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Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders

Molecular psychiatry, 2013-11, Vol.18 (11), p.1153-1165

2013

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Species differences in cannabinoid receptor 2 (CNR2 gene): identification of novel human and rodent CB2 isoforms, differential tissue expression and regulation by cannabinoid receptor ligands

Genes, brain and behavior, 2009-07, Vol.8 (5), p.519-530

2009

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Copy number elevation of 22q11.2 genes arrests the developmental maturation of working memory capacity and adult hippocampal neurogenesis

Molecular psychiatry, 2018-04, Vol.23 (4), p.985-992

2018

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Plasma MMP-9 Levels as the Future Risk of Conversion to Dementia in ApoE4-Positive MCI Patients: Investigation Based on the Alzheimer’s Disease Neuroimaging Initiative Database

The Journal Of Prevention of Alzheimer's Disease, 2022, Vol.9 (2), p.331-337

2022

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Improving polygenic prediction in ancestrally diverse populations

Nature genetics, 2022-05, Vol.54 (5), p.573-580

2022

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A functional polymorphism of the µ-opioid receptor gene is associated with completed suicides

Journal of Neural Transmission, 2008-03, Vol.115 (3), p.531-536

2008

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Alcohol and aldehyde dehydrogenase polymorphisms and risk for suicide: a preliminary observation in the Japanese male population

Genes, brain and behavior, 2010-07, Vol.9 (5), p.498-502

2010

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P03-293 - Alcohol and aldehyde dehydrogenase polymorphisms and risk for suicide

European psychiatry, 2010, Vol.25 (S1), p.1361-1361, Article 25-E1347

2010

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Association between a functional polymorphism in the renin-angiotensin system and completed suicide

Journal of Neural Transmission, 2006-12, Vol.113 (12), p.1915-1920

2006

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P03-446 - Association of FKBP5 gene haplotypes with completed suicide in the Japanese population

European psychiatry, 2011, Vol.26, p.1616-1616

2011

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Association of Two Variable Number of Tandem Repeats in the Monoamine Oxidase A Gene Promoter with Schizophrenia

Neuropsychiatric disease and treatment, 2021-01, Vol.17, p.3315-3323

2021

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Alterations in DNA methylation rates of brain-derived neurotrophic factor in patients with schizophrenia

The European journal of psychiatry, 2021-04, Vol.35 (2), p.67-74

2021

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Investigation of chromosome Y loss in men with schizophrenia

Neuropsychiatric disease and treatment, 2018-01, Vol.14, p.2115-2122

2018

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Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control study

Neuropsychiatric disease and treatment, 2019-08, Vol.15, p.2353-2363

2019

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A cross-sectional study exploring useful indicators for low bone mineral density in male alcoholic patients

Neuropsychiatric disease and treatment, 2018-01, Vol.14, p.663-669

2018

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Association analysis of the Cadherin13 gene with schizophrenia in the Japanese population

Neuropsychiatric disease and treatment, 2015-01, Vol.11 (default), p.1381-1393

2015

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Association study of MIF promoter polymorphisms with suicide completers in the Japanese population

Neuropsychiatric disease and treatment, 2017, Vol.13, p.899-908

2017

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Serotonin transporter regulatory region polymorphism is associated with anorexia nervosa

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-07, Vol.128B (1), p.114-117

2004

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Association of FKBP5 gene haplotypes with completed suicide in the Japanese population

European psychiatry, 2011-03, Vol.26 (S2), p.1616-1616

2011

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Changes of behavioral problems of children at a children's home in Japan, accompanied by the downsizing

Neuropsychiatrie de l'enfance et de l'adolescence, 2012-07, Vol.60 (5), p.S279-S279

2012

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The mental world of autism spectrum disorder through the experience of psychological interview and examination for a case

Neuropsychiatrie de l'enfance et de l'adolescence, 2012-07, Vol.60 (5), p.S302-S302

2012

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A functional polymorphism of the micro-opioid receptor gene is associated with completed suicides

Journal of neural transmission (Vienna, Austria : 1996), 2008, Vol.115 (3), p.531

2008

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Novel missense polymorphism in the regulator of G‐protein signaling 10 gene: analysis of association with schizophrenia

Psychiatry and clinical neurosciences, 2004-10, Vol.58 (5), p.579-581

2004

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A novel polymorphism in the coding region of the DAP-1 gene (HDLG-and-PSD-95 associated protein-1 gene): Analysis of association with schizophrenia

Schizophrenia research, 2003-03, Vol.60 (1), p.93-93

2003

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Neural basis of major depressive disorder: Beyond monoamine hypothesis

Psychiatry and clinical neurosciences, 2018-01, Vol.72 (1), p.3-12

2018

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Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders

Species differences in cannabinoid receptor 2 (CNR2 gene): identification of novel human and rodent CB2 isoforms, differential tissue expression and regulation by cannabinoid receptor ligands

Copy number elevation of 22q11.2 genes arrests the developmental maturation of working memory capacity and adult hippocampal neurogenesis

Plasma MMP-9 Levels as the Future Risk of Conversion to Dementia in ApoE4-Positive MCI Patients: Investigation Based on the Alzheimer’s Disease Neuroimaging Initiative Database

Improving polygenic prediction in ancestrally diverse populations

A functional polymorphism of the µ-opioid receptor gene is associated with completed suicides

Alcohol and aldehyde dehydrogenase polymorphisms and risk for suicide: a preliminary observation in the Japanese male population

P03-293 - Alcohol and aldehyde dehydrogenase polymorphisms and risk for suicide

Association between a functional polymorphism in the renin-angiotensin system and completed suicide

P03-446 - Association of FKBP5 gene haplotypes with completed suicide in the Japanese population

Association of Two Variable Number of Tandem Repeats in the Monoamine Oxidase A Gene Promoter with Schizophrenia

Alterations in DNA methylation rates of brain-derived neurotrophic factor in patients with schizophrenia

Investigation of chromosome Y loss in men with schizophrenia

Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control study

A cross-sectional study exploring useful indicators for low bone mineral density in male alcoholic patients

Association analysis of the Cadherin13 gene with schizophrenia in the Japanese population

Association study of MIF promoter polymorphisms with suicide completers in the Japanese population

Serotonin transporter regulatory region polymorphism is associated with anorexia nervosa

Association of FKBP5 gene haplotypes with completed suicide in the Japanese population

Changes of behavioral problems of children at a children's home in Japan, accompanied by the downsizing

The mental world of autism spectrum disorder through the experience of psychological interview and examination for a case

A functional polymorphism of the micro-opioid receptor gene is associated with completed suicides

Novel missense polymorphism in the regulator of G‐protein signaling 10 gene: analysis of association with schizophrenia

A novel polymorphism in the coding region of the DAP-1 gene (HDLG-and-PSD-95 associated protein-1 gene): Analysis of association with schizophrenia

Neural basis of major depressive disorder: Beyond monoamine hypothesis

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