Anne Girardet

1.2k total citations
49 papers, 804 citations indexed

About

Anne Girardet is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Anne Girardet has authored 49 papers receiving a total of 804 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Pediatrics, Perinatology and Child Health, 21 papers in Genetics and 15 papers in Molecular Biology. Recurrent topics in Anne Girardet's work include Prenatal Screening and Diagnostics (24 papers), Chromosomal and Genetic Variations (14 papers) and Genomic variations and chromosomal abnormalities (9 papers). Anne Girardet is often cited by papers focused on Prenatal Screening and Diagnostics (24 papers), Chromosomal and Genetic Variations (14 papers) and Genomic variations and chromosomal abnormalities (9 papers). Anne Girardet collaborates with scholars based in France, United Kingdom and Switzerland. Anne Girardet's co-authors include Franck Pellestor, B. Andréo, G. Lefort, Lionel Coignet, Mireille Claustres, Jean-Paul Charlieu, Geneviève Lefort, C. Humeau, Marie des Georges and Patrick Petignat and has published in prestigious journals such as International Journal of Molecular Sciences, The American Journal of Human Genetics and Fertility and Sterility.

In The Last Decade

Anne Girardet

46 papers receiving 771 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne Girardet France 18 358 309 269 196 150 49 804
Judy Chernos Canada 15 521 1.5× 286 0.9× 375 1.4× 132 0.7× 180 1.2× 38 859
G. Lefort France 16 377 1.1× 290 0.9× 189 0.7× 217 1.1× 74 0.5× 34 632
Hatem Elghezal Tunisia 20 412 1.2× 281 0.9× 204 0.8× 89 0.5× 463 3.1× 57 992
Tugce Pehlivan United States 17 371 1.0× 666 2.2× 308 1.1× 41 0.2× 371 2.5× 20 1.1k
Frederick W. Luthardt United States 17 318 0.9× 191 0.6× 387 1.4× 99 0.5× 198 1.3× 28 890
Alida C. Knegt Netherlands 14 257 0.7× 232 0.8× 271 1.0× 37 0.2× 120 0.8× 35 652
Frans J. Los Netherlands 22 519 1.4× 1.1k 3.4× 226 0.8× 78 0.4× 374 2.5× 70 1.4k
Celeste M. Krauss United States 12 235 0.7× 156 0.5× 129 0.5× 44 0.2× 79 0.5× 19 496
M. G. J. Jahoda Netherlands 15 283 0.8× 648 2.1× 238 0.9× 86 0.4× 183 1.2× 40 1.0k
G. L. Terzoli Italy 10 397 1.1× 517 1.7× 237 0.9× 143 0.7× 84 0.6× 14 843

Countries citing papers authored by Anne Girardet

Since Specialization
Citations

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

Fields of papers citing papers by Anne Girardet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Girardet

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Girardet. A scholar is included among the top collaborators of Anne Girardet 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 Anne Girardet. Anne Girardet 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.
Sonigo, Charlotte, Noémie Ranisavljevic, T. Anahory, et al.. (2024). Ovarian response in preimplantation genetic testing for myotonic dystrophy type 1. Journal of Assisted Reproduction and Genetics. 42(1). 185–192.
2.
Ranisavljevic, Noémie, et al.. (2020). Are ovarian response and pregnancy rates similar in selected FMR1 premutated and mutated patients undergoing preimplantation genetic testing?. Journal of Assisted Reproduction and Genetics. 37(7). 1675–1683. 5 indexed citations
3.
Girardet, Anne, Stéphanie Plaza, S. Hamamah, et al.. (2017). Thirteen years' experience of 893 PGD cycles for monogenic disorders in a publicly funded, nationally regulated regional hospital service. Reproductive BioMedicine Online. 36(2). 154–163. 9 indexed citations
4.
Guissart, Claire, Caroline Raynal, Anne Girardet, et al.. (2016). Non-invasive prenatal diagnosis (NIPD) of cystic fibrosis: an optimized protocol using MEMO fluorescent PCR to detect the p.Phe508del mutation. Journal of Cystic Fibrosis. 16(2). 198–206. 12 indexed citations
5.
Girardet, Anne, Stéphanie Plaza, Martine De Rycke, et al.. (2015). The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus. European Journal of Human Genetics. 24(4). 469–478. 24 indexed citations
6.
Barat‐Houari, Mouna, Karine Nguyen, Rafaëlle Bernard, et al.. (2009). New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?. European Journal of Human Genetics. 18(5). 533–538. 11 indexed citations
7.
Girardet, Anne, et al.. (2008). Efficient strategies for preimplantation genetic diagnosis of spinal muscular atrophy. Fertility and Sterility. 90(2). 443.e7–443.e12. 17 indexed citations
8.
Taulan‐Cadars, Magali, Anne Girardet, Caroline Guittard, et al.. (2007). Large genomic rearrangements in the CFTRgene contribute to CBAVD. BMC Medical Genetics. 8(1). 22–22. 38 indexed citations
9.
Girardet, Anne, A. Moncla, S. Hamamah, & Mireille Claustres. (2005). Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A gene. Reproductive BioMedicine Online. 10(4). 519–526. 2 indexed citations
10.
Girardet, Anne, et al.. (2003). Short Communication: Rapid Detection of the ΔF508 Mutation in Single Cells Using DHPLC: Implications for Preimplantation Genetic Diagnosis. Journal of Assisted Reproduction and Genetics. 20(4). 153–156. 3 indexed citations
11.
Girardet, Anne. (2003). First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markers. Molecular Human Reproduction. 9(2). 111–116. 37 indexed citations
12.
Girardet, Anne, Sigbjørn Lien, Esther P. Leeflang, et al.. (1999). Direct estimation of the recombination frequency between the RB1 gene and two closely linked microsatellites using sperm typing. European Journal of Human Genetics. 7(2). 239–242. 4 indexed citations
13.
Girardet, Anne, Franck Pellestor, Sylvie Tuffery‐Giraud, et al.. (1997). Amplification of the RB1.20 polymorphism in single spermatozoa. Journal of Assisted Reproduction and Genetics. 14(3). 176–179. 2 indexed citations
14.
Pellestor, Franck, et al.. (1996). Direct detection of disomy in human sperm by the PRINS technique. Human Genetics. 97(1). 21–5. 20 indexed citations
15.
Pellestor, Franck, et al.. (1996). FISH and PRINS, a strategy for rapid chromosome screening: application to the assessment of aneuploidy in human sperm. Cytogenetic and Genome Research. 72(1). 34–36. 27 indexed citations
16.
Pellestor, Franck, et al.. (1996). Preimplantation embryo chromosome analysis by primed in situ labeling method. Fertility and Sterility. 66(5). 781–786. 7 indexed citations
17.
Pellestor, Franck, et al.. (1995). Rapid in situ detection of chromosome 21 by PRINS technique. American Journal of Medical Genetics. 56(4). 393–397. 20 indexed citations
18.
Girardet, Anne, et al.. (1995). [Direct analysis of the frequency of disomy in human sperm using the PRINS technique].. PubMed. 38(2). 85–9. 2 indexed citations
19.
Pellestor, Franck, et al.. (1995). PRINS as a method for rapid chromosomal labeling on human spermatozoa. Molecular Reproduction and Development. 40(3). 333–337. 19 indexed citations
20.
Pellestor, Franck, et al.. (1994). Relationship between morphology and chromosomal constitution in human preimplantation embryo. Molecular Reproduction and Development. 39(2). 141–146. 62 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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