Clarisse Billon

733 total citations
15 papers, 30 citations indexed

About

Clarisse Billon is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Clarisse Billon has authored 15 papers receiving a total of 30 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Pulmonary and Respiratory Medicine and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Clarisse Billon's work include Connective tissue disorders research (5 papers), Aortic Disease and Treatment Approaches (4 papers) and Aortic aneurysm repair treatments (3 papers). Clarisse Billon is often cited by papers focused on Connective tissue disorders research (5 papers), Aortic Disease and Treatment Approaches (4 papers) and Aortic aneurysm repair treatments (3 papers). Clarisse Billon collaborates with scholars based in France, Italy and Canada. Clarisse Billon's co-authors include Valérie Domigo, Nicolas Denarié, Etienne Charpentier, Anne Legrand, Salma Adham, Michael Frank, Xavier Jeunemaı̂tre, A. Millischer, Frederic Galactéros and Flavie Ader and has published in prestigious journals such as SHILAP Revista de lepidopterología, Stroke and Hypertension.

In The Last Decade

Clarisse Billon

9 papers receiving 28 citations

Peers

Clarisse Billon

PRM

NEURO

GENET

CCM

Marzena Romanowska‐Kocejko Poland

Fanchao Wei China

Slavica Trajkova Italy

Jonathan Rosand United States

Holly Snyder United States

Senthil Raghunathan United Kingdom

Sarah Blayney United States

Pilar Galan France

Laurie-Anne Thion France

Duy Ton Vietnam

Marzena Romanowska‐Kocejko Poland

Clarisse Billon

7 ×0.5

PRM

8 ×0.9

NEURO

4 ×0.4

GENET

9 ×1.1

CCM

5 ×0.7

Citations per year, relative to Clarisse Billon Clarisse Billon (= 1×) peers Marzena Romanowska‐Kocejko

Countries citing papers authored by Clarisse Billon

Since Specialization

Citations

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

Fields of papers citing papers by Clarisse Billon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clarisse Billon

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

All Works

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15 of 15 papers shown

Billon, Clarisse, et al.. (2025). Bone graft in bilateral mandibular sagittal split osteotomy: the current state of practice in France. Journal of Stomatology Oral and Maxillofacial Surgery. 126(5). 102419–102419.

Puscas, Tania, Patricia Réant, Erwan Donal, et al.. (2024). Target population for a selective cardiac myosin inhibitor in hypertrophic obstructive cardiomyopathy: Real-life estimation from the French register of hypertrophic cardiomyopathy (REMY). Archives of cardiovascular diseases. 117(6-7). 427–432. 2 indexed citations

Ader, Flavie, Guillaume Jedraszak, Alexandre Janin, et al.. (2024). Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy. Clinical Genetics. 105(6). 676–682. 4 indexed citations

Tetti, Martina, Jacopo Burrello, Marguerite Hureaux, et al.. (2024). Prevalence of Hyperkalemia and Familial Hyperkalemic Hypertension in 5100 Patients Referred to a Tertiary Hypertension Unit. Hypertension. 81(11). 2275–2285.

Billon, Clarisse, Giorgina Barbara Piccoli, Jean‐Madeleine de Sainte Agathe, et al.. (2024). Genome-wide analysis identifies MYH11 compound heterozygous variants leading to visceral myopathy corresponding to late-onset form of megacystis-microcolon-intestinal hypoperistalsis syndrome. Molecular Genetics and Genomics. 299(1). 44–44.

Hagège, Albert, Tania Puscas, Benoît Funalot, et al.. (2024). The French hypertrophic cardiomyopathy gene register: A systematic large gene screening for hypertrophic cardiomyopathy. International Journal of Cardiology. 417. 132542–132542.

Métay, Corinne, Michael Frank, Nicolas Denarié, et al.. (2023). A severe case of PLOD1‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report. SHILAP Revista de lepidopterología. 11(2). e6760–e6760. 2 indexed citations

Eveillard, Jean‐Richard, et al.. (2023). Acquired pseudoxanthoma elasticum-like syndrome and pyruvate kinase deficiency: a case of iron overload?. European Journal of Dermatology. 33(3). 319–320.

Adham, Salma, Anne Debost‐Legrand, Rosa María Bruno, et al.. (2022). Assessment of arterial damage in vascular Ehlers-Danlos syndrome: A retrospective multicentric cohort. Frontiers in Cardiovascular Medicine. 9. 953894–953894. 3 indexed citations

10.

Adham, Salma, A. Legrand, Rosa María Bruno, et al.. (2022). Assessment of arterial damage in vascular Ehlers-Danlos syndrome: a retrospective multicentric cohort. European Heart Journal. 43(Supplement_2).

11.

Chartier, Suzanne, Lucile Boutaud, Caroline Alby, et al.. (2021). Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation. Birth Defects Research. 113(18). 1324–1332. 2 indexed citations

12.

Adham, Salma, Clarisse Billon, Anne Legrand, et al.. (2021). Spontaneous Cervical Artery Dissection in Vascular Ehlers-Danlos Syndrome. Stroke. 52(5). 1628–1635. 13 indexed citations

13.

Albuisson, Juliette, et al.. (2020). Les anévrysmes et dissections héréditaires de l’aorte ascendante. Aspects physiopathologiques, cliniques, syndromologie et classification. Bulletin de l Académie Nationale de Médecine. 204(8). 806–816. 1 indexed citations

14.

Beyaert, C., et al.. (2014). Use of negative heel shoes and pathophysiology of equinus gait in children with cerebral palsy. Gait & Posture. 39. S59–S60. 1 indexed citations

15.

Billon, Clarisse, et al.. (2012). Antibiotic strategy in severe community-acquired pneumococcal pneumonia. Médecine et Maladies Infectieuses. 42(5). 226–234. 2 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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