Frédéric Torès
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetic Associations and Epidemiology 3
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- Genomics and Chromatin Dynamics 3
- Co-authors
- Jörg Hager (9 shared papers)Jérôme Carayol (6 shared papers)Julie Cocquet (3 shared papers)Patrick Nitschké (5 shared papers)Anne Philippi (5 shared papers)Daniel Vaiman (3 shared papers)F. Rousseau (4 shared papers)Karine Fontaine (3 shared papers)
- Journals
- Genetic Epidemiology (2 papers)Journal of Medical Genetics (2 papers)The American Journal of Human Genetics (2 papers)Nature Communications (1 paper)Molecular Biology and Evolution (1 paper)
- Partner nations
- FranceGermanyUnited States
In The Last Decade
Frédéric Torès
24 papers receiving 543 citations
Peers
Comparison fields: 5 of 87
- Genetics 197
- Cognitive Neuroscience 104
- Aging 8
- Urology 25
- Molecular Biology 282
Countries citing papers authored by Frédéric Torès
This map shows the geographic impact of Frédéric Torès'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 Frédéric Torès with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Frédéric Torès more than expected).
Fields of papers citing papers by Frédéric Torès
This network shows the impact of papers produced by Frédéric Torès. 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 Frédéric Torès. The network helps show where Frédéric Torès may publish in the future.
Co-authors
The 25 scholars most cited alongside Frédéric Torès, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 63 | |
| 2 | 2008 | 59 | |
| 3 | 2005 | 53 | |
| 4 | 2015 | 52 | |
| 5 | 2011 | 43 | |
| 6 | 2011 | 38 | |
| 7 | 2017 | 35 | |
| 8 | 2007 | 31 | |
| 9 | 2016 | 26 | |
| 10 | 2007 | 24 | |
| 11 | 2020 | 21 | |
| 12 | 2023 | 16 | |
| 13 | 2010 | 14 | |
| 14 | 2022 | 14 | |
| 15 | 2001 | 13 | |
| 16 | 2010 | 12 | |
| 17 | 2018 | 11 | |
| 18 | 2008 | 9 | |
| 19 | 2009 | 6 | |
| 20 | 2016 | 4 |
About Frédéric Torès
Frédéric Torès is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Nephrology and Plant Science, having authored 24 papers that have together received 555 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Autism Spectrum Disorder Research (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genomics and Chromatin Dynamics (3 papers), Genetic Associations and Epidemiology (3 papers), Chromosomal and Genetic Variations (2 papers) and Renal Diseases and Glomerulopathies (2 papers). The work is most often cited by research in Genetics (197 citations), Cognitive Neuroscience (104 citations), Aging (8 citations), Urology (25 citations) and Molecular Biology (282 citations). Frédéric Torès has collaborated with scholars based in France, Germany and United States. Frequent co-authors include Jörg Hager, Jérôme Carayol, Julie Cocquet, Patrick Nitschké, Anne Philippi, Daniel Vaiman, F. Rousseau, Karine Fontaine, Francis Rousseau and Emmanuel Barillot. Their work appears in journals such as Genetic Epidemiology, Journal of Medical Genetics, The American Journal of Human Genetics, Nature Communications and Molecular Biology and Evolution.
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.