C. Peeters‐Scholte

Cranial Ultrasound Is an Important Tool in the Recognition of Life-Threatening Infratentorial Hemorrhage in Newborns

L. D. de Vries, M. Fumagalli, S. Steggerda, 2020, Neuropediatrics.

Combining advanced MRI and EEG techniques better explains long-term motor outcome after very preterm birth

C. Stam, S. Steggerda, A. A. van den Berg-Huysmans, 2021, Pediatric Research.

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

B. V. van Bon, R. Pfundt, G. Carvill, 2021, American journal of human genetics.

Biallelic ADAM22 pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsy

H. Mefford, A. Paetau, P. Striano, 2022, Brain : a journal of neurology.

Prenatal exome sequencing: A useful tool for the fetal neurologist

E. Bijlsma, E. Verweij, E. Nibbeling, 2021, Clinical genetics.

Social-emotional and behavioural issues after very preterm birth: Parental and teachers experiences.

S. Steggerda, A. van Steenis, M. Rijken, 2022, Journal of child health care : for professionals working with children in the hospital and community.

Recurrent Intracranial Hypertension in a Toddler with Graves’ Disease

C. de Bruin, I. Notting, C. Peeters‐Scholte, 2022, Hormone Research in Paediatrics.

Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism.

R. Pfundt, D. Smedley, S. Robertson, 2021, American Journal of Human Genetics.

Male patients affected by mosaic PCDH19 mutations: five new cases

P. Rump, D. Lindhout, M. Kriek, 2017, neurogenetics.

Putting genome-wide sequencing in neonates into perspective

A. Haeringen, D. Barge-Schaapveld, C. Ruivenkamp, 2018, Genetics in Medicine.

Longitudinal Follow-Up of Children Born Preterm: Neurodevelopment From 2 to 10 Years of Age

R. Vermeiren, S. Steggerda, A. A. van den Berg-Huysmans, 2021, Frontiers in Pediatrics.