Georgia Karadima

1.8k total citations
65 papers, 812 citations indexed

About

Georgia Karadima is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Georgia Karadima has authored 65 papers receiving a total of 812 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Cellular and Molecular Neuroscience, 28 papers in Molecular Biology and 25 papers in Neurology. Recurrent topics in Georgia Karadima's work include Genetic Neurodegenerative Diseases (24 papers), Hereditary Neurological Disorders (20 papers) and Mitochondrial Function and Pathology (12 papers). Georgia Karadima is often cited by papers focused on Genetic Neurodegenerative Diseases (24 papers), Hereditary Neurological Disorders (20 papers) and Mitochondrial Function and Pathology (12 papers). Georgia Karadima collaborates with scholars based in Greece, United Kingdom and Italy. Georgia Karadima's co-authors include Μάριος Πάνας, Georgios Koutsis, Dimitrios Vassilopoulos, Athina Kladi, Dimitrios Avramopoulos, Dimitris Dikeos, E Daskalopoulou, Michael B. Petersen, Dimitris Avramopoulos and Nikolaos Kalfakis and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Georgia Karadima

63 papers receiving 774 citations

Peers

Georgia Karadima

CMN

NEURO

GENET

NEURO

Lena E. Hjermind Denmark

Patrícia de Carvalho Aguiar Brazil

Ilaria Guella Canada

Agnieszka Ciesielska Poland

Vandana Zaman United States

Patrizia Tarantino Italy

Delphine Meffre France

Steven B. Condliffe Italy

Monica M. Oblinger United States

Zihui Xu China

Lena E. Hjermind Denmark

Georgia Karadima

403 ×1.1

CMN

405 ×1.2

388 ×1.6

NEURO

98 ×0.5

GENET

100 ×0.9

NEURO

Citations per year, relative to Georgia Karadima Georgia Karadima (= 1×) peers Lena E. Hjermind

Countries citing papers authored by Georgia Karadima

Since Specialization

Citations

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

Fields of papers citing papers by Georgia Karadima

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Georgia Karadima

This figure shows the co-authorship network connecting the top 25 collaborators of Georgia Karadima. A scholar is included among the top collaborators of Georgia Karadima 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 Georgia Karadima. Georgia Karadima 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

Koutsis, Georgios, David Pellerin, Pablo Iruzubieta, et al.. (2024). Screening for SCA27B, CANVAS and other repeat expansion disorders in Greek patients with late-onset cerebellar ataxia suggests a need to update current diagnostic algorithms. Journal of the Neurological Sciences. 467. 123309–123309. 2 indexed citations

Papagiannakis, Nikolaos, Christos Koros, María Stamelou, et al.. (2024). Parkin mRNA Expression Levels in Peripheral Blood Mononuclear Cells in Parkin‐Related Parkinson's Disease. Movement Disorders. 39(4). 715–722. 3 indexed citations

Pellerin, David, Pablo Iruzubieta, Marie‐Josée Dicaire, et al.. (2024). The FGF14 GAA repeat expansion in Greek patients with late‐onset cerebellar ataxia and an overview of the SCA27B phenotype across populations. Clinical Genetics. 105(4). 446–452. 12 indexed citations

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

Rentzos, Michail, Constantin Potagas, Elisabeth Kapaki, et al.. (2022). Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population. Journal of the Neurological Sciences. 442. 120450–120450. 2 indexed citations

Anagnostou, Evangelos, et al.. (2021). Biallelic RFC1 pentanucleotide repeat expansions in Greek patients with late‐onset ataxia. Clinical Genetics. 100(1). 90–94. 14 indexed citations

Bourbouli, Mara, George P. Paraskevas, Vasiliki Zouvelou, et al.. (2021). Genotyping and Plasma/Cerebrospinal Fluid Profiling of a Cohort of Frontotemporal Dementia–Amyotrophic Lateral Sclerosis Patients. Brain Sciences. 11(9). 1239–1239. 7 indexed citations

Karavasilis, Efstratios, Foteini Christidi, Dimitrios Kasselimis, et al.. (2021). Structural and functional brain changes in X-linked Charcot-Marie-Tooth disease: insights from a multimodal neuroimaging study. Neuroradiology. 64(3). 543–552.

Kasselimis, Dimitrios, Georgia Karadima, Marianthi Breza, et al.. (2020). Evidence for Cognitive Deficits in X-Linked Charcot-Marie-Tooth Disease. Journal of the International Neuropsychological Society. 26(3). 294–302. 4 indexed citations

10.

Breza, Marianthi, Evangelia Emmanouilidou, Anastasia Bougea, et al.. (2020). Elevated Serum α-Synuclein Levels in Huntington’s Disease Patients. Neuroscience. 431. 34–39. 7 indexed citations

11.

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

12.

Hadjigeorgiou, Georgios M., Georgios Koutsis, Vana Tsimourtou, et al.. (2018). Replication study of GWAS risk loci in Greek multiple sclerosis patients. Neurological Sciences. 40(2). 253–260. 25 indexed citations

13.

Chondrogianni, Maria, Frantzeska Frantzeskaki, Evangelos J. Giamarellos‐Bourboulis, et al.. (2018). Three new case reports of Arteriovenous malformation-related Amyotrophic Lateral Sclerosis. Journal of the Neurological Sciences. 393. 58–62. 5 indexed citations

14.

Karadima, Georgia, et al.. (2017). Association of 5-HTTLPR Polymorphism with the Nursing Diagnoses and the Achievement of Nursing Outcomes in Patients with Major Depression. Issues in Mental Health Nursing. 38(10). 798–804. 2 indexed citations

15.

Sarri, Catherine, Sofia Douzgou, Yolanda Gyftodimou, et al.. (2011). Complex distal 10q rearrangement in a girl with mild intellectual disability: Follow up of the patient and review of the literature of non‐acrocentric satellited chromosomes. American Journal of Medical Genetics Part A. 155(11). 2841–2854. 5 indexed citations

16.

Karadima, Georgia, et al.. (2004). A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features. Journal of Neurology. 251(2). 222–223. 6 indexed citations

17.

Papadimitriou, George N., Dimitris Dikeos, Georgia Karadima, et al.. (2001). GABA‐A receptor β3 and α5 subunit gene cluster on chromosome 15q11–q13 and bipolar disorder: A genetic association study. American Journal of Medical Genetics. 105(4). 317–320. 22 indexed citations

18.

Gyftodimou, Jolanda, et al.. (1999). Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction. Clinical Genetics. 55(6). 483–486. 6 indexed citations

19.

Potier, Marie‐Claude, Annie Dutriaux, Georgia Karadima, et al.. (1998). Two Sequence-Ready Contigs Spanning the Two Copies of a 200-kb Duplication on Human 21q: Partial Sequence and Polymorphisms. Genomics. 51(3). 417–426. 16 indexed citations

20.

Economou-Petersen, E, et al.. (1997). Apolipoprotein E polymorphism in the Greek population. Clinical Genetics. 52(4). 216–218. 38 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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