Daniel Vincent
Impact in
- Genetics top 0.2%
- Genetic Associations and Epidemiology
- BRCA gene mutations in cancer
- Cancer Research top 2%
- Breast Cancer Treatment Studies
Papers in
- Genetics 31
- Genetic Associations and Epidemiology 26
- BRCA gene mutations in cancer 20
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- Ovarian cancer diagnosis and treatment 3
- Co-authors
- Guillaume Bourque (1 shared paper)Denis Roy (1 shared paper)François Lefebvre (1 shared paper)Pierre-Éric Lutz (1 shared paper)Jeffrey A. Gross (1 shared paper)Gustavo Turecki (1 shared paper)François Bacot (1 shared paper)Susan G. Stanton (1 shared paper)
- Journals
- Nature Genetics (8 papers)Human Molecular Genetics (4 papers)Nature Communications (3 papers)The American Journal of Human Genetics (3 papers)PLoS Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Daniel Vincent
39 papers receiving 9.4k citations
Daniel Vincent's Hit Papers
Peers
Comparison fields: 5 of 130
- Genetics 5.9k
- Cancer Research 870
- Reproductive Medicine 439
- Oncology 753
- Pulmonary and Respiratory Medicine 751
Countries citing papers authored by Daniel Vincent
This map shows the geographic impact of Daniel Vincent'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 Daniel Vincent with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Vincent more than expected).
Fields of papers citing papers by Daniel Vincent
This network shows the impact of papers produced by Daniel Vincent. 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 Daniel Vincent. The network helps show where Daniel Vincent may publish in the future.
Co-authors
The 13 scholars most cited alongside Daniel Vincent, 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 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A genome-wide association study identifies novel risk loci for type 2 diabetes Hit paper breakdown → | 2007 | 2436 |
| 2 | Association analysis identifies 65 new breast cancer risk loci Hit paper breakdown → | 2017 | 1040 |
| 3 | Large-scale genotyping identifies 41 new loci associated with breast cancer risk Hit paper breakdown → | 2013 | 913 |
| 4 | Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer Hit paper breakdown → | 2015 | 489 |
| 5 | Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer Hit paper breakdown → | 2013 | 468 |
| 6 | Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array Hit paper breakdown → | 2013 | 463 |
| 7 | Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants Hit paper breakdown → | 2015 | 450 |
| 8 | 2013 | 349 | |
| 9 | 2013 | 331 | |
| 10 | Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer Hit paper breakdown → | 2017 | 306 |
| 11 | 2013 | 299 | |
| 12 | 2016 | 269 | |
| 13 | 2013 | 177 | |
| 14 | 2016 | 174 | |
| 15 | 2018 | 165 | |
| 16 | 2013 | 145 | |
| 17 | 2015 | 109 | |
| 18 | 2013 | 98 | |
| 19 | 2013 | 97 | |
| 20 | 2014 | 97 |
About Daniel Vincent
Daniel Vincent is a scholar working on Genetics, Reproductive Medicine, Sensory Systems, Pathology and Forensic Medicine and Oncology, having authored 39 papers that have together received 9.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (26 papers), BRCA gene mutations in cancer (20 papers), Ovarian cancer diagnosis and treatment (3 papers), Prostate Cancer Treatment and Research (2 papers), Breast Lesions and Carcinomas (2 papers), Cancer Risks and Factors (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Epigenetics and DNA Methylation (1 paper). The work is most often cited by research in Genetics (5.9k citations), Cancer Research (870 citations), Reproductive Medicine (439 citations), Oncology (753 citations) and Pulmonary and Respiratory Medicine (751 citations). Daniel Vincent has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Guillaume Bourque, Denis Roy, François Lefebvre, Pierre-Éric Lutz, Jeffrey A. Gross, Gustavo Turecki, François Bacot, Susan G. Stanton, Nicole M. Roslin and Pascale Marquis. Their work appears in journals such as Nature Genetics, Human Molecular Genetics, Nature Communications, The American Journal of Human Genetics and PLoS 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.