Researcher Profile

Renske Oegema

0000-0002-7146-617x

Publications

226

Citations

Co-Authors

Active Years

Publications

Open Access Journal Article Human Molecular Genetics May 27, 2025

KDM2B variants in the CxxC domain impair its DNA-binding ability and cause a distinct neurodevelopmental syndrome

Amber S E van Oirsouw · Michael A Hadders · Martijn Koetsier · Edith D J Peters +27 more

10.1093/hmg/ddaf082 3 citations

Open Access Journal Article Genetics in Medicine Jan 01, 2023

Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature

Richard H. van Jaarsveld · Jack Reilly · Marie-Claire Cornips · Michael A. Hadders +55 more

10.1016/j.gim.2022.09.006 35 citations

Journal Article Journal of Clinical Investigation Feb 04, 2020

Lysine acetyltransferase 8 is involved in cerebral development and syndromic intellectual disability

Lin Li · Mohammad Ghorbani · Monika Weisz-Hubshman · Justine Rousseau +30 more

10.1172/jci131145 61 citations

Open Access Journal Article Nature Reviews Neurology Sep 07, 2020

International consensus recommendations on the diagnostic work-up for malformations of cortical development

Renske Oegema · Tahsin Stefan Barakat · Martina Wilke · Katrien Stouffs +23 more

10.1038/s41582-020-0395-6 127 citations

Publication Timeline

2025

2023

2020

Frequent Co-Authors

Idit Maya

2×

Tahsin Stefan Barakat

2×

Mariëlle Alders

2×

Nurit Assia Batzir

1×

Christopher J. Yuskaitis

1×

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