Joery den Hoed
7PUBLICATIONS
50CO-AUTHORS
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Publications (7)
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|Nov 24, 2025
Multiplexable, High-Throughput DNA-Based Technologies in Screening and Confirmatory Testing of Newborn Conditions: A Scoping Review.Terence Diane Fabella, Joery den Hoed, Lidewij Henneman
|Oct 10, 2025
SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder.Maggie M K Wong, Rosalie A Kampen, Ruth O Braden
|Aug 20, 2025
The NuRD component CHD3 promotes BMP signalling during cranial neural crest cell specification.Zoe H Mitchell, Joery den Hoed, Willemijn Claassen
|Aug 07, 2023
PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework.Alexander J M Dingemans, Max Hinne, Kim M G Truijen
|Dec 29, 2022
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions.Elliot Sollis, Joery den Hoed, Marti Quevedo
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Frequent Collaborators
4 joint publications
Simon E Fisher
2 joint publications
Terence Diane Fabella
2 joint publications
Bert B A de Vries
2 joint publications
Erik A Sistermans
2 joint publications
Elizabeth Palmer
2 joint publications
Philippe M Campeau
1 joint publications
Elliot Sollis
1 joint publications
Jan Schouten
1 joint publications
Dick H W Dekkers
1 joint publications
Jeroen A A Demmers
