Ken Okamura

38PUBLICATIONS
110CO-AUTHORS
Pacific Peoples and disabilityVeterinary medicine (excl. urology)Other Asian languages (excl. South-East Asian)Medical biochemistry - proteins and peptides (incl. medical proteomics)Cardiovascular medicine and haematology not elsewhere classified
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Publications (38)

|Sep 18, 2026
Clinical and Patient-Reported Factors Associated With Impaired Quality of Life in Japanese Patients With Vitiligo: A Multicenter Questionnaire Study Using VitiQoL.

|Jun 01, 2026
Second Guidelines for the Diagnosis and Treatment of Vitiligo in Japan (2025).

|Nov 26, 2025
Updated Analysis of Albinism in Japan: 290 Families With Novel Pathological Variants.

Ken Okamura, Toru Saito, Naoki Oiso

|Oct 23, 2025
Genetic Pigmentary Disorders: From Molecular Mechanisms to Clinical Manifestations.

Ken Okamura, Tamio Suzuki

|Feb 24, 2025
Synonymous but Significant: New Findings of Pathological Variants in Hermansky-Pudlak Syndrome.

Junnosuke Kawaguchi, Ken Okamura, Toru Saito

|Mar 05, 2024
Genetic insights into Tietz albinism-deafness syndrome: A new dominant-negative mutation in MITF.

Kohei Yamamoto, Ken Okamura, Kazumasa Wakamatsu

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Frequent Collaborators

11 joint publications

Toru Saito

10 joint publications

Masahiro Hayashi

8 joint publications

Tamio Suzuki

4 joint publications

Naoki Oiso