Pascal Borry
Impact in
- Genetics top 0.5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
-
- Ethics in Clinical Research
Papers in
-
- Ethics in Clinical Research 72
- Genetics 88
- BRCA gene mutations in cancer 51
- Genomics and Rare Diseases 43
- Co-authors
- Heidi Howard (38 shared papers)Kris Dierickx (35 shared papers)Mahsa Shabani (27 shared papers)Paul Schotsmans (15 shared papers)Danya F. Vears (39 shared papers)Martina C. Cornel (20 shared papers)Karine Sénécal (16 shared papers)Bartha Maria Knoppers (18 shared papers)
- Journals
- European Journal of Human Genetics (30 papers)Genetics in Medicine (9 papers)Accountability in Research (6 papers)PLoS ONE (5 papers)Nature Reviews Genetics (5 papers)
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
Pascal Borry
237 papers receiving 5.0k citations
Peers
Comparison fields: 5 of 160
- Genetics 2.1k
- Public Health, Environmental and Occupational Health 1.6k
- Pediatrics, Perinatology and Child Health 878
- Health Informatics 65
- Physiology 592
Countries citing papers authored by Pascal Borry
This map shows the geographic impact of Pascal Borry'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 Pascal Borry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pascal Borry more than expected).
Fields of papers citing papers by Pascal Borry
This network shows the impact of papers produced by Pascal Borry. 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 Pascal Borry. The network helps show where Pascal Borry may publish in the future.
Co-authors
The 25 scholars most cited alongside Pascal Borry, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 251 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. | 2013 | 272 |
| 2 | 2013 | 259 | |
| 3 | 2016 | 215 | |
| 4 | 2006 | 173 | |
| 5 | 2005 | 150 | |
| 6 | 2009 | 138 | |
| 7 | 2010 | 85 | |
| 8 | 2015 | 83 | |
| 9 | 2017 | 83 | |
| 10 | 2012 | 78 | |
| 11 | 2017 | 74 | |
| 12 | 2005 | 74 | |
| 13 | 2014 | 73 | |
| 14 | 2017 | 70 | |
| 15 | 2014 | 67 | |
| 16 | 2011 | 66 | |
| 17 | 2004 | 64 | |
| 18 | 2011 | 63 | |
| 19 | 2006 | 56 | |
| 20 | 2012 | 55 |
About Pascal Borry
Pascal Borry is a scholar working on Public Health, Environmental and Occupational Health, Genetics, Pediatrics, Perinatology and Child Health, Physiology and General Health Professions, having authored 251 papers that have together received 5.2k indexed citations. Recurring topics across this work include Ethics in Clinical Research (72 papers), BRCA gene mutations in cancer (51 papers), Genomics and Rare Diseases (43 papers), Biomedical Ethics and Regulation (39 papers), Ethics and Legal Issues in Pediatric Healthcare (28 papers), Cystic Fibrosis Research Advances (23 papers), Prenatal Screening and Diagnostics (23 papers) and Ethics in medical practice (18 papers). The work is most often cited by research in Genetics (2.1k citations), Public Health, Environmental and Occupational Health (1.6k citations), Pediatrics, Perinatology and Child Health (878 citations), Health Informatics (65 citations) and Physiology (592 citations). Pascal Borry has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Heidi Howard, Kris Dierickx, Mahsa Shabani, Paul Schotsmans, Danya F. Vears, Martina C. Cornel, Karine Sénécal, Bartha Maria Knoppers, Herman Nys and Carla van El. Their work appears in journals such as European Journal of Human Genetics, Genetics in Medicine, Accountability in Research, PLoS ONE and Nature Reviews Genetics.
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.