Chantal Thys

4.5k total citations
45 papers, 1.1k citations indexed

About

Chantal Thys is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, Chantal Thys has authored 45 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Hematology, 13 papers in Genetics and 12 papers in Molecular Biology. Recurrent topics in Chantal Thys's work include Platelet Disorders and Treatments (21 papers), Blood groups and transfusion (6 papers) and Genetic Syndromes and Imprinting (4 papers). Chantal Thys is often cited by papers focused on Platelet Disorders and Treatments (21 papers), Blood groups and transfusion (6 papers) and Genetic Syndromes and Imprinting (4 papers). Chantal Thys collaborates with scholars based in Belgium, United Kingdom and United States. Chantal Thys's co-authors include Kathleen Freson, Chris Van Geet, Jos Vermylen, Marc Hoylaerts, Christine Wittevrongel, Rita De Vos, Koenraad Devriendt, Cécile Oury, Emese Tóth-Zsámboki and Achiel Van Hoof and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Medicine.

In The Last Decade

Chantal Thys

45 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chantal Thys Belgium 19 501 332 194 175 166 45 1.1k
Christine Wittevrongel Belgium 18 397 0.8× 241 0.7× 175 0.9× 91 0.5× 68 0.4× 36 882
Yoshimitsu Yura Japan 15 323 0.6× 400 1.2× 57 0.3× 143 0.8× 209 1.3× 33 985
Cheryl Y. Gregory United Kingdom 15 365 0.7× 474 1.4× 153 0.8× 44 0.3× 52 0.3× 25 935
Mengfatt Ho United States 14 267 0.5× 612 1.8× 163 0.8× 105 0.6× 109 0.7× 18 1.0k
Frances Donovan United States 8 339 0.7× 442 1.3× 51 0.3× 48 0.3× 154 0.9× 11 1.5k
Toru Kurokawa Japan 20 132 0.3× 589 1.8× 97 0.5× 66 0.4× 81 0.5× 62 1.4k
Katrina Rack United Kingdom 23 484 1.0× 721 2.2× 390 2.0× 25 0.1× 244 1.5× 58 1.6k
Konrad Oexle Germany 20 70 0.1× 609 1.8× 312 1.6× 75 0.4× 114 0.7× 63 1.3k
Strinivasen Naidoo South Africa 17 135 0.3× 252 0.8× 46 0.2× 86 0.5× 376 2.3× 46 740
Sylvie Taviaux France 21 152 0.3× 992 3.0× 312 1.6× 93 0.5× 87 0.5× 42 1.5k

Countries citing papers authored by Chantal Thys

Since Specialization
Citations

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

Fields of papers citing papers by Chantal Thys

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chantal Thys

This figure shows the co-authorship network connecting the top 25 collaborators of Chantal Thys. A scholar is included among the top collaborators of Chantal Thys 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 Chantal Thys. Chantal Thys 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.
Greene, Daniel, Chantal Thys, Ian Berry, et al.. (2024). Mutations in the U4 snRNA gene RNU4-2 cause one of the most prevalent monogenic neurodevelopmental disorders. Nature Medicine. 30(8). 2165–2169. 27 indexed citations
3.
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
4.
Thys, Chantal, Kathelijne Peerlinck, Chris Van Geet, et al.. (2023). Ribosome dysfunction underlies SLFN14-related thrombocytopenia. Blood. 141(18). 2261–2274. 9 indexed citations
5.
Thys, Chantal, Kathleen Freson, Myron G. Best, et al.. (2021). The brain-derived neurotrophic factor prompts platelet aggregation and secretion. Blood Advances. 5(18). 3568–3580. 17 indexed citations
6.
Thys, Chantal, et al.. (2021). Combined transcriptome and proteome profiling of SRC kinase activity in healthy and E527K defective megakaryocytes. Haematologica. 106(12). 3206–3210. 4 indexed citations
7.
Michele, Michela Di, Etienne Waelkens, Chantal Thys, et al.. (2013). Functional studies and proteomics in platelets and fibroblasts reveal a lysosomal defect with increased cathepsin-dependent apoptosis in ATP1A3 defective alternating hemiplegia of childhood. Journal of Proteomics. 86. 53–69. 12 indexed citations
8.
Izzi, Benedetta, Inge François, Veerle Labarque, et al.. (2012). Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction. PLoS ONE. 7(6). e38579–e38579. 19 indexed citations
9.
Jaeken, Jaak, Elena Levtchenko, Chantal Thys, et al.. (2012). Homozygosity for aquaporin 7 G264V in three unrelated children with hyperglyceroluria and a mild platelet secretion defect. Genetics in Medicine. 15(1). 55–63. 26 indexed citations
10.
Régal, Luc, Christine Wittevrongel, Chantal Thys, et al.. (2012). NPC1 defect results in abnormal platelet formation and function: studies in Niemann–Pick disease type C1 patients and zebrafish. Human Molecular Genetics. 22(1). 61–73. 29 indexed citations
11.
Izzi, Benedetta, Francis de Zegher, Inge François, et al.. (2012). No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity. Journal of Human Genetics. 57(4). 277–279. 3 indexed citations
12.
Waele, Liesbeth De, Kathleen Freson, Chantal Thys, et al.. (2010). Severe Gastrointestinal Bleeding and Thrombocytopenia in a Child With an Anti-GATA1 Autoantibody. Pediatric Research. 67(3). 314–319. 5 indexed citations
13.
Michele, Michela Di, Chantal Thys, Christine Wittevrongel, et al.. (2010). Platelet Gs hypofunction and abnormal morphology resulting from a heterozygous RGS2 mutation. Journal of Thrombosis and Haemostasis. 8(7). 1594–1603. 14 indexed citations
14.
Hermans, Cédric, Christine Wittevrongel, Chantal Thys, et al.. (2009). A compound heterozygous mutation in glycoprotein VI in a patient with a bleeding disorder. Journal of Thrombosis and Haemostasis. 7(8). 1356–1363. 75 indexed citations
15.
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
16.
Freson, Kathleen, Chantal Thys, Christine Wittevrongel, & Chris Van Geet. (2006). Mechanisms of Action and Targets for Actual and Future Antiplatelet Drugs. Mini-Reviews in Medicinal Chemistry. 6(6). 719–726. 9 indexed citations
17.
Freson, Kathleen, Hitoshi Hashimoto, Chantal Thys, et al.. (2004). The pituitary adenylate cyclase–activating polypeptide is a physiological inhibitor of platelet activation. Journal of Clinical Investigation. 113(6). 905–912. 48 indexed citations
18.
19.
Hoylaerts, Marc, et al.. (2001). Anti-vWf Antibodies Induce GPIbα and FcγRII Mediated Platelet Aggregation Only at Low Shear Forces. Journal of Thrombosis and Thrombolysis. 12(3). 249–262. 5 indexed citations
20.
Oury, Cécile, Emese Tóth-Zsámboki, Chris Van Geet, et al.. (2000). A Natural Dominant Negative P2X1 Receptor Due to Deletion of a Single Amino Acid Residue. Journal of Biological Chemistry. 275(30). 22611–22614. 46 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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