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List of works by Kazuto Kato

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

scientific article published on 23 December 2019

A review of the key issues associated with the commercialization of biobanks

scientific article (publication date: March 2014)

A second generation human haplotype map of over 3.1 million SNPs

scientific article

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.

scientific article published in June 2018

BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2

scientific article published on 26 December 2018

Consent insufficient for data release

scientific article published on 01 May 2019

Correction to: Ethical Perspectives of Japanese Engineers on Ambient Assisted Living Technologies: Semi-structured Interview

scientific article published on 10 July 2019

Debate on Germline Gene Editing

scientific article published in August 2016

ELSI practices in genomic research in East Asia: implications for research collaboration and public participation

scientific article

Establishing the International Genetic Discrimination Observatory

scientific article published on 23 March 2020

Ethical Perspectives of Japanese Engineers on Ambient Assisted Living Technologies: Semi-structured Interview

scientific article published on 10 July 2019

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

scientific article

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

scientific article published on 15 November 2021

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

scientific article

Ethical issues in personal genome research

scientific article published on March 1, 2013

Ethical issues of personal genome research ⬇️

scientific article published on 01 November 2011

GA4GH: International policies and standards for data sharing across genomic research and healthcare

scientific article published on 10 November 2021

Genome-wide detection and characterization of positive selection in human populations

scientific article

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

scientific article

High-resolution characterization of a hepatocellular carcinoma genome

scientific article

How should the legal framework for the protection of human genomic data be formulated?-Implications from the revision processes of the Act on the Protection of Personal Information (PPI Act).

scientific article published on 15 January 2015

Human genetic research, race, ethnicity and the labeling of populations: recommendations based on an interdisciplinary workshop in Japan.

scientific article published on 23 April 2014

ISSCR Guidelines for Stem Cell Research and Clinical Translation: The 2021 update

scientific article

Including all voices in international data-sharing governance

scientific article published on 7 March 2018

International network of cancer genome projects

scientific article

Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic.

scientific article published on 25 September 2017

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

scientific article published on 04 August 2020

Open science and community norms ⬇️

scientific article published in June 2012

Participant-Centric Initiatives and Medical Research: Scoping Review Protocol.

scientific article published on 12 December 2017

Public attitudes in Japan toward participation in whole genome sequencing studies.

scientific article published on 13 April 2018

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

scientific article published on 23 October 2019

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

scientific article (publication date: November 2013)

Registered access: a 'Triple-A' approach

scientific article

Registered access: authorizing data access

scientific article published on 2 August 2018

Research priorities. ELSI 2.0 for genomics and society

scientific article

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

scientific article published on 20 July 2017

Stem cell research policy and iPS cells

scientific article

The International Cancer Genome Consortium's evolving data-protection policies

scientific article published in June 2014

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

scientific article published on 17 December 2014

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

scientific article

The practice of active patient involvement in rare disease research using ICT: experiences and lessons from the RUDY JAPAN project

scientific article published on 01 February 2021

Toward better governance of human genomic data

scientific article published on 01 January 2021

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

scientific article

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

scientific article

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

scientific article published on 18 March 2022

iPS cells: mapping the policy issues

scientific article published on December 2009

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