about
Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia.Factor structure of the Japanese version of the Edinburgh Postnatal Depression Scale in the postpartum period.Prospective study on the association between harm avoidance and postpartum depressive state in a maternal cohort of Japanese womenCommon variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients.The postpartum depressive state in relation to perceived rearing: a prospective cohort studyResequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders.High-resolution copy number variation analysis of schizophrenia in Japan.What time periods of the day are concerning for parents of children with attention deficit hyperactivity disorder?Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese populationIdentification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.Concerns expressed by parents of children with pervasive developmental disorders for different time periods of the day: a case-control studyRelationship between social support during pregnancy and postpartum depressive state: a prospective cohort study.Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese PopulationInvestigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.Validation and factor analysis of mother-infant bonding questionnaire in pregnant and postpartum women in Japan.Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population.Wisconsin Card Sorting Test scores and clinical and sociodemographic correlates in Schizophrenia: multiple logistic regression analysis.Investigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes.Risk of alcohol use relapse after liver transplantation for alcoholic liver disease.A lack of self-consciousness in autism.Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.Relationship between maternal depression and bonding failure: A prospective cohort study of pregnant women.Exploratory eye movement dysfunction as a discriminator for schizophrenia : a large sample study using a newly developed digital computerized system.Postoperative Psychiatric Complications in Living Liver Donors.Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese populationSocial support helps protect against perinatal bonding failure and depression among mothers: a prospective cohort study.A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility.Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders.Common impairments of emotional facial expression recognition in schizophrenia across French and Japanese cultures.Obsessive-compulsive characteristics in patients with writer's cramp.Influences of an anticholinergic antiparkinsonian drug, parkinsonism, and psychotic symptoms on cardiac autonomic function in schizophrenia.Relationships between exploratory eye movement dysfunction and clinical symptoms in schizophrenia.PM338. Investigation of the association of rare single nucleotide variants in methyl-CpG-binding domain protein 5 (MBD5) with phenotypes of autism spectrum disorders and schizophrenia.Successful Post-Transplant Psychiatric Interventions During Long-Term Follow-Up of Patients Receiving Liver Transplants for Alcoholic Liver Disease.Possible involvement of a cell adhesion molecule, Migfilin, in brain development and pathogenesis of autism spectrum disorders.Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder.Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.A case-control study of the difficulties in daily functioning experienced by children with depressive disorder.Attentional shift by gaze is triggered without awareness.Dorsolateral prefrontal cortical oxygenation during REM sleep in humans.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
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name
Takashi Okada
@ast
Takashi Okada
@en
Takashi Okada
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Takashi Okada
@nl
Takashi Okada
@sl
Такаси Окада
@ru
تاكاشي اوكادا
@ar
type
label
Takashi Okada
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Takashi Okada
@en
Takashi Okada
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Takashi Okada
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Takashi Okada
@sl
Такаси Окада
@ru
تاكاشي اوكادا
@ar
prefLabel
Takashi Okada
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Takashi Okada
@en
Takashi Okada
@es
Takashi Okada
@nl
Takashi Okada
@sl
Такаси Окада
@ru
تاكاشي اوكادا
@ar
P1053
M-8902-2014
P106
P21
P31
P3829
P496
0000-0001-5580-9913