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

PloS one, 2022-03, Vol.17 (3), p.e0265847-e0265847

2022

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

Journal of medical Internet research, 2022-04, Vol.24 (4), p.e33167-e33167

2022

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Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps

Nature medicine, 2021-11, Vol.27 (11), p.1876-1884

2021

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A proposal on the first Japanese practical guidance for the return of individual genomic results in research settings

Journal of human genetics, 2020-03, Vol.65 (3), p.251-261

2020

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Access, autonomy, and affordability: ethical and human rights issues surrounding multigene panel testing for cancer in Japan and Switzerland

Frontiers in genetics, 2024, Vol.15, p.1343720-1343720

2024

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Public reactions to direct-to-consumer genetic health tests: A comparison across the US, UK, Japan and Australia

European journal of human genetics : EJHG, 2020-03, Vol.28 (3), p.339-348

2020

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

Frontiers in genetics, 2021-04, Vol.12, p.646177-646177

2021

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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, 2022-05, Vol.16 (1), p.16-16, Article 16

2022

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High-resolution characterization of a hepatocellular carcinoma genome

Nature genetics, 2011-05, Vol.43 (5), p.464-469

2011

Volltextzugriff (PDF)

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

Frontiers in genetics, 2018-06, Vol.9, p.167-167

2018

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

Frontiers in public health, 2022-07, Vol.10, p.915438-915438

2022

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Ethical, legal and social implications of human genome studies in radiation research: a workshop report for studies on atomic bomb survivors at the Radiation Effects Research Foundation

Journal of radiation research, 2021-07, Vol.62 (4), p.656-661

2021

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

Frontiers in digital health, 2023-09, Vol.5, p.1229308-1229308

2023

Volltextzugriff (PDF)

The inclusion of genomic data in the 2015 revision of Japan's Protection of Personal Information Act: protection of wider range of genomic data as our next challenge

Journal of human genetics, 2018-04, Vol.63 (4), p.537-538

2018

Volltextzugriff (PDF)

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

Asian bioethics review, 2022-04, Vol.14 (2), p.115-131

2022

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Genetic discrimination: introducing the Asian perspective to the debate

Npj genomic medicine, 2021-07, Vol.6 (1), p.54-8, Article 54

2021

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Consent insufficient for data release

Science (American Association for the Advancement of Science), 2019-05, Vol.364 (6439), p.445-446

2019

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Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era

BMC medical ethics, 2016-07, Vol.17 (1), p.39-39, Article 39

2016

Volltextzugriff (PDF)

Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate

PLoS biology, 2013-11, Vol.11 (11), p.e1001699-e1001699

2013

Volltextzugriff (PDF)

Public attitudes in Japan toward participation in whole genome sequencing studies

Human genomics, 2018-04, Vol.12 (1), p.21-21, Article 21

2018

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Including all voices in international data-sharing governance

Human genomics, 2018-03, Vol.12 (1), p.13-13, Article 13

2018

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Machine Learning and Ethics in Plastic Surgery

Plastic and reconstructive surgery. Global open, 2019-03, Vol.7 (3), p.e2162-e2162

2019

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

Frontiers in genetics, 2017-07, Vol.8, p.99-99

2017

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Regulatory Impacts on Stem Cell Research in Japan

Cell stem cell, 2010-05, Vol.6 (5), p.415-418

2010

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ELSI 2.0 for Genomics and Society

Science (American Association for the Advancement of Science), 2012-05, Vol.336 (6082), p.673-674

2012

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

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

Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps

A proposal on the first Japanese practical guidance for the return of individual genomic results in research settings

Access, autonomy, and affordability: ethical and human rights issues surrounding multigene panel testing for cancer in Japan and Switzerland

Public reactions to direct-to-consumer genetic health tests: A comparison across the US, UK, Japan and Australia

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

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

High-resolution characterization of a hepatocellular carcinoma genome

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

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

Ethical, legal and social implications of human genome studies in radiation research: a workshop report for studies on atomic bomb survivors at the Radiation Effects Research Foundation

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

The inclusion of genomic data in the 2015 revision of Japan's Protection of Personal Information Act: protection of wider range of genomic data as our next challenge

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

Genetic discrimination: introducing the Asian perspective to the debate

Consent insufficient for data release

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era

Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate

Public attitudes in Japan toward participation in whole genome sequencing studies

Including all voices in international data-sharing governance

Machine Learning and Ethics in Plastic Surgery

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

Regulatory Impacts on Stem Cell Research in Japan

ELSI 2.0 for Genomics and Society

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