Ohsuke Migita

Functional impact of global rare copy number variation in autism spectrum disorders

Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei et al. · Nature · 2010 · 2K citations · Full text

Autism Spectrum Disorders, Syndromic Autism, Genetics +4

A genome-wide scan for common alleles affecting risk for autism

Richard Anney, Lambertus Klei, Dalila Pinto et al. · Human Molecular Genetics · 2010 · 585 citations · Full text

Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways

Candice K. Silversides, Anath C. Lionel, Gregory Costain et al. · PLoS Genetics · 2012 · 171 citations · Full text

Down Syndrome, Tof Cases, Genome-wide Association Study +15

An association between a missense polymorphism in the close homologue of L1 (CHL1, CALL) gene and schizophrenia

Kenji Sakurai, Ohsuke Migita, Michio Toru et al. · Molecular Psychiatry · 2002 · 109 citations

Psychiatry, Psychotic Disorder, Genetic Disorder +9

Spectrum of mutations and genotype–phenotype analysis in Noonan syndrome patients with RIT1 mutations

Masako Yaoita, Tetsuya Niihori, Seiji Mizuno et al. · Human Genetics · 2015 · 99 citations

Mendelian Disorder, Genetic Disorder, Noonan Syndrome Patients +10