Nicole Corsten-Janssen

5PUBLICATIONS
16CO-AUTHORS
Molecular targetsFoetal development and medicineGene expression (incl. microarray and other genome-wide approaches)GenomicsCardiology (incl. cardiovascular diseases)
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Publications (5)

|Mar 21, 2025
XRCC4-related microcephalic primordial dwarfism: description of a clinical series of 7 cases, phenotype expansion and new diagnostic approaches.

Silvestre Cuinat, Nicolas Chatron, Florence Petit

|Oct 13, 2021
Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancy.

Mirjam Plantinga, Lauren Zwienenberg, Eva van Dijk

|Jul 07, 2020
A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound.

Nicole Corsten-Janssen, Katelijne Bouman, Janouk C D Diphoorn

|Apr 26, 2020
Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging.

Chantal Deden, Kornelia Neveling, Dimitra Zafeiropopoulou

|Nov 01, 2017
Clinical and molecular effects of CHD7 in the heart.

Nicole Corsten-Janssen, Peter J Scambler

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Frequent Collaborators

1 joint publications

Peter J Scambler

1 joint publications

Wendy A G van Zelst-Stams

1 joint publications

Leonie K Duin

1 joint publications

Mirjam Plantinga