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Prenatal Diagnosis|December 4, 2023
Cell-free DNA methylation-based preeclampsia prediction: A journey to improve maternal healthMio Aerden, Marie De Borre, Bernard Thienpont
Clinical Dysmorphology|February 19, 2021
Homozygous missense STRADA mutation in a patient with polyhydramnios, megalencephaly and symptomatic epilepsy syndromeMio Aerden, Lore Vallaeys, Maureen Holvoet, et al.
European Journal of Medical Genetics|August 8, 2020
Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactylyMio Aerden, Marijke Bauters, Kris Van Den Bogaert, et al.
Genome Research|July 22, 2025
Genotype imputation from low-coverage data for medical and population genetic analysesSimone Andrea Biagini, Sara Becelaere, Mio Aerden, et al.
Nature Medicine|August 28, 2023
Cell-free DNA methylome analysis for early preeclampsia predictionMarie De Borre, Huiwen Che, Qian Yu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 30, 2023
Differential alternative splicing analysis links variation in ZRSR2 to a novel type of oral-facial-digital syndromeLaurens Hannes, Marta Atzori, Alice Goldenberg, et al.
International Journal of Molecular Sciences|November 26, 2022
Episignature Mapping of <i>TRIP12</i> Provides Functional Insight into Clark-Baraitser SyndromeLiselot van der Laan, Kathleen Rooney, Mariëlle Alders, et al.
European Journal of Human Genetics : EJHG|February 6, 2023
The neurodevelopmental and facial phenotype in individuals with a TRIP12 variantMio Aerden, Anne-Sophie Denommé-Pichon, Dominique Bonneau, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 28, 2025
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, et al.
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