Soichi Ogishima

8PUBLICATIONS
222CO-AUTHORS
Recommender systemsMajor global burdens of diseaseLanguage documentation and descriptionPacific Peoples life courseGenomics and transcriptomics
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Publications (8)

|Nov 18, 2025
RareLink: scalable REDCap-based framework for rare disease interoperability linking international registries to FHIR and Phenopackets.

Adam S L Graefe, Filip Rehburg, Samer Alkarkoukly

|May 19, 2025
Linking international registries to FHIR and Phenopackets with RareLink: a scalable REDCap-based framework for rare disease data interoperability.

Adam S L Graefe, Filip Rehburg, Samer Alkarkoukly

|May 12, 2025
Integration of Digital Phenotyping and Genomics for Dry Eye Disease: Protocol for a Prospective Cohort Study.

Ken Nagino, Yasutsugu Akasaki, Nobuo Fuse

|Mar 10, 2025
Consistent Performance of GPT-4o in Rare Disease Diagnosis Across Nine Languages and 4967 Cases.

Leonardo Chimirri, J Harry Caufield, Yasemin Bridges

|Aug 12, 2024
Attitudes toward subsequent primary cancer prevention among survivors of childhood, adolescent, and young adult (CAYA) cancer in Japan: results of a comprehensive questionnaire survey on long-term women's health after CAYA cancer.

Mikiko Asai-Sato, Toshifumi Takahashi, Kuniaki Ota

|Nov 12, 2023
The Human Phenotype Ontology in 2024: phenotypes around the world.

Michael A Gargano, Nicolas Matentzoglu, Ben Coleman

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Frequent Collaborators

4 joint publications

Melissa A Haendel

4 joint publications

Christopher J Mungall

4 joint publications

Daniel Danis

4 joint publications

Peter N Robinson