Jeroen Dudink

Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome

Marije Meuwissen, Rachel Schot, Sofija Buta et al. · The Journal of Experimental Medicine · 2016 · 290 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy

Annemieke J.M.H. Verkerk, Rachel Schot, Belinda Dumee et al. · The American Journal of Human Genetics · 2009 · 174 citations · Full text

Medicine, Neurology, Neuroscience +10

Feasibility and safety of intranasally administered mesenchymal stromal cells after perinatal arterial ischaemic stroke in the Netherlands (PASSIoN): a first-in-human, open-label intervention study

Lisanne M. Baak, Nienke Wagenaar, Niek E. van der Aa et al. · The Lancet Neurology · 2022 · 161 citations · Full text

Medicine, Neurology, Neurosurgery +15

COL4A2 mutation associated with familial porencephaly and small-vessel disease

Elly Verbeek, Marije Meuwissen, Frans W. Verheijen et al. · European Journal of Human Genetics · 2012 · 122 citations · Full text

Life Sciences, Genetics, Neuroscience +10

Randomized Controlled Early versus Late Ventricular Intervention Study in Posthemorrhagic Ventricular Dilatation: Outcome at 2 Years

Mehmet Nevzat Çizmeci, Floris Groenendaal, Kian D. Liem et al. · The Journal of Pediatrics · 2020 · 115 citations · Full text

Medicine, Cardiology, Interventional Cardiology +1