about
Oxytocin receptor gene variations predict neural and behavioral response to oxytocin in autism.High-resolution copy number variation analysis of schizophrenia in Japan.A significant causal association between C-reactive protein levels and schizophreniaRare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population.Genome-wide association study identifies 112 new loci for body mass index in the Japanese population.A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility.Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.Genome-wide association studies of bipolar disorder: A systematic review of recent findings and their clinical implications.Transethnic Replication Study to Assess the Association Between Clozapine-Induced Agranulocytosis/Granulocytopenia and Genes at 12p12.2 in a Japanese Population.A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder.Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.DNA methylation analyses of the candidate genes identified by a methylome-wide association study revealed common epigenetic alterations in schizophrenia and bipolar disorder.Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia.Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic EffectGenome-wide Association Analysis of Eye Movement Dysfunction in SchizophreniaGenome-wide association study identifies a novel locus associated with psychological distress in the Japanese populationCorrection: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal gangliaComparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological InsightsRe-evaluating classical body type theories: genetic correlation between psychiatric disorders and body mass index.Assessment of a glyoxalase I frameshift variant, p.P122fs, in Japanese patients with schizophreniaThe genetic architecture of the human cerebral cortexRare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control studyComparative genetic architectures of schizophrenia in East Asian and European populationsIdentification of 28 new susceptibility loci for type 2 diabetes in the Japanese populationGWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architectureGlobal DNA hypomethylation and its correlation to the betaine level in peripheral blood of patients with schizophreniaGWAS of 165,084 Japanese individuals identified nine loci associated with dietary habitsHuman leukocyte antigen DRB1*04:05 and clozapine-induced agranulocytosis/granulocytopeniaThe schizophrenia genetics knowledgebase: a comprehensive update of findings from candidate gene studiesPolygenic risk scores in schizophrenia with clinically significant copy number variantsAssociation of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and CognitionLarge-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
P50
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P50
description
researcher
@en
wetenschapper
@nl
name
Masashi Ikeda
@en
Masashi Ikeda
@nl
type
label
Masashi Ikeda
@en
Masashi Ikeda
@nl
prefLabel
Masashi Ikeda
@en
Masashi Ikeda
@nl
P31
P496
0000-0001-6237-2449