Maayke de Koning
5PUBLICATIONS
11CO-AUTHORS
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Publications (5)
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|Feb 28, 2026
Experiences of Dutch parents undergoing prenatal genomic testing for fetal structural anomalies: A prospective qualitative analysis.Maayke A de Koning, Sarah Long, Holly E Evans
|Feb 10, 2026
"The Way We Do Things is Unsustainable"-Exploring Symptoms of Burnout Among Healthcare Professionals in Prenatal Genomics.Maayke de Koning, Sarah Long, Marit de Vries
|Aug 21, 2025
Prenatal Variants of Uncertain Significance (VUS): to report or not to report?Maayke A de Koning, Malgorzata I Srebniak, Esther J Oldekamp
|Jan 25, 2024
De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops.Maayke A de Koning, Paula A Pimienta Ramirez, Monique C Haak
|Oct 06, 2021
Prenatal exome sequencing: A useful tool for the fetal neurologist.Maayke A de Koning, Mariëtte J V Hoffer, Esther A R Nibbeling
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Frequent Collaborators
4 joint publications
Manon Suerink
3 joint publications
Gijs W E Santen
1 joint publications
Cacha M P C D Peeters-Scholte
1 joint publications
Yunping Lei
1 joint publications
Malgorzata I Srebniak
1 joint publications
Karin E M Diderich
1 joint publications
Hennie T Bruggenwirth
1 joint publications
Mariëtte J V Hoffer
1 joint publications
Lauren Kelada
1 joint publications
Tony Roscioli
