Vassos Neocleous

1.3k total citations
61 papers, 728 citations indexed

About

Vassos Neocleous is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Vassos Neocleous has authored 61 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 30 papers in Genetics and 29 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Vassos Neocleous's work include Sexual Differentiation and Disorders (25 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers) and Hormonal and reproductive studies (16 papers). Vassos Neocleous is often cited by papers focused on Sexual Differentiation and Disorders (25 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers) and Hormonal and reproductive studies (16 papers). Vassos Neocleous collaborates with scholars based in Cyprus, United Kingdom and Greece. Vassos Neocleous's co-authors include Leonidas A. Phylactou, Nicos Skordis, Christos Shammas, Pavlos Fanis, Meropi Toumba, Elisavet Efstathiou, Andreas Kyriakou, Constantinos Deltas, Kyriacos Kyriacou and Alkis Pierides and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Vassos Neocleous

61 papers receiving 720 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vassos Neocleous Cyprus 15 444 261 223 103 74 61 728
Beatrice B. Yaroslavskiy United States 15 681 1.5× 234 0.9× 232 1.0× 12 0.1× 30 0.4× 21 1.3k
Mark J. McCabe United Kingdom 16 331 0.7× 259 1.0× 234 1.0× 13 0.1× 11 0.1× 22 707
Xueping Fan United States 15 462 1.0× 77 0.3× 49 0.2× 68 0.7× 12 0.2× 20 743
J.H.A.M. Tuerlings Netherlands 18 440 1.0× 453 1.7× 45 0.2× 8 0.1× 58 0.8× 49 880
Ludo Deboel Belgium 14 404 0.9× 116 0.4× 135 0.6× 10 0.1× 11 0.1× 24 699
L Wickert Germany 14 329 0.7× 105 0.4× 96 0.4× 12 0.1× 8 0.1× 20 677
Tzipora C. Falik‐Zaccai Israel 19 326 0.7× 191 0.7× 41 0.2× 13 0.1× 39 0.5× 56 809
Marie-Laure Kottler France 15 456 1.0× 406 1.6× 253 1.1× 44 0.4× 3 0.0× 23 981
Albert de la Chapelle Finland 13 544 1.2× 477 1.8× 133 0.6× 35 0.3× 3 0.0× 15 1.3k
Anna Maria Barbieri Italy 17 599 1.3× 336 1.3× 277 1.2× 60 0.6× 10 0.1× 37 1.1k

Countries citing papers authored by Vassos Neocleous

Since Specialization
Citations

This map shows the geographic impact of Vassos Neocleous'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 Vassos Neocleous with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vassos Neocleous more than expected).

Fields of papers citing papers by Vassos Neocleous

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vassos Neocleous. 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 Vassos Neocleous. The network helps show where Vassos Neocleous may publish in the future.

Co-authorship network of co-authors of Vassos Neocleous

This figure shows the co-authorship network connecting the top 25 collaborators of Vassos Neocleous. A scholar is included among the top collaborators of Vassos Neocleous 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 Vassos Neocleous. Vassos Neocleous 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.
Fanis, Pavlos, et al.. (2025). Identification of puberty related miRNAs in the hypothalamus of female mice. Molecular and Cellular Endocrinology. 598. 112468–112468. 1 indexed citations
2.
Neocleous, Vassos, Pavlos Fanis, Savvas Frangos, Nicos Skordis, & Leonidas A. Phylactou. (2023). RET Proto-Oncogene Variants in Patients with Medullary Thyroid Carcinoma from the Mediterranean Basin: A Brief Report. Life. 13(6). 1332–1332. 4 indexed citations
3.
Constantinou, Maria, et al.. (2023). A novel pathogenic variant in ZNF462 gene associated with Weiss–Kruszka syndrome and systemic lupus erythematosus. Lara D. Veeken. 62(8). e249–e250. 3 indexed citations
4.
Kousiappa, Ioanna, Nicoletta Nicolaou, Eleftherios S. Papathanasiou, et al.. (2020). Neurophysiological and Genetic Findings in Patients With Juvenile Myoclonic Epilepsy. Frontiers in Integrative Neuroscience. 14. 45–45. 5 indexed citations
5.
Skordis, Nicos, Pavlos Fanis, Meropi Toumba, et al.. (2018). The Spectrum of Genetic Defects in Congenital Adrenal Hyperplasia in the Population of Cyprus: A Retrospective Analysis. 89. 1 indexed citations
6.
Neocleous, Vassos, Pavlos Fanis, Leonidas A. Phylactou, & Nicos Skordis. (2018). Genotype Is Associated to the Degree of Virilization in Patients With Classic Congenital Adrenal Hyperplasia. Frontiers in Endocrinology. 9. 733–733. 10 indexed citations
7.
Shammas, Christos, et al.. (2017). CDKN2A and MC1R variants found in Cypriot patients diagnosed with cutaneous melanoma. Journal of Genetics. 96(1). 155–160. 4 indexed citations
8.
Skordis, Nicos, Christos Shammas, Andreas Kyriakou, et al.. (2014). Genetic defects of the CYP21A2 gene in girls with premature adrenarche. Journal of Endocrinological Investigation. 38(5). 535–539. 12 indexed citations
9.
Skordis, Nicos, et al.. (2014). Phenotypic variability of hyperandrogenemia in females heterozygous for CYP21A2 mutations. Indian Journal of Endocrinology and Metabolism. 18(7). 72–72. 15 indexed citations
10.
Shammas, Christos, Vassos Neocleous, Marie M. Phelan, et al.. (2013). A report of 2 new cases of MODY2 and review of the literature: Implications in the search for type 2 Diabetes drugs. Metabolism. 62(11). 1535–1542. 10 indexed citations
11.
Shammas, Christos, Vassos Neocleous, Meropi Toumba, et al.. (2012). Overview of Genetic Defects in Endocrinopathies in the Island of Cyprus; Evidence of a Founder Effect. Genetic Testing and Molecular Biomarkers. 16(9). 1073–1079. 14 indexed citations
12.
Neocleous, Vassos, Christos Shammas, Andreas Kyriakou, et al.. (2012). Genetic defects in the cyp21a2 gene in heterozygous girls with premature adrenarche and adolescent females with hyperandrogenemia.. PubMed. 40–7. 9 indexed citations
13.
Riedl, Stefan, Gernot Kriegshäuser, Sabina Baumgartner‐Parzer, et al.. (2012). Reverse-hybridization assay for rapid detection of common CYP21A2 mutations in dried blood spots from newborns with elevated 17-OH progesterone. Clinica Chimica Acta. 414. 211–214. 16 indexed citations
14.
Skordis, Nicos, et al.. (2011). Endocrine profile and phenotype-genotype correlation in unrelated patients with non-classical congenital adrenal hyperplasia. Clinical Biochemistry. 44(12). 959–963. 16 indexed citations
15.
Skordis, Nicos, Vassos Neocleous, Andreas Kyriakou, et al.. (2010). The IVS1- 2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiency. Journal of Endocrinological Investigation. 33(11). 810–814. 16 indexed citations
16.
Neocleous, Vassos, et al.. (2009). Rare mutations in the CYP21A2 gene detected in congenital adrenal hyperplasia. Clinical Biochemistry. 42(13-14). 1363–1367. 12 indexed citations
17.
Neocleous, Vassos, et al.. (2006). High Frequency of 35delG GJB2 Mutation and Absence of del( GJB6-D13S1830 ) in Greek Cypriot Patients with Nonsyndromic Hearing Loss. Genetic Testing. 10(4). 285–289. 19 indexed citations
18.
Neocleous, Vassos, et al.. (2006). Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Greek Cypriot population. International Journal of Pediatric Otorhinolaryngology. 70(8). 1473–1477. 16 indexed citations
19.
Neocleous, Vassos, et al.. (2004). Description of the First Two Seemingly Unrelated Greek Cypriot Families with a Common C618R RET Proto-Oncogene Mutation. Genetic Testing. 8(2). 163–168. 8 indexed citations
20.
Middleton, Lefkos, Kyproula Christodoulou, Amar Mubaidin, et al.. (1999). Distal Hereditary Motor Neuronopathy of the Jerash Type. Annals of the New York Academy of Sciences. 883(1). 439–442. 10 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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