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J-GLOBAL ID:200901080804306732 Update date: Jan. 28, 2025

Yamamoto Anne Beverley

ヤマモト アン ベバリー | Yamamoto Anne Beverley
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Papers (129)

  • Michihiro Hide, Miwa Kishimoto, Ippei Kotera, Akinori Oh, Yoichi Inoue, Beverley Anne Yamamoto, Shinichi Noto. Analysis of disease burden in patients with hereditary angioedema from Japan by patient-reported outcomes. The Journal of Dermatology. 2024
  • Jane Kaye, Nisha Shah, Atsushi Kogetsu, Sarah Coy, Amelia Katirai, Machie Kuroda, Yan Li, Kazuto Kato, Beverley Anne Yamamoto. Moving beyond Technical Issues to Stakeholder Involvement: Key Areas for Consideration in the Development of Human-Centred and Trusted AI in Healthcare. Asian Bioethics Review. 2024
  • Karen L. Woolley, Simon R. Stones, Richard Stephens, Trishna Bharadia, Beverley Yamamoto, Jan Geissler, Bella Yang, Jacqui Oliver, Amanda Boughey, Catherine Elliott, et al. Patient authorship of medical research publications: An evolution, revolution, and solution?. Learned Publishing. 2024
  • Ming Li, Ariunaa Enkhtur, Fei Cheng, Beverley Anne Yamamoto. Ethical implications of ChatGPT in higher education. Journal of Interdisciplinary Studies in Education. 2024. 13. 1. 55-68
  • 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
  • Sinai Harel, Beverley Anne Yamamoto. Comprehensive horizons: examining Japan’s national and regional sexuality education curricula. Sex Education. 2024. 1-18
  • 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
  • Amelia Katirai, Beverley Anne Yamamoto, Atsushi Kogetsu, Kazuto Kato. Perspectives on artificial intelligence in healthcare from a Patient and Public Involvement Panel in Japan: an exploratory study. Frontiers in Digital Health. 2023
  • Beverley Yamamoto, Daisuke Honda, Isao Ohsawa, Kazumasa Iwamoto, Takahiko Horiuchi, Atsushi Fukunaga, Junichi Maehara, Kouhei Yamashita, Michihiro Hide. Burden of illness seen in hereditary angioedema in Japanese patients: Results from a patient reported outcome survey. Intractable & Rare Diseases Research. 2023. 12. 1. 35-44
  • Amelia Katirai, Atsushi Kogetsu, Kazuto Kato, Beverley Yamamoto. Patient involvement in priority-setting for medical research: A mini review of initiatives in the rare disease field. Frontiers in Public Health. 2022. 10
  • Kate Nakasato, Beverley Anne Yamamoto, Kazuto Kato. Evaluating standards for 'serious' disease for preimplantation genetic testing: a multi-case study on regulatory frameworks in Japan, the UK, and Western Australia. Human genomics. 2022. 16. 1. 16-16
  • Rie Ogasawara, Hiroshi Yamanaka, Jun Kobayashi, Sachi Tomokawa, Elli Sugita, Takanori Hirano, Mika Kigawa, Akihiro Nishio, Takeshi Akiyama, Eun Woo Nam, et al. Status of School Health Programs in Asia: National Policy and Implementation. Pediatrics International. 2022. 64. 1. e15146
  • Kazumasa Iwamoto, Beverley Yamamoto, Isao Ohsawa, Daisuke Honda, Takahiko Horiuchi, Akira Tanaka, Atsushi Fukunaga, Junichi Maehara, Kouhei Yamashita, Tomoyuki Akita, et al. The diagnosis and treatment of hereditary angioedema patients in Japan: A patient reported outcome survey. Allergology International. 2021. 70. 2. 235-243
  • 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
  • Kate Nakasato, Beverley Anne Yamamoto, Kazuto Kato. Defining ‘Serious’ Disease for PGT: Standards and regulatory frameworks in Japan, the UK, and Western Australia. 2021. 66
  • Kazumasa Iwamoto, Beverley Yamamoto, Isao Ohsawa, Daisuke Honda, Takahiko Horiuchi, Akira Tanaka, Atsushi Fukunaga, Junichi Maehara, Kouhei Yamashita, Tomoyuki Akita, et al. The diagnosis and treatment of hereditary angioedema patients in Japan: A patient reported outcome survey. Allergology International. 2020. 70. 2. 235-243
  • Nao Hamakawa, Rumiko Nakano, Atsushi Kogetsu, Victoria Coathup, Jane Kaye, Beverley Anne Yamamoto, Kazuto Kato. Landscape of Participant-Centric Initiatives for Medical Research in the United States, the United Kingdom, and Japan: Scoping Review. Journal of Medical Internet Research. 2020. 22. 8. e16441-e16441
  • Lauri Arnstein, Anne Clare Wadsworth, Beverley Anne Yamamoto, Beverley Anne Yamamoto, Richard Stephens, Kawaldip Sehmi, Rachel Jones, Arabella Sargent, Thomas Gegeny, Karen L. Woolley. Patient involvement in preparing health research peer-reviewed publications or results summaries: A systematic review and evidence-based recommendations. Research Involvement and Engagement. 2020. 6. 1
  • Beverley Yamamoto, Hiroshi Yamanaka, Yumi Kimura, Gergely Mohácsi, Rie Ogasawara. Social design for health: Ontological vulnerability, life course and planetary health. Humanistic futures of learning: Perspectives from UNESCO Chairs and UNITWIN Networks. 2020. 91-94
  • Megan Prictor, Megan A. Lewis, Ainsley J. Newson, Matilda Haas, Sachiko Baba, Hannah Kim, Minori Kokado, Jusaku Minari, Fruzsina Molnár-Gábor, Beverley Yamamoto, et al. Dynamic Consent: An Evaluation and Reporting Framework. Journal of Empirical Research on Human Research Ethics. 2019. 1-12

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