Lista de obras -

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

Aberrant endoplasmic reticulum stress response in lymphoblastoid cells from patients with bipolar disorder

artículo científico publicado en 2008

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

Age-Dependent Effects of Catechol-O-Methyltransferase (COMT) Gene Val158Met Polymorphism on Language Function in Developing Children

artículo científico publicado en 2016

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

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 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 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 studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population

artículo científico publicado en 2018

Association study of H2AFZ with schizophrenia in a Japanese case-control sample

artículo científico publicado en 2014

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

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights

artículo científico publicado en 2018

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

artículo científico publicado en 2017

Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis.

artículo científico publicado en 2018

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

Enhanced carbonyl stress in a subpopulation of schizophrenia

artículo científico publicado en 2010

Erratum to: Association study of H2AFZ with schizophrenia in a Japanese case-control sample

artículo científico publicado en 2015

Erratum: Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism.

artículo científico publicado en 2016

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

Fatty acid composition and fatty acid binding protein expression in the postmortem frontal cortex of patients with schizophrenia: A case-control study

artículo científico publicado en 2016

Fatty acid composition of the postmortem prefrontal cortex of patients with schizophrenia, bipolar disorder, and major depressive disorder

artículo científico publicado en 2015

Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies

artículo científico publicado en 2014

Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies

article

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

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

artículo científico publicado en 2011

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 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 and molecular risk factors within the newly identified primate-specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia-associated locus

artículo científico publicado en 2017

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 risks of schizophrenia identified in a matched case-control study

artículo científico publicado en 2020

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 Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect

article

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

Giant subependymoma developed in a patient with aniridia: analyses of PAX6 and tumor-relevant genes

artículo científico publicado en 2010

Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.

artículo científico publicado en 2014

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

Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder.

artículo científico publicado en 2018

Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism

artículo científico publicado en 2015

LDB2 locus disruption on 4p16.1 as a risk factor for schizophrenia and bipolar disorder

scientific article published on 29 September 2020

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

Lipid Pathology of the Corpus Callosum in Schizophrenia and the Potential Role of Abnormal Gene Regulatory Networks with Reduced Microglial Marker Expression

scientific article published on 14 September 2020

Low serum levels of brain-derived neurotrophic factor and epidermal growth factor in patients with chronic schizophrenia

artículo científico publicado en 2008

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

artículo científico publicado en 2002

Peroxisome proliferator-activated receptor α as a novel therapeutic target for schizophrenia

artículo científico publicado en 2020

Polymorphism screening of brain-expressed FABP7, 5 and 3 genes and association studies in autism and schizophrenia in Japanese subjects

artículo científico publicado en 2010

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 of enhanced carbonyl stress in a subpopulation of schizophrenia

artículo científico publicado en 2013

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

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

artículo científico publicado en 2014

VLDL-specific increases of fatty acids in autism spectrum disorder correlate with social interaction

artículo científico publicado en 2020

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 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

Aberrant endoplasmic reticulum stress response in lymphoblastoid cells from patients with bipolar disorder

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

Age-Dependent Effects of Catechol-O-Methyltransferase (COMT) Gene Val158Met Polymorphism on Language Function in Developing Children

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.

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 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 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 studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population

Association study of H2AFZ with schizophrenia in a Japanese case-control sample

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

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights

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

Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis.

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

Enhanced carbonyl stress in a subpopulation of schizophrenia

Erratum to: Association study of H2AFZ with schizophrenia in a Japanese case-control sample

Erratum: Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism.

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

Fatty acid composition and fatty acid binding protein expression in the postmortem frontal cortex of patients with schizophrenia: A case-control study

Fatty acid composition of the postmortem prefrontal cortex of patients with schizophrenia, bipolar disorder, and major depressive disorder

Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies

Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies

Further evidence for the role of MET in autism susceptibility.

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

Gene expression analysis in lymphoblastoid cells as a potential biomarker of 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 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 and molecular risk factors within the newly identified primate-specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia-associated locus

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 risks of schizophrenia identified in a matched case-control study

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 Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect

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.

Giant subependymoma developed in a patient with aniridia: analyses of PAX6 and tumor-relevant genes

Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.

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

Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder.

Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism

LDB2 locus disruption on 4p16.1 as a risk factor for schizophrenia and bipolar disorder

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

Lipid Pathology of the Corpus Callosum in Schizophrenia and the Potential Role of Abnormal Gene Regulatory Networks with Reduced Microglial Marker Expression

Low serum levels of brain-derived neurotrophic factor and epidermal growth factor in patients with chronic schizophrenia

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

Peroxisome proliferator-activated receptor α as a novel therapeutic target for schizophrenia