Laurence M. Boon

16.4k total citations · 1 hit paper
122 papers, 7.3k citations indexed

About

Laurence M. Boon is a scholar working on Surgery, Neurology and Oncology. According to data from OpenAlex, Laurence M. Boon has authored 122 papers receiving a total of 7.3k indexed citations (citations by other indexed papers that have themselves been cited), including 100 papers in Surgery, 53 papers in Neurology and 49 papers in Oncology. Recurrent topics in Laurence M. Boon's work include Vascular Malformations and Hemangiomas (98 papers), Vascular Malformations Diagnosis and Treatment (52 papers) and Vascular Tumors and Angiosarcomas (40 papers). Laurence M. Boon is often cited by papers focused on Vascular Malformations and Hemangiomas (98 papers), Vascular Malformations Diagnosis and Treatment (52 papers) and Vascular Tumors and Angiosarcomas (40 papers). Laurence M. Boon collaborates with scholars based in Belgium, United States and France. Laurence M. Boon's co-authors include Miikka Vikkula, John B. Mulliken, O Enjolras, A. Dompmartin, Pascal Brouillard, Patricia E. Burrows, R Vanwijck, Matthew L. Warman, Bjørn R. Olsen and Nisha Limaye and has published in prestigious journals such as Cell, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Laurence M. Boon

117 papers receiving 7.1k citations

Hit Papers

Vascular Dysmorphogenesis Caused by an Activating Mutatio... 1996 2026 2006 2016 1996 100 200 300 400 500

Peers

Laurence M. Boon
Francine Blei United States
Brian H. Kushner United States
Elisa Boscolo United States
Nisha Limaye Belgium
James C. Nicholson United Kingdom
Kaan Gündüz Türkiye
R. Beverly Raney United States
André M. Oliveira United States
Martin Körbling United States
Francine Blei United States
Laurence M. Boon
Citations per year, relative to Laurence M. Boon Laurence M. Boon (= 1×) peers Francine Blei

Countries citing papers authored by Laurence M. Boon

Since Specialization
Citations

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

Fields of papers citing papers by Laurence M. Boon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laurence M. Boon. 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 Laurence M. Boon. The network helps show where Laurence M. Boon may publish in the future.

Co-authorship network of co-authors of Laurence M. Boon

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence M. Boon. A scholar is included among the top collaborators of Laurence M. Boon 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 Laurence M. Boon. Laurence M. Boon 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.
Andrade, Jorge, Ana Rita Grosso, Rui Benedito, et al.. (2025). Angiopoietin–TIE2 feedforward circuit promotes PIK3CA-driven venous malformations. Nature Cardiovascular Research. 4(7). 801–820. 4 indexed citations
2.
Döring, Yvonne, André Schaller, Erik Vassella, et al.. (2024). Non‐Hotspot PIK3CA Variants Have Higher Variant Allele Frequency and are More Common in Syndromic Vascular Malformations. American Journal of Medical Genetics Part A. 197(2). e63883–e63883. 1 indexed citations
3.
Seront, Emmanuel, Cédric Hermans, Laurence M. Boon, & Miikka Vikkula. (2024). Targeted treatments for vascular malformations: current state of the art. Journal of Thrombosis and Haemostasis. 22(11). 2961–2975. 9 indexed citations
4.
Ivars, Marta, Nicole Revençu, Marie‐Cécile Nassogne, et al.. (2024). Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American Journal of Medical Genetics Part A. 194(6). e63551–e63551. 4 indexed citations
5.
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
6.
Seront, Emmanuel, An Van Damme, Nicole Revençu, et al.. (2023). A case report of sirolimus use in early fetal management of lymphatic malformation. Nature Cardiovascular Research. 2(6). 595–599. 14 indexed citations
7.
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
8.
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
9.
Rößler, Jochen, et al.. (2023). Clinical phenotype of adolescent and adult patients with extracranial vascular malformation. Journal of Vascular Surgery Venous and Lymphatic Disorders. 11(5). 1034–1044.e3. 4 indexed citations
10.
Boon, Laurence M., Liliane Marot, Frank Hammer, et al.. (2022). Case report study of thalidomide therapy in 18 patients with severe arteriovenous malformations. Nature Cardiovascular Research. 1(6). 562–567. 24 indexed citations
11.
Boon, Laurence M., et al.. (2022). Molecular pathways and possible therapies for head and neck vascular anomalies. Journal of Oral Pathology and Medicine. 51(10). 878–887. 4 indexed citations
12.
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
13.
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
14.
Queisser, Angela, Emmanuel Seront, Laurence M. Boon, & Miikka Vikkula. (2021). Genetic Basis and Therapies for Vascular Anomalies. Circulation Research. 129(1). 155–173. 120 indexed citations
15.
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
16.
Seront, Emmanuel, et al.. (2020). Theranostic Advances in Vascular Malformations. Journal of Investigative Dermatology. 140(4). 756–763. 42 indexed citations
17.
Damme, An Van, et al.. (2020). New and Emerging Targeted Therapies for Vascular Malformations. American Journal of Clinical Dermatology. 21(5). 657–668. 67 indexed citations
18.
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
19.
Seront, Emmanuel, Nisha Limaye, Laurence M. Boon, & Miikka Vikkula. (2016). La rapamycine ouvre l’ère des thérapies ciblées dans les malformations veineuses. médecine/sciences. 32(6-7). 574–578. 2 indexed citations
20.
Brouillard, Pascal, Laurence M. Boon, & Miikka Vikkula. (2014). Genetics of lymphatic anomalies. Journal of Clinical Investigation. 124(3). 898–904. 216 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026