Manon Suerink

18PUBLICATIONS
73CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Clinical neuropsychologyCancer geneticsGene expression (incl. microarray and other genome-wide approaches)Haematological tumours
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Publications (18)

|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

|Jan 13, 2026
ERN GENTURIS guideline on counselling on reproductive options for individuals with a cancer predisposition syndrome (including genturis).

Said C Farschtschi, Candy Kumps, Tamara Hussong Milagre

|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

|Oct 17, 2024
ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management.

Chrystelle Colas, Léa Guerrini-Rousseau, Manon Suerink

|Jul 26, 2024
Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.

Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree

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Frequent Collaborators

4 joint publications

Maayke de Koning

3 joint publications

Gijs W E Santen

3 joint publications

Gabriel Capellá Munar

3 joint publications

Esther Nibbeling