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Joery den Hoed

Showing results (1-10 of 18) with videos related to

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Current Opinion in Genetics & Development|July 5, 2020
Genetic pathways involved in human speech disordersJoery den Hoed, Simon E Fisher
EMBO Reports|July 14, 2021
Molecular networks of the FOXP2 transcription factor in the brainJoery den Hoed, Karthikeyan Devaraju, Simon E Fisher
Scientific Reports|September 26, 2018
Functional characterization of TBR1 variants in neurodevelopmental disorderJoery den Hoed, Elliot Sollis, Hanka Venselaar, et al.
International Journal of Neonatal Screening|November 24, 2025
Multiplexable, High-Throughput DNA-Based Technologies in Screening and Confirmatory Testing of Newborn Conditions: A Scoping ReviewTerence Diane Fabella, Joery den Hoed, Lidewij Henneman, et al.
HGG Advances|October 27, 2025
Functional characterization of pathogenic SATB2 missense variants identifies distinct effects on chromatin binding and transcriptional activityJoery den Hoed, Fleur Semmekrot, Jolijn Verseput, et al.
EMBO Reports|August 20, 2025
The NuRD component CHD3 promotes BMP signalling during cranial neural crest cell specificationZoe H Mitchell, Joery den Hoed, Willemijn Claassen, et al.
Cellular and Molecular Life Sciences : CMLS|December 19, 2020
The Ncoa7 locus regulates V-ATPase formation and function, neurodevelopment and behaviourEnrico Castroflorio, Joery den Hoed, Daria Svistunova, et al.
Human Molecular Genetics|December 29, 2022
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactionsElliot Sollis, Joery den Hoed, Marti Quevedo, et al.
Scientific Reports|April 20, 2021
Induced pluripotent stem cells from subjects with Lesch-Nyhan diseaseDiane J Sutcliffe, Ashok R Dinasarapu, Jasper E Visser, et al.
Journal of Medical Genetics|September 26, 2024
Pathogenic <i>SATB2</i> missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypesJoery den Hoed, Hirokazu Hashimoto, Mubeen Khan, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Current Opinion in Genetics & Development|July 5, 2020
Genetic pathways involved in human speech disordersJoery den Hoed, Simon E Fisher
EMBO Reports|July 14, 2021
Molecular networks of the FOXP2 transcription factor in the brainJoery den Hoed, Karthikeyan Devaraju, Simon E Fisher
Scientific Reports|September 26, 2018
Functional characterization of TBR1 variants in neurodevelopmental disorderJoery den Hoed, Elliot Sollis, Hanka Venselaar, et al.
International Journal of Neonatal Screening|November 24, 2025
Multiplexable, High-Throughput DNA-Based Technologies in Screening and Confirmatory Testing of Newborn Conditions: A Scoping ReviewTerence Diane Fabella, Joery den Hoed, Lidewij Henneman, et al.
HGG Advances|October 27, 2025
Functional characterization of pathogenic SATB2 missense variants identifies distinct effects on chromatin binding and transcriptional activityJoery den Hoed, Fleur Semmekrot, Jolijn Verseput, et al.
EMBO Reports|August 20, 2025
The NuRD component CHD3 promotes BMP signalling during cranial neural crest cell specificationZoe H Mitchell, Joery den Hoed, Willemijn Claassen, et al.
Cellular and Molecular Life Sciences : CMLS|December 19, 2020
The Ncoa7 locus regulates V-ATPase formation and function, neurodevelopment and behaviourEnrico Castroflorio, Joery den Hoed, Daria Svistunova, et al.
Human Molecular Genetics|December 29, 2022
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactionsElliot Sollis, Joery den Hoed, Marti Quevedo, et al.
Scientific Reports|April 20, 2021
Induced pluripotent stem cells from subjects with Lesch-Nyhan diseaseDiane J Sutcliffe, Ashok R Dinasarapu, Jasper E Visser, et al.
Journal of Medical Genetics|September 26, 2024
Pathogenic <i>SATB2</i> missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypesJoery den Hoed, Hirokazu Hashimoto, Mubeen Khan, et al.
Pageof 2