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Scientific Reports|September 8, 2022
Survey on experiences and attitudes of parents toward disclosing information to children with genetic syndromes and their siblings in JapanMikiko Kaneko, Daiju Oba, Hirofumi Ohashi
Human Genome Variation|October 28, 2025
Biallelic CPAMD8 variants in a patient with ectopia lentis associated with extraocular systemic features reminiscent of Marfan syndromeDaiju Oba, Mariko Sagara, Sayuri Oda, et al.
Fetal and Pediatric Pathology|May 13, 2026
Utility of Integrating Genome-Wide Postmortem Testing into Clinical Autopsy Practice in Pediatrics: A Retrospective, Single-Center StudyNoriko Watanabe, Kayoko Ichimura, Daiju Oba, et al.
Plos One|March 10, 2022
iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromesSilvia Natsuko Akutsu, Tatsuo Miyamoto, Daiju Oba, et al.
Brain & Development|January 1, 2018
l-Thyroxine-responsive drop attacks in childhood benign hereditary chorea: A case reportTadashi Shiohama, Hirofumi Ohashi, Kenji Shimizu, et al.
Neuropediatrics|March 17, 2020
Use of Perampanel and a Ketogenic Diet in Nonketotic Hyperglycinemia: A Case ReportAtsuro Daida, Shin-Ichiro Hamano, Satoru Ikemoto, et al.
Ebiomedicine|December 20, 2017
Mice with an Oncogenic HRAS Mutation are Resistant to High-Fat Diet-Induced Obesity and Exhibit Impaired Hepatic Energy HomeostasisDaiju Oba, Shin-Ichi Inoue, Sachiko Miyagawa-Tomita, et al.
Seizure|October 15, 2024
Effectiveness of vigabatrin for infantile epileptic spasm syndrome categorized by etiologiesHirokazu Takeuchi, Kenjiro Kikuchi, Rikako Takeda, et al.
Molecular Genetics & Genomic Medicine|January 19, 2020
Possible mitochondrial dysfunction in a patient with deafness, dystonia, and cerebral hypomyelination (DDCH) due to BCAP31 MutationKenji Shimizu, Daiju Oba, Ryusuke Nambu, et al.
Acta Neuropathologica|January 21, 2010
Autopsy study of cerebellar degeneration in siblings with ataxia-telangiectasia-like disorderDaiju Oba, Masaharu Hayashi, Motoyuki Minamitani, et al.
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