Cécile Fourrage

1.2k total citations
12 papers, 145 citations indexed

About

Cécile Fourrage is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Cécile Fourrage has authored 12 papers receiving a total of 145 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Cécile Fourrage's work include Cellular transport and secretion (2 papers), Microtubule and mitosis dynamics (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Cécile Fourrage is often cited by papers focused on Cellular transport and secretion (2 papers), Microtubule and mitosis dynamics (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Cécile Fourrage collaborates with scholars based in France, Switzerland and Netherlands. Cécile Fourrage's co-authors include Evelyn Houliston, Karl Swann, Anthony K. Campbell, Sandra Chevalier, Patrick Nitschké, Mathieu Anheim, Christine Tranchant, Solveig Montaut, Bénédicte Gérard and Tristan Stemmelen and has published in prestigious journals such as PLoS ONE, Journal of Cell Science and Nephrology Dialysis Transplantation.

In The Last Decade

Cécile Fourrage

11 papers receiving 145 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cécile Fourrage France 7 73 50 33 32 19 12 145
Stephen Treaster United States 8 181 2.5× 33 0.7× 33 1.0× 16 0.5× 7 0.4× 9 344
Lorida Llaci United States 8 95 1.3× 25 0.5× 12 0.4× 13 0.4× 13 0.7× 12 170
Mélanie Quilès France 4 152 2.1× 33 0.7× 65 2.0× 28 0.9× 6 0.3× 6 192
Wanxiang Jiang China 7 133 1.8× 48 1.0× 12 0.4× 21 0.7× 5 0.3× 14 196
Kirsi Alakurtti Finland 7 88 1.2× 129 2.6× 17 0.5× 12 0.4× 24 1.3× 9 233
Marisol Mirabelli-Badenier Italy 10 104 1.4× 100 2.0× 14 0.4× 29 0.9× 7 0.4× 13 238
Risa Okada Japan 10 88 1.2× 44 0.9× 33 1.0× 9 0.3× 7 0.4× 19 193
Raffaele Gerlini Germany 10 116 1.6× 29 0.6× 14 0.4× 15 0.5× 6 0.3× 15 210
Christopher Schröder Germany 8 96 1.3× 38 0.8× 21 0.6× 30 0.9× 5 0.3× 15 180
Jan-Willem R. Pott Netherlands 8 293 4.0× 71 1.4× 28 0.8× 38 1.2× 8 0.4× 9 336

Countries citing papers authored by Cécile Fourrage

Since Specialization
Citations

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

Fields of papers citing papers by Cécile Fourrage

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Fourrage

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

All Works

12 of 12 papers shown
1.
Fusaro, Mathieu, Laura Barnabei, Quentin Riller, et al.. (2024). A large deletion in a non-coding regulatory region leads to NFKB1 haploinsufficiency in two adult siblings. Clinical Immunology. 261. 110165–110165. 1 indexed citations
2.
Stos, Bertrand, Patrick Nitschké, Cécile Fourrage, et al.. (2023). Diagnosis of Menke‐Hennekam syndrome by prenatal whole exome sequencing and review of prenatal signs. Molecular Genetics & Genomic Medicine. 11(9). e2219–e2219. 1 indexed citations
3.
Stoupa, Athanasia, Dulanjalee Kariyawasam, Gabor Szinnai, et al.. (2021). High Diagnostic Yield of Targeted Next-Generation Sequencing in a Cohort of Patients With Congenital Hypothyroidism Due to Dyshormonogenesis. Frontiers in Endocrinology. 11. 545339–545339. 17 indexed citations
4.
Perrault, Isabelle, Sylvain Hanein, Xavier Gérard, et al.. (2021). Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic RPGRIP1 Pathologic Variant in the French Leber Congenital Amaurosis Cohort. Genes. 12(2). 287–287. 4 indexed citations
5.
Montaut, Solveig, Christine Tranchant, Nathalie Drouot, et al.. (2018). Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement Disorders. JAMA Neurology. 75(10). 1234–1234. 36 indexed citations
6.
Gribouval, Olivier, Olivia Boyer, Bertrand Knebelmann, et al.. (2018). APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries. Nephrology Dialysis Transplantation. 34(11). 1885–1893. 10 indexed citations
7.
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
8.
Cavallin, Mara, Emilia K. Bijlsma, Sébastien Moutton, et al.. (2016). Recurrent KIF2A mutations are responsible for classic lissencephaly. Neurogenetics. 18(2). 73–79. 21 indexed citations
9.
10.
Lefebvre, Christophe, Céline Largeau, Xavier Michelet, et al.. (2016). The ESCRT-II proteins are involved in shaping the sarcoplasmic reticulum in C. elegans. Journal of Cell Science. 129(7). 1490–1499. 9 indexed citations
11.
12.
Fourrage, Cécile, Sandra Chevalier, & Evelyn Houliston. (2010). A Highly Conserved Poc1 Protein Characterized in Embryos of the Hydrozoan Clytia hemisphaerica: Localization and Functional Studies. PLoS ONE. 5(11). e13994–e13994. 12 indexed citations

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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