Athina Ververi

836 total citations
33 papers, 447 citations indexed

About

Athina Ververi is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Athina Ververi has authored 33 papers receiving a total of 447 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 8 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Athina Ververi's work include Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Autism Spectrum Disorder Research (5 papers). Athina Ververi is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Autism Spectrum Disorder Research (5 papers). Athina Ververi collaborates with scholars based in Greece, United Kingdom and Netherlands. Athina Ververi's co-authors include Dimitrios Zafeiriou, Euthymia Vargìami, A. Antoniadis, Efrosini Kalyva, Michèl A.A.P. Willemsen, Marcel M. Verbeek, Ron A. Wevers, Richard J. Rodenburg, Petra J. W. Pouwels and Georgia Gioula and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Autism and Developmental Disorders and Ultrasound in Obstetrics and Gynecology.

In The Last Decade

Athina Ververi

28 papers receiving 427 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Athina Ververi Greece 11 188 153 136 65 56 33 447
Carmela Scuderi Italy 13 186 1.0× 187 1.2× 146 1.1× 120 1.8× 23 0.4× 34 473
Bàrbara Torrico Spain 8 163 0.9× 196 1.3× 122 0.9× 58 0.9× 20 0.4× 13 351
Aleksandra Djukic United States 14 368 2.0× 382 2.5× 112 0.8× 86 1.3× 23 0.4× 25 597
Markéta Havlovičová Czechia 14 215 1.1× 274 1.8× 244 1.8× 92 1.4× 8 0.1× 33 643
Alena Zumrová Czechia 11 123 0.7× 107 0.7× 129 0.9× 60 0.9× 9 0.2× 29 297
Nancy Govea Spain 13 271 1.4× 129 0.8× 1000 7.4× 47 0.7× 93 1.7× 14 1.5k
Denis Pavăl Romania 6 185 1.0× 110 0.7× 72 0.5× 64 1.0× 6 0.1× 11 303
Eila Airaksinen Finland 13 102 0.5× 67 0.4× 81 0.6× 132 2.0× 13 0.2× 20 409
Margherita Comazzi Italy 9 211 1.1× 215 1.4× 147 1.1× 183 2.8× 8 0.1× 13 528
Assunção Ataíde Portugal 8 501 2.7× 433 2.8× 196 1.4× 157 2.4× 22 0.4× 8 691

Countries citing papers authored by Athina Ververi

Since Specialization
Citations

This map shows the geographic impact of Athina Ververi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Athina Ververi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Athina Ververi more than expected).

Fields of papers citing papers by Athina Ververi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Athina Ververi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Athina Ververi. The network helps show where Athina Ververi may publish in the future.

Co-authorship network of co-authors of Athina Ververi

This figure shows the co-authorship network connecting the top 25 collaborators of Athina Ververi. A scholar is included among the top collaborators of Athina Ververi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Athina Ververi. Athina Ververi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Sotiriadis, Alexandros, et al.. (2025). Incremental yield of exome sequencing over standard prenatal testing in structurally normal fetuses: systematic review and meta‐analysis. Ultrasound in Obstetrics and Gynecology. 65(5). 552–559. 2 indexed citations
3.
Holmes, Nadine, Anne‐Sophie Denommé‐Pichon, Marie Vincent, et al.. (2025). An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical Recommendations. American Journal of Medical Genetics Part A. 197(11). e64157–e64157. 1 indexed citations
4.
Streață, Ioana, Athina Ververi, Ratna Dua Puri, et al.. (2024). Catalogue of inherited autosomal recessive disorders found amongst the Roma population of Europe. European Journal of Medical Genetics. 73. 104989–104989. 2 indexed citations
5.
Ververi, Athina, et al.. (2024). Genomic abnormalities in apparently isolated polyhydramnios and the role of confirmed fetal phenotype: a systematic review and meta-analysis. American Journal of Obstetrics & Gynecology MFM. 6(10). 101469–101469. 2 indexed citations
6.
Tzikos, Georgios, Athina Ververi, Vasileios Rafailidis, et al.. (2023). Bowel Perforation in Vascular EDS: A Case Report and a Comprehensive Review of the Literature. Preprints.org. 1 indexed citations
7.
Tzikos, Georgios, Athina Ververi, Vasileios Rafailidis, et al.. (2023). Bowel Perforation in Vascular Ehlers–Danlos Syndrome: Case Report and Comprehensive Review. Journal of Personalized Medicine. 13(8). 1247–1247.
8.
9.
Kumar, Ajith, Angela F. Brady, Tessa Homfray, et al.. (2022). Expanding the phenotype of TAB2 variants and literature review. American Journal of Medical Genetics Part A. 188(11). 3331–3342. 6 indexed citations
10.
Steel, Dora, Marios Kaliakatsos, Catherine DeVile, et al.. (2020). KIF1A‐related disorders in children: A wide spectrum of central and peripheral nervous system involvement. Journal of the Peripheral Nervous System. 25(2). 117–124. 30 indexed citations
11.
Zafeiriou, Dimitrios, et al.. (2013). Pontocerebellar Hypoplasia in Extreme Prematurity: Clinical and Neuroimaging Findings. Pediatric Neurology. 48(1). 48–51. 8 indexed citations
12.
Zafeiriou, Dimitrios, et al.. (2013). Autism spectrum disorders: The quest for genetic syndromes. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(4). 327–366. 72 indexed citations
13.
Zafeiriou, Dimitrios, et al.. (2012). Recurrent episodes of rhabdomyolysis in pontocerebellar hypoplasia type 2. Neuromuscular Disorders. 23(2). 116–119. 3 indexed citations
14.
Ververi, Athina, et al.. (2011). Clinical and Laboratory Data in a Sample of Greek Children with Autism Spectrum Disorders. Journal of Autism and Developmental Disorders. 42(7). 1470–1476. 24 indexed citations
15.
Printza, Nikoleta, et al.. (2011). Life-Threatening Hyponatremia and Acute Renal Failure due to Iatrogenic Neonatal Bladder Rupture. Urologia Internationalis. 88(2). 238–240. 4 indexed citations
16.
Ververi, Athina, et al.. (2010). Childhood Autism and Auditory System Abnormalities. Pediatric Neurology. 42(5). 309–314. 69 indexed citations
17.
Zafeiriou, Dimitrios, et al.. (2009). Tyrosine hydroxylase deficiency with severe clinical course. Molecular Genetics and Metabolism. 97(1). 18–20. 30 indexed citations
18.
Zafeiriou, Dimitrios, et al.. (2009). The Serotonergic System: Its Role in Pathogenesis and Early Developmental Treatment of Autism. Current Neuropharmacology. 7(2). 150–157. 64 indexed citations
19.
Zafeiriou, Dimitrios, Richard J. Rodenburg, Hans Scheffer, et al.. (2008). MR Spectroscopy and Serial Magnetic Resonance Imaging in a Patient with Mitochondrial Cystic Leukoencephalopathy due to Complex I Deficiency andNDUFV1Mutations and Mild Clinical Course. Neuropediatrics. 39(3). 172–175. 28 indexed citations
20.
Zafeiriou, Dimitrios, et al.. (2008). Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation. European Journal of Paediatric Neurology. 13(2). 191–193. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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