Ilse Feenstra

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 49 publications

Unsolicited findings in genomic testing: what do we tell the patient?

Unsolicited findings in genomic testing: what do we tell the patient?

Journal: Nederlands tijdschrift voor geneeskunde

Published: December 24, 2025

Exome sequencing in fetuses with congenital diaphragmatic hernia in a nationwide cohort.

Exome sequencing in fetuses with congenital diaphragmatic hernia in a nationwide cohort.

Journal: Prenatal diagnosis

Published: March 14, 2024

Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter Study.

Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter Study.

Journal: Prenatal diagnosis

Published: February 13, 2024

Lessons learned from rapid exome sequencing for 575 critically ill patients across the broad spectrum of rare disease.

Lessons learned from rapid exome sequencing for 575 critically ill patients across the broad spectrum of rare disease.

Journal: Frontiers in genetics

Published: September 29, 2023

Downgrades: a potential source of moral tension.

Downgrades: a potential source of moral tension.

Journal: Journal of medical ethics

Published: July 21, 2023

All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experience.

All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experience.

Journal: Prenatal diagnosis

Published: October 07, 2022

TSHZ1-dependent gene regulation is essential for olfactory bulb development and olfaction.

TSHZ1-dependent gene regulation is essential for olfactory bulb development and olfaction.

Journal: The Journal of clinical investigation

Published: August 15, 2022

Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.

Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.

Journal: American journal of human genetics

Published: July 08, 2022

Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.

Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.

Journal: American journal of human genetics

Published: January 24, 2022

Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individuals.

Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individuals.

Journal: European journal of human genetics : EJHG

Published: April 11, 2021

Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging.

Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging.

Journal: Prenatal diagnosis

Published: December 23, 2019

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.

Journal: American journal of human genetics

Published: June 24, 2019

Showing 1-12 of 49

Last Updated: 09/26/2026