Manon Suerink

Leiden, ZH, Netherlands

Last Updated: 09/26/2026

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Found 47 publications

ERN GENTURIS guideline on counselling on reproductive options for individuals with a cancer predisposition syndrome (including genturis).

ERN GENTURIS guideline on counselling on reproductive options for individuals with a cancer predisposition syndrome (including genturis).

Journal: European journal of human genetics : EJHG

Published: October 22, 2025

"The Way We Do Things is Unsustainable"-Exploring Symptoms of Burnout Among Healthcare Professionals in Prenatal Genomics.

"The Way We Do Things is Unsustainable"-Exploring Symptoms of Burnout Among Healthcare Professionals in Prenatal Genomics.

Journal: Prenatal diagnosis

Published: September 29, 2025

Experiences of Dutch parents undergoing prenatal genomic testing for fetal structural anomalies: A prospective qualitative analysis.

Experiences of Dutch parents undergoing prenatal genomic testing for fetal structural anomalies: A prospective qualitative analysis.

Journal: Journal of genetic counseling

Published: June 06, 2025

Prenatal Variants of Uncertain Significance (VUS): to report or not to report?

Prenatal Variants of Uncertain Significance (VUS): to report or not to report?

Journal: European journal of human genetics : EJHG

Published: February 20, 2025

Prevalence and Consequences of APC Mosaicism in Patients With Colorectal Adenomas.

Prevalence and Consequences of APC Mosaicism in Patients With Colorectal Adenomas.

Journal: Gastroenterology

Published: February 12, 2025

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

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

Journal: European journal of human genetics : EJHG

Published: July 26, 2024

Prenatal Ultrasonographic Features Associated With ARSL and X-Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series.

Prenatal Ultrasonographic Features Associated With ARSL and X-Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series.

Journal: Prenatal diagnosis

Published: April 04, 2024

Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study.

Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study.

Journal: European journal of human genetics : EJHG

Published: April 02, 2024

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

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

Journal: European journal of human genetics : EJHG

Published: March 27, 2024

Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.

Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.

Journal: European journal of human genetics : EJHG

Published: February 03, 2024

Delineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndrome.

Delineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndrome.

Journal: Genes, chromosomes & cancer

Published: December 14, 2023

De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops.

De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops.

Journal: Journal of medical genetics

Published: October 17, 2023

Showing 1-12 of 47

Last Updated: 09/26/2026