Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndromeJ. K. J. VAN HOUDT, Joris Vermeesch, Matthew A. Deardorff et al.|Nature Genetics|2012Cited by 244
Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidiesNathalie Brison, Joris Vermeesch|Genetics in Medicine|2016Cited by 60
Genomewide copy number alteration screening of circulating plasma DNA: potential for the detection of incipient tumorsLiesbeth Lenaerts, Joris Vermeesch|Annals of Oncology|2018Cited by 57
Extreme enrichment of VNTR-associated polymorphicity in human subtelomeres: genes with most VNTRs are predominantly expressed in the brainJasper Linthorst, Henne Holstege, Wim Meert et al.|Translational Psychiatry|2020Cited by 26
Novel STIL Compound Heterozygous Mutations Cause Severe Fetal Microcephaly and Centriolar LengtheningFrancesca Cristofoli, Hilde Van Esch, B. De Keersmaecker et al.|Molecular Syndromology|2017Cited by 21