Luc Dehaspe
Impact in
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
Papers in
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- Prenatal Screening and Diagnostics 10
- Fetal and Pediatric Neurological Disorders 3
- Genetics 5
- Genomic variations and chromosomal abnormalities 4
- BRCA gene mutations in cancer 1
- Co-authors
- Joris Vermeesch (20 shared papers)Nathalie Brison (14 shared papers)Eric Legius (9 shared papers)Kris Van Den Bogaert (10 shared papers)Koenraad Devriendt (10 shared papers)Peter Vandenberghe (6 shared papers)Magali Verheecke (5 shared papers)Vincent Vandecaveye (5 shared papers)
- Journals
- npj Genomic Medicine (2 papers)Annals of Oncology (2 papers)European Journal of Human Genetics (2 papers)Genetics in Medicine (2 papers)Blood Advances (1 paper)
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
Luc Dehaspe
21 papers receiving 585 citations
Peers
Comparison fields: 5 of 39
- Pediatrics, Perinatology and Child Health 283
- Cancer Research 183
- Pathology and Forensic Medicine 114
- Genetics 123
- Oncology 103
Countries citing papers authored by Luc Dehaspe
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
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-authors
The 25 scholars most cited alongside Luc Dehaspe, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 138 | |
| 2 | 2015 | 101 | |
| 3 | 2015 | 95 | |
| 4 | 2018 | 50 | |
| 5 | 2016 | 39 | |
| 6 | 2015 | 36 | |
| 7 | 2018 | 29 | |
| 8 | 2012 | 27 | |
| 9 | 2021 | 21 | |
| 10 | 2019 | 19 | |
| 11 | 2020 | 11 | |
| 12 | 2019 | 11 | |
| 13 | 2022 | 10 | |
| 14 | 2016 | 7 | |
| 15 | 2021 | 5 | |
| 16 | High-throughput sample identification and tracking for exome and custom targeted sequencing projects | 2013 | 2 |
| 17 | 2018 | 2 | |
| 18 | 2017 | 1 | |
| 19 | 2013 | 1 | |
| 20 | : Incidence of uncommon fetal aneuploidies detected by non-invasive prenatal testing | 2017 | 1 |
About Luc Dehaspe
Luc Dehaspe is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Cancer Research and Surgery, having authored 21 papers that have together received 607 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (10 papers), Cancer Genomics and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Fetal and Pediatric Neurological Disorders (3 papers), Congenital heart defects research (2 papers), Demographic Trends and Gender Preferences (1 paper), Gene expression and cancer classification (1 paper) and BRCA gene mutations in cancer (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (283 citations), Cancer Research (183 citations), Pathology and Forensic Medicine (114 citations), Genetics (123 citations) and Oncology (103 citations). Luc Dehaspe has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Joris Vermeesch, Nathalie Brison, Eric Legius, Kris Van Den Bogaert, Koenraad Devriendt, Peter Vandenberghe, Magali Verheecke, Vincent Vandecaveye, Daan Dierickx and Thomas Tousseyn. Their work appears in journals such as npj Genomic Medicine, Annals of Oncology, European Journal of Human Genetics, Genetics in Medicine and Blood Advances.
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.