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Multiple dose pharmacokinetics of tiludronate in healthy volunteers

European journal of clinical pharmacology, 1996, Vol.51 (2), p.175-181

1996

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Disposition and clinical pharmacokinetics of microcrystalline theophylline

European journal of clinical pharmacology, 1980-09, Vol.17 (5), p.379-384

1980

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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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Protective effect of oral oxyphenonium bromide, terbutaline and theophylline against the bronchial obstructive effects of inhaled histamine, acetylcholine and propranolol

European journal of clinical pharmacology, 1984-01, Vol.26 (4), p.435-441

1984

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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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Clinical pharmacokinetics of intramuscular thiazinamium methyl sulfate

International journal of clinical pharmacology, therapy, and toxicology, 1983-09, Vol.21 (9), p.454

1983

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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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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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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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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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Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations

Journal of human genetics, 2012-10, Vol.57 (10), p.654-659

2012

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Strong influence of variants near MC4R on adiposity in children and adults: a cross-sectional study in Indian population

Journal of human genetics, 2013-01, Vol.58 (1), p.27-32

2013

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Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation

Journal of human genetics, 2012-08, Vol.57 (8), p.485-493

2012

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Association of CARD8 with inflammatory bowel disease in Koreans

Journal of human genetics, 2011-03, Vol.56 (3), p.217-223

2011

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Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation

Journal of human genetics, 2011-09, Vol.56 (9), p.660-665

2011

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Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes

Journal of human genetics, 2011-11, Vol.56 (11), p.759-764

2011

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Polymorphisms of transforming growth factor-β signaling pathway and Kawasaki disease in the Taiwanese population

Journal of human genetics, 2011-12, Vol.56 (12), p.840-845

2011

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TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion

Journal of human genetics, 2012-09, Vol.57 (9), p.587-592

2012

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USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1

Journal of human genetics, 2012-10, Vol.57 (10), p.633-637

2012

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Association of the arginine vasopressin receptor 1A ( ) haplotypes with listening to music

Journal of human genetics, 2011-04, Vol.56 (4), p.324-329

2011

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Multiple dose pharmacokinetics of tiludronate in healthy volunteers

Disposition and clinical pharmacokinetics of microcrystalline theophylline

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

Protective effect of oral oxyphenonium bromide, terbutaline and theophylline against the bronchial obstructive effects of inhaled histamine, acetylcholine and propranolol

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

Clinical pharmacokinetics of intramuscular thiazinamium methyl sulfate

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

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

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

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

Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations

Strong influence of variants near MC4R on adiposity in children and adults: a cross-sectional study in Indian population

Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation

Association of CARD8 with inflammatory bowel disease in Koreans

Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation

Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes

Polymorphisms of transforming growth factor-β signaling pathway and Kawasaki disease in the Taiwanese population

TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion

USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1

Association of the arginine vasopressin receptor 1A ( ) haplotypes with listening to music

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