Françoise Clerget‐Darpoux

10.7k total citations · 1 hit paper
168 papers, 4.7k citations indexed

About

Françoise Clerget‐Darpoux is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Françoise Clerget‐Darpoux has authored 168 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Genetics, 52 papers in Molecular Biology and 31 papers in Immunology. Recurrent topics in Françoise Clerget‐Darpoux's work include Genetic Associations and Epidemiology (50 papers), Diabetes and associated disorders (22 papers) and Genetic Mapping and Diversity in Plants and Animals (21 papers). Françoise Clerget‐Darpoux is often cited by papers focused on Genetic Associations and Epidemiology (50 papers), Diabetes and associated disorders (22 papers) and Genetic Mapping and Diversity in Plants and Animals (21 papers). Françoise Clerget‐Darpoux collaborates with scholars based in France, United States and Italy. Françoise Clerget‐Darpoux's co-authors include Catherine Bonaïti‐Pellié, Emmanuelle Génin, Marie‐Claude Babron, Joëlle Hochez, María Martínez, Dominique Campion, Alexis Brice, Didier Hannequin, Bernard Prum and Michèle Puel and has published in prestigious journals such as Science, PLoS ONE and Neurology.

In The Last Decade

Françoise Clerget‐Darpoux

164 papers receiving 4.5k citations

Hit Papers

Early-Onset Autosomal Dominant Alzheimer Disease: Prevale... 1999 2026 2008 2017 1999 100 200 300 400 500
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.

  1. 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 Career Trend Papers Cites
Françoise Clerget‐Darpoux France 36 2.2k 1.4k 905 630 627 168 4.7k
Giulio Genovese United States 33 1.8k 0.8× 2.6k 1.9× 334 0.4× 526 0.8× 209 0.3× 67 6.8k
Marcella Devoto Italy 45 1.8k 0.8× 2.7k 1.9× 260 0.3× 316 0.5× 125 0.2× 161 6.6k
Stephen Sawcer United Kingdom 40 1.1k 0.5× 1.6k 1.2× 714 0.8× 2.5k 3.9× 136 0.2× 130 7.1k
Thomas S. Jacques United Kingdom 41 487 0.2× 2.1k 1.5× 427 0.5× 382 0.6× 69 0.1× 148 5.8k
Jean-Marc Lalouel United States 41 2.2k 1.0× 2.1k 1.5× 404 0.4× 535 0.8× 29 0.0× 111 7.2k
Patrick Edery France 33 1.6k 0.7× 2.4k 1.7× 126 0.1× 205 0.3× 131 0.2× 117 4.5k
Adrian Clark United Kingdom 49 1.7k 0.8× 3.5k 2.5× 647 0.7× 426 0.7× 35 0.1× 137 8.2k
Stephen Donoghue United Kingdom 18 703 0.3× 541 0.4× 441 0.5× 602 1.0× 48 0.1× 35 2.6k
Arif B. Ekici Germany 42 1.6k 0.7× 2.6k 1.9× 311 0.3× 779 1.2× 34 0.1× 195 5.1k
J.-M. Lalouel United States 26 2.9k 1.3× 3.3k 2.4× 340 0.4× 274 0.4× 29 0.0× 99 7.4k

Countries citing papers authored by Françoise Clerget‐Darpoux

Since Specialization
Citations

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

Fields of papers citing papers by Françoise Clerget‐Darpoux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Françoise Clerget‐Darpoux

This figure shows the co-authorship network connecting the top 25 collaborators of Françoise Clerget‐Darpoux. A scholar is included among the top collaborators of Françoise Clerget‐Darpoux 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 Clerget‐Darpoux. Françoise Clerget‐Darpoux 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.
Génin, Emmanuelle & Françoise Clerget‐Darpoux. (2015). Revisiting the Polygenic Additive Liability Model through the Example of Diabetes Mellitus. Human Heredity. 80(4). 171–177. 11 indexed citations
2.
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
3.
Bourgey, Mathieu, Hervé Perdry, & Françoise Clerget‐Darpoux. (2007). Modeling the effect of PTPN22in rheumatoid arthritis. BMC Proceedings. 1(S1). S37–S37. 10 indexed citations
4.
Leutenegger, Anne‐Louise, Audrey Labalme, Emmanuelle Génin, et al.. (2006). Using Genomic Inbreeding Coefficient Estimates for Homozygosity Mapping of Rare Recessive Traits: Application to Taybi-Linder Syndrome. The American Journal of Human Genetics. 79(1). 62–66. 35 indexed citations
5.
Babron, Marie‐Claude, Catherine Bourgain, Anne‐Louise Leutenegger, & Françoise Clerget‐Darpoux. (2005). Detection of susceptibility loci by genome-wide linkage analysis. BMC Genetics. 6(S1). S18–S18. 5 indexed citations
6.
Bourgain, Catherine, Emmanuelle Génin, P. Holopainen, et al.. (2001). Use of Closely Related Affected Individuals for the Genetic Study of Complex Diseases in Founder Populations. The American Journal of Human Genetics. 68(1). 154–159. 39 indexed citations
7.
Clerget‐Darpoux, Françoise. (2000). Unraveling the Genetic Component of Multifactorial Diseases: Dream or Reality. International Statistical Review. 68(1). 45–51. 2 indexed citations
8.
Hannequin, Didier, Dominique Campion, Cécile Dumanchin, et al.. (1998). Génétique de la maladie d'Alzheimer. Revue Neurologique. 154. 1 indexed citations
9.
Greco, Luigi, Selvaggia Percopo, Fabienne Clot, et al.. (1998). Lack of Correlation Between Genotype and Phenotype in Celiac Disease. Journal of Pediatric Gastroenterology and Nutrition. 26(3). 286–290. 1 indexed citations
10.
Génin, Emmanuelle & Françoise Clerget‐Darpoux. (1998). Reply to Weeks and Sinsheimer. The American Journal of Human Genetics. 62(3). 731–736. 5 indexed citations
11.
Martínez, María, Dominique Campion, Alexis Brice, et al.. (1998). Apolipoprotein E ϵ4 Allele and Familial Aggregation of Alzheimer Disease. Archives of Neurology. 55(6). 810–810. 45 indexed citations
12.
Clerget‐Darpoux, Françoise. (1998). Overview of strategies for complex genetic diseases. Kidney International. 53(6). 1441–1445. 5 indexed citations
13.
Didierjean, Olivier, María Martínez, Dominique Campion, et al.. (1997). No effect of the alpha 1-antichymotrypsin A allele in Alzheimer's disease. Journal of Neurology Neurosurgery & Psychiatry. 63(1). 103–105. 14 indexed citations
14.
Génin, Emmanuelle & Françoise Clerget‐Darpoux. (1996). Association studies in consanguineous populations.. PubMed Central. 58(4). 861–6. 18 indexed citations
15.
Génin, Emmanuelle, María Martínez, & Françoise Clerget‐Darpoux. (1995). Posterior probability of linkage and maximal lod score. Annals of Human Genetics. 59(1). 123–132. 9 indexed citations
16.
Deschamps, I, J Hors, Françoise Clerget‐Darpoux, et al.. (1990). Excess of maternal HLA-DR3 antigens in HLA DR3,4 positive Type 1 (insulin-dependent) diabetic patients. Diabetologia. 33(7). 425–430. 24 indexed citations
17.
Clerget‐Darpoux, Françoise, et al.. (1990). Hereditary retinoblastoma: can balanced insertion entirely explain the differences of expressivity among families?. Human Genetics. 86(2). 203–8. 6 indexed citations
18.
Spielman, Richard S., Max P. Baur, & Françoise Clerget‐Darpoux. (1989). Genetic analysis of IDDM: Summary of GAW5 IDDM results. Genetic Epidemiology. 6(1). 43–58. 45 indexed citations
19.
Dizier, Marie‐Hélène, Françoise Clerget‐Darpoux, & Joëlle Hochez. (1989). Segregation analysis of two genetic markers in IDDM families under two‐locus models. Genetic Epidemiology. 6(1). 71–75. 5 indexed citations
20.
Clerget‐Darpoux, Françoise. (1983). Genealogical and genetic structure. The American Journal of Human Genetics. 35(1). 158–159. 3 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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