Get started
Author

Athina Ververi

Observed names: A Ververi, A. Ververi, A., Ververi, Ververi, Athina, Αθηνά Βερβέρη, Βέρβερη, Αθηνά, Βέρβερη, Αθηνά Φωτίου
Observed institutions: Aristotle University of Thessaloniki, Great Ormond Street Hospital, Great Ormond Street Hospital for Children NHS Foundation Trust, London North West Healthcare NHS Trust, Papageorgiou General Hospital, Ippokrateio General Hospital of Thessaloniki, G. Papanikolaou General Hospital, Hippocration General Hospital
ORCID: 0000-0002-8393-4444
Observed ORCIDs: 0000-0002-8393-4444, 0009-0004-0974-5006
OpenAlex ID: A5001392750
Autism spectrum disorders: The quest for genetic syndromes
2013 · Dimitrios I. Zafeiriou, Athina Ververi, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 118
Childhood Autism and Auditory System Abnormalities
2010 · Magdalini Hitoglou, Athina Ververi, et al. · Pediatric Neurology · 104
Data-driven consideration of genetic disorders for global genomic newborn screening programs
2025 · Thomas Minten, Sarah Bick, et al. · Genetics in Medicine · 91
The Serotonergic System: Its Role in Pathogenesis and Early Developmental Treatment of Autism
2009 · D. Zafeiriou, A. Ververi, et al. · Current Neuropharmacology · 87
PDF
Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome
2013 · Euthymia Vargiami, Athina Ververi, et al. · American Journal of Medical Genetics Part A · 55
KIF1A‐related disorders in children: A wide spectrum of central and peripheral nervous system involvement
2020 · Tarishi Nemani, Dora Steel, et al. · Journal of the Peripheral Nervous System · 54
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability
2024 · María del Rocío Pérez Baca, Eva Z. Jacobs, et al. · The American Journal of Human Genetics · 47
Tyrosine hydroxylase deficiency with severe clinical course
2009 · D.I. Zafeiriou, M.A. Willemsen, et al. · Molecular Genetics and Metabolism · 46
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome
2020 · Reham Alharatani, Athina Ververi, et al. · Human Molecular Genetics · 42
PDF
Bi-allelic Variants in the GPI Transamidase Subunit PIGK Cause a Neurodevelopmental Syndrome with Hypotonia, Cerebellar Atrophy, and Epilepsy
2020 · Thi Tuyet Mai Nguyen, Yoshiko Murakami, et al. · The American Journal of Human Genetics · 39
PDF
Clinical and Laboratory Data in a Sample of Greek Children with Autism Spectrum Disorders
2011 · Athina Ververi, Efthymia Vargiami, et al. · Journal of Autism and Developmental Disorders · 37
MR Spectroscopy and Serial Magnetic Resonance Imaging in a Patient with Mitochondrial Cystic Leukoencephalopathy due to Complex I Deficiency andNDUFV1Mutations and Mild Clinical Course
2008 · D. Zafeiriou, R. Rodenburg, et al. · Neuropediatrics · 37
l-2-Hydroxyglutaric aciduria presenting with severe autistic features
2008 · D.I. Zafeiriou, A. Ververi, et al. · Brain and Development · 28
Phenotypic spectrum associated with de novo mutations in QRICH1 gene
2017 · A. Ververi, M. Splitt, et al. · Clinical Genetics · 23
The Effect of Maternal Diet and Physical Activity on the Epigenome of the Offspring
2024 · Anastasia Panagiotidou, Christos Chatzakis, et al. · Genes · 22
PDF
Brainstem Auditory Evoked Potentials in Boys with Autism: Still Searching for the Hidden Truth.
2015 · Athina Ververi, Euthymia Vargiami, et al. · Iranian journal of child neurology. · 20
PDF
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria
2022 · Athina Ververi, Sara Zagaglia, et al. · Human Molecular Genetics · 18
PDF
Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation
2008 · D.I. Zafeiriou, F. Lehmann-Horn, et al. · European Journal of Paediatric Neurology · 13
Incremental yield of exome sequencing over standard prenatal testing in structurally normal fetuses: systematic review and meta‐analysis
2025 · A. Sotiriadis, E. Demertzidou, et al. · Ultrasound in Obstetrics and Gynecology · 12
PDF
Expanding the phenotype of TAB2 variants and literature review
2022 · Emily Woods, Imogen Marson, et al. · American Journal of Medical Genetics Part A · 12
PDF
Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies
2025 · Sébastien Küry, Janelle E. Stanton, et al. · Nature Communications · 11
PDF
Pontocerebellar Hypoplasia in Extreme Prematurity: Clinical and Neuroimaging Findings
2013 · Dimitrios I. Zafeiriou, Athina Ververi, et al. · Pediatric Neurology · 11
PDF
An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical Recommendations
2025 · E. Woods, N. Holmes, et al. · American Journal of Medical Genetics Part A · 9
PDF
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome
2023 · Vincenzo Salpietro, Reza Maroofian, et al. · The American Journal of Human Genetics · 9
PDF
Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy
2021 · Stella Mouskou, Adamantios Katerelos, et al. · Molecular Syndromology · 8
PDF
Works count: 79
Citation count: 1,030
H-index: 17
I10-index: 22
Year
Topic
Type