Lista de obras -

A case control association study and cognitive function analysis of neuropilin and tolloid-like 1 gene and schizophrenia in the Japanese population

artículo científico publicado en 2011

A family-based and case-control association study of SOX10 in schizophrenia

artículo científico publicado en 2006

A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia

artículo científico publicado en 2005

A microsatellite repeat in the promoter of the N-methyl-D-aspartate receptor 2A subunit (GRIN2A) gene suppresses transcriptional activity and correlates with chronic outcome in schizophrenia

artículo científico publicado en 2003

A novel missense mutation (Leu46Val) of PAX6 found in an autistic patient

artículo científico publicado en 2009

A novel scale including strabismus and 'cuspidal ear' for distinguishing schizophrenia patients from controls using minor physical anomalies

artículo científico publicado en 2006

A population-specific uncommon variant in GRIN3A associated with schizophrenia.

artículo científico publicado en 2012

A promoter haplotype of the inositol monophosphatase 2 gene (IMPA2) at 18p11.2 confers a possible risk for bipolar disorder by enhancing transcription

artículo científico publicado en 2007

Ablation of Mrds1/Ofcc1 Induces Hyper-γ-Glutamyl Transpeptidasemia without Abnormal Head Development and Schizophrenia-Relevant Behaviors in Mice ⬇️

artículo científico publicado el 29 de diciembre de 2011

Analysis of a cluster of polymorphisms in AKT1 gene in bipolar pedigrees: a family-based association study

artículo científico publicado en 2003

Analysis of correlation between serum D-serine levels and functional promoter polymorphisms of GRIN2A and GRIN2B genes.

artículo científico publicado en 2005

Analysis of strain‐dependent prepulse inhibition points to a role for Shmt1 (SHMT1) in mice and in schizophrenia ⬇️

artículo científico publicado el 26 de octubre de 2010

Association analyses between brain-expressed fatty-acid binding protein (FABP) genes and schizophrenia and bipolar disorder.

artículo científico publicado en 2010

Association analysis of ATF4 and ATF5, genes for interacting-proteins of DISC1, in bipolar disorder

artículo científico publicado en 2007

Association analysis of FEZ1 variants with schizophrenia in Japanese cohorts.

artículo científico publicado en 2004

Association analysis of HSP90B1 with bipolar disorder

artículo científico publicado en 2007

Association analysis of SOD2 variants with methamphetamine psychosis in Japanese and Taiwanese populations.

artículo científico publicado en 2006

Association and synergistic interaction between promoter variants of the DRD4 gene in Japanese schizophrenics

artículo científico publicado en 2006

Association between polymorphisms in the promoter region of the sialyltransferase 8B (SIAT8B) gene and schizophrenia

artículo científico publicado en 2005

Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B.

artículo científico publicado en 2004

Association of Transcription Factor Gene LMX1B with Autism ⬇️

artículo científico publicado el 25 de agosto de 2011

Association of an orexin 1 receptor 408Val variant with polydipsia-hyponatremia in schizophrenic subjects

artículo científico publicado en 2005

Association of decreased prefrontal hemodynamic response during a verbal fluency task with EGR3 gene polymorphism in patients with schizophrenia and in healthy individuals

artículo científico publicado en 2013

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder in Japanese and the National Institute of Mental Health pedigrees.

artículo científico publicado en 2004

Association of neural cell adhesion molecule 1 gene polymorphisms with bipolar affective disorder in Japanese individuals

artículo científico publicado en 2004

Association studies and gene expression analyses of the DISC1-interacting molecules, pericentrin 2 (PCNT2) and DISC1-binding zinc finger protein (DBZ), with schizophrenia and with bipolar disorder

artículo científico publicado en 2009

Association study between the Down syndrome cell adhesion molecule (DSCAM) gene and bipolar disorder

scientific article published on 01 February 2008

Association study of Nogo‐related genes with schizophrenia in a Japanese case–control sample ⬇️

artículo científico publicado el 11 de mayo de 2011

Association study of polymorphisms in the 5' upstream region of human DISC1 gene with schizophrenia

artículo científico publicado en 2004

Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population ⬇️

artículo científico publicado el 17 de septiembre de 2011

Association study of the short tandem repeat in the 5' upstream region of the cholecystokinin gene with mood disorders in the Japanese population

artículo científico publicado en 2002

Brain region-specific altered expression and association of mitochondria-related genes in autism

artículo científico publicado en 2012

C18orf1 located on chromosome 18p11.2 may confer susceptibility to schizophrenia.

artículo científico publicado en 2003

Case-control association study of human netrin G1 gene in Japanese schizophrenia

artículo científico publicado en 2004

Comprehensive association analysis of 27 genes from the GABAergic system in Japanese individuals affected with schizophrenia

artículo científico publicado en 2017

DNA methylation status of SOX10 correlates with its downregulation and oligodendrocyte dysfunction in schizophrenia.

artículo científico publicado en 2005

Distinguishable haplotype blocks in the HTR3A and HTR3B region in the Japanese reveal evidence of association of HTR3B with female major depression

artículo científico publicado en 2006

Distribution of haplotypes derived from three common variants of the NR4A2 gene in Japanese patients with schizophrenia

artículo científico publicado en 2003

Evidence of association between gamma-aminobutyric acid type A receptor genes located on 5q34 and female patients with mood disorders

artículo científico publicado en 2003

Evidence that variation in the peripheral benzodiazepine receptor (PBR) gene influences susceptibility to panic disorder

artículo científico publicado en 2006

Exon resequencing of H3K9 methyltransferase complex genes, EHMT1, EHTM2 and WIZ, in Japanese autism subjects

artículo científico publicado en 2014

Extended analyses support the association of a functional (GT)n polymorphism in the GRIN2A promoter with Japanese schizophrenia

artículo científico publicado en 2005

Fabp7 maps to a quantitative trait locus for a schizophrenia endophenotype

artículo científico publicado en 2007

Failure to confirm genetic association of the CHI3L1 gene with schizophrenia in Japanese and Chinese populations

artículo científico publicado en 2009

Failure to confirm genetic association of the FXYD6 gene with schizophrenia: the Japanese population and meta-analysis.

artículo científico publicado en 2010

Failure to support a genetic contribution of AKT1 polymorphisms and altered AKT signaling in schizophrenia

artículo científico publicado en 2006

Functional polymorphisms of HSPA5: possible association with bipolar disorder

artículo científico publicado en 2005

Further evidence for the role of MET in autism susceptibility.

artículo científico publicado en 2010

Gene and expression analyses reveal enhanced expression of pericentrin 2 (PCNT2) in bipolar disorder

artículo científico publicado en 2007

Genetic analyses of roundabout (ROBO) axon guidance receptors in autism.

artículo científico publicado en 2008

Genetic analyses of the brain-derived neurotrophic factor (BDNF) gene in autism

artículo científico publicado en 2007

Genetic analysis of a functional GRIN2A promoter (GT)n repeat in bipolar disorder pedigrees in humans

artículo científico publicado en 2003

Genetic analysis of the calcineurin pathway identifies members of the EGR gene family, specifically EGR3, as potential susceptibility candidates in schizophrenia

artículo científico publicado en 2007

Genetic analysis of the glyoxalase system in schizophrenia

artículo científico publicado en 2015

Genetic and expression analyses of FZD3 in schizophrenia

scientific article published on 01 September 2004

Genetic and expression analyses of the STOP (MAP6) gene in schizophrenia

artículo científico publicado en 2006

Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism.

artículo científico publicado en 2008

Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson's disease

artículo científico publicado en 2005

Genetic association study between the detected risk variants based upon type II diabetes GWAS and psychotic disorders in the Japanese population

artículo científico publicado en 2013

Genetic examination of the PLXNA2 gene in Japanese and Chinese people with schizophrenia.

artículo científico publicado en 2007

Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.

artículo científico publicado en 2013

Genome-Wide Association Study of Schizophrenia in Japanese Population ⬇️

artículo científico publicado el 6 de junio de 2011

Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations

artículo científico publicado en 2015

Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.

artículo científico publicado en 2005

Identification of multiple serine racemase (SRR) mRNA isoforms and genetic analyses of SRR and DAO in schizophrenia and D-serine levels

artículo científico publicado en 2005

Increased stathmin1 expression in the dentate gyrus of mice causes abnormal axonal arborizations

artículo científico publicado en 2010

Lack of association between polymorphisms in the 5' upstream region of the DISC1 gene and mood disorders

artículo científico publicado en 2007

Lack of association of EGR2 variants with bipolar disorder in Japanese population

artículo científico publicado en 2013

Linkage disequilibrium analysis of the CHRNA7 gene and its partially duplicated region in schizophrenia

artículo científico publicado en 2006

Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder

artículo científico publicado en 2004

Mitochondrial DNA haplogroup analysis in patients with bipolar disorder

scientific article published on 01 March 2009

Molecular analysis, mutation screening, and association study of adenylate cyclase type 9 gene (ADCY9) in mood disorders

artículo científico publicado en 2002

Mutation screening and assessment of the effect of genetic variations on expression and RNA editing of serotonin receptor 2C in the human brain

artículo científico publicado en 2009

No association between the Val66Met polymorphism of the brain-derived neurotrophic factor gene and bipolar disorder in a Japanese population: a multicenter study.

artículo científico publicado en 2004

Nominal association between a polymorphism in DGKH and bipolar disorder detected in a meta-analysis of East Asian case-control samples.

artículo científico publicado en 2011

Population-dependent contribution of the major histocompatibility complex region to schizophrenia susceptibility

artículo científico publicado en 2015

Population-specific haplotype association of the postsynaptic density gene DLG4 with schizophrenia, in family-based association studies

artículo científico publicado en 2013

Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene (GABRA1) and mood disorders

artículo científico publicado en 2004

Preliminary genome-wide association study of bipolar disorder in the Japanese population.

artículo científico publicado en 2009

Protocadherin α (PCDHA) as a novel susceptibility gene for autism

artículo científico publicado en 2013

Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis.

artículo científico publicado en 2014

Replication study of Japanese cohorts supports the role of STX1A in autism susceptibility.

artículo científico publicado en 2010

SNP analyses of growth factor genes EGF, TGFbeta-1, and HGF reveal haplotypic association of EGF with autism

artículo científico publicado en 2007

Sequencing and expression analyses of the synaptic lipid raft adapter gene PAG1 in schizophrenia

artículo científico publicado en 2014

The chitinase 3-like 1 gene and schizophrenia: evidence from a multi-center case-control study and meta-analysis

artículo científico publicado en 2010

Transcriptional activities of cholecystokinin promoter haplotypes and their relevance to panic disorder susceptibility

artículo científico publicado en 2003

Two genetic variants of CD38 in subjects with autism spectrum disorder and controls.

artículo científico publicado en 2010

Utility of Scalp Hair Follicles as a Novel Source of Biomarker Genes for Psychiatric Illnesses.

artículo científico publicado en 2014

Variable number of tandem repeat polymorphisms of DRD4: re-evaluation of selection hypothesis and analysis of association with schizophrenia

artículo científico publicado en 2008

Zinc finger protein 804A (ZNF804A) and verbal deficits in individuals with autism.

artículo científico publicado en 2014

Lista de obras de

A case control association study and cognitive function analysis of neuropilin and tolloid-like 1 gene and schizophrenia in the Japanese population

A family-based and case-control association study of SOX10 in schizophrenia

A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia

A microsatellite repeat in the promoter of the N-methyl-D-aspartate receptor 2A subunit (GRIN2A) gene suppresses transcriptional activity and correlates with chronic outcome in schizophrenia

A novel missense mutation (Leu46Val) of PAX6 found in an autistic patient

A novel scale including strabismus and 'cuspidal ear' for distinguishing schizophrenia patients from controls using minor physical anomalies

A population-specific uncommon variant in GRIN3A associated with schizophrenia.

A promoter haplotype of the inositol monophosphatase 2 gene (IMPA2) at 18p11.2 confers a possible risk for bipolar disorder by enhancing transcription

Ablation of Mrds1/Ofcc1 Induces Hyper-γ-Glutamyl Transpeptidasemia without Abnormal Head Development and Schizophrenia-Relevant Behaviors in Mice ⬇️

Analysis of a cluster of polymorphisms in AKT1 gene in bipolar pedigrees: a family-based association study

Analysis of correlation between serum D-serine levels and functional promoter polymorphisms of GRIN2A and GRIN2B genes.

Analysis of strain‐dependent prepulse inhibition points to a role for Shmt1 (SHMT1) in mice and in schizophrenia ⬇️

Association analyses between brain-expressed fatty-acid binding protein (FABP) genes and schizophrenia and bipolar disorder.

Association analysis of ATF4 and ATF5, genes for interacting-proteins of DISC1, in bipolar disorder

Association analysis of FEZ1 variants with schizophrenia in Japanese cohorts.

Association analysis of HSP90B1 with bipolar disorder

Association analysis of SOD2 variants with methamphetamine psychosis in Japanese and Taiwanese populations.

Association and synergistic interaction between promoter variants of the DRD4 gene in Japanese schizophrenics

Association between polymorphisms in the promoter region of the sialyltransferase 8B (SIAT8B) gene and schizophrenia

Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B.

Association of Transcription Factor Gene LMX1B with Autism ⬇️

Association of an orexin 1 receptor 408Val variant with polydipsia-hyponatremia in schizophrenic subjects

Association of decreased prefrontal hemodynamic response during a verbal fluency task with EGR3 gene polymorphism in patients with schizophrenia and in healthy individuals

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder in Japanese and the National Institute of Mental Health pedigrees.

Association of neural cell adhesion molecule 1 gene polymorphisms with bipolar affective disorder in Japanese individuals

Association studies and gene expression analyses of the DISC1-interacting molecules, pericentrin 2 (PCNT2) and DISC1-binding zinc finger protein (DBZ), with schizophrenia and with bipolar disorder

Association study between the Down syndrome cell adhesion molecule (DSCAM) gene and bipolar disorder

Association study of Nogo‐related genes with schizophrenia in a Japanese case–control sample ⬇️

Association study of polymorphisms in the 5' upstream region of human DISC1 gene with schizophrenia

Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population ⬇️

Association study of the short tandem repeat in the 5' upstream region of the cholecystokinin gene with mood disorders in the Japanese population

Brain region-specific altered expression and association of mitochondria-related genes in autism

C18orf1 located on chromosome 18p11.2 may confer susceptibility to schizophrenia.

Case-control association study of human netrin G1 gene in Japanese schizophrenia

Comprehensive association analysis of 27 genes from the GABAergic system in Japanese individuals affected with schizophrenia

DNA methylation status of SOX10 correlates with its downregulation and oligodendrocyte dysfunction in schizophrenia.

Distinguishable haplotype blocks in the HTR3A and HTR3B region in the Japanese reveal evidence of association of HTR3B with female major depression

Distribution of haplotypes derived from three common variants of the NR4A2 gene in Japanese patients with schizophrenia

Evidence of association between gamma-aminobutyric acid type A receptor genes located on 5q34 and female patients with mood disorders

Evidence that variation in the peripheral benzodiazepine receptor (PBR) gene influences susceptibility to panic disorder

Exon resequencing of H3K9 methyltransferase complex genes, EHMT1, EHTM2 and WIZ, in Japanese autism subjects

Extended analyses support the association of a functional (GT)n polymorphism in the GRIN2A promoter with Japanese schizophrenia

Fabp7 maps to a quantitative trait locus for a schizophrenia endophenotype

Failure to confirm genetic association of the CHI3L1 gene with schizophrenia in Japanese and Chinese populations

Failure to confirm genetic association of the FXYD6 gene with schizophrenia: the Japanese population and meta-analysis.

Failure to support a genetic contribution of AKT1 polymorphisms and altered AKT signaling in schizophrenia

Functional polymorphisms of HSPA5: possible association with bipolar disorder

Further evidence for the role of MET in autism susceptibility.

Gene and expression analyses reveal enhanced expression of pericentrin 2 (PCNT2) in bipolar disorder

Genetic analyses of roundabout (ROBO) axon guidance receptors in autism.

Genetic analyses of the brain-derived neurotrophic factor (BDNF) gene in autism

Genetic analysis of a functional GRIN2A promoter (GT)n repeat in bipolar disorder pedigrees in humans

Genetic analysis of the calcineurin pathway identifies members of the EGR gene family, specifically EGR3, as potential susceptibility candidates in schizophrenia

Genetic analysis of the glyoxalase system in schizophrenia

Genetic and expression analyses of FZD3 in schizophrenia

Genetic and expression analyses of the STOP (MAP6) gene in schizophrenia

Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism.

Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson's disease

Genetic association study between the detected risk variants based upon type II diabetes GWAS and psychotic disorders in the Japanese population

Genetic examination of the PLXNA2 gene in Japanese and Chinese people with schizophrenia.

Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.

Genome-Wide Association Study of Schizophrenia in Japanese Population ⬇️

Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations

Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.

Identification of multiple serine racemase (SRR) mRNA isoforms and genetic analyses of SRR and DAO in schizophrenia and D-serine levels

Increased stathmin1 expression in the dentate gyrus of mice causes abnormal axonal arborizations

Lack of association between polymorphisms in the 5' upstream region of the DISC1 gene and mood disorders

Lack of association of EGR2 variants with bipolar disorder in Japanese population

Linkage disequilibrium analysis of the CHRNA7 gene and its partially duplicated region in schizophrenia

Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder

Mitochondrial DNA haplogroup analysis in patients with bipolar disorder

Molecular analysis, mutation screening, and association study of adenylate cyclase type 9 gene (ADCY9) in mood disorders

Mutation screening and assessment of the effect of genetic variations on expression and RNA editing of serotonin receptor 2C in the human brain

No association between the Val66Met polymorphism of the brain-derived neurotrophic factor gene and bipolar disorder in a Japanese population: a multicenter study.

Nominal association between a polymorphism in DGKH and bipolar disorder detected in a meta-analysis of East Asian case-control samples.

Population-dependent contribution of the major histocompatibility complex region to schizophrenia susceptibility

Population-specific haplotype association of the postsynaptic density gene DLG4 with schizophrenia, in family-based association studies

Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene (GABRA1) and mood disorders

Preliminary genome-wide association study of bipolar disorder in the Japanese population.