Y. Iwayama

Elucidation of the mechanism of byproduct DNA synthesis in whole-transcript amplification by poly-A tagging and development of its specific suppression
20250 citationsauthor #2
Distinctiveness and continuity in transcriptome and connectivity in the anterior-posterior axis of the paraventricular nucleus of the thalamus.
202320 citationsauthor #5
Author Correction: Single-cell transcriptomics uncovers EGFR signaling-mediated gastric progenitor cell differentiation in stomach homeostasis
20230 citationsauthor #5
Taq1A polymorphism in patients with bipolar disorder: A candidate gene study based on the dopamine hypothesis
20231 citationsauthor #14
Single-cell transcriptomics uncovers EGFR signaling-mediated gastric progenitor cell differentiation in stomach homeostasis
202318 citationsauthor #5
Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder
20228 citationsauthor #11
SLITRK1-mediated noradrenergic projection suppression in the neonatal prefrontal cortex
20229 citationsauthor #6
Differential genetic associations and expression of PAPST1/SLC35B2 in bipolar disorder and schizophrenia
20222 citationsauthor #6
Cooperation of LIM domain‐binding 2 (LDB2) with EGR in the pathogenesis of schizophrenia
20217 citationsauthor #12
Abnormal gene expression of BDNF, but not BDNF-AS, in iPSC, neural stem cells and postmortem brain samples from bipolar disorder.
20216 citationsauthor #3
Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia
202114 citationsauthor #5
Glyoxalase I disruption and external carbonyl stress impair mitochondrial function in human induced pluripotent stem cells and derived neurons
202123 citationsauthor #5
A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brain
202119 citationsauthor #2
Lipid Pathology of the Corpus Callosum in Schizophrenia and the Potential Role of Abnormal Gene Regulatory Networks with Reduced Microglial Marker Expression
202028 citationsauthor #5
Evaluation of the role of fatty acid-binding protein 7 in controlling schizophrenia-relevant phenotypes using newly established knockout mice.
202016 citationsauthor #8
LDB2 locus disruption on 4p16.1 as a risk factor for schizophrenia and bipolar disorder
20200 citationsauthor #4
LDB2 locus disruption on 4p16.1 as a risk factor for schizophrenia and bipolar disorder
20204 citationsauthor #4
Genetic Deciphering of Prepulse Inhibition Reveals the Putative Role of an Atypical Cadherin in Schizophrenia Pathogenesis
20202 citationsauthor #5
A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders
202024 citationsauthor #16
Evidence for Altered Metabolism of Sphingosine-1-Phosphate in the Corpus Callosum of Patients with Schizophrenia
202034 citationsauthor #3
Peroxisome proliferator-activated receptor α as a novel therapeutic target for schizophrenia
202024 citationsauthor #7
Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition and Implication of CDH23 in Schizophrenia
20202 citationsauthor #5
A potential role of fatty acid binding protein 4 in the pathophysiology of autism spectrum disorder
202016 citationsauthor #14
Genetic risks of schizophrenia identified in a matched case–control study
20203 citationsauthor #5
Investigation of betaine as a novel psychotherapeutic for schizophrenia
201964 citationsauthor #7
Key role of soluble epoxide hydrolase in the neurodevelopmental disorders of offspring after maternal immune activation
201950 citationsauthor #10
Genetic risks of schizophrenia identified in a matched case-control study
20192 citationsauthor #5
Excess hydrogen sulfide and polysulfides production underlies a schizophrenia pathophysiology
201963 citationsauthor #7
Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation
201848 citationsauthor #4
Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis.
20180 citationsauthor #7
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
2018132 citationsauthor #10
Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis.
201834 citationsauthor #7
O2-H-1-2 Zic2 hypomorphic mutant mice as a schizophre- nia model and ZIC2 mutations identified in schizophrenia patients
201821 citationsauthor #3
Association studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population
20182 citationsauthor #3
Genetic and molecular risk factors within the newly identified primate‐specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia‐associated locus
201716 citationsauthor #6
A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility
201725 citationsauthor #6
A spontaneous and novel Pax3 mutant mouse that models Waardenburg syndrome and neural tube defects.
201710 citationsauthor #5
Autism-like behaviours and enhanced memory formation and synaptic plasticity in Lrfn2/SALM1-deficient mice
201765 citationsauthor #9
Polyunsaturated fatty acid deficiency during neurodevelopment in mice models the prodromal state of schizophrenia through epigenetic changes in nuclear receptor genes
201769 citationsauthor #3
Comprehensive association analysis of 27 genes from the GABAergic system in Japanese individuals affected with schizophrenia.
201712 citationsauthor #3
Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders
201770 citationsauthor #5
Scientific Summaries for Families with ASD
20160 citationsauthor #10
Cerebrospinal fluid metabolomics identifies a key role of isocitrate dehydrogenase in bipolar disorder: evidence in support of mitochondrial dysfunction hypothesis
2016107 citationsauthor #4
Age-Dependent Effects of Catechol-O-Methyltransferase (COMT) Gene Val158Met Polymorphism on Language Function in Developing Children
201618 citationsauthor #4
Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population
201624 citationsauthor #13
Fatty acid composition and fatty acid binding protein expression in the postmortem frontal cortex of patients with schizophrenia: A case-control study.
201626 citationsauthor #4
Analysis of induced pluripotent stem cells carrying 22q11.2 deletion
2016101 citationsauthor #9
Genome‐wide Association Study of Autism Spectrum Disorder in the East Asian Populations
201699 citationsauthor #11
Erratum: Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism
20160 citationsauthor #2
Erratum to: Association study of H2AFZ with schizophrenia in a Japanese case–control sample
20150 citationsauthor #3
Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism
201521 citationsauthor #2
Utility of Scalp Hair Follicles as a Novel Source of Biomarker Genes for Psychiatric Illnesses.
201551 citationsauthor #5
Sequencing and expression analyses of the synaptic lipid raft adapter gene PAG1 in schizophrenia
20153 citationsauthor #2
Genetic analysis of the glyoxalase system in schizophrenia.
201513 citationsauthor #4
Association study of H2AFZ with schizophrenia in a Japanese case–control sample
20153 citationsauthor #3
Population-dependent contribution of the major histocompatibility complex region to schizophrenia susceptibility.
20157 citationsauthor #3
Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.
201532 citationsauthor #7
Reduced cortical expression of a newly identified splicing variant of the DLG1 gene in patients with early-onset schizophrenia
201523 citationsauthor #3
22q11.2 deletion carriers and schizophrenia-associated novel variants
201419 citationsauthor #2
schizophrenia and autism spectrum disorder and mouse behavioral studies
201410 citationsauthor #7
Exon resequencing of H3K9 methyltransferase complex genes, EHMT1, EHTM2 and WIZ, in Japanese autism subjects
201432 citationsauthor #2
Defective Craniofacial Development and Brain Function in a Mouse Model for Depletion of Intracellular Inositol Synthesis*
201430 citationsauthor #6
Replication and cross‐phenotype study based upon schizophrenia GWASs data in the Japanese population: Support for association of MHC region with psychosis
201428 citationsauthor #3
Association of decreased prefrontal hemodynamic response during a verbal fluency task with EGR3 gene polymorphism in patients with schizophrenia and in healthy individuals
201432 citationsauthor #11
Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies
201499 citationsauthor #7
Intracellular Inositol Synthesis Brain Function in a Mouse Model for Defective Craniofacial Development and Neurobiology :
20140 citationsauthor #2
Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizures
2014121 citationsauthor #10
Zinc finger protein 804A (ZNF804A) and verbal deficits in individuals with autism.
201433 citationsauthor #7
Population-Specific Haplotype Association of the Postsynaptic Density Gene DLG4 with Schizophrenia, in Family-Based Association Studies
201323 citationsauthor #4
Lack of association of EGR2 variants with bipolar disorder in Japanese population.
20131 citationsauthor #3
Genetic association study between the detected risk variants based upon type II diabetes GWAS and psychotic disorders in the Japanese population
20138 citationsauthor #4
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
201310 citationsauthor #8
Protocadherin α (PCDHA) as a novel susceptibility gene for autism.
201355 citationsauthor #5
A population-specific uncommon variant in GRIN3A associated with schizophrenia.
201347 citationsauthor #2
Genetic Variants on 3q21 and in the Sp8 Transcription Factor Gene (SP8) as Susceptibility Loci for Psychotic Disorders: A Genetic Association Study
201320 citationsauthor #5
Brain region-specific altered expression and association of mitochondria-related genes in autism
2012140 citationsauthor #5
Association study of Nogo‐related genes with schizophrenia in a Japanese case–control sample
201120 citationsauthor #3
Genome-Wide Association Study of Schizophrenia in Japanese Population
2011167 citationsauthor #2
Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population
201152 citationsauthor #2
Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population
20110 citationsauthor #2
Association of Transcription Factor Gene LMX1B with Autism
201110 citationsauthor #6
Replication study of Japanese cohorts supports the role of STX1A in autism susceptibility.
201139 citationsauthor #9
Nominal association between a polymorphism in DGKH and bipolar disorder detected in a meta‐analysis of East Asian case–control samples
201117 citationsauthor #3
Schizophrenia with the 22q11.2 deletion and additional genetic defects: case history
201134 citationsauthor #4
Ablation of Mrds1/Ofcc1 Induces Hyper-γ-Glutamyl Transpeptidasemia without Abnormal Head Development and Schizophrenia-Relevant Behaviors in Mice
20119 citationsauthor #7
Association analyses between brain‐expressed fatty‐acid binding protein (FABP) genes and schizophrenia and bipolar disorder
201042 citationsauthor #1
Further evidence for the role of MET in autism susceptibility.
201055 citationsauthor #9
Enhanced carbonyl stress in a subpopulation of schizophrenia.
2010160 citationsauthor #6
Excessive ingestion of long-chain polyunsaturated fatty acids during developmental stage causes strain- and sex-dependent eye abnormalities in mice.
20100 citationsauthor #2
Behavioral analyses of transgenic mice harboring bipolar disorder candidate genes, IMPA1 and IMPA2.
201011 citationsauthor #4
Polymorphism screening of brain-expressed FABP7, 5 and 3 genes and association studies in autism and schizophrenia in Japanese subjects
201045 citationsauthor #2
Analysis of strain‐dependent prepulse inhibition points to a role for Shmt1 (SHMT1) in mice and in schizophrenia
201017 citationsauthor #5
Failure to confirm genetic association of the FXYD6 gene with schizophrenia: The Japanese population and meta‐analysis
20107 citationsauthor #3
Giant Subependymoma Developed in a Patient with Aniridia: Analyses of PAX6 and Tumor‐relevant Genes
201011 citationsauthor #3
Functional (GT)n polymorphisms in promoter region of N‐methyl‐d‐aspartate receptor 2A subunit (GRIN2A) gene affect hippocampal and amygdala volumes
201012 citationsauthor #5
A novel missense mutation (Leu46Val) of PAX6 found in an autistic patient.
200941 citationsauthor #2
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
200938 citationsauthor #4
Failure to confirm genetic association of the CHI3L1 gene with schizophrenia in Japanese and Chinese populations
200910 citationsauthor #3
GENETIC AND EXPRESSION ANALYSES OF SEROTONERGIC FACTORS IN AUTISM
20090 citationsauthor #11
Evidence of association of serotonin transporter gene polymorphisms with schizophrenia in a South Indian population
200941 citationsauthor #2

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