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European Journal of Medical Genetics|August 14, 2016
Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factorJeroen Breckpot, Marieke Vercruyssen, Eddy Weyts, et al.
Clinical Chemistry|June 30, 2022
Pan-Cancer Detection and Typing by Mining Patterns in Large Genome-Wide Cell-Free DNA Sequencing DatasetsHuiwen Che, Tatjana Jatsenko, Liesbeth Lenaerts, et al.
Prenatal Diagnosis|May 22, 2020
Prenatally detected copy number variants in a national cohort: A postnatal follow-up studyJoke Muys, Yves Jacquemyn, Bettina Blaumeiser, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 10, 2021
Outcome of publicly funded nationwide first-tier noninvasive prenatal screeningKris Van Den Bogaert, Lore Lannoo, Nathalie Brison, et al.
Prenatal Diagnosis|October 19, 2018
The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrationsJoke Muys, Bettina Blaumeiser, Yves Jacquemyn, et al.
Obstetrics and Gynecology|May 6, 2021
Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple GestationsMargot van Riel, Nathalie Brison, Machteld Baetens, et al.
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