Jeroen Breckpot

5.6k citations
56 papers · 900 indexed · h-index 19
Topics
Genomic variations and chromosomal abnormalities (25 papers)Congenital heart defects research (19 papers)Genomics and Rare Diseases (9 papers)

In The Last Decade

Jeroen Breckpot

52 papers receiving 878 citations

Peers

Jeroen Breckpot
Comparison fields: 5 of 85
  • Molecular Biology 562
  • Genetics 392
  • Epidemiology 221
  • Pediatrics, Perinatology and Child Health 140
  • Cardiology and Cardiovascular Medicine 96
Replace Vimla S. Aggarwal with:
Vimla S. Aggarwal United States
Boris Keren France
Kerry K. Brown United States
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Shagun Aggarwal India
Qi Tian China
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Judith Goodship United Kingdom
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Citations per field
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Citations per year

Countries citing papers authored by Jeroen Breckpot

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Jeroen Breckpot

This figure shows the co-authorship network connecting the top 25 collaborators of Jeroen Breckpot. A scholar is included among the top collaborators of Jeroen Breckpot 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 Jeroen Breckpot. Jeroen Breckpot 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
#WorkIndexed citations
1 10
2 0
3 1
4 1
5 6
6 15
7 46
8 3
9 25
10 3
11 19
12 16
13 13
14
Massive parallel Sequencing in non-syndromic familial CHD
1
15
Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1
0
16 3
17 9
18 6
19 23
20 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) and Genomics and Rare Diseases (9 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.

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