Satoshi Morioke, Tatsuki Aikyo, Akio Tanaka, Daiki Matsubara, Ryo Saito, Kazumasa Iwamoto, Chisato Yamasaki, Atsushi Kogetsu, Nao Hamakawa, Moeko Isono, et al. Survey of hereditary angioedema episodes and quality of life impairment through a patient-participatory registry. Journal of Cutaneous Immunology and Allergy. 2024. 7
Atsushi Kogetsu, Moeko Isono, Tatsuki Aikyo, Junichi Furuta, Dai Goto, Nao Hamakawa, Michihiro Hide, Risa Hori, Noriko Ikeda, Keiko Inoi, et al. Enhancing evidence-informed policymaking in medicine and healthcare: stakeholder involvement in the Commons Project for rare diseases in Japan. Research involvement and engagement. 2023. 9. 1. 107-107
Jonathan Lawson, Moran N Cabili, Giselle Kerry, Tiffany Boughtwood, Adrian Thorogood, Pinar Alper, Sarion R Bowers, Rebecca R Boyles, Anthony J Brookes, Matthew Brush, et al. The Data Use Ontology to streamline responsible access to human biomedical datasets. Cell genomics. 2021. 1. 2. None
Heidi L Rehm, Angela J H Page, Lindsay Smith, Jeremy B Adams, Gil Alterovitz, Lawrence J Babb, Maxmillian P Barkley, Michael Baudis, Michael J S Beauvais, Tim Beck, et al. GA4GH: International policies and standards for data sharing across genomic research and healthcare. Cell genomics. 2021. 1. 2
Nao Hamakawa, Atsushi Kogetsu, Moeko Isono, Chisato Yamasaki, Shirou Manabe, Toshihiro Takeda, Kazumasa Iwamoto, Tomoya Kubota, Joe Barrett, Nathanael Gray, et al. The practice of active patient involvement in rare disease research using ICT: experiences and lessons from the RUDY JAPAN project. Research involvement and engagement. 2021. 7. 1. 9-9
