Joris Vermeesch

30.4k citations

381 papers · 13.3k indexed · 5 hit papers · h-index 59

Molecular Biology top 0.5%
Genetics top 0.05%
Pediatrics, Perinatology and Child Health top 0.1%
Plant Science top 1%
Cancer Research top 1%

Co-authors: Koenraad Devriendt Thierry Voet Jean‐Pierre Fryns Matthew S. Hestand Yves Moreau Simon Ardui Thomy de Ravel Peter Marynen
Topics: Genomic variations and chromosomal abnormalities (198 papers)Prenatal Screening and Diagnostics (123 papers)Chromosomal and Genetic Variations (76 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Science Nucleic Acids Research Journal of Biological Chemistry
Partner nations: Belgium United States Netherlands

In The Last Decade

Joris Vermeesch

366 papers receiving 12.8k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

22q11.2 deletion syndrome

2015 791 citations Donna M. McDonald‐McGinn, Ann Swillen et al. profile →
Chromosome instability is common in human cleavage-stage embryos

2009 601 citations Thierry Voet, Cindy Melotte et al. Nature Medicine profile →
Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics

2018 493 citations Simon Ardui, Joris Vermeesch et al. profile →
Mosaic Copy Number Variation in Human Neurons

2013 380 citations Michael J. McConnell, Michael Lindberg et al. Science profile →
Position statement from the International Society for Prenatal Diagnosis on the use of non‐invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies

2023 58 citations Mark D. Pertile, Joris Vermeesch et al. Prenatal Diagnosis profile →

Peers

Countries citing papers authored by Joris Vermeesch

Since Specialization

Citations

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

Fields of papers citing papers by Joris Vermeesch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joris Vermeesch. 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 Joris Vermeesch. The network helps show where Joris Vermeesch may publish in the future.

Co-authorship network of co-authors of Joris Vermeesch

This figure shows the co-authorship network connecting the top 25 collaborators of Joris Vermeesch. A scholar is included among the top collaborators of Joris Vermeesch 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 Joris Vermeesch. Joris Vermeesch is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Origin and development of uniparental and polyploid blastomeres 2025 ·iScience ·(unknown),(unknown),(unknown),Tatjana Jatsenko,(unknown),(unknown),(unknown),Thierry Voet,Olga Tšuiko,Ants Kurg,Katrien Smits,Ann Van Soom,Joris Vermeesch	1
2	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
3	Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndrome 2024 ·Genome Research ·(unknown),Nicolas Dierckxsens,(unknown),(unknown),Erika Souche,(unknown),Tracy Heung,Koenraad Devriendt,Hilde Peeters,Donna M. McDonald‐McGinn,Ann Swillen,Jeroen Breckpot,Beverly S. Emanuel,Hilde Van Esch,Anne S. Bassett,Joris Vermeesch	1
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	Cell-free DNA methylome analysis for early preeclampsia prediction 2023 ·Nature Medicine ·(unknown),Huiwen Che,Qian Yu,Lore Lannoo,(unknown),Leen Vancoillie,Pauline Dreesen,(unknown),(unknown),Eva Galle,Jeroen Breckpot,Joachim Van Keirsbilck,Wilfried Gyselaers,Koenraad Devriendt,Joris Vermeesch,Kristel Van Calsteren,Bernard Thienpont	46
6	Primary mediastinal large B‐cell lymphoma is characterized by large‐scale copy‐neutral loss of heterozygosity 2022 ·Genes Chromosomes and Cancer ·(unknown),Koen Debackere,Lukas Marcelis,Nicolas Dierckxsens,Jonas Demeulemeester,Eftychia Dimitriadou,Daan Dierickx,Pierre Lefesvre,Karen Deraedt,Carlos Graux,Lucienne Michaux,Jan Cools,Thomas Tousseyn,Joris Vermeesch,Iwona Włodarska	3
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	Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples 2021 ·PLoS Computational Biology ·(unknown),(unknown),Amin Ardeshirdavani,(unknown),Joris Vermeesch,Andres Salumets,Kaarel Krjutškov,Priit Palta	5
9	The landscape of copy number variations in classical Hodgkin lymphoma: a joint KU Leuven and LYSA study on cell-free DNA 2021 ·Blood Advances ·(unknown),Iwona Włodarska,(unknown),Olivier Gheysens,Luc Dehaspe,Thomas Tousseyn,Luc‐Matthieu Fornecker,Julien Lazarovici,Olivier Casasnovas,Anne‐Claire Gac,Christophe Bonnet,Kamal Bouabdallah,Christiane Copie‐Bergman,Bettina Fabiani,Daan Dierickx,Lukas Marcelis,Joris Vermeesch,Marc André,Peter Vandenberghe	18
10	MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells 2020 ·Human Molecular Genetics ·(unknown),(unknown),Simon Ardui,Yannick De Vlaeminck,Joke Allemeersch,(unknown),Claudia Spits,Fien Vanroye,Pierre Hilven,(unknown),Joris Vermeesch,Alexander Gheldof,Karen Sermon	5
11	LEF1 haploinsufficiency causes ectodermal dysplasia 2020 ·Clinical Genetics ·Jonathan Lévy,Yline Capri,(unknown),Céline Dupont,Joris Vermeesch,Koenraad Devriendt,Alain Verloès,Anne‐Claude Tabet,Isabelle Bailleul‐Forestier	12
12	International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies 2020 ·Prenatal Diagnosis ·Glenn E. Palomaki,Rossa W. K. Chiu,Mark D. Pertile,Erik A. Sistermans,Yuval Yaron,Joris Vermeesch,Neeta L. Vora,Robert G. Best,Louise Wilkins‐Haug	41
13	Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition 2019 ·Genetics in Medicine ·Marta Unolt,Molka Kammoun,Beata Nowakowska,Gail E. Graham,T. Blaine Crowley,Matthew S. Hestand,(unknown),Maciej Geremek,Beverly S. Emanuel,Elaine H. Zackai,Joris Vermeesch,Donna M. McDonald‐McGinn	7
14	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
15	NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies 2018 ·Scientific Reports ·(unknown),Olga Žilina,Ants Kurg,(unknown),Maire Peters,(unknown),Anne Mari Roost,(unknown),Priit Palta,Nathalie Brison,Joris Vermeesch,Kaarel Krjutškov,Andres Salumets,Lauris Kaplinski	12
16	Mosaic Copy Number Variation in Human Neuronsbreakdown → 2013 ·Science ·Michael J. McConnell,Michael Lindberg,Kristen Brennand,(unknown),Thierry Voet,(unknown),(unknown),Roger S. Lasken,Joris Vermeesch,Ira M. Hall,Fred H. Gage	380
17	Genomic microarrays: a technology overview 2012 ·Prenatal Diagnosis ·Paul Brady,Joris Vermeesch	42
18	Array-CGH: A novel tool in genetic diagnosis of individuals with congenital heart defects 2006 ·European Journal of Human Genetics ·Bernard Thienpont,Luc Mertens,Peter Van Loo,Bénédicte Eyskens,Derize Boshoff,(unknown),Thomy de Ravel,Jean‐Pierre Fryns,Marc Gewillig,Joris Vermeesch,Koenraad Devriendt	0
19	Molecular karkyotyping detecs structural low grade mosaics in 4 % of patietns with idiopathic mental retardation and multiple congenital aberrations 2005 ·European Journal of Human Genetics ·(unknown),Björn Menten,Cindy Melotte,Bernard Thienpont,Karen Buysse,(unknown),Peter Marynen,Anne De Paepe,Jean‐Pierre Fryns,Geert Mortier,Koenraad Devriendt,Frank Speleman,Joris Vermeesch	2
20	Telomere length regulation in telomerase positive murine cell line 1998 ·Ghent University Academic Bibliography (Ghent University) ·Sofie Bekaert,Joris Vermeesch,Peter Marynen,Patric Van Oostveldt	1

About Joris Vermeesch

Joris Vermeesch is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Developmental Biology, having authored 381 papers that have together received 13.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (198 papers), Prenatal Screening and Diagnostics (123 papers) and Chromosomal and Genetic Variations (76 papers). The work is most often cited by research in Genetics (6.4k citations), Pediatrics, Perinatology and Child Health (3.6k citations) and Molecular Biology (6.6k citations). Joris Vermeesch has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Koenraad Devriendt, Thierry Voet, Jean‐Pierre Fryns, Matthew S. Hestand, Yves Moreau, Simon Ardui, Thomy de Ravel, Peter Marynen, Hilde Van Esch and Adam Ameur. Their work appears in journals such as Science, Nucleic Acids Research and Journal of Biological Chemistry.

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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