Ken Okamura

37PUBLICATIONS
95CO-AUTHORS
Veterinary medicine (excl. urology)Other Asian languages (excl. South-East Asian)Medical biochemistry - proteins and peptides (incl. medical proteomics)Cardiovascular medicine and haematology not elsewhere classifiedGene and molecular therapy
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Publications (37)

|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

|Nov 05, 2023
Rational design of a JAK1-selective siRNA inhibitor for the modulation of autoimmunity in the skin.

Qi Tang, Hassan H Fakih, Mohammad Zain Ui Abideen

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