Stéphane Bourgeois
Impact in
- Pharmacology top 0.5%
- Pharmacogenetics and Drug Metabolism
- Genetics top 10%
- Forensic and Genetic Research
- Genetic Associations and Epidemiology
- Race, Genetics, and Society
Papers in
- Genetics 10
- Forensic and Genetic Research 5
- Genetic Associations and Epidemiology 4
- Race, Genetics, and Society 3
- Genetic diversity and population structure 3
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- Pharmacogenetics and Drug Metabolism 6
- Co-authors
- Damian Labuda (8 shared papers)Panos Deloukas (6 shared papers)Mia Wadelius (4 shared papers)Fumihiko Takeuchi (1 shared paper)Jonatan D. Lindh (1 shared paper)Niclas Eriksson (1 shared paper)William McLaren (1 shared paper)Vasudev Kumanduri (1 shared paper)
- Journals
- Annals of Human Genetics (2 papers)Genome Medicine (2 papers)American Journal of Physical Anthropology (1 paper)Pharmacogenomics (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomCanadaUnited States
In The Last Decade
Stéphane Bourgeois
18 papers receiving 1.1k citations
Stéphane Bourgeois's Hit Papers
Peers
Comparison fields: 5 of 117
- Pharmacology 465
- Genetics 314
- Biochemistry 77
- Endocrinology, Diabetes and Metabolism 163
- Statistics and Probability 53
Countries citing papers authored by Stéphane Bourgeois
This map shows the geographic impact of Stéphane Bourgeois'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 Stéphane Bourgeois with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stéphane Bourgeois more than expected).
Fields of papers citing papers by Stéphane Bourgeois
This network shows the impact of papers produced by Stéphane Bourgeois. 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 Stéphane Bourgeois. The network helps show where Stéphane Bourgeois may publish in the future.
Co-authors
The 25 scholars most cited alongside Stéphane Bourgeois, 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 | A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose Hit paper breakdown → | 2009 | 475 |
| 2 | 2006 | 175 | |
| 3 | 1996 | 67 | |
| 4 | 2016 | 42 | |
| 5 | 2005 | 41 | |
| 6 | 2011 | 34 | |
| 7 | 2013 | 31 | |
| 8 | 2015 | 30 | |
| 9 | 2003 | 29 | |
| 10 | 2012 | 26 | |
| 11 | 2005 | 25 | |
| 12 | 2005 | 23 | |
| 13 | 2017 | 20 | |
| 14 | 2003 | 17 | |
| 15 | 2020 | 13 | |
| 16 | 2009 | 13 | |
| 17 | 2017 | 8 | |
| 18 | 2021 | 5 |
About Stéphane Bourgeois
Stéphane Bourgeois is a scholar working on Genetics, Pharmacology, Molecular Biology, Cellular and Molecular Neuroscience and Surgery, having authored 18 papers that have together received 1.1k indexed citations. Recurring topics across this work include Pharmacogenetics and Drug Metabolism (6 papers), Forensic and Genetic Research (5 papers), Genetic Associations and Epidemiology (4 papers), Race, Genetics, and Society (3 papers), Genetic diversity and population structure (3 papers), Hormonal Regulation and Hypertension (2 papers), African history and culture analysis (2 papers) and Hereditary Neurological Disorders (1 paper). The work is most often cited by research in Pharmacology (465 citations), Genetics (314 citations), Biochemistry (77 citations), Endocrinology, Diabetes and Metabolism (163 citations) and Statistics and Probability (53 citations). Stéphane Bourgeois has collaborated with scholars based in United Kingdom, Canada and United States. Frequent co-authors include Damian Labuda, Panos Deloukas, Mia Wadelius, Fumihiko Takeuchi, Jonatan D. Lindh, Niclas Eriksson, William McLaren, Vasudev Kumanduri, Lennart Holm and Nicole Soranzo. Their work appears in journals such as Annals of Human Genetics, Genome Medicine, American Journal of Physical Anthropology, Pharmacogenomics and European Journal of Human 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.