Joris Vermeesch

Students28

• Benjamin Huremagic“Analysis and Sharing of Whole Genome Sequencing Data”2026 · doctoral
• Antoine Passemiers“Multimodal Analysis of Cell-Free DNA for Early and Sensitive Cancer Detection”2026 · doctoral
• Kate Elizabeth Stanley“Cell free DNA fragmentation in health and disease”2025 · doctoral
• Stefania Tuveri“cfDNA genome-wide methylation profiling for pre-symptomatic cancer detection and typing”2025 · doctoral
• Yan Zhao“Unravelling the mechanisms of chromosomal instability during early embryogenesis.”2025 · doctoral
• Adrian Odrzywolski“The molecular basis of human disease: glioblastoma and skeletal dysplasia”2024 · doctoral
• Maria Siermann“Polygenic Risk Scores in Preimplantation Genetic Testing (PGT-P): Stakeholder Perspectives and Ethical Challenges”2024 · doctoral
• Elia Fernandez Gallardo“A multi-omics genome-plus-transcriptome single-cell atlas of human preimplantation development”2023 · doctoral
• Tine De Coster“Determination of the molecular causes of the incidence of chromosomal instability”2023 · doctoral
• Margot van Riel“Exploring the possibility of non-invasive prenatal diagnosis using cervical cells”2023 · doctoral
• Huiwen Che“Genomic profiling of cell-free DNA”2022 · doctoral
• Lisanne Vervoort“Low copy repeats flanking chromosome 22q11.2 deletion syndrome”2022 · doctoral
• M. Kammoun“Genomic analysis of Congenital Diaphragamatic Hernia”2019 · doctoral
• S. Ardui“Determination of the Variability and Associated Epigenetic Signature of Tandem Repeats by Single Molecule Sequencing”2018 · doctoral
• F. Cristofoli“Identification and functional characterization of novel genes causing syndromic microcephaly”2018 · doctoral
• A. Zablotskaya“Characterization of tandem repeats in human genome and their role in disease”2018 · doctoral
• Amin Ardeshirdavani“A Development Framework for Data Analytics in Genomics”2017 · doctoral
• Alejandro Sifrim“Interpretation and Prioritization of Genomic Single-Nucleotide Variation”2016 · doctoral
• M. Isrie“Discovery of Novel Genes for Intellectual Disability and Multiple Congenital Anomalies in the Next Generation Sequencing Era”2016 · doctoral
• Masoud Zamani Esteki“Haplarithmisis to study haplotypes genome-wide to single-cell resolution, enabling a generic method for preimplantation genectic diagnosis in the clinic and novel fundamental genome research.”2015 · doctoral
• Niels Van der Aa“Sequencen van individuele cellen voor het bestuderen van chromosoom instabiliteit in embryos en de origine van structurele genetische variatie”2015 · doctoral
• Paul Brady“Prenatal Chromosomal Microarray Analysis and Identification of Genetic Variants in Congenital Diaphragmatic Hernia.”2014 · doctoral
• Caroline Robberecht“Copy number variations as cause of infertility and embryonic lethality.”2012 · doctoral
• Femke Hannes“The Molecular Dissection of Contiguous Gene Syndromes with a Focus on 4p16 Deletion Syndrome”2011 · doctoral
• Liesbeth Backx“Implementation of array painting for the identification of candidate genes for (non-)syndromic intellectual disability”2010 · doctoral
• Irina Balikova“The role of copy number variations in the etiology of congenital ocular malformations”2010 · doctoral
• Bernard Thienpont“Improving our Insight in the Genetic Origin of Congenital Heart defects using Array Comparative Genome Hybridization.”2009 · doctoral
• Nicole Maas“Microarray Comparative Genome Hybridization in mental retardation / congenital malformations”2008 · doctoral

Sat beside the lineage

Theses where they were a committee member, examiner or in another role, not as advisor.

• Josefin Johansson“Advanced Genomic Tools in Translational Research of Neurodevelopmental Disorders”opponent · 2022 · Uppsala universitet · doctoral