Lista de obras -

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility

artículo científico publicado en 2017

ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk

artículo científico publicado en 2020

An essential role of the aPKC-Aurora A-NDEL1 pathway in neurite elongation by modulation of microtubule dynamics

scientific journal article

An unbiased data-driven age-related structural brain parcellation for the identification of intrinsic brain volume changes over the adult lifespan.

artículo científico publicado en 2017

Assessment of a glyoxalase I frameshift variant, p.P122fs, in Japanese patients with schizophrenia

artículo científico publicado en 2018

Author Correction: Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

artículo científico publicado en 2019

Behavioral alterations associated with targeted disruption of exons 2 and 3 of the Disc1 gene in the mouse.

artículo científico publicado en 2011

Cell body shape and directional movement stability in human-induced pluripotent stem cell-derived dopaminergic neurons

scientific article published on 02 April 2020

Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus

artículo científico publicado en 2020

Dysregulation of schizophrenia-related aquaporin 3 through disruption of paranode influences neuronal viability

artículo científico publicado en 2018

Effect of intranasal oxytocin on the core social symptoms of autism spectrum disorder: a randomized clinical trial

artículo científico publicado en 2018

Evaluation of resting state networks in patients with gliomas: connectivity changes in the unaffected side and its relation to cognitive function

artículo científico publicado en 2015

Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia

scientific article published on 17 September 2020

Generation and analysis of novel Reln-deleted mouse model corresponding to exonic Reln deletion in schizophrenia

artículo científico publicado en 2020

High-resolution copy number variation analysis of schizophrenia in Japan.

artículo científico publicado en 2016

Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility

artículo científico publicado en 2016

Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder

artículo científico publicado en 2022

In Vitro Modeling of the Bipolar Disorder and Schizophrenia Using Patient-Derived Induced Pluripotent Stem Cells with Copy Number Variations of PCDH15 and RELN

artículo científico publicado en 2019

Induced pluripotent stem cells derived from a schizophrenia patient with ASTN2 deletion

artículo científico publicado en 2018

Inhibition of calpain increases LIS1 expression and partially rescues in vivo phenotypes in a mouse model of lissencephaly

artículo científico publicado en 2009

Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.

artículo científico publicado en 2016

Investigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes.

artículo científico publicado en 2016

Krüppel-like factor 5 is essential for blastocyst development and the normal self-renewal of mouse ESCs.

artículo científico publicado en 2008

LIS1 and NDEL1 coordinate the plus-end-directed transport of cytoplasmic dynein.

artículo científico publicado en 2008

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

artículo científico publicado en 2016

Possible involvement of a cell adhesion molecule, Migfilin, in brain development and pathogenesis of autism spectrum disorders.

artículo científico publicado en 2017

Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

artículo científico publicado en 2019

Psychiatric-disorder-related behavioral phenotypes and cortical hyperactivity in a mouse model of 3q29 deletion syndrome

scientific article published on 19 June 2019

Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.

artículo científico publicado en 2017

Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder

artículo científico publicado en 2020

Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.

artículo científico publicado en 2018

Reorganization of brain networks and its association with general cognitive performance over the adult lifespan

artículo científico publicado en 2019

Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders

artículo científico publicado en 2016

Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant

scientific article published on 19 July 2018

Lista de obras de

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility

ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk

An essential role of the aPKC-Aurora A-NDEL1 pathway in neurite elongation by modulation of microtubule dynamics

An unbiased data-driven age-related structural brain parcellation for the identification of intrinsic brain volume changes over the adult lifespan.

Assessment of a glyoxalase I frameshift variant, p.P122fs, in Japanese patients with schizophrenia

Author Correction: Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

Behavioral alterations associated with targeted disruption of exons 2 and 3 of the Disc1 gene in the mouse.

Cell body shape and directional movement stability in human-induced pluripotent stem cell-derived dopaminergic neurons

Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus

Dysregulation of schizophrenia-related aquaporin 3 through disruption of paranode influences neuronal viability

Effect of intranasal oxytocin on the core social symptoms of autism spectrum disorder: a randomized clinical trial

Evaluation of resting state networks in patients with gliomas: connectivity changes in the unaffected side and its relation to cognitive function

Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia

Generation and analysis of novel Reln-deleted mouse model corresponding to exonic Reln deletion in schizophrenia

High-resolution copy number variation analysis of schizophrenia in Japan.

Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility

Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder

In Vitro Modeling of the Bipolar Disorder and Schizophrenia Using Patient-Derived Induced Pluripotent Stem Cells with Copy Number Variations of PCDH15 and RELN

Induced pluripotent stem cells derived from a schizophrenia patient with ASTN2 deletion

Inhibition of calpain increases LIS1 expression and partially rescues in vivo phenotypes in a mouse model of lissencephaly

Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.

Investigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes.

Krüppel-like factor 5 is essential for blastocyst development and the normal self-renewal of mouse ESCs.

LIS1 and NDEL1 coordinate the plus-end-directed transport of cytoplasmic dynein.

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

Possible involvement of a cell adhesion molecule, Migfilin, in brain development and pathogenesis of autism spectrum disorders.

Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

Psychiatric-disorder-related behavioral phenotypes and cortical hyperactivity in a mouse model of 3q29 deletion syndrome

Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.

Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder

Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.

Reorganization of brain networks and its association with general cognitive performance over the adult lifespan

Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders

Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant