Athina Xaidara

510 total citations
21 papers, 355 citations indexed

About

Athina Xaidara is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Athina Xaidara has authored 21 papers receiving a total of 355 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Physiology and 4 papers in Genetics. Recurrent topics in Athina Xaidara's work include Carbohydrate Chemistry and Synthesis (3 papers), Porphyrin Metabolism and Disorders (3 papers) and Lysosomal Storage Disorders Research (3 papers). Athina Xaidara is often cited by papers focused on Carbohydrate Chemistry and Synthesis (3 papers), Porphyrin Metabolism and Disorders (3 papers) and Lysosomal Storage Disorders Research (3 papers). Athina Xaidara collaborates with scholars based in Greece, United States and France. Athina Xaidara's co-authors include Sotiris Youroukos, Emmanuel Kanavakis, Justine E Johnson, Kathryn J. Swoboda, Louis J. Ptáček, Mark Leppert, Kenneth Silver, Talia Kakourou, Polyxeni Nicolaidou and Athanasios G. Kaditis and has published in prestigious journals such as Annals of Neurology, The Journal of Urology and Developmental Medicine & Child Neurology.

In The Last Decade

Athina Xaidara

21 papers receiving 346 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 Xaidara Greece 10 121 114 60 55 55 21 355
Hamìt Özyürek Türkiye 10 223 1.8× 61 0.5× 35 0.6× 30 0.5× 221 4.0× 34 461
Pascal Sabouraud France 11 116 1.0× 143 1.3× 27 0.5× 23 0.4× 50 0.9× 25 385
Satoko Nakahara Japan 10 102 0.8× 88 0.8× 119 2.0× 17 0.3× 79 1.4× 12 391
Susana Boronat Spain 13 61 0.5× 46 0.4× 124 2.1× 37 0.7× 94 1.7× 47 335
Veena Rajaram United States 5 71 0.6× 87 0.8× 17 0.3× 24 0.4× 28 0.5× 7 443
Gianluca Casara Italy 11 98 0.8× 111 1.0× 23 0.4× 23 0.4× 57 1.0× 20 296
A Martínez-Bermejo Spain 14 274 2.3× 120 1.1× 65 1.1× 114 2.1× 120 2.2× 40 650
Gabriele Spinelli Italy 10 187 1.5× 120 1.1× 39 0.7× 122 2.2× 29 0.5× 35 543
Noboru Habu Japan 11 72 0.6× 57 0.5× 70 1.2× 54 1.0× 19 0.3× 28 372
E H Jellinek United Kingdom 12 70 0.6× 36 0.3× 137 2.3× 74 1.3× 33 0.6× 26 506

Countries citing papers authored by Athina Xaidara

Since Specialization
Citations

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

Fields of papers citing papers by Athina Xaidara

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Athina Xaidara

This figure shows the co-authorship network connecting the top 25 collaborators of Athina Xaidara. A scholar is included among the top collaborators of Athina Xaidara 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 Xaidara. Athina Xaidara 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.
Mavridou, Irene, Evangelia Dimitriou, Marie T. Vanier, et al.. (2017). The Spectrum of Niemann-Pick Type C Disease in Greece. JIMD Reports. 36. 41–48. 10 indexed citations
2.
Giannakopoulos, Aristeidis, Helen Fryssira, Maria Tzetis, Athina Xaidara, & Christina Kanaka‐Gantenbein. (2016). Central precocious puberty in a boy with 22q13 deletion syndrome and NOTCH-1 gene duplication. Journal of Pediatric Endocrinology and Metabolism. 0(0). 1307–1311. 8 indexed citations
3.
Tanou, Kalliopi, Athina Xaidara, & Athanasios G. Kaditis. (2015). Efficacy of pulse methylprednisolone in a pediatric case of postinfectious bronchiolitis obliterans. Pediatric Pulmonology. 50(5). E13–E16. 14 indexed citations
4.
Mavridou, Irene, Mónica Cozar, Sofia Douzgou, et al.. (2013). Niemann–Pick type C disease: a novel NPC1 mutation segregating in a Greek island. Clinical Genetics. 85(6). 543–547. 8 indexed citations
5.
Kakourou, Talia, et al.. (2013). Retrospective Analysis of the Relationship Between Infantile Seborrheic Dermatitis and Atopic Dermatitis. Pediatric Dermatology. 31(2). 125–130. 26 indexed citations
6.
Xaidara, Athina, et al.. (2012). Propranolol treatment for severe infantile hemangiomas: a single‐centre 3‐year experience. Acta Paediatrica. 101(10). e469–74. 27 indexed citations
7.
Pons, Roser, Ester Cuenca-León, Elena Miravet, et al.. (2011). Paroxysmal non-kinesigenic dyskinesia due to a PNKD recurrent mutation: Report of two Southern European families. European Journal of Paediatric Neurology. 16(1). 86–89. 15 indexed citations
8.
Iatrou, Christos, et al.. (2010). Evolution of Fabry disease in male patients: The Greek experience. Clinical Nephrology. 73(1). 58–63. 3 indexed citations
9.
Xaidara, Athina, et al.. (2009). Chitotriosidase plasma activity in nephropathic cystinosis. Journal of Inherited Metabolic Disease. 32(S1). 157–159. 5 indexed citations
10.
11.
Kakourou, Talia, Fotini Psychou, Antonis Voutetakis, et al.. (2004). Low serum insulin values in children with multiple lesions of granuloma annulare: a prospective study. Journal of the European Academy of Dermatology and Venereology. 19(1). 30–34. 9 indexed citations
12.
Swoboda, Kathryn J., Emmanuel Kanavakis, Athina Xaidara, et al.. (2004). Alternating hemiplegia of childhood or familial hemiplegic migraine?: A novel ATP1A2 mutation. Annals of Neurology. 55(6). 884–887. 119 indexed citations
13.
Kanavakis, Emmanuel, et al.. (2003). Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait. Developmental Medicine & Child Neurology. 45(12). 833–6. 23 indexed citations
14.
Kanavakis, Emmanuel, et al.. (2003). Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait. Developmental Medicine & Child Neurology. 45(12). 833–836. 21 indexed citations
15.
Papassotiriou, Ioannis, Joanne Traeger‐Synodinos, Danièlle Promé, et al.. (2001). Hb SITIA [β128(H6)Ala→Val]: AN UNSTABLE VARIANT WITH A SUBSTITUTION IN THE α1β1 INTERFACE. Hemoglobin. 25(1). 45–56. 3 indexed citations
16.
Dacou‐Voutetakis, Catherine, Amalia Sertedaki, Catherine Sarri, et al.. (1999). Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in a boy with a ring chromosome 18: additional evidence of autoimmunity or IDDM gene(s) on chromosome 18. Journal of Medical Genetics. 36(2). 156–158. 19 indexed citations
17.
Nicolaidou, Polyxeni, et al.. (1996). Family Pattern of Idiopathic Hypercalciuria and its Subtypes. The Journal of Urology. 1042–1044. 1 indexed citations
18.
D’Angio, Giulio J., et al.. (1996). Neuroblastoma metastatic to brain. Medical and Pediatric Oncology. 26(3). 208–214. 4 indexed citations
19.
Nicolaidou, Polyxeni, et al.. (1996). Family Pattern of Idiopathic Hypercalciuria and its Subtypes. The Journal of Urology. 155(3). 1042–1044. 23 indexed citations
20.
Tzortzatou‐Stathopoulou, Fotini, et al.. (1995). Effect of trimethoprim‐sulphamethoxazole in langerhans' cell histiocytosis: Preliminary observations. Medical and Pediatric Oncology. 25(2). 74–78. 8 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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