Yoshihiro Nawa
0000-0003-3164-2519
Meijo University
10 papers found
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Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case–control study
Analysis of human neuronal cells carrying ASTN2 deletion: A cross-disorder risk variant of schizophrenia, autism spectrum disorder, and bipolar disorder
Treatment‐resistant schizophrenia in patients with 3q29 deletion: A case series of four patients
Exome sequencing of Japanese schizophrenia multiplex families supports the involvement of calcium ion channels
Cross-disorder analysis of genic and regulatory copy number variations in bipolar disorder, schizophrenia, and autism spectrum disorder
Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population
Resequencing and association analysis of GAP43 with autism spectrum disorder and schizophrenia in a Japanese population
Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder
Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility
Lateralized interictal epileptiform discharges during rapid eye movement sleep correlate with epileptogenic hemisphere in children with intractable epilepsy secondary to tuberous sclerosis complex
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