Nobuhiko Okamoto

49PUBLICATIONS
98CO-AUTHORS
Aerospace materialsPerformance artDevelopmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Adolescent health
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Publications (49)

|Aug 11, 2026
Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

|Apr 18, 2026
Pierson syndrome with numerous dilated tubules masquerading as autosomal recessive polycystic kidney disease: a case report.

|Feb 02, 2026
A Patient With Intellectual Disability, Agenesis of Corpus Callosum, and Congenital Heart Disease Associated With Chromosome 10p11.2 Microdeletion.

Nobuhiko Okamoto, Eriko Nishi, Yuiko Hasegawa

|Jan 16, 2026
Cerebral blood flow and benzodiazepine receptor distribution in a patient with ALG6-congenital disorder of glycosylation.

Ryuki Matsuura, Kenjiro Kikuchi, Azusa Oba

|Nov 29, 2025
Co-Occurrence of Urogenital Anomalies and Congenital Heart Disease in a Child With Alpha-Thalassemia Mental Retardation Syndrome Associated With Chromosome 16 Abnormalities due to Partial Monosomy 16p13.3 and Partial Trisomy 16q22.1-q24.3.

Hideki Tamaru, Yuki Sasaki, Takamasa Miyoshi

|Jul 02, 2025
Approaches to diagnostic screening for congenital disorders of glycosylation and its prevalence in Japan.

Nobuhiko Okamoto, Machiko Kadoya, Yoshinao Wada

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Frequent Collaborators

7 joint publications

Naomichi Matsumoto

6 joint publications

Toshiyuki Yamamoto

5 joint publications

Tadashi Kaname

4 joint publications

Yuri Uchiyama