Françoise Devillard

2.7k total citations
27 papers, 431 citations indexed

About

Françoise Devillard is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Françoise Devillard has authored 27 papers receiving a total of 431 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 14 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Françoise Devillard's work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Chromosomal and Genetic Variations (5 papers). Françoise Devillard is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Chromosomal and Genetic Variations (5 papers). Françoise Devillard collaborates with scholars based in France, Italy and Germany. Françoise Devillard's co-authors include Florence Amblard, Véronique Satre, Charles Coutton, Pierre‐Simon Jouk, Gaëlle Vieville, Sophie Rousseaux, B Sèle, Edith Chevret, J. Cozzi and J. Lespinasse and has published in prestigious journals such as The EMBO Journal, International Journal of Molecular Sciences and Human Reproduction.

In The Last Decade

Françoise Devillard

25 papers receiving 404 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Françoise Devillard France 11 247 152 148 142 107 27 431
B Delobel France 11 313 1.3× 170 1.1× 60 0.4× 117 0.8× 61 0.6× 18 451
Jean Pierre Siffroi France 16 483 2.0× 387 2.5× 376 2.5× 171 1.2× 173 1.6× 35 792
Tsvia Frumkin Israel 9 198 0.8× 294 1.9× 44 0.3× 209 1.5× 121 1.1× 16 505
M. Codina‐Pascual Spain 11 256 1.0× 175 1.2× 95 0.6× 164 1.2× 70 0.7× 15 411
Michelle Merrill United States 6 295 1.2× 261 1.7× 68 0.5× 331 2.3× 164 1.5× 8 629
Tamar Schwartz Israel 11 136 0.6× 273 1.8× 97 0.7× 103 0.7× 118 1.1× 18 481
Alpesh Doshi United Kingdom 14 149 0.6× 143 0.9× 221 1.5× 254 1.8× 251 2.3× 24 562
Teija Peura Australia 14 245 1.0× 490 3.2× 72 0.5× 73 0.5× 289 2.7× 35 651
Vikram Jaswaney United States 7 424 1.7× 245 1.6× 60 0.4× 154 1.1× 16 0.1× 12 489
Xiechao He China 9 73 0.3× 315 2.1× 57 0.4× 31 0.2× 121 1.1× 13 401

Countries citing papers authored by Françoise Devillard

Since Specialization
Citations

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

Fields of papers citing papers by Françoise Devillard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Françoise Devillard

This figure shows the co-authorship network connecting the top 25 collaborators of Françoise Devillard. A scholar is included among the top collaborators of Françoise Devillard 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 Devillard. Françoise Devillard 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.
Troadec, Marie‐Bérengère, Françoise Devillard, David Geneviève, et al.. (2024). Use of Prenatal Exome Sequencing: Opinion Statement of the French Federation of Human Genetics Working Group. Prenatal Diagnosis. 45(3). 299–309. 6 indexed citations
2.
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
3.
Désir, Julie, Damien Haye, Pauline Le Tanno, et al.. (2022). Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis. Clinical Genetics. 103(5). 560–565. 3 indexed citations
4.
Bonati, Maria Teresa, Chiara Castronovo, M. Crippa, et al.. (2019). 9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression. Neurogenetics. 20(3). 145–154. 11 indexed citations
5.
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
6.
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
7.
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
8.
Poreau, Brice, Klaus Dieterich, Véronique Satre, et al.. (2015). 13q31.1 microdeletion: A prenatal case report with macrocephaly and macroglossia. European Journal of Medical Genetics. 58(10). 526–530. 2 indexed citations
9.
David, Marie, Françoise Devillard, Klaus Dieterich, et al.. (2015). Parcours scolaire et prise en charge médico-éducative des enfants avec déficience intellectuelle légère. Archives de Pédiatrie. 22(3). 223–234. 3 indexed citations
10.
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
11.
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
12.
Kocher, Laurence, Jocelyne Brun, Françoise Devillard, Éric Azabou, & Bruno Claustrat. (2014). Phase advance of circadian rhythms in Smith–Magenis syndrome: A case study in an adult man. Neuroscience Letters. 585. 144–148. 6 indexed citations
13.
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
14.
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
15.
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
16.
Devillard, Françoise, Vincent Guinchat, Daniel Moreno‐De‐Luca, et al.. (2010). Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism. American Journal of Medical Genetics Part A. 152A(9). 2346–2354. 14 indexed citations
17.
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
18.
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
19.
Devillard, Françoise. (2002). Polyploidy in large-headed sperm: FISH study of three cases. Human Reproduction. 17(5). 1292–1298. 86 indexed citations
20.
Rousseaux, Sophie, Edith Chevret, Michèle Monteil, et al.. (1995). Meiotic segregation in males heterozygote for reciprocal translocations: analysis of sperm nuclei by two and three colour fluorescence in situ hybridization. Cytogenetic and Genome Research. 71(3). 240–246. 54 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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