Jeroen Breckpot
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 25
- Genomics and Rare Diseases 9
- Genetics and Neurodevelopmental Disorders 8
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- Congenital heart defects research 19
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- Prenatal Screening and Diagnostics 6
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- Congenital Heart Disease Studies 8
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- Cardiomyopathy and Myosin Studies 5
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- Chromosomal and Genetic Variations 5
- Co-authors
- Koenraad DevriendtJoris VermeeschBernard ThienpontMarc GewilligHilde PeetersLéon-Charles TrancheventYves MoreauKarel Allegaert
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
Jeroen Breckpot
52 papers receiving 878 citations
Peers
Comparison fields: 5 of 85
- Genetics 392
- Molecular Biology 562
- Pediatrics, Perinatology and Child Health 140
- Epidemiology 221
- Developmental Biology 11
Countries citing papers authored by Jeroen Breckpot
This map shows the geographic impact of Jeroen Breckpot'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 Jeroen Breckpot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jeroen Breckpot more than expected).
Fields of papers citing papers by Jeroen Breckpot
This network shows the impact of papers produced by Jeroen Breckpot. 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 Jeroen Breckpot. The network helps show where Jeroen Breckpot may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Jeroen Breckpot, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 10 | |
| 2 | 2025 | 0 | |
| 3 | 2024 | 1 | |
| 4 | 2024 | 1 | |
| 5 | 2023 | 6 | |
| 6 | 2023 | 15 | |
| 7 | 2023 | 46 | |
| 8 | 2023 | 3 | |
| 9 | 2022 | 25 | |
| 10 | 2020 | 3 | |
| 11 | 2019 | 19 | |
| 12 | 2018 | 16 | |
| 13 | 2017 | 13 | |
| 14 | Massive parallel Sequencing in non-syndromic familial CHD | 2013 | 1 |
| 15 | Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1 | 2013 | 0 |
| 16 | 2010 | 3 | |
| 17 | 2010 | 9 | |
| 18 | 2009 | 6 | |
| 19 | 2009 | 23 | |
| 20 | 2008 | 5 |
About Jeroen Breckpot
Jeroen Breckpot is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 56 papers that have together received 900 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (25 papers), Congenital heart defects research (19 papers), Genomics and Rare Diseases (9 papers), Congenital Heart Disease Studies (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Prenatal Screening and Diagnostics (6 papers), Cardiomyopathy and Myosin Studies (5 papers) and Chromosomal and Genetic Variations (5 papers). The work is most often cited by research in Genetics (392 citations), Molecular Biology (562 citations) and Pediatrics, Perinatology and Child Health (140 citations). Jeroen Breckpot has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Koenraad Devriendt, Joris Vermeesch, Bernard Thienpont, Marc Gewillig, Hilde Peeters, Léon-Charles Tranchevent, Yves Moreau, Karel Allegaert, Thomy de Ravel and Anniek Corveleyn. Their work appears in journals such as Nature Medicine, Scientific Reports and Genome Research.
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.