Fanny Pelluard

1.2k total citations
27 papers, 305 citations indexed

About

Fanny Pelluard is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Surgery. According to data from OpenAlex, Fanny Pelluard has authored 27 papers receiving a total of 305 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pediatrics, Perinatology and Child Health, 10 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in Fanny Pelluard's work include Prenatal Screening and Diagnostics (10 papers), Pregnancy and preeclampsia studies (7 papers) and Congenital heart defects research (5 papers). Fanny Pelluard is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Pregnancy and preeclampsia studies (7 papers) and Congenital heart defects research (5 papers). Fanny Pelluard collaborates with scholars based in France, Republic of the Congo and United States. Fanny Pelluard's co-authors include Dominique Carles, Gwenaëlle André, Annie Laquerrière, Louise Devisme, J. Horovitz, Véronique David, Pascale Marcorelles, Claude Bendavid, Sylvie Odent and Laurent Pasquier and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Fanny Pelluard

27 papers receiving 301 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fanny Pelluard France 9 164 74 71 71 50 27 305
B. Bessières France 12 118 0.7× 41 0.6× 61 0.9× 79 1.1× 23 0.5× 23 352
Claudine Le Vaillant France 12 192 1.2× 112 1.5× 73 1.0× 164 2.3× 46 0.9× 45 400
Naohiro Kanayama Japan 8 124 0.8× 50 0.7× 63 0.9× 115 1.6× 80 1.6× 12 369
Necat İmirzalıoğlu Türkiye 11 146 0.9× 64 0.9× 159 2.2× 29 0.4× 60 1.2× 31 429
Christel Eckmann-Scholz Germany 11 85 0.5× 83 1.1× 45 0.6× 107 1.5× 22 0.4× 39 318
Doerte W. Luedders Germany 10 58 0.4× 46 0.6× 56 0.8× 139 2.0× 39 0.8× 29 331
Toby N. Fay United Kingdom 12 136 0.8× 128 1.7× 60 0.8× 159 2.2× 118 2.4× 19 463
S.‐T. Joseph Huang United States 7 72 0.4× 73 1.0× 58 0.8× 135 1.9× 156 3.1× 7 340
Elliott G. Richards United States 15 87 0.5× 145 2.0× 68 1.0× 126 1.8× 67 1.3× 49 565
Hitomi Arahori Japan 11 190 1.2× 62 0.8× 139 2.0× 26 0.4× 18 0.4× 19 642

Countries citing papers authored by Fanny Pelluard

Since Specialization
Citations

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

Fields of papers citing papers by Fanny Pelluard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fanny Pelluard

This figure shows the co-authorship network connecting the top 25 collaborators of Fanny Pelluard. A scholar is included among the top collaborators of Fanny Pelluard 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 Fanny Pelluard. Fanny Pelluard 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.
Ader, Flavie, Caroline Rooryck, Fanny Pelluard, et al.. (2023). Morphological and genetic causes of fetal cardiomyopathies. Clinical Genetics. 104(1). 63–72. 2 indexed citations
2.
Coste, Thibault, Catherine Vincent‐Delorme, Louise Devisme, et al.. (2022). COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage. Prenatal Diagnosis. 42(5). 601–610. 11 indexed citations
3.
Legendre, Marine, et al.. (2021). An Atypical Case of Congenital Erythropoietic Porphyria. Genes. 12(11). 1828–1828. 1 indexed citations
4.
Trimouille, Aurélien, Florent Marguet, Eulalie Lasseaux, et al.. (2020). Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination. Acta Neuropathologica Communications. 8(1). 48–48. 6 indexed citations
5.
Patrier, Sophie, Jacqueline Aziza, Louise Devisme, et al.. (2020). p57-discordant villi in hydropic products of conception: a clinicopathological study of 70 cases. Human Pathology. 101. 18–30. 13 indexed citations
6.
Mattuizzi, Aurélien, Gwenaëlle André, Dominique Carles, et al.. (2020). Adverse perinatal outcomes of chronic intervillositis of unknown etiology: an observational retrospective study of 122 cases. Scientific Reports. 10(1). 12611–12611. 25 indexed citations
7.
Pelluard, Fanny, et al.. (2018). Truncus arteriosus communis: report of three cases and review of literature. African Health Sciences. 18(1). 147–147. 3 indexed citations
8.
Marguet, Florent, Caroline Rooryck, Marie‐Laure Vuillaume, et al.. (2017). Early fetal presentation of Koolen-de Vries: Case report with literature review. European Journal of Medical Genetics. 60(11). 605–609. 1 indexed citations
9.
Delmas, Yahsou, P. Chabanier, Fanny Pelluard, et al.. (2015). Incidence of obstetrical thrombotic thrombocytopenic purpura in a retrospective study within thrombocytopenic pregnant women. A difficult diagnosis and a treatable disease. BMC Pregnancy and Childbirth. 15(1). 19 indexed citations
10.
Carles, Dominique, et al.. (2014). Choriocarcinome gestationnel intra-placentaire de découverte fortuite sur un placenta à terme. Annales de Pathologie. 34(2). 119–123. 4 indexed citations
11.
Pelluard, Fanny, Anne‐Lise Delezoide, Louise Devisme, et al.. (2014). Fetal phenotype associated with the 22q11 deletion. American Journal of Medical Genetics Part A. 164(11). 2724–2731. 33 indexed citations
12.
Toutain, Jérôme, Martina Prochazkova‐Carlotti, David Cappellen, et al.. (2013). Reduced Placental Telomere Length during Pregnancies Complicated by Intrauterine Growth Restriction. PLoS ONE. 8(1). e54013–e54013. 39 indexed citations
13.
Carles, Dominique, et al.. (2013). Anatomie pathologique de l’insuffisance vasculaire utéroplacentaire. Annales de Pathologie. 33(4). 230–236. 3 indexed citations
14.
Carles, Dominique, et al.. (2013). L’artère sous-clavière droite aberrante (arteria lusoria) et le risque de trisomie 21. Analyse rétrospective de 11 479 examens fœtopathologiques. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 43(9). 698–703. 8 indexed citations
15.
Carles, Dominique, et al.. (2012). Tamponnade sur thrombose de la veine interventriculaire antérieure compliquant un cathétérisme veineux central chez un nouveau-né. Annales de Pathologie. 32(3). 217–219. 2 indexed citations
16.
Golfier, François, Jérôme Clerc, Touria Hajri, et al.. (2011). Contribution of referent pathologists to the quality of trophoblastic diseases diagnosis. Human Reproduction. 26(10). 2651–2657. 32 indexed citations
17.
Pelluard, Fanny. (2010). Pathologie du placenta. Cas n° 6. Dysplasie mésenchymateuse du placenta. Annales de Pathologie. 30(4). 301–305. 2 indexed citations
18.
Carles, Dominique, et al.. (2009). Intérêt et limites de l’examen histopathologique des biopsies de villosités choriales. Bulletin de l Académie Nationale de Médecine. 193(3). 675–690. 2 indexed citations
19.
Pasquier, Laurent, Pascale Marcorelles, Philippe Loget, et al.. (2008). Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases. Acta Neuropathologica. 117(2). 185–200. 54 indexed citations
20.
Carles, Dominique, et al.. (2004). Syndrome de Di George, étude rétrospective de 52 cas. Archives de Pédiatrie. 12(3). 254–257. 7 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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