Athina Kladi

518 total citations
20 papers, 388 citations indexed

About

Athina Kladi is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Athina Kladi has authored 20 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Cellular and Molecular Neuroscience, 12 papers in Neurology and 10 papers in Molecular Biology. Recurrent topics in Athina Kladi's work include Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (8 papers) and Neurological disorders and treatments (7 papers). Athina Kladi is often cited by papers focused on Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (8 papers) and Neurological disorders and treatments (7 papers). Athina Kladi collaborates with scholars based in Greece, Cyprus and United Kingdom. Athina Kladi's co-authors include Μάριος Πάνας, Georgia Karadima, Dimitrios Vassilopoulos, Georgios Koutsis, Evangelos Vassos, Kyproula Christodoulou, Nikolaos Karandreas, Panagiota Manta, Konstantinos Spengos and Georgios Tsivgoulis and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Neurology.

In The Last Decade

Athina Kladi

19 papers receiving 375 citations

Peers

Athina Kladi

CMN

MB

NEURO

GENET

HEMAT

Marcos Barbosa Portugal

Takashi Kimura Japan

Toniella Giallongo Italy

Karima Ghorab France

Masanori Gomi Japan

Rocco Adiutori United Kingdom

Ana Sierra Spain

Xinghua Luan China

Emanuele Panza Italy

Bilal Malik United States

Marcos Barbosa Portugal

Athina Kladi

101 ×0.5

CMN

187 ×1.0

MB

169 ×1.2

NEURO

232 ×3.1

GENET

23 ×0.6

HEMAT

Citations per year, relative to Athina Kladi Athina Kladi (= 1×) peers Marcos Barbosa

Countries citing papers authored by Athina Kladi

Since Specialization

Citations

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

Fields of papers citing papers by Athina Kladi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Athina Kladi

This figure shows the co-authorship network connecting the top 25 collaborators of Athina Kladi. A scholar is included among the top collaborators of Athina Kladi 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 Kladi. Athina Kladi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

1.

Papadimas, George K., Constantinos Papadopoulos, Kyriaki Kekou, et al.. (2022). A Greek National Cross-Sectional Study on Myotonic Dystrophies. International Journal of Molecular Sciences. 23(24). 15507–15507. 1 indexed citations

2.

Anagnostou, Evangelos, et al.. (2019). Disentangling balance impairments in spinal and bulbar muscular atrophy. Neuroscience Letters. 705. 94–98. 9 indexed citations

3.

Fostira, Florentia, Athina Kladi, Daniel L. Edelstein, et al.. (2019). Blood-based testing of mutations in patients with head and neck squamous cell carcinoma (HNSCC) using highly sensitive SafeSEQ technology. Annals of Oncology. 30. v469–v469. 4 indexed citations

4.

Messaritakis, Ippokratis, Maria Sfakianaki, Chara Papadaki, et al.. (2018). Prognostic significance of CEACAM5mRNA-positive circulating tumor cells in patients with metastatic colorectal cancer. Cancer Chemotherapy and Pharmacology. 82(5). 767–775. 18 indexed citations

5.

Koutsis, Georgios, Georgia Karadima, Athina Kladi, & Μάριος Πάνας. (2014). Late-onset Huntington's disease: Diagnostic and prognostic considerations. Parkinsonism & Related Disorders. 20(7). 726–730. 27 indexed citations

6.

Koutsis, Georgios, et al.. (2014). C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population. Neurobiology of Aging. 36(1). 547.e13–547.e16. 29 indexed citations

7.

Koutsis, Georgios, Μάριος Πάνας, George P. Paraskevas, et al.. (2014). From Mild Ataxia to Huntington Disease Phenocopy: The Multiple Faces of Spinocerebellar Ataxia 17. SHILAP Revista de lepidopterología. 2014. 1–4. 8 indexed citations

8.

Koutsis, Georgios, Athina Kladi, Georgia Karadima, et al.. (2013). Friedreich's ataxia and other hereditary ataxias in Greece: An 18-year perspective. Journal of the Neurological Sciences. 336(1-2). 87–92. 15 indexed citations

9.

Koutsis, Georgios, Georgia Karadima, Athina Kladi, & Μάριος Πάνας. (2013). The challenge of juvenile Huntington disease. Neurology. 80(11). 990–996. 9 indexed citations

10.

Koutsis, Georgios, Sally Pemble, Mary G. Sweeney, et al.. (2012). Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia. Journal of the Neurological Sciences. 318(1-2). 178–180. 7 indexed citations

11.

Balatsouras, Dimitrios G., Μάριος Πάνας, John Xenellis, et al.. (2012). Inner ear dysfunction in myotonic dystrophy type 1. Acta Neurologica Scandinavica. 127(5). 337–343. 8 indexed citations

12.

Πάνας, Μάριος, Georgia Karadima, Evangelos Vassos, et al.. (2010). Huntington's disease in Greece: the experience of 14 years. Clinical Genetics. 80(6). 586–590. 37 indexed citations

13.

Dardiotis, Efthimios, Eleni Zamba Papanicolaou, Filia Vonta, et al.. (2009). Epidemiological, clinical and genetic study of familial amyloidotic polyneuropathy in Cyprus. Amyloid. 16(1). 32–37. 33 indexed citations

14.

Christodoulou, Kyproula, Georgia Xiromerisiou, Μάριος Πάνας, et al.. (2009). Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene. Neurological Sciences. 31(3). 393–397. 4 indexed citations

15.

Vassos, Evangelos, Μάριος Πάνας, Athina Kladi, & Dimitrios Vassilopoulos. (2007). Higher Levels of Extroverted Hostility Detected in Gene Carriers at Risk for Huntington’s Disease. Biological Psychiatry. 62(12). 1347–1352. 17 indexed citations

16.

Vassos, Evangelos, Μάριος Πάνας, Athina Kladi, & Dimitrios Vassilopoulos. (2007). Effect of CAG repeat length on psychiatric disorders in Huntington’s disease. Journal of Psychiatric Research. 42(7). 544–549. 43 indexed citations

17.

Tsivgoulis, Georgios, Konstantinos Spengos, Nikolaos Karandreas, et al.. (2006). Presymptomatic Neuromuscular Disorders Disclosed Following Statin Treatment. Archives of Internal Medicine. 166(14). 1519–1519. 55 indexed citations

18.

Πάνας, Μάριος, Georgia Karadima, Nikolaos Kalfakis, et al.. (2000). Genotyping of presenilin-1 polymorphism in amyotrophic lateral sclerosis. Journal of Neurology. 247(12). 940–942. 7 indexed citations

19.

Economou-Petersen, E, Athanassios Aessopos, Athina Kladi, et al.. (1998). Apolipoprotein E 4 Allele as a Genetic Risk Factor for Left Ventricular Failure in Homozygous β-Thalassemia. Blood. 92(9). 3455–3459. 1 indexed citations

20.

Economou-Petersen, E, Athanassios Aessopos, Athina Kladi, et al.. (1998). Apolipoprotein E 4 Allele as a Genetic Risk Factor for Left Ventricular Failure in Homozygous β-Thalassemia. Blood. 92(9). 3455–3459. 56 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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