S. Ardui

Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells

J. Joung, S. Seneca, J. Vermeesch, 2018, Nucleic acids research.

Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single‐Molecule Sequencing

K. Devriendt, J. Vermeesch, M. Hestand, 2017, Human mutation.

Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management

H. Peeters, K. Devriendt, J. Vermeesch, 2015, European Journal of Human Genetics.

Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics

A. Ameur, J. Vermeesch, M. Hestand, 2018, Nucleic acids research.

The Future of Prenatal Cytogenetics: From Copy Number Variations to Non-invasive Prenatal Testing

J. Vermeesch, S. Ardui, P. Brady, 2013, Current Genetic Medicine Reports.

MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells.

J. Vermeesch, K. Sermon, C. Spits, 2020, Human Molecular Genetics.

MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells

J. Vermeesch, K. Sermon, C. Spits, 2020, bioRxiv.

Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical Experience

T. de Ravel, K. Devriendt, J. Vermeesch, 2018, Front. Genet..