List of works by Itaru Kushima

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

scientific article

A network of networks approach for modeling interconnected brain tissue-specific networks

scientific article published on 01 September 2019

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

scientific article published on 22 August 2017

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

scientific article published on 22 July 2020

Aberrant functional connectivity between the thalamus and visual cortex is related to attentional impairment in schizophrenia

scientific article published on 21 June 2018

Analysis of the VAV3 as candidate gene for schizophrenia: evidences from voxel-based morphometry and mutation screening

scientific article published on 13 March 2012

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

scientific article published on 01 October 2018

Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia

scientific article published on 7 February 2016

Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population

scientific article

Association study of bromodomain-containing 1 gene with schizophrenia in Japanese population

scientific article

Association study of ubiquitin-specific peptidase 46 (USP46) with bipolar disorder and schizophrenia in a Japanese population

scientific article published on 29 January 2010

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

scientific article published on 03 May 2019

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

scientific article published on 02 April 2020

Characterization of a schizophrenia patient with a rare RELN deletion by combining genomic and patient-derived cell analyses

scientific article published on 14 December 2019

Clinical manifestations of schizophrenia in four patients with variants in voltage‐gated calcium channel‐encoding genes: a case series

scientific article published in 2022

Common Variants in BCL9 Gene and Schizophrenia in a Japanese Population: Association Study, Meta-Analysis and Cognitive Function Analysis / UOBIČAJENE VARIJANTE BCL9 GENA I ŠIZOFRENIJA U JAPANSKOJ POPULACIJI: ŠTUDIJA POVEZANOSTI, METAANALIZA I ANA

article

Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients

scientific article

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

scientific article published on 01 September 2018

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

scientific article published on 05 February 2020

Copy number variant in the region of adenosine kinase (ADK) and its possible contribution to schizophrenia susceptibility

scientific article published on 6 November 2017

Cutting-edge morphological studies of post-mortem brains of patients with schizophrenia and potential applications of X-ray nanotomography (nano-CT)

scientific article published on 11 December 2019

Definition and refinement of the 7q36.3 duplication region associated with schizophrenia.

scientific article published on January 2013

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

scientific article published on 29 August 2018

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

scientific article published on 29 June 2018

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

scientific article published on 17 February 2020

Genetic and animal model analyses reveal the pathogenic role of a novel deletion of RELN in schizophrenia

scientific article published in Scientific Reports

Genetic association study of KREMEN1 and DKK1 and schizophrenia in a Japanese population

scientific article published on 11 February 2010

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 a Japanese population

scientific article published on 15 September 2010

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

scientific article

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

scientific article

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

scientific article published on 29 August 2016

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

scientific article published on 26 February 2022

Implications of germline copy-number variations in psychiatric disorders: review of large-scale genetic studies

scientific article published on 21 September 2020

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

scientific article published on 01 September 2019

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

scientific article published on 19 May 2018

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

scientific article published in January 2018

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

scientific article

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

scientific article published on December 2016

Loss of function studies in mice and genetic association link receptor protein tyrosine phosphatase α to schizophrenia

scientific article published on 10 August 2011

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

scientific article

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia.

scientific article

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.

scientific article

Polygenic risk scores in schizophrenia with clinically significant copy number variants

scientific article published on 30 September 2019

Possible association between ubiquitin-specific peptidase 46 gene and major depressive disorders in the Japanese population

scientific article published on 12 June 2011

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

scientific article published on 8 November 2017

Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

scientific article published on 22 April 2019

Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder

scientific article published on 14 July 2020

Quantitative facial expression analysis revealed the efficacy and time course of oxytocin in autism

scientific article published on 01 July 2019

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

scientific article

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

scientific article published on 05 December 2020

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

scientific article published on 10 January 2018

Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder

scientific article

Replication of enhanced carbonyl stress in a subpopulation of schizophrenia

scientific article published on 28 October 2013

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

scientific article published on 7 June 2016

Resequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders.

scientific article

Resequencing and association analysis of the KALRN and EPHB1 genes and their contribution to schizophrenia susceptibility

scientific article published in November 2010

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

scientific article published on 19 July 2018

Single-neuron and genetic correlates of autistic behavior in macaque.

scientific article

The regulation of soluble receptor for AGEs contributes to carbonyl stress in schizophrenia

scientific article published on 15 September 2016

Three lines of induced pluripotent stem cells derived from a 15q11.2-q13.1 duplication syndrome patient

scientific article published on 10 August 2018

Three-dimensional alteration of neurites in schizophrenia

scientific article published on 12 February 2019

White matter microstructure between the pre-SMA and the cingulum bundle is related to response conflict in healthy subjects

scientific article

X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization

scientific article published in 2022

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