Lista de obras -

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 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

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 FEZ1 variants with schizophrenia in Japanese cohorts.

artículo científico publicado en 2004

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

artículo científico publicado en 2006

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

artículo científico publicado en 2004

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 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

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

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

Further evidence for the role of MET in autism susceptibility.

artículo científico publicado en 2010

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 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 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 expression analysis detects eight genes with robust alterations specific to bipolar I disorder: relevance to neuronal network perturbation

artículo científico publicado en 2006

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

artículo científico publicado en 2002

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

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

artículo científico publicado en 2009

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

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

artículo científico publicado en 2003

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

artículo científico publicado en 2008

Lista de obras de

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 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

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 FEZ1 variants with schizophrenia in Japanese cohorts.

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

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

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

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

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.

Further evidence for the role of MET in autism susceptibility.

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

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

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 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 expression analysis detects eight genes with robust alterations specific to bipolar I disorder: relevance to neuronal network perturbation

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

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

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

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

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

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

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

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