Florence Petit

5.5k total citations
61 papers, 1.0k citations indexed

About

Florence Petit is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Florence Petit has authored 61 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 32 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Florence Petit's work include Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (11 papers) and Congenital limb and hand anomalies (9 papers). Florence Petit is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (11 papers) and Congenital limb and hand anomalies (9 papers). Florence Petit collaborates with scholars based in France, United Kingdom and United States. Florence Petit's co-authors include Nadav Ahituv, Karen E. Sears, Sylvie Manouvrier‐Hanu, Muriel Holder‐Espinasse, Fabienne Escande, Joris Andrieux, Nicole Porchet, Anne‐Sophie Jourdain, Jamal Ghoumid and Didier Lacombe and has published in prestigious journals such as Nature Communications, The Journal of Experimental Medicine and PLoS ONE.

In The Last Decade

Florence Petit

56 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florence Petit France 20 610 461 107 105 92 61 1.0k
Mona Aglan Egypt 22 802 1.3× 992 2.2× 82 0.8× 111 1.1× 57 0.6× 70 1.6k
Louise Brueton United Kingdom 24 908 1.5× 604 1.3× 154 1.4× 205 2.0× 59 0.6× 34 1.5k
Sevim Balcı Türkiye 17 552 0.9× 463 1.0× 200 1.9× 181 1.7× 160 1.7× 70 1.2k
Christian Babbs United Kingdom 19 842 1.4× 444 1.0× 88 0.8× 69 0.7× 37 0.4× 35 1.2k
Yves Lacassie United States 18 475 0.8× 425 0.9× 174 1.6× 92 0.9× 29 0.3× 70 952
Stavit A. Shalev Israel 19 519 0.9× 416 0.9× 107 1.0× 84 0.8× 21 0.2× 44 962
Tuula Rinne Netherlands 15 601 1.0× 253 0.5× 101 0.9× 48 0.5× 25 0.3× 32 997
Riyana Babul‐Hirji Canada 15 785 1.3× 522 1.1× 62 0.6× 121 1.2× 40 0.4× 31 1.2k
Laurence Taine France 21 428 0.7× 398 0.9× 147 1.4× 274 2.6× 86 0.9× 46 924
Patrice Bourgeois France 17 810 1.3× 549 1.2× 146 1.4× 28 0.3× 35 0.4× 45 1.4k

Countries citing papers authored by Florence Petit

Since Specialization
Citations

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

Fields of papers citing papers by Florence Petit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florence Petit

This figure shows the co-authorship network connecting the top 25 collaborators of Florence Petit. A scholar is included among the top collaborators of Florence Petit 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 Florence Petit. Florence Petit 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.
Choi, Tae‐Ik, Yu‐Ri Lee, Laurie Robak, et al.. (2024). RFC2 may contribute to the pathogenicity of Williams syndrome revealed in a zebrafish model. Journal of genetics and genomics. 51(12). 1389–1403. 1 indexed citations
2.
Vanlerberghe, Clémence, Frédéric Frénois, Thomas Smol, et al.. (2024). RPL26 variants: A rare cause of Diamond-Blackfan anemia syndrome with multiple congenital anomalies at the forefront. Genetics in Medicine. 26(12). 101266–101266.
3.
Vanlerberghe, Clémence, Frédéric Frénois, Emilie Ait‐Yahya, et al.. (2024). Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome. Genetics in Medicine. 26(12). 101267–101267.
4.
Poirier, Karine, Richard Belvindrah, Imane Moutkine, et al.. (2022). Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development. Nature Communications. 13(1). 2746–2746. 4 indexed citations
5.
Smol, Thomas, Perrine Brunelle, Roseline Caumes, et al.. (2022). TRIT1 deficiency: Two novel patients with four novel variants. European Journal of Medical Genetics. 65(11). 104603–104603. 2 indexed citations
6.
Ghoumid, Jamal, Thomas Smol, Perrine Brunelle, et al.. (2021). Le test de concordance de script à l’heure de la réforme du second cycle des études médicales en France : étude pilote en génétique médicale. Pédagogie médicale. 22(2). 67–72.
7.
Zhang, Yichi, Chenling Xiong, Jingjing Zhao, et al.. (2021). Deletion of CTCF sites in the SHH locus alters enhancer–promoter interactions and leads to acheiropodia. Nature Communications. 12(1). 2282–2282. 35 indexed citations
8.
Haro, Endika, Florence Petit, Fabienne Escande, et al.. (2021). Identification of limb-specific Lmx1b auto-regulatory modules with Nail-patella syndrome pathogenicity. Nature Communications. 12(1). 5533–5533. 15 indexed citations
9.
Morlot, Susanne, Gunnar Schmidt, Bernd Auber, et al.. (2020). De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopenia. Clinical Genetics. 98(4). 374–378. 5 indexed citations
10.
Becker, Lena‐Luise, Hormos Salimi Dafsari, Jens Schallner, et al.. (2020). The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification. Journal of Human Genetics. 65(11). 1003–1017. 31 indexed citations
11.
Quelennec, Eddy, Jeanne Amiel, Sandrine Marlin, et al.. (2020). Generation of an iPSC line (IMAGINi022-A) from a patient carrying a SOX10 missense mutation and presenting with deafness, depigmentation and progressive neurological impairment. Stem Cell Research. 48. 101936–101936. 2 indexed citations
12.
Rodero, Mathieu P., Cécile Conrad, Mathieu Maurin, et al.. (2019). Bloom syndrome protein restrains innate immune sensing of micronuclei by cGAS. The Journal of Experimental Medicine. 216(5). 1199–1213. 86 indexed citations
13.
Syx, Delfien, Florence Petit, Nathalie Goemans, et al.. (2019). Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers–Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrix. Genetics in Medicine. 22(1). 112–123. 38 indexed citations
14.
Ghoumid, Jamal, Florence Petit, Odile Boute‐Bénéjean, et al.. (2017). Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder. European Journal of Human Genetics. 25(8). 1011–1014. 10 indexed citations
15.
Andrieux, Joris, Florence Petit, Sonia Bouquillon, et al.. (2014). ELNgene triplication responsible for familial supravalvular aortic aneurysm. Cardiology in the Young. 25(4). 712–717. 17 indexed citations
16.
Petit, Florence, Ghislaine Plessis, Matthieu Décamp, et al.. (2014). 21q21 deletion involving NCAM2: Report of 3 cases with neurodevelopmental disorders. European Journal of Medical Genetics. 58(1). 44–46. 27 indexed citations
17.
Petit, Florence, Joris Andrieux, Geneviève Baujat, et al.. (2013). Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families. Clinical Genetics. 85(5). 464–469. 17 indexed citations
18.
Petit, Florence, Joris Andrieux, Muriel Holder‐Espinasse, et al.. (2011). Xq12q13.1 microduplication encompassing the EFNB1 gene in a boy with congenital diaphragmatic hernia. European Journal of Medical Genetics. 54(5). e525–e527. 8 indexed citations
19.
Bonneau, Dominique, Muriel Holder‐Espinasse, Cyril Goizet, et al.. (2009). Oculo-dento-digital dysplasia: Lack of genotype–phenotype correlation for GJA1 mutations and usefulness of neuro-imaging. European Journal of Medical Genetics. 53(1). 19–22. 17 indexed citations
20.
Andrieux, Joris, Steven Richebourg, Bénédicte Duban‐Bedu, et al.. (2008). Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delay. European Journal of Medical Genetics. 51(4). 373–381. 11 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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