Yasuhisa Ohata

assistant professor

Osaka University

Japan

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Dr. Yasuhisa Ohata is an assistant professor at Osaka University, Japan. His research focuses on the characterization of genetic disorders affecting bone health, including osteogenesis imperfecta and hypophosphatemia. He has contributed to the understanding of bone fragility in children and adolescents, as well as the therapeutic evaluations of growth hormone replacement and the management of glucocorticoid-induced osteoporosis.

Articles (16)

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2025

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2024

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2024

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2024

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2020

Collaborators (3)

Yoshitomo Hoshino

University of Tokyo Hospital

JAPAN

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Yuki Taniguchi

University of Tokyo Hospital

JAPAN

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MAKOTO FUJIWARA

Osaka University

JAPAN

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Yasuhisa Ohata

Research Interests

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Articles (16)

Characterization of a Novel Col1a1G643S/+ Osteogenesis Imperfecta Mouse Model with Insights into Skeletal Phenotype, Fragility, and Therapeutic Evaluations

Effect of Mutation Type on Ectopic Ossification Among Adult Patients With X-Linked Hypophosphatemia

Effective growth hormone replacement with once‐weekly somapacitan in Japanese children with growth hormone deficiency: Results from REAL4, a phase 3 clinical trial

The 2023 Guidelines for the management and treatment of glucocorticoid-induced osteoporosis

Association of trabecular bone score and bone mineral apparent density with the severity of bone fragility in children and adolescents with osteogenesis imperfecta: A cross-sectional study

A patient with pachydermoperiostosis harboring SLCO2A1 variants with a history of differentiating from acromegaly

Assessment of body fat mass, anthropometric measurement and cardiometabolic risk in children and adolescents with achondroplasia and hypochondroplasia

A case of hyperphosphatemic familial tumoral calcinosis due to maternal uniparental disomy of a GALNT3 variant

Pathogenic variants of the <i>GNAS</i> gene introduce an abnormal amino acid sequence in the β6 strand/α5 helix of Gsα, causing pseudohypoparathyroidism type 1A and pseudopseudohypoparathyroidism in two unrelated Japanese families.

Pathogenic Variants of the PHEX Gene

Phosphate promotes osteogenic differentiation through non-canonical Wnt signaling pathway in human mesenchymal stem cells

Genotype–phenotype analysis, and assessment of the importance of the zinc-binding site in PHEX in Japanese patients with X-linked hypophosphatemic rickets using 3D structure modeling

Neonatal cholestasis can be the first symptom of McCune–Albright syndrome: A case report

4-Phenylbutyric acid enhances the mineralization of osteogenesis imperfecta iPSC-derived osteoblasts

Alkaline phosphatase in pediatric patients with genu varum caused by vitamin D-deficient rickets

A case of HDR syndrome coexisting with tetralogy of Fallot, with a novel GATA3 mutation, which manifested as a renal abscess.

Collaborators (3)

Yoshitomo Hoshino

Yuki Taniguchi

MAKOTO FUJIWARA

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