藤田医科大学 · 医学部 / 医学研究科 · 助教

研究关键词hereditary cancer・genetic counseling・large language models・copy number variation・liquid biopsy・neurofibromatosis type 1・homologous recombination deficiency・PARP inhibitors

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• Barriers and facilitators for online genetic care for hereditary cancer in Japan: findings from surveys of both clients and medical professionals.2026
• Evaluating and Enhancing Japanese Large Language Models for Genetic Counseling Support: Comparative Study of Domain Adaptation and the Development of an Expert-Evaluated Dataset.2025
• Genotypes and phenotypes of neurofibromatosis type 1 patients in Japan: A Hereditary Tumor Cohort Study.2024
• Copy number variant detection using next-generation sequencing in EYS-associated retinitis pigmentosa.2024

• AIを用いた遺伝性腫瘍のリスク評価システムの開発

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