Francis Rousseau

2.6k total citations · 1 hit paper
21 papers, 1.5k citations indexed

About

Francis Rousseau is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Francis Rousseau has authored 21 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 8 papers in Cognitive Neuroscience. Recurrent topics in Francis Rousseau's work include Autism Spectrum Disorder Research (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Colorectal Cancer Treatments and Studies (5 papers). Francis Rousseau is often cited by papers focused on Autism Spectrum Disorder Research (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Colorectal Cancer Treatments and Studies (5 papers). Francis Rousseau collaborates with scholars based in France, United States and United Kingdom. Francis Rousseau's co-authors include Laurence Legeai‐Mallet, Anna Pelet, Jacky Bonaventure, P Maroteaux, Arnold Münnich, Jean‐Michel Rozet, Pierre Laurent‐Puig, Alexis Laurent, Jessica Zucman‐Rossi and Thomas Decaens and has published in prestigious journals such as Nature, Science and Nature Genetics.

In The Last Decade

Francis Rousseau

21 papers receiving 1.5k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

1994 689 citations Francis Rousseau, Jacky Bonaventure et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Francis Rousseau France	13	902	736	213	165	160	21	1.5k
Palma Finelli Italy	29	1.2k 1.4×	1.0k 1.4×	171 0.8×	42 0.3×	53 0.3×	95	2.2k
Marko Uutela Finland	11	998 1.1×	227 0.3×	237 1.1×	53 0.3×	173 1.1×	13	1.8k
Jacqueline Schoumans Sweden	29	1.2k 1.3×	1.6k 2.1×	193 0.9×	19 0.1×	162 1.0×	73	2.5k
Nessa Hawkins United States	16	971 1.1×	343 0.5×	150 0.7×	19 0.1×	50 0.3×	22	2.4k
Margherita Silengo Italy	29	2.0k 2.2×	1.7k 2.3×	177 0.8×	16 0.1×	146 0.9×	114	3.3k
Zunyi Zhang China	22	847 0.9×	217 0.3×	260 1.2×	115 0.7×	53 0.3×	58	1.3k
Nada Al Tassan Saudi Arabia	22	1.1k 1.2×	582 0.8×	496 2.3×	12 0.1×	137 0.9×	58	2.4k
Steven Y. Cheng China	19	1.4k 1.5×	309 0.4×	278 1.3×	13 0.1×	71 0.4×	46	1.7k
Yu Hou China	16	969 1.1×	183 0.2×	376 1.8×	21 0.1×	53 0.3×	32	1.8k
A. Moseley United States	5	834 0.9×	890 1.2×	80 0.4×	8 0.0×	68 0.4×	10	1.6k

Countries citing papers authored by Francis Rousseau

Since Specialization

Citations

This map shows the geographic impact of Francis Rousseau'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 Francis Rousseau with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Francis Rousseau more than expected).

Fields of papers citing papers by Francis Rousseau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Francis Rousseau. 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 Francis Rousseau. The network helps show where Francis Rousseau may publish in the future.

Co-authorship network of co-authors of Francis Rousseau

This figure shows the co-authorship network connecting the top 25 collaborators of Francis Rousseau. A scholar is included among the top collaborators of Francis Rousseau 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 Francis Rousseau. Francis Rousseau is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

David, Catherine, Karine Fontaine, Charles Marcaillou, et al.. (2018). Technical Validation of a Reverse-Transcription Quantitative Polymerase Chain Reaction In Vitro Diagnostic Test for the Determination of MiR-31-3p Expression Levels in Formalin-Fixed Paraffin-Embedded Metastatic Colorectal Cancer Tumor Specimens. Biomarker Insights. 13. 4203060573–4203060573. 10 indexed citations

Pugh, S., Raphaële Thiébaut, John Bridgewater, et al.. (2017). Association between miR-31-3p expression and cetuximab efficacy in patients with KRAS wild-type metastatic colorectal cancer: a post-hoc analysis of the New EPOC trial. Oncotarget. 8(55). 93856–93866. 33 indexed citations

Laurent‐Puig, Pierre, Volker Heinemann, Franck Bonnetain, et al.. (2016). MiR 31 3p as a predictive biomarker of cetuximab efficacy effect in metastatic colorectal cancer (mCRC) patients enrolled in FIRE-3 study.. Journal of Clinical Oncology. 34(15_suppl). 3516–3516. 9 indexed citations

Carayol, Jérôme, Gerard D. Schellenberg, Beth A. Dombroski, et al.. (2014). A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism. Frontiers in Genetics. 5. 33–33. 7 indexed citations

Gabriele, Stefano, Federica Lombardi, Roberto Sacco, et al.. (2014). The GLO1 C332 (Ala111) allele confers autism vulnerability: Family-based genetic association and functional correlates. Journal of Psychiatric Research. 59. 108–116. 18 indexed citations

Laurent‐Puig, Pierre, John Bridgewater, John Primrose, et al.. (2014). Mir-31-3p as a predictive biomarker of cetuximab effects in a post hoc analysis of new EPOC phase III trial.. Journal of Clinical Oncology. 32(15_suppl). 3523–3523. 2 indexed citations

Nault, Jean‐Charles, Aurélien de Reyniès, Augusto Villanueva, et al.. (2013). A Hepatocellular Carcinoma 5-Gene Score Associated With Survival of Patients After Liver Resection. Gastroenterology. 145(1). 176–187. 245 indexed citations

Edery, Patrick, Charles Marcaillou, Mourad Sahbatou, et al.. (2011). Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA. Science. 332(6026). 240–243. 159 indexed citations

Carayol, Jérôme, Gerard D. Schellenberg, Beth A. Dombroski, et al.. (2011). Autism risk assessment in siblings of affected children using sex-specific genetic scores. Molecular Autism. 2(1). 17–17. 17 indexed citations

10.

Dubern, B., Corneliu Hénégar, Lavinia Paternoster, et al.. (2011). Association between CST3 rs2424577 Polymorphism and Corpulence Related Phenotypes during Lifetime in Populations of European Ancestry. Obesity Facts. 4(2). 131–144. 3 indexed citations

11.

Rousseau, Francis, et al.. (2011). Territorial assemblages simulation for territorial intelligence. HAL (Le Centre pour la Communication Scientifique Directe). 2 indexed citations

12.

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

13.

Napolioni, Valerio, Federica Lombardi, Roberto Sacco, et al.. (2010). Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes. European Journal of Human Genetics. 19(3). 353–359. 39 indexed citations

14.

Brooks, Peter, Charles Marcaillou, Jean‐Paul Saraiva, et al.. (2009). Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta. BMC Genetics. 10(1). 16–16. 6 indexed citations

15.

Sacco, Roberto, Jörg Hager, Francis Rousseau, et al.. (2007). Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1. BMC Medical Genetics. 8(1). 11–11. 45 indexed citations

16.

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

17.

Cancel‐Tassin, Géraldine, Alain Latil, Francis Rousseau, et al.. (2003). Association Study of Polymorphisms in the Human Estrogen Receptor Alpha Gene and Prostate Cancer Risk. European Urology. 44(4). 487–490. 24 indexed citations

18.

Rousseau, Francis, Jacky Bonaventure, Laurence Legeai‐Mallet, et al.. (1996). Mutations of the Fibroblast Growth Factor Receptor-3 Gene in Achondroplasia. Hormone Research. 45(1-2). 108–110. 38 indexed citations

19.

Merrer, Martine Le, Francis Rousseau, Laurence Legeai‐Mallet, et al.. (1994). A gene for achondroplasia–hypochondroplasia maps to chromosome 4p. Nature Genetics. 6(3). 318–321. 89 indexed citations

20.

Rousseau, Francis, Jacky Bonaventure, Laurence Legeai‐Mallet, et al.. (1994). Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Nature. 371(6494). 252–254. 689 indexed citations breakdown →

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.

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