Florian Privé
Impact in
- Genetics top 2%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Genetic diversity and population structure
- Statistics and Probability top 5%
Papers in
- Genetics 21
- Genetic Associations and Epidemiology 20
- Genetic Mapping and Diversity in Plants and Animals 11
- Genetic and phenotypic traits in livestock 10
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- Epigenetics and DNA Methylation 3
- Bioinformatics and Genomic Networks 3
- Co-authors
- Bjarni J. Vilhjálmsson (17 shared papers)Michaël G. B. Blum (5 shared papers)Julyan Arbel (3 shared papers)Hugues Aschard (9 shared papers)Keurcien Luu (3 shared papers)Andrey Ziyatdinov (2 shared papers)Qianqian Zhang (1 shared paper)Doug Speed (1 shared paper)
- Journals
- Bioinformatics (6 papers)The American Journal of Human Genetics (4 papers)Nature Communications (3 papers)Human Genetics and Genomics Advances (2 papers)Nature Genetics (1 paper)
- Partner nations
- DenmarkUnited StatesFrance
In The Last Decade
Florian Privé
25 papers receiving 1.5k citations
Florian Privé's Hit Papers
Peers
Comparison fields: 5 of 128
- Genetics 1.0k
- Statistics and Probability 83
- Psychiatry and Mental health 92
- Molecular Biology 392
- Cancer Research 70
Countries citing papers authored by Florian Privé
This map shows the geographic impact of Florian Privé'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 Florian Privé with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Florian Privé more than expected).
Fields of papers citing papers by Florian Privé
This network shows the impact of papers produced by Florian Privé. 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 Florian Privé. The network helps show where Florian Privé may publish in the future.
Co-authors
The 25 scholars most cited alongside Florian Privé, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | LDpred2: better, faster, stronger Hit paper breakdown → | 2020 | 323 |
| 2 | 2018 | 188 | |
| 3 | 2020 | 162 | |
| 4 | Portability of 245 polygenic scores when derived from the UK Biobank and applied to 9 ancestry groups from the same cohort Hit paper breakdown → | 2022 | 135 |
| 5 | 2019 | 99 | |
| 6 | Polygenic scoring accuracy varies across the genetic ancestry continuum Hit paper breakdown → | 2023 | 90 |
| 7 | 2021 | 82 | |
| 8 | 2020 | 67 | |
| 9 | 2021 | 56 | |
| 10 | 2019 | 43 | |
| 11 | 2022 | 36 | |
| 12 | 2022 | 32 | |
| 13 | 2021 | 26 | |
| 14 | 2023 | 25 | |
| 15 | 2020 | 25 | |
| 16 | 2020 | 23 | |
| 17 | 2023 | 22 | |
| 18 | 2022 | 18 | |
| 19 | 2023 | 16 | |
| 20 | 2021 | 13 |
About Florian Privé
Florian Privé is a scholar working on Genetics, Molecular Biology, Health, Toxicology and Mutagenesis, Oncology and Epidemiology, having authored 27 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (20 papers), Genetic Mapping and Diversity in Plants and Animals (11 papers), Genetic and phenotypic traits in livestock (10 papers), Epigenetics and DNA Methylation (3 papers), Bioinformatics and Genomic Networks (3 papers), Health, Environment, Cognitive Aging (3 papers), Statistical Methods and Inference (2 papers) and Attention Deficit Hyperactivity Disorder (2 papers). The work is most often cited by research in Genetics (1.0k citations), Statistics and Probability (83 citations), Psychiatry and Mental health (92 citations), Molecular Biology (392 citations) and Cancer Research (70 citations). Florian Privé has collaborated with scholars based in Denmark, United States and France. Frequent co-authors include Bjarni J. Vilhjálmsson, Michaël G. B. Blum, Julyan Arbel, Hugues Aschard, Keurcien Luu, Andrey Ziyatdinov, Qianqian Zhang, Doug Speed, Bogdan Paşaniuc and Clive Hoggart. Their work appears in journals such as Bioinformatics, The American Journal of Human Genetics, Nature Communications, Human Genetics and Genomics Advances and Nature 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.