Andreas Kyriakou

1.1k total citations
44 papers, 706 citations indexed

About

Andreas Kyriakou is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Andreas Kyriakou has authored 44 papers receiving a total of 706 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 14 papers in Genetics and 12 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Andreas Kyriakou's work include Sexual Differentiation and Disorders (21 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and LGBTQ Health, Identity, and Policy (6 papers). Andreas Kyriakou is often cited by papers focused on Sexual Differentiation and Disorders (21 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and LGBTQ Health, Identity, and Policy (6 papers). Andreas Kyriakou collaborates with scholars based in United Kingdom, Cyprus and Greece. Andreas Kyriakou's co-authors include Nicos Skordis, S. Faisal Ahmed, Avril Mason, Leonidas A. Phylactou, Meropi Toumba, Vassos Neocleous, Angela Lucas-Herald, Ruth McGowan, Elisavet Efstathiou and Yiannis Ioannou and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The Journal of Pediatrics and Human Reproduction.

In The Last Decade

Andreas Kyriakou

44 papers receiving 698 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreas Kyriakou United Kingdom 17 357 191 146 142 108 44 706
Nurçin Saka Türkiye 18 307 0.9× 265 1.4× 441 3.0× 58 0.4× 48 0.4× 63 961
Christine Derzko Canada 15 131 0.4× 156 0.8× 624 4.3× 31 0.2× 40 0.4× 30 1.2k
Heba Elsedfy Egypt 18 166 0.5× 117 0.6× 172 1.2× 23 0.2× 395 3.7× 66 995
Nilgün Yarış Türkiye 12 310 0.9× 169 0.9× 108 0.7× 78 0.5× 30 0.3× 33 649
C. C. M. Beerendonk Netherlands 22 415 1.2× 214 1.1× 129 0.9× 75 0.5× 17 0.2× 67 1.6k
Rasha T. Hamza Egypt 17 119 0.3× 138 0.7× 148 1.0× 17 0.1× 30 0.3× 44 587
Vincenzina Bruni Italy 15 125 0.4× 149 0.8× 101 0.7× 32 0.2× 16 0.1× 47 762
Nuvarte Setian Brazil 15 248 0.7× 360 1.9× 283 1.9× 39 0.3× 34 0.3× 63 731
Lefkothea Karaviti United States 17 433 1.2× 323 1.7× 397 2.7× 118 0.8× 23 0.2× 61 985
Maria G. Vogiatzi United States 13 189 0.5× 106 0.6× 124 0.8× 39 0.3× 11 0.1× 33 582

Countries citing papers authored by Andreas Kyriakou

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Kyriakou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Kyriakou

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Kyriakou. A scholar is included among the top collaborators of Andreas Kyriakou 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 Andreas Kyriakou. Andreas Kyriakou 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.
Shaikh, M Guftar, Timothy Barrett, Nicola Bridges, et al.. (2024). Prader–Willi syndrome: guidance for children and transition into adulthood. Endocrine Connections. 13(8). 3 indexed citations
2.
Henderson, A. Cortney, Anne‐Marie Childs, Jennifer Dunne, et al.. (2023). Reporting of paediatric osteoporotic vertebral fractures in Duchenne muscular dystrophy and potential impact on clinical management: the need for standardised and structured reporting. Pediatric Radiology. 54(1). 117–126. 1 indexed citations
3.
Smith, Simon S., et al.. (2021). An appraisal of current service delivery and future models of care for young people with gender dysphoria. European Journal of Pediatrics. 180(9). 2969–2976. 14 indexed citations
4.
Kyriakou, Andreas, et al.. (2021). Levels of physical activity and barriers to sport participation in young people with gender dysphoria. Journal of Pediatric Endocrinology and Metabolism. 34(6). 747–753. 12 indexed citations
5.
Skordis, Nicos, et al.. (2020). Gender dysphoria in children and adolescents: an overview. HORMONES. 19(3). 267–276. 21 indexed citations
6.
Ali, Salma, Melissa Gardner, Yiqiao Xin, et al.. (2020). Parent-reported outcomes in young children with disorders/differences of sex development. International Journal of Pediatric Endocrinology. 2020(1). 3–3. 6 indexed citations
7.
Gerasimidis, Konstantinos, et al.. (2019). Impact of Pubertal Suppression on Body Composition and Bone Mineral Density in Adolescents with Gender Dysphoria. 92. 1 indexed citations
8.
Fanis, Pavlos, Nicos Skordis, Meropi Toumba, et al.. (2019). Central Precocious Puberty Caused by Novel Mutations in the Promoter and 5′-UTR Region of the Imprinted MKRN3 Gene. Frontiers in Endocrinology. 10. 677–677. 26 indexed citations
9.
Sanders, Caroline, J. Camille Hall, Caroline Sanders, et al.. (2018). Involving Individuals with Disorders of Sex Development and Their Parents in Exploring New Models of Shared Learning: Proceedings from a DSDnet COST Action Workshop. Sexual Development. 12(5). 225–231. 13 indexed citations
10.
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
11.
Chiriţă-Emandi, Adela, et al.. (2017). A retrospective analysis of longitudinal changes in bone mineral content in cystic fibrosis. Journal of Pediatric Endocrinology and Metabolism. 30(8). 807–814. 9 indexed citations
12.
Dessens, Arianne B., Guilherme Guaragna‐Filho, Andreas Kyriakou, et al.. (2017). Understanding the needs of professionals who provide psychosocial care for children and adults with disorders of sex development. BMJ Paediatrics Open. 1(1). e000132–e000132. 21 indexed citations
13.
Kyriakou, Andreas, Arianne B. Dessens, Jillian Bryce, et al.. (2016). Current models of care for disorders of sex development – results from an International survey of specialist centres. Orphanet Journal of Rare Diseases. 11(1). 155–155. 59 indexed citations
14.
Kyriakou, Andreas, Arianne B. Dessens, Jillian Bryce, et al.. (2015). Diagnostic Approach to a Newborn with Suspected DSD: Results From an International Survey of Specialist Care for DSD. 84. 1 indexed citations
15.
Chiriţă-Emandi, Adela, et al.. (2014). Longitudinal Changes of Bone Mineral Content in Children with Cystic Fibrosis. 82. 1 indexed citations
16.
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
17.
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
18.
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
19.
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
20.
Skordis, Nicos, et al.. (2008). Effect of bisphosphonate treatment on bone mineral density in patients with thalassaemia major.. PubMed. 6 Suppl 1. 144–8. 24 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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