Jelle Vlaeminck
Brussels, BRU, Belgium
Last Updated: 09/26/2026
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Found 9 publications
Phenotypic and genotypic analysis of pediatric patients with congenital isolated growth hormone deficiency resulting from biallelic variants in the GHRHR gene: a Belgian registry study.
Journal: European journal of pediatrics
Published: March 01, 2026
Case Report: A first case of desmin-related myofibrillar myopathy due to inheritance from a confirmed mosaic asymptomatic carrier.
Journal: Frontiers in genetics
Published: March 21, 2025
Genetic variants associated with ventricular arrhythmias during ajmaline test in Brugada syndrome.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: March 03, 2025
Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variants.
Journal: Journal of assisted reproduction and genetics
Published: September 20, 2024
Case report: A case of severe capecitabine toxicity due to confirmed in trans compound heterozygosity of a common and rare DPYD variant.
Journal: Frontiers in pharmacology
Published: July 04, 2024
Variant-Specific Landscape of Mutual Exclusivity Among BRAF, EGFR, and KRAS Oncogenes Reveals Overlap With Functionally Antagonistic Mutant Pairs.
Journal: International journal of cancer
Published: May 10, 2024
Genomic analysis of methicillin-resistant Staphylococcus aureus clonal complex 239 isolated from Danish patients with and without an international travel history.
Journal: Frontiers in microbiology
Published: August 11, 2022
The dynamic transcriptome during maturation of biofilms formed by methicillin-resistant Staphylococcus aureus.
Journal: Frontiers in microbiology
Published: February 23, 2022
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Last Updated: 09/26/2026