Mélanie Eyries

6.0k total citations
54 papers, 1.9k citations indexed

About

Mélanie Eyries is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Surgery. According to data from OpenAlex, Mélanie Eyries has authored 54 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Pulmonary and Respiratory Medicine, 20 papers in Genetics and 14 papers in Surgery. Recurrent topics in Mélanie Eyries's work include Pulmonary Hypertension Research and Treatments (24 papers), Vascular Anomalies and Treatments (19 papers) and Vascular Malformations and Hemangiomas (8 papers). Mélanie Eyries is often cited by papers focused on Pulmonary Hypertension Research and Treatments (24 papers), Vascular Anomalies and Treatments (19 papers) and Vascular Malformations and Hemangiomas (8 papers). Mélanie Eyries collaborates with scholars based in France, United States and Australia. Mélanie Eyries's co-authors include Florent Soubrier, David Montani, Marc Humbert, Barbara Girerd, Florence Coulet, Monique Agrapart, David‐Alexandre Trégouët, Kévin Montagne, Olivier Sitbon and Gérald Simonneau and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Mélanie Eyries

52 papers receiving 1.9k citations

Peers

Mélanie Eyries
Neil Davie United Kingdom
Yoshikazu Nakaoka Japan
Sonia Bergaya France
Xinmin Zhou China
Raphaël Thuillet France
Michael W. Pauciulo United States
Wolfgang Bergmeier United States
Roger A. Wagner United States
Jan-Renier Moonen United States
Valerie Schulte Germany
Neil Davie United Kingdom
Mélanie Eyries
Citations per year, relative to Mélanie Eyries Mélanie Eyries (= 1×) peers Neil Davie

Countries citing papers authored by Mélanie Eyries

Since Specialization
Citations

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

Fields of papers citing papers by Mélanie Eyries

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mélanie Eyries

This figure shows the co-authorship network connecting the top 25 collaborators of Mélanie Eyries. A scholar is included among the top collaborators of Mélanie Eyries 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 Mélanie Eyries. Mélanie Eyries 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.
Bisdorff, Annouk, Alexandre Perrier, Erell Guillerm, et al.. (2025). Identification of Somatic Genetic Variants in Superficial Vascular Malformations by Liquid Biopsy in a Cohort of 88 Patients from a French Hospital. Molecular Diagnosis & Therapy. 29(3). 367–380.
2.
Boucly, Athénaïs, Antoine Beurnier, Xavier Jaïs, et al.. (2024). Outcomes and risk assessment in pulmonary veno-occlusive disease. ERJ Open Research. 10(1). 612–2023. 7 indexed citations
3.
Bogaard, Harm Jan, Mélanie Eyries, Olivier Meyrignac, et al.. (2024). Pulmonary vascular phenotype identified in patients withGDF2(BMP9) orBMP10variants: an international multicentre study. European Respiratory Journal. 63(4). 2301634–2301634. 9 indexed citations
4.
Tusseau, Maud, Mélanie Eyries, Nicolas Chatron, et al.. (2024). Genome sequencing identify chromosome 9 inversions disrupting ENG in 2 unrelated HHT families. European Journal of Medical Genetics. 68. 104919–104919. 3 indexed citations
5.
Guilhem, A, Sophie Dupuis‐Girod, Olivier Espitia, et al.. (2023). Seven cases of hereditary haemorrhagic telangiectasia-like hepatic vascular abnormalities associated with EPHB4 pathogenic variants. Journal of Medical Genetics. 60(9). 905–909. 2 indexed citations
6.
Leclercq, Delphine, Lucas Di Meglio, Clémence Marois, et al.. (2023). Late-Onset Status Epilepticus Associated With Isolated Leptomeningeal Angioma and Sturge-Weber Syndrome–Related GNA11 Pathogenic Variation. Neurology. 101(22). 1021–1022. 1 indexed citations
7.
Eyries, Mélanie, et al.. (2023). Isolated Pulmonary Arteriovenous Malformations Associated With BMPR2 Pathogenic Variants. CHEST Journal. 164(2). e23–e26. 2 indexed citations
8.
Adão, Rui, Carmen Brás‐Silva, Mélanie Eyries, et al.. (2023). Physiological and pathophysiological roles of the KCNK3 potassium channel in the pulmonary circulation and the heart. The Journal of Physiology. 601(17). 3717–3737. 5 indexed citations
9.
Starnoni, Daniele, Stanislas Smajda, Alexandre Vivanti, et al.. (2022). Arteriovenous Cerebral High Flow Shunts in Children: From Genotype to Phenotype. Frontiers in Pediatrics. 10. 871565–871565. 5 indexed citations
10.
Giraud, Sophie, Claire Bardel, Sophie Dupuis‐Girod, et al.. (2020). Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia. Orphanet Journal of Rare Diseases. 15(1). 254–254. 5 indexed citations
11.
Guillaumot, Anne, E. Gomez, Mélanie Eyries, et al.. (2020). Une maladie veino-occlusive pulmonaire familiale avec mutation biallélique hétérozygote composite d’EIF2AK4. Revue des Maladies Respiratoires. 37(10). 823–828. 2 indexed citations
12.
Eyries, Mélanie, David Montani, Sophie Nadaud, et al.. (2018). Widening the landscape of heritable pulmonary hypertension mutations in paediatric and adult cases. European Respiratory Journal. 53(3). 1801371–1801371. 66 indexed citations
13.
Eyries, Mélanie & Florent Soubrier. (2016). Diagnóstico genético molecular de la hipertensión arterial pulmonar: una complejidad creciente. Revista Española de Cardiología. 69(11). 1003–1004. 2 indexed citations
14.
Girerd, Barbara, David Montani, Xavier Jaïs, et al.. (2015). Genetic counselling in a national referral centre for pulmonary hypertension. European Respiratory Journal. 47(2). 541–552. 70 indexed citations
15.
Ma, Lijiang, Danilo Roman‐Campos, Eric D. Austin, et al.. (2013). A Novel Channelopathy in Pulmonary Arterial Hypertension. New England Journal of Medicine. 369(4). 351–361. 315 indexed citations
16.
Mustapha, Sélima Fourati Ben, Florence Coulet, Mélanie Eyries, et al.. (2013). In Vitro fertilization failure of normozoospermic men: search for a lack of testicular isozyme of angiotensin-converting enzyme. Basic and Clinical Andrology. 23(1). 4–4. 3 indexed citations
17.
Eyries, Mélanie, Florence Coulet, Barbara Girerd, et al.. (2011). ACVRL1 germinal mosaic with two mutant alleles in hereditary hemorrhagic telangiectasia associated with pulmonary arterial hypertension. Clinical Genetics. 82(2). 173–179. 21 indexed citations
18.
Coulet, Florence, Jérémie H. Lefèvre, Chrystelle Colas, et al.. (2011). Unexplained polyposis: a challenge for geneticists, pathologists and gastroenterologists. Clinical Genetics. 81(1). 38–46. 32 indexed citations
19.
Eyries, Mélanie, Tucker Collins, & Levon M. Khachigian. (2004). Modulation of Growth Factor Gene Expression in Vascular Cells by Oxidative Stress. Endothelium. 11(2). 133–139. 48 indexed citations
20.
Eyries, Mélanie, Annie Michaud, Jaap Deinum, et al.. (2001). Increased Shedding of Angiotensin-converting Enzyme by a Mutation Identified in the Stalk Region. Journal of Biological Chemistry. 276(8). 5525–5532. 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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