Pascal Brouillard

3.0k total citations
46 papers, 1.7k citations indexed

About

Pascal Brouillard is a scholar working on Oncology, Surgery and Pathology and Forensic Medicine. According to data from OpenAlex, Pascal Brouillard has authored 46 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Oncology, 19 papers in Surgery and 18 papers in Pathology and Forensic Medicine. Recurrent topics in Pascal Brouillard's work include Vascular Malformations and Hemangiomas (16 papers), Lymphatic System and Diseases (15 papers) and Soft tissue tumors and treatment (14 papers). Pascal Brouillard is often cited by papers focused on Vascular Malformations and Hemangiomas (16 papers), Lymphatic System and Diseases (15 papers) and Soft tissue tumors and treatment (14 papers). Pascal Brouillard collaborates with scholars based in Belgium, United States and France. Pascal Brouillard's co-authors include Miikka Vikkula, Laurence M. Boon, John B. Mulliken, Bjørn R. Olsen, Matthew L. Warman, O Enjolras, Raphaël Helaers, Michella Ghassibe‐Sabbagh, Oon Tian Tan and Alexandre Irrthum and has published in prestigious journals such as Circulation, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Pascal Brouillard

44 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pascal Brouillard Belgium 22 870 776 438 418 298 46 1.7k
Göran Stenman Sweden 26 410 0.5× 613 0.8× 425 1.0× 317 0.8× 819 2.7× 52 2.2k
Penny McKelvie Australia 22 332 0.4× 336 0.4× 360 0.8× 428 1.0× 215 0.7× 84 1.7k
Carmo Martins Portugal 21 433 0.5× 498 0.6× 90 0.2× 216 0.5× 440 1.5× 43 1.2k
Andréï Tchirkov France 22 307 0.4× 389 0.5× 266 0.6× 174 0.4× 702 2.4× 88 1.7k
Eileen Boye United States 17 546 0.6× 305 0.4× 254 0.6× 132 0.3× 429 1.4× 21 1.2k
Charles D. Bangs United States 19 143 0.2× 580 0.7× 138 0.3× 247 0.6× 605 2.0× 44 1.6k
Ulrike Bockmühl Germany 23 572 0.7× 465 0.6× 145 0.3× 187 0.4× 686 2.3× 68 1.6k
Yu Oyama United States 19 166 0.2× 306 0.4× 109 0.2× 483 1.2× 278 0.9× 44 1.5k
Fausto Zorzi Italy 15 508 0.6× 339 0.4× 127 0.3× 157 0.4× 471 1.6× 48 1.4k
Marilu Nelson United States 24 309 0.4× 446 0.6× 116 0.3× 340 0.8× 734 2.5× 51 2.0k

Countries citing papers authored by Pascal Brouillard

Since Specialization
Citations

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

Fields of papers citing papers by Pascal Brouillard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pascal Brouillard

This figure shows the co-authorship network connecting the top 25 collaborators of Pascal Brouillard. A scholar is included among the top collaborators of Pascal Brouillard 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 Pascal Brouillard. Pascal Brouillard 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.
Lebeau, Alizée, Elitsa Ivanova, Silvia Blacher, et al.. (2025). Targeting uPARAP Modifies Lymphatic Vessel Architecture and Attenuates Lymphedema. Circulation. 151(19). 1412–1429. 1 indexed citations
2.
Martin, Manon, Dominique Beckers, Marie-Christine Lebrethon, et al.. (2024). A New Tool to Identify Pediatric Patients with Atypical Diabetes Associated with Gene Polymorphisms. Diabetes & Metabolism Journal. 48(5). 949–959.
3.
Brouillard, Pascal, Aino Murtomäki, Veli‐Matti Leppänen, et al.. (2024). Loss-of-function mutations of the TIE1 receptor tyrosine kinase cause late-onset primary lymphedema. Journal of Clinical Investigation. 134(14). 2 indexed citations
4.
Queisser, Angela, A. Dompmartin, Raphaël Helaers, et al.. (2024). Somatic Loss-of-Function PIK3R1 and Activating Non-hotspot PIK3CA Mutations Associated with Capillary Malformation with Dilated Veins (CMDV). Journal of Investigative Dermatology. 144(9). 2066–2077.e6. 4 indexed citations
5.
Seront, Emmanuel, An Van Damme, Catherine Legrand, et al.. (2023). Preliminary results of the European multicentric phase III trial regarding sirolimus in slow-flow vascular malformations. JCI Insight. 8(21). 28 indexed citations
6.
Giacalone, Guido, Raphaël Helaers, Salma Adham, et al.. (2023). Ureteropelvic junction obstruction with primary lymphoedema associated with CELSR1 variants. Journal of Medical Genetics. 60(12). 1161–1168. 3 indexed citations
7.
Pollet, Hélène, Bénédicte Brichard, Catherine Lambert, et al.. (2023). Splenectomy improves erythrocyte functionality in spherocytosis based on septin abundance, but not maturation defects. Blood Advances. 7(17). 4705–4720. 2 indexed citations
8.
Niyazov, Dmitriy, et al.. (2021). Hypotrichosis‐lymphedema‐telangiectasia syndrome: Report of ileal atresia associated with a SOX18 de novo pathogenic variant and review of the phenotypic spectrum. American Journal of Medical Genetics Part A. 185(7). 2153–2159. 4 indexed citations
9.
Helaers, Raphaël, Christine Galant, Laurence M. Boon, et al.. (2021). KRAS-driven model of Gorham-Stout disease effectively treated with trametinib. JCI Insight. 6(15). 53 indexed citations
10.
Brouillard, Pascal, Matthieu J. Schlögel, Raphaël Helaers, et al.. (2021). Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations. Orphanet Journal of Rare Diseases. 16(1). 267–267. 32 indexed citations
11.
Brouillard, Pascal, Marlys H. Witte, Robert P. Erickson, et al.. (2021). Primary lymphoedema. Nature Reviews Disease Primers. 7(1). 77–77. 53 indexed citations
12.
Smeland, Marie Falkenberg, Pascal Brouillard, Trine Prescott, et al.. (2021). Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis. Journal of Medical Genetics. 60(1). 57–64. 5 indexed citations
13.
d’Avila-Levy, Claudia M., Bertrand Bearzatto, Jérôme Ambroise, et al.. (2020). First Draft Genome of the Trypanosomatid Herpetomonas muscarum ingenoplastis through MinION Oxford Nanopore Technology and Illumina Sequencing. Tropical Medicine and Infectious Disease. 5(1). 25–25. 5 indexed citations
14.
Martínez‐Corral, Inés, Yan Zhang, Henrik Ortsäter, et al.. (2020). Blockade of VEGF-C signaling inhibits lymphatic malformations driven by oncogenic PIK3CA mutation. Nature Communications. 11(1). 2869–2869. 70 indexed citations
15.
Revençu, Nicole, Marie Ravoet, Raphaël Helaers, et al.. (2019). RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation. Journal of Medical Genetics. 57(1). 48–52. 46 indexed citations
16.
Jha, Sawan Kumar, Terhi Kärpänen, Veli‐Matti Leppänen, et al.. (2017). Efficient activation of the lymphangiogenic growth factor VEGF-C requires the C-terminal domain of VEGF-C and the N-terminal domain of CCBE1. Scientific Reports. 7(1). 4916–4916. 66 indexed citations
17.
Brouillard, Pascal, Laurence M. Boon, & Miikka Vikkula. (2014). Genetics of lymphatic anomalies. Journal of Clinical Investigation. 124(3). 898–904. 216 indexed citations
18.
Brouillard, Pascal, Louis Boon, O Enjolras, et al.. (2001). Somatic second hit-hypothesis is true for glomuvenous malformations.. The American Journal of Human Genetics. 69(4). 604–604.
19.
Vikkula, Miikka, et al.. (2001). Truncating mutations in the glomulin gene cause glomuvenous malformations.. The American Journal of Human Genetics. 69(4). 183–183. 2 indexed citations
20.
Brouillard, Pascal, Bjørn R. Olsen, & Miikka Vikkula. (2000). High-Resolution Physical and Transcript Map of the Locus for Venous Malformations with Glomus Cells (VMGLOM) on Chromosome 1p21–p22. Genomics. 67(1). 96–101. 29 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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