Veerle Labarque

1.6k total citations
54 papers, 516 citations indexed

About

Veerle Labarque is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, Veerle Labarque has authored 54 papers receiving a total of 516 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Hematology, 14 papers in Genetics and 10 papers in Molecular Biology. Recurrent topics in Veerle Labarque's work include Platelet Disorders and Treatments (10 papers), Blood Coagulation and Thrombosis Mechanisms (9 papers) and Hemoglobinopathies and Related Disorders (8 papers). Veerle Labarque is often cited by papers focused on Platelet Disorders and Treatments (10 papers), Blood Coagulation and Thrombosis Mechanisms (9 papers) and Hemoglobinopathies and Related Disorders (8 papers). Veerle Labarque collaborates with scholars based in Belgium, Netherlands and Democratic Republic of the Congo. Veerle Labarque's co-authors include Chris Van Geet, Kathleen Freson, Chantal Thys, Christine Wittevrongel, Benedetta Izzi, Lambertus P. van den Heuvel, Elena Levtchenko, Victor S. Blanchette, Anne Uyttebroeck and Manuel Carção and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Veerle Labarque

47 papers receiving 505 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Veerle Labarque Belgium 14 210 123 85 74 62 54 516
Marina Baldini Italy 15 174 0.8× 70 0.6× 179 2.1× 104 1.4× 35 0.6× 52 666
Nicoletta Masera Italy 14 236 1.1× 108 0.9× 246 2.9× 138 1.9× 101 1.6× 37 547
Valentina Pierini Italy 11 158 0.8× 150 1.2× 63 0.7× 31 0.4× 36 0.6× 31 484
Kunihiko Aya Japan 9 78 0.4× 193 1.6× 119 1.4× 39 0.5× 133 2.1× 13 909
Jacob Katz Israel 13 119 0.6× 106 0.9× 62 0.7× 48 0.6× 49 0.8× 30 629
Andrew Loughney United Kingdom 13 57 0.3× 135 1.1× 70 0.8× 84 1.1× 88 1.4× 24 513
N Weber Australia 10 51 0.2× 159 1.3× 82 1.0× 43 0.6× 45 0.7× 31 488
H. C. M. Haanen Netherlands 10 203 1.0× 65 0.5× 82 1.0× 25 0.3× 21 0.3× 13 851
Ivan Macciocca Australia 16 95 0.5× 211 1.7× 86 1.0× 80 1.1× 319 5.1× 36 928
Dale Owens United Kingdom 11 457 2.2× 77 0.6× 181 2.1× 45 0.6× 101 1.6× 18 846

Countries citing papers authored by Veerle Labarque

Since Specialization
Citations

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

Fields of papers citing papers by Veerle Labarque

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Veerle Labarque

This figure shows the co-authorship network connecting the top 25 collaborators of Veerle Labarque. A scholar is included among the top collaborators of Veerle Labarque 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 Veerle Labarque. Veerle Labarque 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.
Lavend’homme, Renaud, Chantal Thys, Sam Noppen, et al.. (2025). Functional assessment of genetic variants in thrombomodulin detected in patients with bleeding and thrombosis. Blood. 145(17). 1929–1942. 3 indexed citations
2.
Sirachainan, Nongnuch, C. Heleen van Ommen, Shoshana Revel‐Vilk, et al.. (2025). International Perspectives on Vitamin K Deficiency Bleeding in Infants: A Cross‐Sectional Questionnaire‐Based Survey. Pediatric Blood & Cancer. 72(10). e31889–e31889.
3.
Geet, Chris Van, Peter Verhamme, Thomas Vanassche, et al.. (2025). Clinical utility of panel-based genetic sequencing for von Willebrand disease. Research and Practice in Thrombosis and Haemostasis. 9(2). 102730–102730. 2 indexed citations
4.
5.
Tshilolo, Léon, et al.. (2024). Relevance of repeated analyses of albuminuria and glomerular filtration rate in African children with sickle cell anaemia. British Journal of Haematology. 205(3). 1137–1146. 1 indexed citations
6.
Labarque, Veerle & Emmanuel Okocha. (2024). Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease. International Journal of Molecular Sciences. 25(10). 5427–5427. 2 indexed citations
7.
Labarque, Veerle, et al.. (2024). Thrombosed massive portal vein aneurysm in an adolescent boy. Pediatric Radiology. 54(11). 1928–1932.
8.
Labarque, Veerle, et al.. (2024). Chinese and Belgian pediatricians’ perspectives toward pediatric palliative care: an online survey. BMC Palliative Care. 23(1). 106–106. 1 indexed citations
9.
Jacquemin, Marc, Veerle Labarque, Chantal Thys, et al.. (2023). Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experience. Journal of Thrombosis and Haemostasis. 21(4). 887–895. 13 indexed citations
10.
11.
Heuvel, Lambertus P. van den, et al.. (2022). Glomerular hyperfiltration: part 2—clinical significance in children. Pediatric Nephrology. 38(8). 2529–2547. 13 indexed citations
12.
Labarque, Veerle, et al.. (2022). Long-Term Outcome of Single-Session, Ultrasound-Guided, Radiofrequency Ablation for Symptomatic Small, Lower Limb, Venous Malformations. SHILAP Revista de lepidopterología. 106(1). 68–68. 2 indexed citations
13.
Ekulu, Pépé Mfutu, et al.. (2022). HIV-associated nephropathy in children: challenges in a resource-limited setting. Pediatric Nephrology. 38(8). 2509–2521. 1 indexed citations
14.
15.
Morren, Marie‐Anne, et al.. (2018). Phosphatidylinositol‐4,5‐bisphosphate 3‐kinase catalytic subunit alpha (PIK3CA)‐related overgrowth spectrum: A brief report. Pediatric Dermatology. 35(3). e186–e188. 9 indexed citations
16.
Labarque, Veerle, et al.. (2016). The Factor VIII to Von Willebrand Factor Antigen (FVIII/VWF:Ag) ratio could be helpful in identifying carriers of hemophilia A. Haemophilia. 22(4). 16. 1 indexed citations
17.
Lemiere, Jurgen, et al.. (2014). Follow-up study of intellectual functioning in children treated for a brain tumor. Pediatric Blood & Cancer. 61. 3 indexed citations
18.
Williams, Suzan, et al.. (2013). Portal vein thrombosis in children and adolescents. Journal of Thrombosis and Haemostasis. 11(2). 1012. 2 indexed citations
19.
Geet, Chris Van, Benedetta Izzi, Veerle Labarque, & Kathleen Freson. (2009). Human platelet pathology related to defects in the G-protein signaling cascade. Journal of Thrombosis and Haemostasis. 7. 282–286. 20 indexed citations
20.
Freson, Kathleen, Benedetta Izzi, Veerle Labarque, et al.. (2008). GNAS Defects Identified by Stimulatory G Protein α-Subunit Signalling Studies in Platelets. The Journal of Clinical Endocrinology & Metabolism. 93(12). 4851–4859. 30 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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