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Ohsuke Migita

Functional impact of global rare copy number variation in autism spectrum disorders
2010 · Dalila Pinto, Alistair T. Pagnamenta, et al. · Nature · 2,013
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A genome-wide scan for common alleles affecting risk for autism
2010 · R. Anney, L. Klei, et al. · Human Molecular Genetics · 593
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Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways
2012 · Candice K. Silversides, Anath C. Lionel, et al. · PLoS Genetics · 168
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An association between a missense polymorphism in the close homologue of L1 (CHL1, CALL) gene and schizophrenia
2002 · K Sakurai, O Migita, et al. · Molecular Psychiatry · 110
Spectrum of mutations and genotype–phenotype analysis in Noonan syndrome patients with RIT1 mutations
2015 · Masako Yaoita, Tetsuya Niihori, et al. · Human Genetics · 101
Two distinctive classic genetic syndromes, 22q11.2 deletion syndrome and Angelman syndrome, occurring within the same family
2009 · Rika Kosaki, Ohsuke Migita, et al. · American Journal of Medical Genetics Part A · 74
Mechanisms of Formation of Structural Variation in a Fully Sequenced Human Genome
2012 · Andy Wing Chun Pang, Ohsuke Migita, et al. · Human Mutation · 50
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The CASK gene harbored in a deletion detected by array‐CGH as a potential candidate for a gene causative of X‐linked dominant mental retardation
2008 · Shin Hayashi, Seiji Mizuno, et al. · American Journal of Medical Genetics Part A · 48
Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)
2021 · Mari Minatogawa, Ai Unzaki, et al. · Journal of Medical Genetics · 44
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Newborn screening for Pompe disease in Japan
2011 · Eri Oda, Toju Tanaka, et al. · Molecular Genetics and Metabolism · 39
ADRB2 Polymorphisms and Asthma Susceptibility: Transmission Disequilibrium Test and Meta-Analysis
2004 · Ohsuke Migita, Emiko Noguchi, et al. · International Archives of Allergy and Immunology · 38
Association between a polymorphism in cysteinyl leukotriene receptor 2 on chromosome 13q14 and atopic asthma
2004 · Hiromi Fukai, Yoshino Ogasawara, et al. · Pharmacogenetics · 37
Association of ZNF74 gene genotypes with age-at-onset of schizophrenia
2001 · K. Takase, T. Ohtsuki, et al. · Schizophrenia Research · 37
Haplotype analysis of a 100 kb region spanning TNF–LTA identifies a polymorphism in the LTA promoter region that is associated with atopic asthma susceptibility in Japan
2005 · O. Migita, E. Noguchi, et al. · Clinical & Experimental Allergy · 34
Determination of structure and transcriptional regulation of CYSLTR1 and an association study with asthma and rhinitis
2005 · Jian Zhang, Ohsuke Migita, et al. · Pediatric Allergy and Immunology · 28
Novel SIN3A mutation identified in a Japanese patient with Witteveen-Kolk syndrome
2018 · Yoko Narumi-Kishimoto, Naomi Araki, et al. · European Journal of Medical Genetics · 22
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Association of a haplotype block spanning SDAD1 gene and CXC chemokine genes with allergic rhinitis
2005 · Jian Zhang, Emiko Noguchi, et al. · Journal of Allergy and Clinical Immunology · 21
Analysis of chromosome microstructures in products of conception associated with recurrent miscarriage
2018 · Taisuke Sato, Ohsuke Migita, et al. · Reproductive BioMedicine Online · 20
Novel TFAP2A mutation in a Japanese family with Branchio-oculo-facial syndrome
2018 · Taisuke Sato, Osamu Samura, et al. · Human Genome Variation · 19
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Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform Mole
2015 · Yuki Ito, Kayoko Maehara, et al. · Gynecologic and Obstetric Investigation · 19
X-linked inhibitor of apoptosis protein deficiency complicated with Crohn's disease-like enterocolitis and Takayasu arteritis: A case report
2020 · Ichiro Takeuchi, Toshinao Kawai, et al. · Clinical Immunology · 17
Amplicon Sequencing-Based Noninvasive Fetal Genotyping for RHD-Positive D Antigen-Negative Alleles
2019 · Ken Takahashi, Ohsuke Migita, et al. · Clinical Chemistry · 17
A novel heterozygous ITGB3 p.T720del inducing spontaneous activation of integrin αIIbβ3 in autosomal dominant macrothrombocytopenia with aggregation dysfunction
2018 · Naohiro Miyashita, Masahiro Onozawa, et al. · Annals of Hematology · 11
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Cytogenetic analysis of spontaneously discharged products of conception by array-based comparative genomic hybridization
2016 · Nobuaki Ozawa, Haruhiko Sago, et al. · SpringerPlus · 11
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Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants
2023 · Shiena Watanabe, Ming Lei, et al. · Brain and Development · 10
Works count: 73
Citation count: 3,684
H-index: 19
I10-index: 26
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