| Childhood autism and associated comorbidities DI Zafeiriou, A Ververi, E Vargiami Brain and development 29 (5), 257-272, 2007 | 312 | 2007 |
| Autism spectrum disorders: the quest for genetic syndromes DI Zafeiriou, A Ververi, V Dafoulis, E Kalyva, E Vargiami American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 …, 2013 | 127 | 2013 |
| Childhood autism and auditory system abnormalities M Hitoglou, A Ververi, A Antoniadis, DI Zafeiriou Pediatric neurology 42 (5), 309-314, 2010 | 122 | 2010 |
| The serotonergic system: its role in pathogenesis and early developmental treatment of autism DI Zafeiriou, A Ververi, E Vargiami Current neuropharmacology 7 (2), 150-157, 2009 | 106 | 2009 |
| KIF1A‐related disorders in children: A wide spectrum of central and peripheral nervous system involvement T Nemani, D Steel, M Kaliakatsos, C DeVile, A Ververi, R Scott, S Getov, ... Journal of the Peripheral Nervous System 25 (2), 117-124, 2020 | 55 | 2020 |
| Clinical and laboratory data in a sample of Greek children with autism spectrum disorders A Ververi, E Vargiami, V Papadopoulou, D Tryfonas, DI Zafeiriou Journal of autism and developmental disorders 42, 1470-1476, 2012 | 48 | 2012 |
| Tyrosine hydroxylase deficiency with severe clinical course DI Zafeiriou, MA Willemsen, MM Verbeek, E Vargiami, A Ververi, ... Molecular genetics and metabolism 97 (1), 18-20, 2009 | 48 | 2009 |
| MR spectroscopy and serial magnetic resonance imaging in a patient with mitochondrial cystic leukoencephalopathy due to complex I deficiency and NDUFV1 mutations and mild … DI Zafeiriou, RJT Rodenburg, H Scheffer, LP van den Heuvel, ... Neuropediatrics 39 (03), 172-175, 2008 | 42 | 2008 |
| L-2-Hydroxyglutaric aciduria presenting with severe autistic features DI Zafeiriou, A Ververi, GS Salomons, E Vargiami, D Haas, ... Brain and Development 30 (4), 305-307, 2008 | 40 | 2008 |
| Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome R Alharatani, A Ververi, A Beleza-Meireles, W Ji, E Mis, QT Patterson, ... Human molecular genetics 29 (11), 1900-1921, 2020 | 39 | 2020 |
| Bi-allelic variants in the GPI transamidase subunit PIGK cause a neurodevelopmental syndrome with hypotonia, cerebellar atrophy, and epilepsy TTM Nguyen, Y Murakami, S Mobilio, M Niceta, G Zampino, C Philippe, ... The American Journal of Human Genetics 106 (4), 484-495, 2020 | 33 | 2020 |
| Brainstem auditory evoked potentials in boys with autism: still searching for the hidden truth A Ververi, E Vargiami, V Papadopoulou, D Tryfonas, D Zafeiriou Iranian Journal of Child Neurology 9 (2), 21, 2015 | 23 | 2015 |
| Phenotypic spectrum associated with de novo mutations in QRICH1 gene A Ververi, M Splitt, JCS Dean, DDD Study, AF Brady Clinical genetics 93 (2), 286-292, 2018 | 21 | 2018 |
| Severe clinical presentation in monozygotic twins with 10p15. 3 microdeletion syndrome E Vargiami, A Ververi, M Kyriazi, E Papathanasiou, G Gioula, S Gerou, ... American Journal of Medical Genetics Part A 164 (3), 764-768, 2014 | 20 | 2014 |
| Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation DI Zafeiriou, F Lehmann-Horn, E Vargiami, E Teflioudi, A Ververi, ... european journal of paediatric neurology 13 (2), 191-193, 2009 | 14 | 2009 |
| Pontocerebellar hypoplasia in extreme prematurity: clinical and neuroimaging findings DI Zafeiriou, A Ververi, A Anastasiou, V Soubasi, E Vargiami Pediatric Neurology 48 (1), 48-51, 2013 | 12 | 2013 |
| Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability MRP Baca, EZ Jacobs, L Vantomme, P Leblanc, E Bogaert, A Dheedene, ... The American Journal of Human Genetics 111 (3), 509-528, 2024 | 10 | 2024 |
| Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria A Ververi, S Zagaglia, L Menzies, J Baptista, R Caswell, S Baulac, ... Human Molecular Genetics 32 (4), 580-594, 2023 | 8 | 2023 |
| Flash VEP findings in children with bilateral spastic cerebral palsy: Correlation with clinico-radiological parameters E Vargiami, DI Zafeiriou, N Kozeis, A Ververi, E Kontopoulos, ... Journal of Pediatric Neurology 6 (4), 329-339, 2008 | 7 | 2008 |
| Life-threatening hyponatremia and acute renal failure due to iatrogenic neonatal bladder rupture N Printza, A Ververi, M Bandouraki, E Vargiami, D Gidaris, F Papachristou Urologia Internationalis 88 (2), 238-240, 2012 | 6 | 2012 |
