Motomu Hashimoto is an expert in Rheumatology at Osaka Metropolitan University Hospital (Japan). As of October 2026, ScienceLeadR ranks Motomu Hashimoto in the top 1% of experts worldwide for Autoimmune Diseases, Arthritis and Epidemiologic Studies. Motomu Hashimoto has authored 330 publications, the most recent in 2026, and is an investigator in 5 clinical trials, 1 of them ongoing. SLR score: 1,107 (community average: 125). How the SLR is computed.

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Rheumatology

Subspecialties: Immunology - Internal Medicine - Biochemistry

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Short Biography

Trained under Prof. Shimon Sakaguchi, the 2025 Nobel Laureate recognized for the discovery of regulatory T cells, Prof. Motomu Hashimoto has advanced pioneering research bridging basic and clinical immunology. His work using a monogenic autoimmune mouse model has elucidated mechanisms through which genetic and environmental factors determine disease phenotypes—including rheumatoid arthritis, systemic lupus erythematosus, and spondyloarthritis. In clinical research, Prof. Hashimoto established the ANSWER cohort, Japan’s largest rheumatoid arthritis registry, generating real-world evidence that informs the optimal use of molecular targeted therapies. His major contributions integrating bench and bedside research were honored with the 2025 Japan College of Rheumatology Scientific Award.


Key Research Achievements

Basic research

1. Yoshida T, Hashimoto M. et al. Arthritis Res Ther. 2025 ;27(1):143

2. Katsushima M, Hashimoto M. et al. Rheumatology (Oxford). 2025 ;64(5):3104-3115

3. Shirakashi M, Hashimoto M. et al. Arthritis Rheumatol. 2022 ;74(4):641-653.

4. Tabuchi Y, Hashimoto M. et al. Arthritis Res Ther. 2022 ;24(1):176.

5. Matsuo T, Hashimoto M. et al. J Immunol. 2019;202(11):3161-3172.

6. Hirota K, Hashimoto M, et al. Immunity. 2018: S1074-7613(18)30146-8.

7. Ito Y, Hashimoto M, et al. Science. 2014;346(6207):363-8.

8. Hashimoto M, et al. J Exp Med. 2010;207(6):1135-43.


Clinical Research

1. Torii M, Hashimoto M. et al. Arthritis Res Ther. 2026;28(1):66.

2. Smolen JS, Hashimoto M, Taylor PC, et al. RMD Open. 2026 ;12(1):e006094

3. Fujisawa Y, Hashimoto M. et al. Rheumatology (Oxford). 2026 ;65(2):keaf602.

4. Watanabe R, Hashimoto M. et al. Rheumatology (Oxford). 2024 ;63(9):2418-2426.

5. Nakayama Y, Hashimoto M. et al. Rheumatology (Oxford). 2024; 63(2):349-357.

6. Iwasaki T, Hashimoto M. et al. Front Immunol. 2022 6;13:901437.

7. Nakayama Y, Hashimoto M. et al. Rheumatol Int. 2022 ;42(7):1227-1234.

8. Hashimoto M, et al. Arthritis Res Ther. 2018;20(1):165. .

9. Hashimoto M, et al. PLoS One. 2015;10:e0122121.


Organizations

Career arc: 2000 - 2026

Source: PubMed

Osaka Metropolitan University

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 330

Citations

Citations: 9 272 1st author: 13 Last author: 68 Unique author: 3


Breakdown by type

Click a legend label to hide or show it in the chart.

Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Comparative effectiveness and safety of five Janus kinase inhibitors in real-world clinical practice: the multicentre ANSWER cohort.
PMID 42949113 — safety, rheumatic diseases, drug-related side effects and adverse reactions, janus kinases, therapeutics, janus kinase inhibitors
Rheumatology (Oxford)20260
Burden of herpes zoster and recombinant zoster vaccine willingness in systemic lupus erythematosus: A single-center cohort study.
PMID 42803531 — vaccines, azathioprine, cohort studies, lupus erythematosus, systemic, herpes zoster, diagnosis, herpes zoster vaccine, immunosuppression therapy
Lupus20260
Reasons-stratified treatment retention after JAK inhibitor discontinuation in rheumatoid arthritis: the ANSWER cohort study.
PMID 42900496 — pharmaceutical preparations, arthritis, cohort studies, rheumatic diseases, arthritis, rheumatoid, therapeutics, janus kinase inhibitors, retention, psychology
Rheumatology (Oxford)20260
CD40-CD40L interactions in systemic autoimmune diseases.
PMID 42885554 — rheumatic diseases, lupus erythematosus, systemic, cd40 ligand, autoimmune diseases, arthritis, rheumatoid, blood platelets, tissues
Rheumatology (Oxford)20260
Comment on: early rheumatoid factor decline predicts subsequent clinical remission in rheumatoid arthritis: the ANSWER cohort: Reply.
PMID 42886529 — arthritis, rheumatic diseases, arthritis, rheumatoid, rheumatoid factor
Rheumatology (Oxford)20260

Clinical Studies 5

Sources: ClinicalTrials, EU CTIS

Synthesis

Principal Investigator: 1

By phase:

Phase 2 2
Phase 3 2
Phase 4 1

By status:

Completed 3
Active not recruiting 1
Unknown 1

By type:

Interventional 5

By Monocentric/Multicentric:

monocentric 0
multicentric2to4 0
multicentric5to9 0
multicentricup10 5

Main Topics

Ongoing Clinical Trials

Ongoing trial started since 2021, where this expert is an investigator

Source: ClinicalTrials

Study Phase Status Start
A Study to Evaluate Effectiveness and Safety of Deucravacitinib (BMS 986165) Compared With Placebo in Participants With Active Systemic Lupus Erythematosus
NCT05620407 — safety, connective tissue, connective tissue diseases, lupus erythematosus, systemic, immune system diseases, immune system, autoimmune diseases, tissues
Phase 3Active not recruiting2023

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