Yann Joly
Impact in
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- Ethics in Clinical Research
- Health Informatics top 5%
Papers in
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- Ethics in Clinical Research 68
- Biotechnology and Related Fields 12
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- Intellectual Property and Patents 20
- Co-authors
- Bartha Maria KnoppersJacques SimardIda Ngueng FezeFrancine DurocherEdward S. DoveCharles DuprasKatie M. SaulnierGabrielle Bertier
- Journals
- The Journal of Law Medicine & Ethics (10 papers)European Journal of Human Genetics (6 papers)Frontiers in Genetics (6 papers)Genome Medicine (5 papers)New Genetics and Society (5 papers)
- Partner nations
- CanadaUnited KingdomUnited States
In The Last Decade
Yann Joly
155 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 137
- Public Health, Environmental and Occupational Health 884
- Health Informatics 40
- Genetics 755
- Physiology 408
- Business and International Management 29
Countries citing papers authored by Yann Joly
This map shows the geographic impact of Yann Joly's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Yann Joly with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yann Joly more than expected).
Fields of papers citing papers by Yann Joly
This network shows the impact of papers produced by Yann Joly. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Yann Joly. The network helps show where Yann Joly may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Yann Joly, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2024 | 6 | |
| 3 | 2024 | 1 | |
| 4 | 2023 | 0 | |
| 5 | 2023 | 3 | |
| 6 | 2023 | 8 | |
| 7 | 2022 | 3 | |
| 8 | 2021 | 7 | |
| 9 | 2021 | 22 | |
| 10 | 2021 | 4 | |
| 11 | 2021 | 5 | |
| 12 | Erring in Law and in Fact: The Supreme Court of Canada’s Reference re Genetic Non-Discrimination Act | 2021 | 1 |
| 13 | 2021 | 24 | |
| 14 | THE CONTESTED FUTURES OF BIOBANKS AND INTELLECTUAL PROPERTY | 2020 | 0 |
| 15 | 2017 | 1 | |
| 16 | Protecting the Privacy of Canadians’ Health Information in the Cloud | 2016 | 5 |
| 17 | 2015 | 10 | |
| 18 | Approval of new pharmacogenomic tests: is the Canadian regulatory process adequate? | 2010 | 1 |
| 19 | Life Insurers' Access to Genetic Information: A Way out of the Stalemate? | 2006 | 1 |
| 20 | Genetics and life insurance in Canada: points to consider | 2003 | 6 |
About Yann Joly
Yann Joly is a scholar working on Public Health, Environmental and Occupational Health, Management of Technology and Innovation, Genetics, Reproductive Medicine and Physiology, having authored 171 papers that have together received 2.1k indexed citations. Recurring topics across this work include Ethics in Clinical Research (68 papers), Biomedical Ethics and Regulation (45 papers), BRCA gene mutations in cancer (28 papers), Intellectual Property and Patents (20 papers), Cancer Genomics and Diagnostics (14 papers), CRISPR and Genetic Engineering (13 papers), Genomics and Rare Diseases (12 papers) and Biotechnology and Related Fields (12 papers). The work is most often cited by research in Public Health, Environmental and Occupational Health (884 citations), Health Informatics (40 citations), Genetics (755 citations), Physiology (408 citations) and Business and International Management (29 citations). Yann Joly has collaborated with scholars based in Canada, United Kingdom and United States. Frequent co-authors include Bartha Maria Knoppers, Jacques Simard, Ida Ngueng Feze, Francine Durocher, Edward S. Dove, Charles Dupras, Katie M. Saulnier, Gabrielle Bertier, Stephanie O. M. Dyke and Gratien Dalpé. Their work appears in journals such as The Journal of Law Medicine & Ethics, European Journal of Human Genetics, Frontiers in Genetics, Genome Medicine and New Genetics and Society.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.