What should scientists do outside the laboratory? lessons on science communication from the Japanese genome research project

por Itoh, Machiko, Kato, Kazuto
Publicado 2005

Framework and Practical Guidance for the Ethical Use of Electronic Methods for Communication With Participants in Medical Research

por Kogetsu, Atsushi, Kato, Kazuto
Publicado 2022

Stakeholder Involvement in the Governance of Human Genome Editing in Japan

por Aikyo, Tatsuki, Kogetsu, Atsushi, Kato, Kazuto
Publicado 2023

Ethical considerations of research policy for personal genome analysis: the approach of the Genome Science Project in Japan

por Minari, Jusaku, Shirai, Tetsuya, Kato, Kazuto
Publicado 2014

Ethical acceptability of research on human-animal chimeric embryos: summary of opinions by the Japanese Expert Panel on Bioethics

por Mizuno, Hiroshi, Akutsu, Hidenori, Kato, Kazuto
Publicado 2015

Authentication of Patients and Participants in Health Information Exchange and Consent for Medical Research: A Key Step for Privacy Protection, Respect for Autonomy, and Trustworth...

por Kogetsu, Atsushi, Ogishima, Soichi, Kato, Kazuto
Publicado 2018

Machine Learning and Ethics in Plastic Surgery

por Koimizu, Jungen, Numajiri, Toshiaki, Kato, Kazuto
Publicado 2019

Institutional and Social Issues Surrounding Genetic Counselors in Japan: Current Challenges and Implications for the Global Community

por Aizawa, Yayoi, Watanabe, Atsushi, Kato, Kazuto
Publicado 2021

Why does it take so long for rare disease patients to get an accurate diagnosis?—A qualitative investigation of patient experiences of hereditary angioedema

por Isono, Moeko, Kokado, Minori, Kato, Kazuto
Publicado 2022

Evaluating standards for ‘serious’ disease for preimplantation genetic testing: a multi-case study on regulatory frameworks in Japan, the UK, and Western Australia

por Nakasato, Kate, Yamamoto, Beverley Anne, Kato, Kazuto
Publicado 2022

Ethical and Social Issues for Health Care Providers in the Intensive Care Unit during the Early Stages of the COVID-19 Pandemic in Japan: a Questionnaire Survey

por Seino, Yusuke, Aizawa, Yayoi, Kogetsu, Atsushi, Kato, Kazuto
Publicado 2021

Patient involvement in priority-setting for medical research: A mini review of initiatives in the rare disease field

por Katirai, Amelia, Kogetsu, Atsushi, Kato, Kazuto, Yamamoto, Beverley
Publicado 2022

Perspectives on artificial intelligence in healthcare from a Patient and Public Involvement Panel in Japan: an exploratory study

por Katirai, Amelia, Yamamoto, Beverley Anne, Kogetsu, Atsushi, Kato, Kazuto
Publicado 2023

The emerging need for family-centric initiatives for obtaining consent in personal genome research

por Minari, Jusaku, Teare, Harriet, Mitchell, Colin, Kaye, Jane, Kato, Kazuto
Publicado 2014

Social and Communicative Functions of Informed Consent Forms in East Asia and Beyond

por Yoshizawa, Go, Sasongko, Teguh H., Ho, Chih-Hsing, Kato, Kazuto
Publicado 2017

Public attitudes in Japan toward participation in whole genome sequencing studies

por Okita, Taketoshi, Ohashi, Noriko, Kabata, Daijiro, Shintani, Ayumi, Kato, Kazuto
Publicado 2018

Participant-Centric Initiatives and Medical Research: Scoping Review Protocol

por Coathup, Victoria, Hamakawa, Nao, Finlay, Teresa, Bell, Jessica, Kaye, Jane, Kato, Kazuto
Publicado 2017

Registered access: a ‘Triple-A' approach

por Dyke, Stephanie O M, Kirby, Emily, Shabani, Mahsa, Thorogood, Adrian, Kato, Kazuto, Knoppers, Bartha M
Publicado 2016

Landscape of Participant-Centric Initiatives for Medical Research in the United States, the United Kingdom, and Japan: Scoping Review

por Hamakawa, Nao, Nakano, Rumiko, Kogetsu, Atsushi, Coathup, Victoria, Kaye, Jane, Yamamoto, Beverley Anne, Kato, Kazuto
Publicado 2020

Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan

por Coathup, Victoria, Teare, Harriet J. A., Minari, Jusaku, Yoshizawa, Go, Kaye, Jane, Takahashi, Masanori P., Kato, Kazuto
Publicado 2016