Géraldine Viot

3.5k total citations
56 papers, 1.4k citations indexed

About

Géraldine Viot is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Géraldine Viot has authored 56 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 27 papers in Pediatrics, Perinatology and Child Health and 19 papers in Molecular Biology. Recurrent topics in Géraldine Viot's work include Prenatal Screening and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (13 papers) and Assisted Reproductive Technology and Twin Pregnancy (10 papers). Géraldine Viot is often cited by papers focused on Prenatal Screening and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (13 papers) and Assisted Reproductive Technology and Twin Pregnancy (10 papers). Géraldine Viot collaborates with scholars based in France, United Kingdom and United States. Géraldine Viot's co-authors include Arnold Münnich, Michel Vekemans, Valérie Cormier‐Daire, Stanislas Lyonnet, Véronica Cusin, Annick Toutain, Delphine Girlich, Martine Le Merrer, Anne Moncla and Jürgen‐Christoph von Kleist-Retzow and has published in prestigious journals such as Nature Genetics, American Journal of Obstetrics and Gynecology and The Journal of Pediatrics.

In The Last Decade

Géraldine Viot

53 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Géraldine Viot France 21 674 647 280 144 121 56 1.4k
Graziella Pinto France 26 1.0k 1.5× 717 1.1× 238 0.8× 324 2.3× 105 0.9× 65 2.1k
Mehmet Alikaşifoğlu Türkiye 21 602 0.9× 485 0.7× 126 0.5× 180 1.3× 74 0.6× 115 1.5k
Nicos Skordis Cyprus 24 664 1.0× 569 0.9× 370 1.3× 201 1.4× 69 0.6× 109 1.9k
Piero Pirazzoli Italy 25 686 1.0× 430 0.7× 301 1.1× 245 1.7× 121 1.0× 64 1.7k
Emmanuelle Lemyre Canada 22 550 0.8× 879 1.4× 276 1.0× 129 0.9× 86 0.7× 52 1.3k
Silvia Tabano Italy 25 832 1.2× 470 0.7× 394 1.4× 166 1.2× 84 0.7× 70 1.8k
Helen Kingston United Kingdom 24 839 1.2× 645 1.0× 161 0.6× 122 0.8× 137 1.1× 63 1.9k
Agnes Bankier Australia 27 767 1.1× 990 1.5× 357 1.3× 389 2.7× 126 1.0× 80 2.0k
Paul Kruszka United States 20 453 0.7× 397 0.6× 138 0.5× 120 0.8× 121 1.0× 66 1.1k
P Rochiccioli France 25 562 0.8× 512 0.8× 474 1.7× 183 1.3× 56 0.5× 111 1.7k

Countries citing papers authored by Géraldine Viot

Since Specialization
Citations

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

Fields of papers citing papers by Géraldine Viot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Géraldine Viot

This figure shows the co-authorship network connecting the top 25 collaborators of Géraldine Viot. A scholar is included among the top collaborators of Géraldine Viot 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 Géraldine Viot. Géraldine Viot 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.
Boyer, M., Patricia Fauque, J. de Mouzon, et al.. (2023). Risk factors associated with preterm birth in singletons born after IVF: a national cohort study. Reproductive BioMedicine Online. 46(4). 750–759.
2.
Fauque, Patricia, J. de Mouzon, A. Devaux, et al.. (2020). Reproductive technologies, female infertility, and the risk of imprinting-related disorders. Clinical Epigenetics. 12(1). 191–191. 20 indexed citations
3.
Pessione, Fabienne, J. de Mouzon, Sylvie Epelboin, et al.. (2020). Risques de morbidité maternelle et périnatale en fécondation in vitro : une étude nationale de cohorte française. Gynécologie Obstétrique Fertilité & Sénologie . 48(4). 351–358. 7 indexed citations
4.
Lévy, Jonathan, Aurélie Coussement, Céline Dupont, et al.. (2017). Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome. American Journal of Medical Genetics Part A. 173(8). 2081–2087. 15 indexed citations
5.
Poirier, Karine, et al.. (2017). Loss of Function of KCNC1 is associated with intellectual disability without seizures. European Journal of Human Genetics. 25(5). 560–564. 23 indexed citations
6.
Jacquemard, F., et al.. (2016). Le dépistage prénatal non invasif de la trisomie 21. Étude rétrospective à propos de 8821 patientes. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 45(9). 1127–1132. 3 indexed citations
7.
Streuli, Isabelle, et al.. (2012). FMR1 gene alleles in infertile women with primary ovarian insufficiency, diminished ovarian reserve and poor response to ovarian stimulation. Fertility and Sterility. 98(3). S131–S132. 1 indexed citations
8.
Viot, Géraldine, et al.. (2012). Prenatal diagnosis as a tool and support for eugenics: myth or reality in contemporary French society?. Medicine Health Care and Philosophy. 16(1). 83–91. 5 indexed citations
9.
Budișteanu, Magdalena, Sorina Mihaela Papuc, Jean‐Michel Dupont, et al.. (2012). Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architecture. Psychiatry Research. 197(3). 356–357. 1 indexed citations
10.
Khung‐Savatovsky, Suonavy, Géraldine Viot, Julia Tantau, et al.. (2011). Fetopathologic examination for early termination of pregnancy: dogma or necessity?. American Journal of Obstetrics and Gynecology. 205(5). 467.e1–467.e9. 3 indexed citations
11.
Dupont, Céline, Aziza Lebbar, Cécile Teinturier, et al.. (2007). First reported case of intrachromosomal cryptic inv dup del Xp in a boy with developmental retardation. American Journal of Medical Genetics Part A. 143A(11). 1236–1243. 11 indexed citations
12.
Grangé, G., et al.. (2006). Fréquence des malformations associées à la trisomie 21: À propos de 101 cas fcetopathologiques. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 35(5). 477–482. 2 indexed citations
13.
Hubert, D., Catherine Patrat, Juliette Guibert, et al.. (2006). Results of assisted reproductive technique in men with cystic fibrosis. Human Reproduction. 21(5). 1232–1236. 29 indexed citations
14.
Grangé, G., et al.. (2006). Fréquence des malformations associées à la trisomie 21. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 35(5). 477–482. 4 indexed citations
15.
Viot, Géraldine, Pascale Sonigo, Isabelle Simon, et al.. (2003). Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different. American Journal of Medical Genetics Part A. 126A(2). 123–128. 23 indexed citations
16.
Pannier, E., Géraldine Viot, M. C. Aubry, et al.. (2002). Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygroma. Prenatal Diagnosis. 23(1). 25–30. 19 indexed citations
17.
Viot, Géraldine, Didier Lacombe, Albert David, et al.. (2002). Osteopathia striata cranial sclerosis: Non‐random X‐inactivation suggestive of X‐linked dominant inheritance. American Journal of Medical Genetics. 107(1). 1–4. 28 indexed citations
18.
Leersnyder, Hélène De, Marie‐Christine de Blois, Bruno Claustrat, et al.. (2001). Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome. The Journal of Pediatrics. 139(1). 111–116. 124 indexed citations
19.
Faivre, Laurence, Isabelle Radford, Géraldine Viot, et al.. (2000). Cerebellar ataxia and mental retardation in a child with an inherited satellited chromosome 4q. Annales de Génétique. 43(1). 35–38. 16 indexed citations
20.
Dufourcq-Lagelouse, Rémi, Nathalie Lambert, Michel Duval, et al.. (1999). Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1. European Journal of Human Genetics. 7(6). 633–637. 40 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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