Kris Van Den Bogaert

1.8k citations

36 papers · 998 indexed · h-index 16

Pediatrics, Perinatology and Child Health top 2%
Molecular Biology
Genetics top 10%
Cancer Research top 10%
Otorhinolaryngology top 2%

Co-authors: Joris Vermeesch Nathalie Brison Eric Legius Koenraad Devriendt Guy Van Camp Luc Dehaspe Thomy de Ravel Hilde Van Esch
Topics: Prenatal Screening and Diagnostics (19 papers)Genomic variations and chromosomal abnormalities (12 papers)Fetal and Pediatric Neurological Disorders (8 papers)
Cited by: Otorhinolaryngology Pediatrics, Perinatology and Child Health Sensory Systems
Journals: Nature Communications Scientific Reports The American Journal of Human Genetics
Partner nations: Belgium United States Netherlands

In The Last Decade

Kris Van Den Bogaert

36 papers receiving 950 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical evaluation of long-read sequencing-based episignature detection in developmental disorders 2025 ·Genome Medicine ·(unknown),(unknown),Erika Souche,Jeroen Breckpot,Koenraad Devriendt,Hilde Peeters,Griet Van Buggenhout,Hilde Van Esch,Kris Van Den Bogaert,Joris Vermeesch	10
2	Chromosomal analysis and short-term outcome of prenatally diagnosed congenital heart disease 2025 ·Scientific Reports ·(unknown),(unknown),Koen Devriendt,Kris Van Den Bogaert,Björn Cools,Luc De Catte,Marc Gewillig,Jeroen Breckpot	1
3	Cell type signatures in cell-free DNA fragmentation profiles reveal disease biology 2024 ·Nature Communications ·Kate E. Stanley,Tatjana Jatsenko,(unknown),(unknown),Lore Lannoo,Kristel Van Calsteren,(unknown),Ilse Parijs,(unknown),Kris Van Den Bogaert,Rodrigo A. Toledo,Liesbeth Lenaerts,Sabine Tejpar,Kevin Punie,(unknown),Peter Vandenberghe,Bernard Thienpont,Joris Vermeesch	35
4	What helps define outcomes in persistent uninterpretable non‐invasive prenatal testing: Maternal factors, fetal fraction or quality scores? 2023 ·Prenatal Diagnosis ·Lore Lannoo,(unknown),Nathalie Brison,Ilse Parijs,Leen Vancoillie,Kris Van Den Bogaert,Joris Vermeesch,Koenraad Devriendt,Kristel Van Calsteren	1
5	Inactivating TDP2 missense mutation in siblings with congenital abnormalities reminiscent of fanconi anemia 2023 ·Human Genetics ·Guido Zagnoli-Vieira,Jan Bražina,Kris Van Den Bogaert,(unknown),Guy Molenaers,Keith W. Caldecott,Hilde Van Esch	5
6	Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles 2023 ·European Journal of Human Genetics ·Ilse Parijs,Nathalie Brison,Leen Vancoillie,Machteld Baetens,Bettina Blaumeiser,(unknown),Julie Désir,Boyan Dimitrov,Nathalie Fieremans,Katrien Janssens,Sandra Janssens,(unknown),Björn Menten,(unknown),(unknown),Ann Van Den Bogaert,Koenraad Devriendt,Kris Van Den Bogaert,Joris Vermeesch	2
7	Machine learning-based detection of immune-mediated diseases from genome-wide cell-free DNA sequencing datasets 2022 ·npj Genomic Medicine ·Huiwen Che,Tatjana Jatsenko,Lore Lannoo,(unknown),Luc Dehaspe,Leen Vancoillie,Nathalie Brison,Ilse Parijs,Kris Van Den Bogaert,Koenraad Devriendt,(unknown),Ellen De Langhe,Séverine Vermeire,Bram Verstockt,Kristel Van Calsteren,Joris Vermeesch	9
8	Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge 2022 ·European Journal of Human Genetics ·Lore Lannoo,(unknown),Jeroen Breckpot,Nathalie Brison,Luc De Catte,Eftychia Dimitriadou,Eric Legius,Hilde Peeters,Ilse Parijs,Olga Tšuiko,Leen Vancoillie,Joris Vermeesch,Griet Van Buggenhout,Kris Van Den Bogaert,Kristel Van Calsteren,Koenraad Devriendt	25
9	A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC) 2021 ·Molecular Cytogenetics ·(unknown),Marta Deperas-Kamińska,Ewa Obersztyn,(unknown),Nathalie Brison,Kris Van Den Bogaert,Tomasz Roszkowski,(unknown),Magdalena Bartnik,(unknown),(unknown),Joris Vermeesch,Beata Nowakowska	2
10	Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA 2020 ·Genetics in Medicine ·Huiwen Che,(unknown),Eftychia Dimitriadou,Cindy Melotte,Nathalie Brison,(unknown),Kris Van Den Bogaert,Olga Tšuiko,Koenraad Devriendt,Eric Legius,Masoud Zamani Esteki,Thierry Voet,Joris Vermeesch	21
11	Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening 2019 ·Genetics in Medicine ·Nathalie Brison,(unknown),(unknown),Kristl G. Claeys,Luc Dehaspe,Thomy de Ravel,Liesbeth De Waele,Nathalie Goemans,Eric Legius,Hilde Peeters,Hilde Van Esch,Valérie Race,Joris Vermeesch,Koenraad Devriendt,Kris Van Den Bogaert	19
12	Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M 2018 ·Human Reproduction ·Aspasia Destouni,Eftychia Dimitriadou,(unknown),Sophie Debrock,Cindy Melotte,Kris Van Den Bogaert,Masoud Zamani Esteki,Jia Ding,Thierry Voet,Ellen Denayer,Thomy de Ravel,Eric Legius,Christel Meuleman,Karen Peeraer,Joris Vermeesch	45
13	Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies 2016 ·Genetics in Medicine ·Nathalie Brison,Kris Van Den Bogaert,Luc Dehaspe,(unknown),Katrien Janssens,Bettina Blaumeiser,Hilde Peeters,Hilde Van Esch,Griet Van Buggenhout,Annick Vogels,Thomy de Ravel,Eric Legius,Koenraad Devriendt,Joris Vermeesch	39
14	Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management 2015 ·European Journal of Human Genetics ·(unknown),Luc Dehaspe,Nathalie Brison,Paul Brady,Simon Ardui,Molka Kammoun,(unknown),Klaske D. Lichtenbelt,Kris Van Den Bogaert,Jeroen Van Houdt,Hilde Peeters,Hilde Van Esch,Thomy de Ravel,Eric Legius,Koenraad Devriendt,Joris Vermeesch	98
15	A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1 2007 ·European Journal of Human Genetics ·Melissa Thys,Kris Van Den Bogaert,Vasiliki Iliadou,Kathleen Vanderstraeten,Nele Dieltjens,Isabelle Schrauwen,Wenjie Chen,(unknown),Maria Grigoriadou,Robert J. Pauw,(unknown),Richard J. Smith,Michael B. Petersen,Guy Van Camp	44
16	The Phenotype of the First Otosclerosis Family Linked to OTSC5 2006 ·Otology & Neurotology ·Robert J. Pauw,Els De Leenheer,Kris Van Den Bogaert,P.L.M. Huygen,Guy Van Camp,F.B.M. Joosten,Cor W. R. J. Cremers	3
17	Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease 2006 ·The American Journal of Human Genetics ·Regina C. Betz,Laura Planko,Sibylle Eigelshoven,S. Hanneken,Sandra M. Pasternack,Heinrich Büssow,Kris Van Den Bogaert,Joerg Wenzel,Markus Braun‐Falco,Arno Rütten,Michael A. Rogers,Thomas Ruzicka,Markus M. Nöthen,Thomas M. Magin,Roland Kruse	145
18	Mutation analysis of the GJB2 (Connexin 26) gene in Egypt 2005 ·Human Mutation ·Rikkert L. Snoeckx,(unknown),Nadia Kamal,Kris Van Den Bogaert,Guy Van Camp	49
19	Monogenic nonsyndromic otosclerosis: Audiological and linkage analysis in a large Greek pedigree 2005 ·International Journal of Pediatric Otorhinolaryngology ·Vasiliki Iliadou,Kris Van Den Bogaert,(unknown),(unknown),Kathleen Vanderstraeten,Erik Fransén,Melissa Thys,Maria Grigoriadou,Ανδρέας Παμπάνος,John R. Economides,(unknown),Guy Van Camp,Michael B. Petersen	8
20	A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36 2001 ·The American Journal of Human Genetics ·Kris Van Den Bogaert,Paul Govaerts,Isabelle Schatteman,Matthew Brown,(unknown),F.E. Offeciers,Thomas Somers,Frank Declau,Paul Coucke,Paul Van de Heyning,Richard J. Smith,Guy Van Camp	78

About Kris Van Den Bogaert

Kris Van Den Bogaert is a scholar working on Otorhinolaryngology, Sensory Systems and Pediatrics, Perinatology and Child Health, having authored 36 papers that have together received 998 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (12 papers) and Fetal and Pediatric Neurological Disorders (8 papers). The work is most often cited by research in Otorhinolaryngology (162 citations), Pediatrics, Perinatology and Child Health (404 citations) and Sensory Systems (88 citations). Kris Van Den Bogaert has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Joris Vermeesch, Nathalie Brison, Eric Legius, Koenraad Devriendt, Guy Van Camp, Luc Dehaspe, Thomy de Ravel, Hilde Van Esch, Hilde Peeters and Paul Brady. Their work appears in journals such as Nature Communications, Scientific Reports and The American Journal of Human Genetics.

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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