Florence Amblard

917 total citations
21 papers, 276 citations indexed

About

Florence Amblard is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Florence Amblard has authored 21 papers receiving a total of 276 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 10 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Florence Amblard's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Florence Amblard is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Florence Amblard collaborates with scholars based in France and Netherlands. Florence Amblard's co-authors include Françoise Devillard, Véronique Satre, Charles Coutton, Pierre‐Simon Jouk, Gaëlle Vieville, Sophie Brouillet, Sylviane Hennebicq, Chantal Desmaze, F Ledeist and Suzanne Demczuk and has published in prestigious journals such as International Journal of Molecular Sciences, Human Reproduction and European Journal of Human Genetics.

In The Last Decade

Florence Amblard

19 papers receiving 264 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 Amblard France 10 147 122 78 75 60 21 276
Nicole Morichon France 9 149 1.0× 164 1.3× 83 1.1× 134 1.8× 57 0.9× 10 367
Nicole Joyé France 10 118 0.8× 74 0.6× 54 0.7× 105 1.4× 63 1.1× 17 223
Denise Molina‐Gomes France 12 162 1.1× 101 0.8× 157 2.0× 130 1.7× 133 2.2× 32 406
Capucine Hyon France 12 262 1.8× 210 1.7× 89 1.1× 98 1.3× 64 1.1× 21 376
Antonios Garas Greece 12 73 0.5× 64 0.5× 88 1.1× 78 1.0× 81 1.4× 39 332
Judy F.C. Chow Hong Kong 11 119 0.8× 146 1.2× 72 0.9× 157 2.1× 131 2.2× 22 338
Katherine L. Palmerola United States 8 75 0.5× 225 1.8× 59 0.8× 125 1.7× 102 1.7× 22 401
Michelle C. French New Zealand 10 126 0.9× 227 1.9× 34 0.4× 73 1.0× 113 1.9× 15 378
Stéphane Serero France 8 188 1.3× 133 1.1× 62 0.8× 110 1.5× 59 1.0× 15 328

Countries citing papers authored by Florence Amblard

Since Specialization
Citations

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

Fields of papers citing papers by Florence Amblard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florence Amblard

This figure shows the co-authorship network connecting the top 25 collaborators of Florence Amblard. A scholar is included among the top collaborators of Florence Amblard 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 Amblard. Florence Amblard 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.
Perrin, Aurore, Fréderic Morel, Françoise Devillard, et al.. (2023). Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry. International Journal of Molecular Sciences. 24(4). 3664–3664. 1 indexed citations
2.
Bricout, Véronique‐Aurélie, Michel Guinot, A. Favre‐Juvin, Florence Amblard, & Françoise Devillard. (2021). A Successful Harmonious Development by Sport of a Child with Down Syndrome: Fifteen Years of Sport Medical Follow-Up. 5(3). 1 indexed citations
3.
Martinez, Guillaume, Françoise Devillard, Véronique Satre, et al.. (2018). Is sperm FISH analysis still useful for Robertsonian translocations? Meiotic analysis for 23 patients and review of the literature. Basic and Clinical Andrology. 28(1). 5–5. 9 indexed citations
4.
Lorès, Patrick, Hervé Sartelet, Brice Poreau, et al.. (2018). Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction. Clinical Genetics. 94(6). 575–580. 5 indexed citations
5.
Zouari, Raoudha, Sélima Fourati Ben Mustapha, Guillaume Martinez, et al.. (2016). Patients with multiple morphological abnormalities of the sperm flagella due toDNAH1mutations have a good prognosis following intracytoplasmic sperm injection. Human Reproduction. 31(6). 1164–1172. 75 indexed citations
6.
Devillard, Françoise, Véronique Satre, Klaus Dieterich, et al.. (2015). Microdeletion del(22)(q12.1) excluding the MN1 gene in a patient with craniofacial anomalies. American Journal of Medical Genetics Part A. 170(2). 498–503. 5 indexed citations
7.
Tanno, Pauline Le, Brice Poreau, Françoise Devillard, et al.. (2014). Maternal complex chromosomal rearrangement leads to TCF12 microdeletion in a patient presenting with coronal craniosynostosis and intellectual disability. American Journal of Medical Genetics Part A. 164(6). 1530–1536. 13 indexed citations
8.
Coutton, Charles, Klaus Dieterich, Véronique Satre, et al.. (2014). Array-CGH in children with mild intellectual disability: a population-based study. European Journal of Pediatrics. 174(1). 75–83. 15 indexed citations
9.
Stasia, Marie José, Cécile Martel, Véronique Satre, et al.. (2013). Functional and genetic characterization of two extremely rare cases of Williams–Beuren Syndrome associated with chronic granulomatous disease. European Journal of Human Genetics. 21(10). 1079–1084. 14 indexed citations
10.
Coutton, Charles, Brice Poreau, Françoise Devillard, et al.. (2013). Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH Gene. Molecular Syndromology. 5(1). 25–31. 8 indexed citations
11.
Coutton, Charles, Françoise Devillard, Gaëlle Vieville, et al.. (2012). 17p13.1 microduplication in a boy with Silver–Russell syndrome features and intellectual disability. American Journal of Medical Genetics Part A. 158A(10). 2564–2570. 25 indexed citations
12.
Boulet, Sheree L., Valérie Delorme, M. Althuser, et al.. (2010). Chimérisme tétragamétique : à propos d’un cas. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 40(1). 77–80. 3 indexed citations
13.
Faure, A.K., Isabelle Aknin‐Seifer, Véronique Satre, et al.. (2007). Fine mapping of re-arranged Y chromosome in three infertile patients with non-obstructive azoospermia/cryptozoospermia. Human Reproduction. 22(7). 1854–1860. 9 indexed citations
14.
15.
Satre, Véronique, et al.. (2004). Prenatal diagnosis of DMD in a female foetus affected by Turner syndrome. Prenatal Diagnosis. 24(11). 913–917. 14 indexed citations
16.
Cans, C., et al.. (1998). Population screening for aneuploidy using maternal age and ultrasound. Prenatal Diagnosis. 18(7). 683–692. 13 indexed citations
17.
Amblard, Florence & P Jalbert. (1994). Les Hommes XYY. Andrologie. 4(2). 197–204.
18.
Desmaze, Chantal, M Prieur, Florence Amblard, et al.. (1993). Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.. PubMed. 53(6). 1239–49. 45 indexed citations
19.
Cohen, Olivier, et al.. (1992). Human reciprocal translocations: a new computer system for genetic counseling.. PubMed. 35(4). 193–201. 4 indexed citations
20.
Jalbert, P, et al.. (1989). [Role of karyotype in studying male infertility].. PubMed. 18(6). 724–8. 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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