Françoise Charbonnier

2.4k total citations · 1 hit paper
23 papers, 1.3k citations indexed

About

Françoise Charbonnier is a scholar working on Molecular Biology, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, Françoise Charbonnier has authored 23 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Cancer Research and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Françoise Charbonnier's work include Cancer Genomics and Diagnostics (7 papers), Genetic factors in colorectal cancer (6 papers) and RNA Research and Splicing (4 papers). Françoise Charbonnier is often cited by papers focused on Cancer Genomics and Diagnostics (7 papers), Genetic factors in colorectal cancer (6 papers) and RNA Research and Splicing (4 papers). Françoise Charbonnier collaborates with scholars based in France, United States and Réunion. Françoise Charbonnier's co-authors include Thierry Frébourg, Cosette Martin, Dominique Campion, Alexis Brice, Didier Hannequin, Grégory Raux, Serge Belliard, Agnès Camuzat, Agnès Michon and Valérie Mesnage and has published in prestigious journals such as Nucleic Acids Research, Molecular Cell and Oncogene.

In The Last Decade

Françoise Charbonnier

21 papers receiving 1.3k citations

Hit Papers

align trajectories

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.

Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

1999 544 citations Dominique Campion, Cécile Dumanchin et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Françoise Charbonnier France	15	615	445	271	270	268	23	1.3k
Alonso Martínez Colombia	10	965 1.6×	414 0.9×	57 0.2×	132 0.5×	202 0.8×	22	1.4k
Alejandro Abuin United States	15	998 1.6×	280 0.6×	104 0.4×	233 0.9×	115 0.4×	17	1.3k
Lasse Sinkkonen Luxembourg	20	1.0k 1.7×	220 0.5×	255 0.9×	194 0.7×	403 1.5×	39	1.7k
Jackelien van Scheppingen Netherlands	19	386 0.6×	233 0.5×	52 0.2×	133 0.5×	134 0.5×	23	859
Guanghong Liao United States	19	887 1.4×	317 0.7×	72 0.3×	79 0.3×	116 0.4×	29	1.7k
Sonia Podvin United States	17	562 0.9×	205 0.5×	77 0.3×	370 1.4×	96 0.4×	38	1.3k
Chunyu Wang China	22	599 1.0×	143 0.3×	61 0.2×	79 0.3×	131 0.5×	71	1.3k
Parham Nejad United States	9	583 0.9×	248 0.6×	109 0.4×	91 0.3×	280 1.0×	18	1.0k
Tingting Yu China	19	651 1.1×	132 0.3×	63 0.2×	350 1.3×	117 0.4×	108	1.3k
Rita Cittadella Italy	18	274 0.4×	197 0.4×	233 0.9×	141 0.5×	36 0.1×	36	1.0k

Countries citing papers authored by Françoise Charbonnier

Since Specialization

Citations

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

Fields of papers citing papers by Françoise Charbonnier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Françoise Charbonnier

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Lecoquierre, François, Nathalie Drouot, Sophie Coutant, et al.. (2025). Parental germline mosaicism in genome-wide phased de novo variants: Recurrence risk assessment and implications for precision genetic counselling. PLoS Genetics. 21(3). e1011651–e1011651.

Thibaut, L, Stéphanie Vasseur, Olivier Quenez, et al.. (2025). Bridging the Diagnostic Gap in Hereditary Cancers with Simple, Cost-Effective, High-Throughput RNA Splicing Analysis. Journal of Molecular Diagnostics. 27(10). 954–968.

Lecoquierre, François, Kévin Cassinari, Nathalie Drouot, et al.. (2024). Assessment of parental mosaicism rates in neurodevelopmental disorders caused by apparent de novo pathogenic variants using deep sequencing. Scientific Reports. 14(1). 5289–5289. 2 indexed citations

Cassinari, Kévin, Élodie Alessandri-Gradt, Pascal Chambon, et al.. (2020). Assessment of Multiplex Digital Droplet RT-PCR as a Diagnostic Tool for SARS-CoV-2 Detection in Nasopharyngeal Swabs and Saliva Samples. Clinical Chemistry. 67(5). 736–741. 30 indexed citations

Coutant, Sophie, Céline Derambure, Françoise Charbonnier, et al.. (2020). Blood functional assay for rapid clinical interpretation of germline TP53 variants. Journal of Medical Genetics. 58(12). 796–805. 11 indexed citations

Charbonnier, Françoise, Aymeric Douillard, Valérie Macioce, et al.. (2018). Efficiency of physiotherapy with Caycedian Sophrology on children with asthma: A randomized controlled trial. Pediatric Pulmonology. 53(5). 559–566. 4 indexed citations

Coutant, Sophie, Émilie Angot, Jean‐Christophe Sabourin, et al.. (2016). Familial solitary chondrosarcoma resulting from germline EXT2 mutation. Genes Chromosomes and Cancer. 56(2). 128–134. 5 indexed citations

Marguet, Florent, Annie Laquerrière, Alice Goldenberg, et al.. (2016). Clinical and pathologic features of Aicardi–Goutières syndrome due to an IFIH1 mutation: A pediatric case report. American Journal of Medical Genetics Part A. 170(5). 1317–1324. 14 indexed citations

Mungamuri, Sathish Kumar, Dorthe Cartier, Ravi Sachidanandam, et al.. (2016). CRISPR-Barcoding for Intratumor Genetic Heterogeneity Modeling and Functional Analysis of Oncogenic Driver Mutations. Molecular Cell. 63(3). 526–538. 51 indexed citations

10.

Charbonnier, Françoise, Estelle Houivet, Marie‐Pierre Buisine, et al.. (2011). Evaluation of Lynch syndrome modifier genes in 748 MMR mutation carriers. European Journal of Human Genetics. 19(8). 887–892. 17 indexed citations

11.

Charbonnier, Françoise, Pascal Chambon, Jean‐Baptiste Latouche, et al.. (2011). Pitfalls in the use of DGV for CNV interpretation. American Journal of Medical Genetics Part A. 155(10). 2593–2596. 12 indexed citations

12.

Lefébure, B., Françoise Charbonnier, Frédéric Di Fiore, et al.. (2010). Prognostic Value of Circulating Mutant DNA in Unresectable Metastatic Colorectal Cancer. Annals of Surgery. 251(2). 275–280. 41 indexed citations

13.

Tournier, Isabelle, Myriam Vézain, Alexandra Martins, et al.. (2008). A large fraction of unclassified variants of the mismatch repair genesMLH1andMSH2is associated with splicing defects. Human Mutation. 29(12). 1412–1424. 126 indexed citations

14.

Charbonnier, Françoise, Stéphanie Baert‐Desurmont, Ping Liang, et al.. (2005). The 5′ region of theMSH2gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences. Human Mutation. 26(3). 255–261. 27 indexed citations

15.

Faivre, Laurence, Pascale Saugier-Véber, Jean-Paul Paı̈s de Barros, et al.. (2005). Variable expressivity of the clinical and biochemical phenotype associated with the apolipoprotein E p.Leu149del mutation. European Journal of Human Genetics. 13(11). 1186–1191. 26 indexed citations

16.

Campion, Dominique, Cécile Dumanchin, Didier Hannequin, et al.. (1999). Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum. The American Journal of Human Genetics. 65(3). 664–670. 544 indexed citations breakdown →

17.

Bonnet‐Brilhault, Frédérique, Claudine Laurent, Dominique Campion, et al.. (1999). No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia. European Journal of Human Genetics. 7(2). 247–250. 24 indexed citations

18.

Campion, Dominique, Florence Thibaut, Sonia Dollfus, et al.. (1996). Association study between schizophrenia and monoamine oxidase A and B DNA polymorphisms. Psychiatry Research. 62(3). 221–226. 23 indexed citations

19.

Campion, Dominique, Cosette Martin, Roland Heilig, et al.. (1995). The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease. Genomics. 26(2). 254–257. 79 indexed citations

20.

Flaman, Jean‐Michel, Thierry Frébourg, Viviane Moreau, et al.. (1994). A rapid PCR fidelity assay. Nucleic Acids Research. 22(15). 3259–3260. 89 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.

Explore authors with similar magnitude of impact