Joris Vermeesch

Professor

KULeuven

Belgium

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About

Joris Vermeesch is a Professor at KULeuven in Belgium. His research primarily focuses on non-invasive prenatal testing, prenatal cell-free DNA analysis, and the clinical management of high-risk pregnancies. Recent articles authored by Professor Vermeesch explore the implications of genetic screening and the experiences of healthcare professionals in this field.

Articles (16)

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2025

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2025

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2024

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2021

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2021

Collaborators (7)

Priit Palta

University of Helsinki

FINLAND

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Kristel Van Calsteren

BELGIUM

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Mark Pertile

Head, Divisions of Reproductive Genetics and Biochemical Genetics

AUSTRALIA

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Lisa Hui

Associate Professor

University of Melbourne

AUSTRALIA

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Andres Salumets

Professor of reproductive medicine

Karolinska Institutet-Huddinge Campus

SWEDEN

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Pascal Borry

Prof. Dr. at KU Leuven

KU Leuven

BELGIUM

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Neeta Vora

Professor

University of North Carolina at Chapel Hill

UNITED STATES

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Joris Vermeesch

Research Interests

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About

Articles (16)

BinDel

Persistent Uninterpretable or Failed Prenatal Cell‐Free DNA Screening Indicates a High‐Risk Pregnancy and is Associated With Biological Factors Interfering With cfDNA‐Analysis: A Prospective Cohort Study

Healthcare professionals’ experiences with expanded noninvasive prenatal screening: challenges and solutions

Comprehensive Recommendations for the Clinical Management of Pregnant Women With Noninvasive Prenatal Test Results Suspicious of a Maternal Malignancy

Gollop–Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11

Ultrasensitive Microhaplotype-Based Detection of Minor Alleles in Cervical Samples of Pregnant Women Identifies Sperm Rather Than Fetal DNA

What helps define outcomes in persistent uninterpretable non‐invasive prenatal testing: Maternal factors, fetal fraction or quality scores?

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

Low copy repeats in the genome: from neglected to respected

Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores

Non-invasive prenatal testing: when results suggests maternal cancer

The 22q11.2 Low Copy Repeats

Commentary on Multiple Copy Number Variants Detected by Noninvasive Prenatal Testing

The Hunt for the Chromosome 22q11.2 Deletion Syndrome Schizophrenia Genes

Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples

International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies

Collaborators (7)

Priit Palta

Kristel Van Calsteren

Mark Pertile

Lisa Hui

Andres Salumets

Pascal Borry

Neeta Vora

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