Kris Van Den Bogaert

1.8k total citations
36 papers, 998 citations indexed

About

Kris Van Den Bogaert is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Kris Van Den Bogaert has authored 36 papers receiving a total of 998 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Pediatrics, Perinatology and Child Health, 15 papers in Molecular Biology and 15 papers in Genetics. Recurrent topics in Kris Van Den Bogaert's work include Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (12 papers) and Fetal and Pediatric Neurological Disorders (8 papers). Kris Van Den Bogaert is often cited by papers focused on Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (12 papers) and Fetal and Pediatric Neurological Disorders (8 papers). Kris Van Den Bogaert collaborates with scholars based in Belgium, United States and Netherlands. Kris Van Den Bogaert's co-authors include Joris Vermeesch, Nathalie Brison, Eric Legius, Koenraad Devriendt, Guy Van Camp, Luc Dehaspe, Thomy de Ravel, Hilde Van Esch, Paul Brady and Hilde Peeters and has published in prestigious journals such as Nature Communications, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Kris Van Den Bogaert

36 papers receiving 950 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kris Van Den Bogaert Belgium 16 404 322 269 191 162 36 998
Erik Huys Netherlands 11 293 0.7× 808 2.5× 1.2k 4.3× 77 0.4× 38 0.2× 20 1.9k
Jeroen Knijnenburg Netherlands 22 201 0.5× 473 1.5× 578 2.1× 111 0.6× 7 0.0× 47 1.4k
M Shohat Israel 15 134 0.3× 329 1.0× 387 1.4× 65 0.3× 4 0.0× 29 911
Paul Bossuyt Belgium 13 37 0.1× 440 1.4× 157 0.6× 77 0.4× 12 0.1× 15 796
Ruth M. Liberfarb United States 18 136 0.3× 283 0.9× 571 2.1× 45 0.2× 7 0.0× 29 880
Christian N. Paxton United States 14 82 0.2× 227 0.7× 74 0.3× 66 0.3× 8 0.0× 33 631
D Donnai United Kingdom 14 70 0.2× 447 1.4× 576 2.1× 40 0.2× 20 0.1× 22 1.2k
Hermann‐Josef Lüdecke Germany 19 117 0.3× 937 2.9× 864 3.2× 149 0.8× 17 0.1× 39 1.8k
Denise Batista United States 21 190 0.5× 429 1.3× 510 1.9× 72 0.4× 27 0.2× 59 1.5k
Gillian L. Hall United Kingdom 18 25 0.1× 304 0.9× 44 0.2× 165 0.9× 378 2.3× 32 1.0k

Countries citing papers authored by Kris Van Den Bogaert

Since Specialization
Citations

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

Fields of papers citing papers by Kris Van Den Bogaert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kris Van Den Bogaert. 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 Kris Van Den Bogaert. The network helps show where Kris Van Den Bogaert may publish in the future.

Co-authorship network of co-authors of Kris Van Den Bogaert

This figure shows the co-authorship network connecting the top 25 collaborators of Kris Van Den Bogaert. A scholar is included among the top collaborators of Kris Van Den Bogaert 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 Kris Van Den Bogaert. Kris Van Den Bogaert 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.
Devriendt, Koen, Kris Van Den Bogaert, Björn Cools, et al.. (2025). Chromosomal analysis and short-term outcome of prenatally diagnosed congenital heart disease. Scientific Reports. 15(1). 3923–3923. 1 indexed citations
2.
Souche, Erika, Jeroen Breckpot, Koenraad Devriendt, et al.. (2025). Clinical evaluation of long-read sequencing-based episignature detection in developmental disorders. Genome Medicine. 17(1). 1–1. 10 indexed citations
3.
Buggenhout, Griet Van, et al.. (2024). Expanding the phenotype of copy number variations involving NR0B1 (DAX1). European Journal of Human Genetics. 32(4). 421–425. 1 indexed citations
4.
Stanley, Kate E., Tatjana Jatsenko, Lore Lannoo, et al.. (2024). Cell type signatures in cell-free DNA fragmentation profiles reveal disease biology. Nature Communications. 15(1). 2220–2220. 35 indexed citations
5.
Lannoo, Lore, Nathalie Brison, Ilse Parijs, et al.. (2023). What helps define outcomes in persistent uninterpretable non‐invasive prenatal testing: Maternal factors, fetal fraction or quality scores?. Prenatal Diagnosis. 43(10). 1333–1343. 1 indexed citations
6.
Parijs, Ilse, Nathalie Brison, Leen Vancoillie, et al.. (2023). Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles. European Journal of Human Genetics. 32(1). 31–36. 2 indexed citations
7.
Lannoo, Lore, Jeroen Breckpot, Nathalie Brison, et al.. (2022). Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge. European Journal of Human Genetics. 30(12). 1323–1330. 25 indexed citations
8.
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
9.
Lannoo, Lore, Liesbeth Lenaerts, Kris Van Den Bogaert, et al.. (2021). Non‐invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?. Prenatal Diagnosis. 41(10). 1264–1272. 15 indexed citations
10.
Deperas-Kamińska, Marta, Ewa Obersztyn, Nathalie Brison, et al.. (2021). A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC). Molecular Cytogenetics. 14(1). 18–18. 2 indexed citations
11.
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
12.
Destouni, Aspasia, Eftychia Dimitriadou, Sophie Debrock, et al.. (2018). Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M. Human Reproduction. 33(12). 2302–2311. 45 indexed citations
13.
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
14.
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
15.
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
16.
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
17.
18.
Thys, Melissa, Kris Van Den Bogaert, Vasiliki Iliadou, et al.. (2007). A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1. European Journal of Human Genetics. 15(3). 362–368. 44 indexed citations
19.
Pauw, Robert J., Els De Leenheer, Kris Van Den Bogaert, et al.. (2006). The Phenotype of the First Otosclerosis Family Linked to OTSC5. Otology & Neurotology. 27(3). 308–315. 3 indexed citations
20.
Bogaert, Kris Van Den, Paul Govaerts, Isabelle Schatteman, et al.. (2001). A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36. The American Journal of Human Genetics. 68(2). 495–500. 78 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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