Frédéric Torès

6.5k total citations
22 papers, 478 citations indexed

About

Frédéric Torès is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Frédéric Torès has authored 22 papers receiving a total of 478 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Cognitive Neuroscience. Recurrent topics in Frédéric Torès's work include Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Frédéric Torès is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Frédéric Torès collaborates with scholars based in France, Germany and United States. Frédéric Torès's co-authors include Jörg Hager, Jérôme Carayol, Daniel Vaiman, Julie Cocquet, Anne Philippi, Patrick Nitschké, Francis Rousseau, F. Rousseau, Karine Fontaine and Emmanuel Barillot and has published in prestigious journals such as Nature Communications, Bioinformatics and Gut.

In The Last Decade

Frédéric Torès

22 papers receiving 466 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Frédéric Torès France 13 260 209 110 59 44 22 478
Birgitte Bertelsen Denmark 13 244 0.9× 195 0.9× 56 0.5× 73 1.2× 56 1.3× 26 525
Sureni V. Mullegama United States 15 315 1.2× 308 1.5× 65 0.6× 34 0.6× 26 0.6× 27 564
Reenal Pattni United States 12 384 1.5× 335 1.6× 80 0.7× 157 2.7× 34 0.8× 20 732
Sara Loddo Italy 13 277 1.1× 402 1.9× 73 0.7× 19 0.3× 36 0.8× 39 639
Eva Rossier Germany 13 406 1.6× 392 1.9× 74 0.7× 26 0.4× 17 0.4× 21 644
Megan T. Cho United States 20 508 2.0× 462 2.2× 79 0.7× 32 0.5× 22 0.5× 27 838
Sylvie Jaillard France 16 435 1.7× 397 1.9× 31 0.3× 45 0.8× 51 1.2× 54 802
Ian Blumenthal United States 8 386 1.5× 406 1.9× 143 1.3× 36 0.6× 17 0.4× 9 663
J CLARK United States 8 127 0.5× 127 0.6× 115 1.0× 32 0.5× 31 0.7× 12 446
Tessa Walcher Germany 5 271 1.0× 87 0.4× 38 0.3× 49 0.8× 24 0.5× 5 430

Countries citing papers authored by Frédéric Torès

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Frédéric Torès

This figure shows the co-authorship network connecting the top 25 collaborators of Frédéric Torès. A scholar is included among the top collaborators of Frédéric Torès based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Frédéric Torès. Frédéric Torès is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Morinière, Vincent, Laurence Heidet, Olivier Gribouval, et al.. (2023). VNtyper enables accurate alignment-free genotyping of MUC1 coding VNTR using short-read sequencing data in autosomal dominant tubulointerstitial kidney disease. iScience. 26(7). 107171–107171. 12 indexed citations
2.
Kornobis, Étienne, Frédéric Torès, Patrick Nitschké, et al.. (2022). Complex regulation of Gephyrin splicing is a determinant of inhibitory postsynaptic diversity. Nature Communications. 13(1). 3507–3507. 13 indexed citations
3.
Ialy‐Radio, Côme, Robin C. Friedman, Christophe Battail, et al.. (2020). Battle of the Sex Chromosomes: Competition between X and Y Chromosome-Encoded Proteins for Partner Interaction and Chromatin Occupancy Drives Multicopy Gene Expression and Evolution in Muroid Rodents. Molecular Biology and Evolution. 37(12). 3453–3468. 21 indexed citations
4.
Cagnard, Nicolas, Marine Gil, Fernando E. Sepulveda, et al.. (2018). Tetratricopeptide repeat domain 7A is a nuclear factor that modulates transcription and chromatin structure. Cell Discovery. 4(1). 61–61. 11 indexed citations
5.
Steffann, Julie, Aurore Pouliet, Christine Bole, et al.. (2017). No correlation between mtDNA amount and methylation levels at the CpG island of POLG exon 2 in wild-type and mutant human differentiated cells. Journal of Medical Genetics. 54(5). 324–329. 4 indexed citations
6.
Ialy‐Radio, Côme, Tatiana Soboleva, Frédéric Torès, et al.. (2017). SLY regulates genes involved in chromatin remodeling and interacts with TBL1XR1 during sperm differentiation. Cell Death and Differentiation. 24(6). 1029–1044. 33 indexed citations
7.
Vaiman, Daniel, et al.. (2016). Expression and epigenomic landscape of the sex chromosomes in mouse post-meiotic male germ cells. Epigenetics & Chromatin. 9(1). 47–47. 25 indexed citations
8.
Toubiana, Julie, Emilie Courtine, Frédéric Torès, et al.. (2016). Association of REL polymorphisms and outcome of patients with septic shock. Annals of Intensive Care. 6(1). 28–28. 4 indexed citations
9.
Gougèlet, Angélique, Chiara Sartor, Laura Bachelot, et al.. (2015). Antitumour activity of an inhibitor of miR-34a in liver cancer with β-catenin-mutations. Gut. 65(6). 1024–1034. 52 indexed citations
10.
Jeanpierre, Marc, G. Macé, Mélanie Parisot, et al.. (2011). RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects. Journal of Medical Genetics. 48(7). 497–504. 37 indexed citations
11.
Carayol, Jérôme, Roberto Sacco, Frédéric Torès, et al.. (2011). Converging Evidence for an Association of ATP2B2 Allelic Variants with Autism in Male Subjects. Biological Psychiatry. 70(9). 880–887. 42 indexed citations
12.
Carayol, Jérôme, Frédéric Torès, Inke R. König, Jörg Hager, & Andreas Ziegler. (2010). Evaluating diagnostic accuracy of genetic profiles in affected offspring families. Statistics in Medicine. 29(22). 2359–2368. 12 indexed citations
13.
Spielmann, Nadine, David M. Mutch, F. Rousseau, et al.. (2008). Cathepsin S genotypes are associated with Apo‐A1 and HDL‐cholesterol in lean and obese French populations. Clinical Genetics. 74(2). 155–163. 8 indexed citations
14.
Maussion, Gilles, Jérôme Carayol, Aude-Marie Lepagnol-Bestel, et al.. (2008). Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism. Human Molecular Genetics. 17(16). 2541–2551. 58 indexed citations
15.
Philippi, Anne, Frédéric Torès, Jérôme Carayol, et al.. (2007). Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis. BMC Medical Genetics. 8(1). 74–74. 30 indexed citations
16.
Bertrais, Sandrine, Vincent Frochot, Michèle Guerre-Millo, et al.. (2007). Promoter adiponectin polymorphisms and waist/hip ratio variation in a prospective French adults study. International Journal of Obesity. 32(4). 669–675. 24 indexed citations
17.
Carayol, Jérôme, Anne Philippi, & Frédéric Torès. (2006). Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment. Genetic Epidemiology. 30(8). 666–676. 3 indexed citations
18.
Philippi, Anne, Frédéric Torès, Pierre Lindenbaum, et al.. (2005). Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism. Molecular Psychiatry. 10(10). 950–960. 53 indexed citations
19.
Torès, Frédéric & Emmanuel Barillot. (2001). The art of pedigree drawing: algorithmic aspects. Bioinformatics. 17(2). 174–179. 13 indexed citations
20.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Birgitte Bertelsen Breakdown of academic impact, for papers by Sureni V. Mullegama Breakdown of academic impact, for papers by Reenal Pattni Breakdown of academic impact, for papers by Sara Loddo Breakdown of academic impact, for papers by Eva Rossier Breakdown of academic impact, for papers by Megan T. Cho Breakdown of academic impact, for papers by Sylvie Jaillard Breakdown of academic impact, for papers by Ian Blumenthal Breakdown of academic impact, for papers by J CLARK Breakdown of academic impact, for papers by Tessa Walcher
Rankless by CCL
2026