Joris R Vermeesch is an expert in Genetics at Universitair Ziekenhuis Leuven (Belgium). As of October 2026, ScienceLeadR ranks Joris R Vermeesch in the top 1% of experts worldwide for Congenital Abnormalities and Genetic Services. Joris R Vermeesch has authored 548 publications, the most recent in 2026, and is an investigator in 1 clinical trial. SLR score: 1,600 (community average: 125). How the SLR is computed.

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Joris R Vermeesch Universitair Ziekenhuis Leuven Belgium
1 600 ScienceLeadR Reputation 1600
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Genetics

Subspecialties: Biochemistry - Obstetrics - Gynecology

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Expert Rankings

Top experts on the MeSH terms this expert works on

Organizations

Career arc: 1995 - 2026

Source: PubMed

KU Leuven

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 548

Citations

Citations: 27 666 1st author: 24 Last author: 168 Unique author: 6


Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
A nationwide prospective randomized trial for diagnosing developmental disorders demonstrates genome sequencing outperforms standard of care.
PMID 42830293 — genomics, genome
Genome Med20260
The uneven landscape of cognitive domains in 22q11.2 deletion syndrome: A large consortium study.
PMID 42765380 — psychology, clinical
Psychol Med20261
Prevalence and mechanistic origins of genome-wide ploidy abnormalities in ICSI derived human preimplantation embryos.
PMID 42709939 — blastocyst, genome, biopsy, prevalence, haploidy, cytogenetics, sperm injections, intracytoplasmic, ploidies, genetics, medical, triploidy
Hum Mol Genet20260
Cell-free DNA fragmentome analysis informs pregnancy outcome in patients with immune-mediated disease.
PMID 42616843 — cells, pregnancy, triage, pregnancy outcome, cell-free nucleic acids, risk factors
Sci Transl Med20261
Multicentric Longitudinal Performance Monitoring of Different Prenatal Cell-Free DNA Screening Technologies in Belgium.
PMID 42607131 — cells, trisomy, down syndrome, cell-free nucleic acids, dna
Prenat Diagn20260

Clinical Studies 1

Sources: ClinicalTrials, EU CTIS

Synthesis

Principal Investigator: 1

By phase:

N/A 1

By status:

Unknown 1

By type:

Observational 1

By Monocentric/Multicentric:

monocentric 1
multicentric2to4 0
multicentric5to9 0
multicentricup10 0

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