Lista de obras -

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

artículo científico publicado en 2006

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

A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders

artículo científico publicado en 2020

A spontaneous and novel Pax3 mutant mouse that models Waardenburg syndrome and neural tube defects

artículo científico publicado en 2016

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 t(18;21)(p11.1;p11.1) translocation in a family with schizophrenia

artículo científico publicado en 2009

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

artículo científico publicado en 2006

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

scientific article published on 01 February 2008

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

artículo científico publicado el 17 de septiembre de 2011

Autism-like behaviours and enhanced memory formation and synaptic plasticity in Lrfn2/SALM1-deficient mice

artículo científico publicado en 2017

Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients.

artículo científico publicado en 2007

Behavioral analyses of transgenic mice harboring bipolar disorder candidate genes, IMPA1 and IMPA2.

artículo científico publicado en 2010

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

artículo científico publicado en 2012

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

Defective craniofacial development and brain function in a mouse model for depletion of intracellular inositol synthesis

artículo científico publicado en 2014

Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation.

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

Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizures.

artículo científico publicado en 2014

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 of association of serotonin transporter gene polymorphisms with schizophrenia in a South Indian population

artículo científico publicado en 2009

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

artículo científico publicado en 2006

Excessive ingestion of long-chain polyunsaturated fatty acids during developmental stage causes strain- and sex-dependent eye abnormalities in mice.

artículo científico publicado en 2010

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

artículo científico publicado en 2014

Expression analysis of actin-related genes as an underlying mechanism for mood disorders

artículo científico publicado en 2006

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

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

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 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 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

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

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

artículo científico publicado en 2010

Human myo‐inositol monophosphatase 2 rescues the nematode thermotaxis mutant ttx‐7 more efficiently than IMPA1: functional and evolutionary considerations of the two mammalian myo‐inositol monophosphatase genes ⬇️

artículo científico publicado el 26 de diciembre de 2012

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

artículo científico publicado en 2014

Investigation of betaine as a novel psychotherapeutic for schizophrenia

scientific article published on 26 June 2019

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

artículo científico publicado en 2015

Key role of soluble epoxide hydrolase in the neurodevelopmental disorders of offspring after maternal immune activation

scientific article published on 19 March 2019

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 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

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

Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population

artículo científico publicado en 2016

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

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

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

Spatial expression patterns and biochemical properties distinguish a second myo-inositol monophosphatase IMPA2 from IMPA1

artículo científico publicado en 2007

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

Zic2 hypomorphic mutant mice as a schizophrenia model and ZIC2 mutations identified in schizophrenia patients

artículo científico publicado en 2011

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

artículo científico publicado en 2014

Lista de obras de

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

A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders

A spontaneous and novel Pax3 mutant mouse that models Waardenburg syndrome and neural tube defects

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 t(18;21)(p11.1;p11.1) translocation in a family with schizophrenia

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

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

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

Autism-like behaviours and enhanced memory formation and synaptic plasticity in Lrfn2/SALM1-deficient mice

Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients.

Behavioral analyses of transgenic mice harboring bipolar disorder candidate genes, IMPA1 and IMPA2.

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

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.

Defective craniofacial development and brain function in a mouse model for depletion of intracellular inositol synthesis

Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation.

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

Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizures.

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 of association of serotonin transporter gene polymorphisms with schizophrenia in a South Indian population

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

Excessive ingestion of long-chain polyunsaturated fatty acids during developmental stage causes strain- and sex-dependent eye abnormalities in mice.

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

Expression analysis of actin-related genes as an underlying mechanism for mood disorders

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

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

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 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 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

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

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

Human myo‐inositol monophosphatase 2 rescues the nematode thermotaxis mutant ttx‐7 more efficiently than IMPA1: functional and evolutionary considerations of the two mammalian myo‐inositol monophosphatase genes ⬇️

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

Investigation of betaine as a novel psychotherapeutic for schizophrenia

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

Key role of soluble epoxide hydrolase in the neurodevelopmental disorders of offspring after maternal immune activation

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

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

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

Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population

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

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

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