Luc Dehaspe

1.1k total citations
21 papers, 593 citations indexed

About

Luc Dehaspe is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Luc Dehaspe has authored 21 papers receiving a total of 593 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pediatrics, Perinatology and Child Health, 8 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Luc Dehaspe's work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (7 papers) and Cancer Genomics and Diagnostics (6 papers). Luc Dehaspe is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (7 papers) and Cancer Genomics and Diagnostics (6 papers). Luc Dehaspe collaborates with scholars based in Belgium, United States and Netherlands. Luc Dehaspe's co-authors include Joris Vermeesch, Nathalie Brison, Eric Legius, Kris Van Den Bogaert, Koenraad Devriendt, Peter Vandenberghe, Daan Dierickx, Vincent Vandecaveye, Magali Verheecke and Frédéric Amant and has published in prestigious journals such as Cancer Research, Annals of Oncology and Clinical Chemistry.

In The Last Decade

Luc Dehaspe

21 papers receiving 570 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luc Dehaspe Belgium 11 297 223 191 189 124 21 593
Anthony T. Gordon United Kingdom 13 470 1.6× 143 0.6× 309 1.6× 297 1.6× 151 1.2× 19 878
Fiona S. Togneri United Kingdom 7 226 0.8× 96 0.4× 197 1.0× 115 0.6× 27 0.2× 9 440
Wing‐Shan Lee Hong Kong 10 145 0.5× 328 1.5× 68 0.4× 289 1.5× 39 0.3× 12 506
Rachel T. Klein United States 10 48 0.2× 205 0.9× 354 1.9× 204 1.1× 299 2.4× 15 600
Katie Beierl United States 15 216 0.7× 209 0.9× 89 0.5× 167 0.9× 104 0.8× 24 683
Iris H.I.M. Hollink Netherlands 19 50 0.2× 162 0.7× 130 0.7× 684 3.6× 41 0.3× 35 1.2k
Natalie Banet United States 11 106 0.4× 44 0.2× 51 0.3× 152 0.8× 42 0.3× 33 519
C. R. Bartram Germany 11 142 0.5× 60 0.3× 60 0.3× 183 1.0× 110 0.9× 17 696
Ji Cheng United States 3 56 0.2× 80 0.4× 93 0.5× 263 1.4× 35 0.3× 7 534
E. Renate Panzer-Grümayer Austria 14 244 0.8× 78 0.3× 40 0.2× 203 1.1× 243 2.0× 20 1.0k

Countries citing papers authored by Luc Dehaspe

Since Specialization
Citations

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

Fields of papers citing papers by Luc Dehaspe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luc Dehaspe

This figure shows the co-authorship network connecting the top 25 collaborators of Luc Dehaspe. A scholar is included among the top collaborators of Luc Dehaspe 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 Luc Dehaspe. Luc Dehaspe 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.
Che, Huiwen, Tatjana Jatsenko, Lore Lannoo, et al.. (2022). Machine learning-based detection of immune-mediated diseases from genome-wide cell-free DNA sequencing datasets. npj Genomic Medicine. 7(1). 55–55. 9 indexed citations
2.
Włodarska, Iwona, Olivier Gheysens, Luc Dehaspe, et al.. (2021). The landscape of copy number variations in classical Hodgkin lymphoma: a joint KU Leuven and LYSA study on cell-free DNA. Blood Advances. 5(7). 1991–2002. 18 indexed citations
3.
Delforge, Michel, Luc Dehaspe, Thomas Tousseyn, et al.. (2021). Ultra-low coverage whole genome sequencing of ccfDNA in multiple myeloma: A tool for laboratory routine?. Cancer Treatment and Research Communications. 28. 100380–100380. 5 indexed citations
4.
Brison, Nathalie, Kristl G. Claeys, Luc Dehaspe, et al.. (2019). Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening. Genetics in Medicine. 21(12). 2774–2780. 19 indexed citations
5.
Che, Huiwen, Marijke Van Ghelue, Luc Dehaspe, et al.. (2019). Fetal sex determination in twin pregnancies using non-invasive prenatal testing. npj Genomic Medicine. 4(1). 15–15. 10 indexed citations
6.
Lenaerts, Liesbeth, Peter Vandenberghe, Nathalie Brison, et al.. (2018). Genomewide copy number alteration screening of circulating plasma DNA: potential for the detection of incipient tumors. Annals of Oncology. 30(1). 85–95. 29 indexed citations
7.
Brison, Nathalie, Luc Dehaspe, Kris Van Den Bogaert, et al.. (2018). Predicting fetoplacental chromosomal mosaicism during non‐invasive prenatal testing. Prenatal Diagnosis. 38(4). 258–266. 47 indexed citations
8.
Lenaerts, Liesbeth, Nathalie Brison, Huiwen Che, et al.. (2018). Unbiased genomewide screening of circulating plasma DNA for cancer detection. Annals of Oncology. 29. viii479–viii479. 2 indexed citations
9.
Brison, Nathalie, Kris Van Den Bogaert, Luc Dehaspe, et al.. (2017). : Incidence of uncommon fetal aneuploidies detected by non-invasive prenatal testing. VUBIR (Vrije Universiteit Brussel). 100–100. 1 indexed citations
10.
Brison, Nathalie, Kris Van Den Bogaert, Luc Dehaspe, et al.. (2017). Accuracy and Clinical Value of Maternal Incidental Findings During Noninvasive Prenatal Testing for Fetal Aneuploidies. Obstetrical & Gynecological Survey. 72(8). 469–470. 1 indexed citations
11.
Brison, Nathalie, Kris Van Den Bogaert, Luc Dehaspe, et al.. (2016). Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies. Genetics in Medicine. 19(3). 306–313. 39 indexed citations
12.
Hestand, Matthew S., Beata Nowakowska, Elfi Vergaelen, et al.. (2016). A catalog of hemizygous variation in 127 22q11 deletion patients. Human Genome Variation. 3(1). 15065–15065. 7 indexed citations
13.
Brison, Nathalie, Kris Van Den Bogaert, Luc Dehaspe, et al.. (2016). Maternal incidental findings during non-invasive prenatal testing for fetal aneuploidies. 32–32. 1 indexed citations
14.
Dehaspe, Luc, Nathalie Brison, Paul Brady, et al.. (2015). Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management. European Journal of Human Genetics. 23(10). 1286–1293. 98 indexed citations
15.
Louw, Jacoba, Jeroen Breckpot, Bert Callewaert, et al.. (2015). The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects. American Journal of Medical Genetics Part A. 167(8). 1822–1829. 36 indexed citations
16.
Vandenberghe, Peter, Iwona Włodarska, Thomas Tousseyn, et al.. (2015). Non-invasive detection of genomic imbalances in Hodgkin/Reed-Sternberg cells in early and advanced stage Hodgkin's lymphoma by sequencing of circulating cell-free DNA: a technical proof-of-principle study. The Lancet Haematology. 2(2). e55–e65. 94 indexed citations
17.
Amant, Frédéric, Magali Verheecke, Iwona Włodarska, et al.. (2015). Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing. JAMA Oncology. 1(6). 814–814. 136 indexed citations
18.
Houdt, Jeroen Van, et al.. (2013). High-throughput sample identification and tracking for exome and custom targeted sequencing projects. European Journal of Human Genetics. 21. 165–165. 2 indexed citations
19.
Bosch, Linda J.W., Geert Trooskens, Pétur Snæbjörnsson, et al.. (2013). Abstract 1155: Promoter CpG island hypermethylation of Decoy Receptor 1 (DCR1) is associated with poor response to irinotecan in colorectal cancer.. Cancer Research. 73(8_Supplement). 1155–1155. 1 indexed citations
20.
Michils, G, Luc Dehaspe, Jeroen Van Houdt, et al.. (2012). Molecular Analysis of the Breast Cancer Genes BRCA1 and BRCA2 Using Amplicon-Based Massive Parallel Pyrosequencing. Journal of Molecular Diagnostics. 14(6). 623–630. 27 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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