| De novo coding variants are strongly associated with Tourette disorder AJ Willsey, TV Fernandez, D Yu, RA King, A Dietrich, J Xing, SJ Sanders, ... Neuron 94 (3), 486-499. e9, 2017 | 184 | 2017 |
| Perinatal motor behaviour and neurological outcome in spina bifida aperta DA Sival, JH Begeer, AL Staal-Schreinemachers, JME Vos-Niël, ... Early human development 50 (1), 27-37, 1997 | 156 | 1997 |
| Fetal endoscopic myelomeningocele closure preserves segmental neurological function RJ Verbeek, A Heep, NM Maurits, R Cremer, EW Hoving, OF Brouwer, ... Developmental Medicine & Child Neurology 54 (1), 15-22, 2012 | 126 | 2012 |
| Long‐term outcome in pyridoxine‐dependent epilepsy LA Bok, FJ Halbertsma, S Houterman, RA Wevers, C Vreeswijk, C Jakobs, ... Developmental Medicine & Child Neurology 54 (9), 849-854, 2012 | 125 | 2012 |
| The effect of intrauterine growth retardation on the quality of general movements in the human fetus DA Sival, GHA Visser, HFR Prechtl Early human development 28 (2), 119-132, 1992 | 116 | 1992 |
| A novel diagnostic approach to patients with myoclonus R Zutt, ME Van Egmond, JW Elting, PJ Van Laar, OF Brouwer, DA Sival, ... Nature Reviews Neurology 11 (12), 687-697, 2015 | 110 | 2015 |
| A cell junction pathology of neural stem cells leads to abnormal neurogenesis and hydrocephalus EM Rodríguez, MM Guerra, K Vío, C González, A Ortloff, LF Bátiz, ... Biological research 45 (3), 231-241, 2012 | 102 | 2012 |
| Ventricular zone disruption in human neonates with intraventricular hemorrhage JP McAllister, MM Guerra, LC Ruiz, AJ Jimenez, D Dominguez-Pinos, ... Journal of Neuropatholgy & Experimental Neurology 76 (5), 358-375, 2017 | 101 | 2017 |
| Cell junction pathology of neural stem cells is associated with ventricular zone disruption, hydrocephalus, and abnormal neurogenesis MM Guerra, R Henzi, A Ortloff, N Lichtin, K Vio, AJ Jimenez, ... Journal of Neuropathology & Experimental Neurology 74 (7), 653-671, 2015 | 98 | 2015 |
| Ataxia rating scales are age‐dependent in healthy children R Brandsma, AH Spits, MJ Kuiper, RJ Lunsing, H Burger, HP Kremer, ... Developmental Medicine & Child Neurology 56 (6), 556-563, 2014 | 94 | 2014 |
| Does reduction of amniotic fluid affect fetal movements? DA Sival, GHA Visser, HFR Prechtl Early human development 23 (3), 233-246, 1990 | 92 | 1990 |
| Dystonia in children and adolescents: a systematic review and a new diagnostic algorithm ME Van Egmond, A Kuiper, H Eggink, RJ Sinke, OF Brouwer, ... Journal of Neurology, Neurosurgery & Psychiatry 86 (7), 774-781, 2015 | 91 | 2015 |
| Neuroependymal denudation is in progress in full‐term human foetal spina bifida aperta DA Sival, M Guerra, WFA den Dunnen, LF Bátiz, G Alvial, ... Brain pathology 21 (2), 163-179, 2011 | 91 | 2011 |
| Neonatal loss of motor function in human spina bifida aperta DA Sival, TW Weerden, JSH Vles, A Timmer, WFA Dunnen, ... Pediatrics 114 (2), 427-434, 2004 | 80 | 2004 |
| Functional magnetic resonance imaging of the sensorimotor system in preterm infants A Heep, L Scheef, J Jankowski, M Born, N Zimmermann, D Sival, A Bos, ... Pediatrics 123 (1), 294-300, 2009 | 78 | 2009 |
| Shah-Waardenburg syndrome and PCWH associated with SOX10 mutations: a case report and review of the literature JBGM Verheij, DA Sival, JH van der Hoeven, YJ Vos, LC Meiners, ... European Journal of Paediatric Neurology 10 (1), 11-17, 2006 | 77 | 2006 |
| The EEG response to pyridoxine‐IV neither identifies nor excludes pyridoxine‐dependent epilepsy LA Bok, NM Maurits, MA Willemsen, C Jakobs, LK Teune, BT Poll‐The, ... Epilepsia 51 (12), 2406-2411, 2010 | 72 | 2010 |
| Ramsay hunt syndrome: Clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation ME van Egmond, CC Verschuuren‐Bemelmans, EA Nibbeling, JWJ Elting, ... Movement disorders 29 (1), 139-143, 2014 | 63 | 2014 |
| Intraspinal dermoid and epidermoid tumors: report of 18 cases and reappraisal of the literature J van Aalst, F Hoekstra, EAM Beuls, EMJ Cornips, JW Weber, DA Sival, ... Pediatric neurosurgery 45 (4), 281-290, 2009 | 58 | 2009 |
| Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction D Tiosano, HN Baris, A Chen, MM Hitzert, M Schueler, F Gulluni, ... PLoS genetics 15 (4), e1008088, 2019 | 56 | 2019 |
