus for schizophrenia and bipolar affective disorder in South Indian population

Journal of human genetics, 2012-08, Vol.57 (8), p.523-530

2012

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The prevalence of CYP2D6 and CYP2C19 genotypes in a population of healthy Dutch volunteers

CYP2D6 and CYP2C19 activity in a large population of Dutch healthy volunteers : indications for oral contraceptive-related gender differences

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

Ambulatory accelerometry to quantify involuntary movements and tics in the syndrome of Gilles de la Tourette

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

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

Identification of 15 loci influencing height in a Korean population

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

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

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

Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors

Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree

hOGG1 Ser326Cys polymorphism and risk of lung cancer by histological type

The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea

Genome-wide association study of copy number variation identified gremlin1 as a candidate gene for lean body mass

Gene expression analysis in lymphoblastoid cells as a potential biomarker of bipolar disorder

Association between type 2 diabetes genetic susceptibility loci and visceral and subcutaneous fat area as determined by computed tomography

A genome-wide CNV association study on panic disorder in a Japanese population

HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome

Estimation of carrier frequencies of six autosomal-recessive Mendelian disorders in the Korean population

Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome

High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis

Gender-specific association of TSNAX/DISC1 locus for schizophrenia and bipolar affective disorder in South Indian population

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