Séverine Audebert‐Bellanger

997 total citations
11 papers, 103 citations indexed

About

Séverine Audebert‐Bellanger is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Séverine Audebert‐Bellanger has authored 11 papers receiving a total of 103 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Séverine Audebert‐Bellanger's work include Genomic variations and chromosomal abnormalities (3 papers), Cystic Fibrosis Research Advances (2 papers) and Neurofibromatosis and Schwannoma Cases (2 papers). Séverine Audebert‐Bellanger is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Cystic Fibrosis Research Advances (2 papers) and Neurofibromatosis and Schwannoma Cases (2 papers). Séverine Audebert‐Bellanger collaborates with scholars based in France, United Kingdom and Morocco. Séverine Audebert‐Bellanger's co-authors include Claude Férec, L. Misery, C. Abasq‐Thomas, I. Duguépéroux, Martine Blayau, E. Brenaut, P. Wolkenstein, S. Ferkal, Marie‐Pierre Audrézet and Virginie Scotet and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Journal of Medical Genetics and Acta Dermato Venereologica.

In The Last Decade

Séverine Audebert‐Bellanger

10 papers receiving 92 citations

Peers

Séverine Audebert‐Bellanger

NEURO

PRM

GENET

SURGE

PPCH

Manali Chitre United Kingdom

Andrea Dieckmann Germany

C. Cancès France

Alice Masurel France

Sandhya Parkash Canada

Charles D. Madsen United States

Yonit A. Addissie United States

Paulette Barahona Australia

Sui Chien Wong United Kingdom

Kévin Cassinari France

Manali Chitre United Kingdom

Séverine Audebert‐Bellanger

46 ×1.4

NEURO

18 ×0.6

PRM

10 ×0.4

GENET

5 ×0.2

SURGE

14 ×0.6

PPCH

Citations per year, relative to Séverine Audebert‐Bellanger Séverine Audebert‐Bellanger (= 1×) peers Manali Chitre

Countries citing papers authored by Séverine Audebert‐Bellanger

Since Specialization

Citations

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

Fields of papers citing papers by Séverine Audebert‐Bellanger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Séverine Audebert‐Bellanger. 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 Séverine Audebert‐Bellanger. The network helps show where Séverine Audebert‐Bellanger may publish in the future.

Co-authorship network of co-authors of Séverine Audebert‐Bellanger

This figure shows the co-authorship network connecting the top 25 collaborators of Séverine Audebert‐Bellanger. A scholar is included among the top collaborators of Séverine Audebert‐Bellanger 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 Séverine Audebert‐Bellanger. Séverine Audebert‐Bellanger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Uguen, Kévin, Sylvia Redon, Karen Rouault, et al.. (2024). An unusual diagnosis of alpha‐mannosidosis with ocular anomalies: Behind the scenes of a hidden copy number variation. American Journal of Medical Genetics Part A. 194(5). e63532–e63532.

Plaisancié, Julie, Jelena Martinović, Sandra Whalen, et al.. (2023). Clinical, genetic and biochemical signatures of RBP4-related ocular malformations. Journal of Medical Genetics. 61(1). 84–92. 2 indexed citations

Marguet, Florent, Myriam Vézain, Pascale Marcorelles, et al.. (2021). Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants. Acta Neuropathologica Communications. 9(1). 104–104. 15 indexed citations

Édouard, Thomas, Séverine Audebert‐Bellanger, Cindy Colson, et al.. (2021). Joint involvement in Noonan syndrome. A retrospective paediatric descriptive study. Joint Bone Spine. 89(1). 105270–105270. 3 indexed citations

Audebert‐Bellanger, Séverine, Patrick Vourc’h, Sylvie Fraitag, et al.. (2018). Multiple capillary malformations of progressive onset: Capillary malformation–arteriovenous malformation syndrome (CM-AVM). Annales de Dermatologie et de Vénéréologie. 145(8-9). 486–491. 3 indexed citations

Audebert‐Bellanger, Séverine, et al.. (2017). Post-traumatic Stress Disorder in Patients and Relatives Following a Diagnosis of De novo Neurofibromatosis Type 1. Acta Dermato Venereologica. 98(2). 291–293. 3 indexed citations

Brenaut, E., Séverine Audebert‐Bellanger, S. Ferkal, et al.. (2015). Clinical Characteristics of Pruritus in Neurofibromatosis 1. Acta Dermato Venereologica. 96(3). 398–399. 26 indexed citations

Redon, Sylvia, Caroline Bénech, Séverine Audebert‐Bellanger, et al.. (2013). A small de novo 16q24.1 duplication in a woman with severe clinical features. European Journal of Medical Genetics. 56(4). 211–215. 16 indexed citations

Duguépéroux, I., Marie‐Pierre Audrézet, Philippe Parent, et al.. (2012). Cascade testing in families of carriers identified through newborn screening in Western Brittany (France). Journal of Cystic Fibrosis. 12(4). 338–344. 1 indexed citations

10.

Basinko, Audrey, Séverine Audebert‐Bellanger, Nathalie Douet‐Guilbert, et al.. (2011). Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: Molecular characterization of two der(11)t(11;16). American Journal of Medical Genetics Part A. 155(9). 2281–2287. 8 indexed citations

11.

Scotet, Virginie, I. Duguépéroux, Marie‐Pierre Audrézet, et al.. (2010). Focus on cystic fibrosis and other disorders evidenced in fetuses with sonographic finding of echogenic bowel: 16-year report from Brittany, France. American Journal of Obstetrics and Gynecology. 203(6). 592.e1–592.e6. 26 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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