Geneviève Lefort

659 total citations
29 papers, 375 citations indexed

About

Geneviève Lefort is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Geneviève Lefort has authored 29 papers receiving a total of 375 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 15 papers in Pediatrics, Perinatology and Child Health and 10 papers in Plant Science. Recurrent topics in Geneviève Lefort's work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (15 papers) and Chromosomal and Genetic Variations (10 papers). Geneviève Lefort is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (15 papers) and Chromosomal and Genetic Variations (10 papers). Geneviève Lefort collaborates with scholars based in France, United Kingdom and Germany. Geneviève Lefort's co-authors include Franck Pellestor, Jacques Puechberty, B. Andréo, Pierre Sarda, Anne Girardet, David Geneviève, Patricia Blanchet, Vincent Gâtinois, Thomas Liehr and Anja Weise and has published in prestigious journals such as Fertility and Sterility, Molecular Human Reproduction and European Journal of Human Genetics.

In The Last Decade

Geneviève Lefort

27 papers receiving 345 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Geneviève Lefort France 13 262 160 148 105 34 29 375
Ioannis Papoulidis Greece 13 251 1.0× 195 1.2× 116 0.8× 51 0.5× 33 1.0× 52 388
Barbara Delle Chiaie Belgium 7 251 1.0× 136 0.8× 195 1.3× 38 0.4× 19 0.6× 10 423
Maria Paola Recalcati Italy 11 240 0.9× 89 0.6× 191 1.3× 46 0.4× 19 0.6× 21 378
Monika Ziegler Germany 13 261 1.0× 117 0.7× 116 0.8× 169 1.6× 20 0.6× 36 345
D A Couzin United Kingdom 12 226 0.9× 124 0.8× 135 0.9× 117 1.1× 26 0.8× 23 367
Vikram Jaswaney United States 7 424 1.6× 154 1.0× 245 1.7× 51 0.5× 16 0.5× 12 489
Peter M. Kroisel Austria 14 381 1.5× 248 1.6× 231 1.6× 59 0.6× 17 0.5× 18 500
Amelia Villa Spain 9 176 0.7× 75 0.5× 83 0.6× 50 0.5× 25 0.7× 12 241
Claudine Fear United Kingdom 10 229 0.9× 74 0.5× 147 1.0× 36 0.3× 15 0.4× 16 312
Catherine Metaxotou Greece 12 188 0.7× 140 0.9× 130 0.9× 66 0.6× 18 0.5× 35 334

Countries citing papers authored by Geneviève Lefort

Since Specialization
Citations

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

Fields of papers citing papers by Geneviève Lefort

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Geneviève Lefort

This figure shows the co-authorship network connecting the top 25 collaborators of Geneviève Lefort. A scholar is included among the top collaborators of Geneviève Lefort 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 Geneviève Lefort. Geneviève Lefort 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.
Ravel, Jean‐Marie, M. Renaud, Jean Muller, et al.. (2023). Clinical utility of periodic reinterpretation of CNVs of uncertain significance: an 8-year retrospective study. Genome Medicine. 15(1). 39–39. 7 indexed citations
2.
Gâtinois, Vincent, Nicole Bigi, E. Mousty, et al.. (2019). Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations. Molecular Genetics & Genomic Medicine. 7(11). e00895–e00895.
3.
Pellestor, Franck, Vincent Gâtinois, Jacques Puechberty, David Geneviève, & Geneviève Lefort. (2014). Chromothripsis: potential origin in gametogenesis and preimplantation cell divisions. A review. Fertility and Sterility. 102(6). 1785–1796. 49 indexed citations
4.
Mau‐Them, Frédéric Tran, Mouna Barat‐Houari, Claire Jeandel, et al.. (2013). Dysspondyloenchondromatosis without COL2A1 mutation: Possible genetic heterogeneity. American Journal of Medical Genetics Part A. 164(3). 769–773. 3 indexed citations
5.
Pinson, Lucile, Linda Mannini, Marjolaine Willems, et al.. (2013). CEP57 mutation in a girl with mosaic variegated aneuploidy syndrome. American Journal of Medical Genetics Part A. 164(1). 177–181. 20 indexed citations
6.
Pellestor, Franck, Jacques Puechberty, Anja Weise, et al.. (2011). Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier. Fertility and Sterility. 95(7). 2433.e17–2433.e22. 31 indexed citations
7.
Schneider, Anouck, Anne‐Marie Chaze, Nicole Bigi, et al.. (2009). Epiphyseal punctate calcifications (stippling) in complete trisomy 9. Prenatal Diagnosis. 29(11). 1085–1088. 2 indexed citations
8.
Bhatt, Samarth, Kamran Moradkhani, Kristin Mrasek, et al.. (2008). Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. European Journal of Human Genetics. 17(1). 44–50. 14 indexed citations
9.
Rigolet, Muriel, Geneviève Lefort, Patricia Blanchet, et al.. (2007). Early prenatal diagnosis of ICF syndrome by mutation detection. Prenatal Diagnosis. 27(11). 1075–1078. 7 indexed citations
10.
Roubertie, Agathe, et al.. (2006). Partial Epilepsy and 47,XXX Karyotype: Report of Four Cases. Pediatric Neurology. 35(1). 69–74. 10 indexed citations
11.
Pellestor, Franck, B. Andréo, Jacques Puechberty, Geneviève Lefort, & Pierre Sarda. (2006). Analysis of Sperm Aneuploidy by PRINS. Humana Press eBooks. 334. 49–60. 7 indexed citations
12.
Moradkhani, Kamran, Jacques Puechberty, Patricia Blanchet, et al.. (2006). Mosaic trisomy 16 in a fetus: the complex relationship between phenotype and genetic mechanisms. Prenatal Diagnosis. 26(12). 1179–1182. 9 indexed citations
13.
Lefort, Geneviève, Patricia Blanchet, François Rivier, et al.. (2002). Stable dicentric duplication‐deficiency chromosome 14 resulting from crossing‐over within a maternal paracentric inversion. American Journal of Medical Genetics. 113(4). 333–338. 24 indexed citations
14.
Solassol, Jérôme, et al.. (2002). Rapid detection of common autosomal aneuploidies by quantitative fluorescent PCR on uncultured amniocytes. European Journal of Human Genetics. 10(8). 462–466. 16 indexed citations
15.
Orsetti, Béatrice, Geneviève Lefort, Pierre Boulot, B. Andréo, & Franck Pellestor. (1998). Fetal cells in maternal blood: the use of primedin situ (PRINS) labelling technique for fetal cell detection and sex assessment. Prenatal Diagnosis. 18(10). 1014–1022. 17 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.. (1996). Rapid chromosome detection in human gametes, zygotes, and preimplantation embryos using the PRINS technique. Journal of Assisted Reproduction and Genetics. 13(8). 675–680. 9 indexed citations
18.
Pellestor, Franck, et al.. (1996). The PRINS technique: potential use for rapid preimplantation embryo chromosome screening. Molecular Human Reproduction. 2(2). 135–138. 15 indexed citations
19.
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
20.
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

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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