A. Papadimitriou

1.2k total citations
21 papers, 745 citations indexed

About

A. Papadimitriou is a scholar working on Molecular Biology, Neurology and Clinical Biochemistry. According to data from OpenAlex, A. Papadimitriou has authored 21 papers receiving a total of 745 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Neurology and 5 papers in Clinical Biochemistry. Recurrent topics in A. Papadimitriou's work include Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (5 papers) and ATP Synthase and ATPases Research (4 papers). A. Papadimitriou is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (5 papers) and ATP Synthase and ATPases Research (4 papers). A. Papadimitriou collaborates with scholars based in Greece, Italy and United States. A. Papadimitriou's co-authors include Andreina Bordoni, Giacomo P. Comi, Valeria Tiranti, Massimo Zeviani, António Toscano, Nereo Bresolin, Maurizio Moggio, Serenella Servidei, Francesco Bono and Eleonora Lamantea and has published in prestigious journals such as Neurology, Annals of Neurology and Behavioral Neuroscience.

In The Last Decade

A. Papadimitriou

21 papers receiving 726 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Papadimitriou Greece 14 570 324 112 92 66 21 745
Hanna Mierzewska Poland 15 444 0.8× 126 0.4× 98 0.9× 105 1.1× 127 1.9× 57 728
Birgit Uhlenberg Germany 10 529 0.9× 273 0.8× 55 0.5× 84 0.9× 175 2.7× 16 981
Veronika Karcagi Hungary 13 461 0.8× 100 0.3× 84 0.8× 79 0.9× 101 1.5× 32 616
Franco Carrara Italy 20 1.6k 2.8× 894 2.8× 75 0.7× 144 1.6× 126 1.9× 28 1.8k
Gert Van Goethem Belgium 12 1.0k 1.8× 649 2.0× 73 0.7× 230 2.5× 145 2.2× 13 1.2k
Cristina Jou Spain 15 405 0.7× 111 0.3× 40 0.4× 66 0.7× 68 1.0× 65 637
R. M. Chalmers United Kingdom 13 733 1.3× 305 0.9× 180 1.6× 273 3.0× 109 1.7× 16 1.1k
M G Sweeney United Kingdom 18 1.0k 1.8× 577 1.8× 128 1.1× 314 3.4× 85 1.3× 21 1.2k
F. Carrara Italy 13 1.4k 2.4× 895 2.8× 42 0.4× 140 1.5× 116 1.8× 19 1.5k
Niranjanan Nirmalananthan United Kingdom 11 293 0.5× 67 0.2× 177 1.6× 159 1.7× 30 0.5× 23 537

Countries citing papers authored by A. Papadimitriou

Since Specialization
Citations

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

Fields of papers citing papers by A. Papadimitriou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Papadimitriou

This figure shows the co-authorship network connecting the top 25 collaborators of A. Papadimitriou. A scholar is included among the top collaborators of A. Papadimitriou 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 A. Papadimitriou. A. Papadimitriou 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.
Korfias, Stefanos, A. Papadimitriou, Georgios Stranjalis, et al.. (2009). Serum Biochemical Markers of Brain Injury. Mini-Reviews in Medicinal Chemistry. 9(2). 227–234. 23 indexed citations
2.
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
3.
Magos, Adam, et al.. (2009). V28 Ovarian artery clamp: A new clamp to reduce bleeding at open myomectomy. International Journal of Gynecology & Obstetrics. 107(S2). 1 indexed citations
4.
Ronchi, Dario, George Hadjigeorgiou, Andreina Bordoni, et al.. (2008). Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia. Journal of Neurology. 255(9). 1384–1391. 31 indexed citations
5.
Galbiati, Sara, Andreina Bordoni, Dimitra Papadimitriou, et al.. (2006). New Mutations in TK2 Gene Associated With Mitochondrial DNA Depletion. Pediatric Neurology. 34(3). 177–185. 47 indexed citations
6.
Korfias, Stefanos, Georgios Stranjalis, A. Papadimitriou, et al.. (2006). Serum S-100B Protein as A Biochemical Marker of Brain Injury: A Review of Current Concepts. Current Medicinal Chemistry. 13(30). 3719–3731. 91 indexed citations
7.
Papadimitriou, A., et al.. (2005). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a Greek family. Neurological Sciences. 26(4). 278–281. 4 indexed citations
8.
Lamantea, Eleonora, Valeria Tiranti, Andreina Bordoni, et al.. (2002). Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia. Annals of Neurology. 52(2). 211–219. 215 indexed citations
9.
10.
Napoli, Laura, Andreina Bordoni, Massimo Zeviani, et al.. (2001). A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family. Neurology. 57(12). 2295–2298. 77 indexed citations
11.
Hadjigeorgiou, George, Giacomo P. Comi, Andreina Bordoni, et al.. (1999). Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa. Journal of Inherited Metabolic Disease. 22(6). 762–763. 15 indexed citations
12.
Papadimitriou, A., et al.. (1998). Continuous muscle fiber activity associated with morphea (localized scleroderma). Neurology. 51(6). 1763–1764. 1 indexed citations
13.
Papadimitriou, A., Giacomo P. Comi, George Hadjigeorgiou, et al.. (1998). Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome. Neurology. 51(4). 1086–1092. 86 indexed citations
14.
Rose, Michael, D. N. Landon, A. Papadimitriou, & J A Morgan-Hughes. (1997). A rapidly progressive adolescent‐onset oculopharyngeal somatic syndrome with rimmed vacuoles in two siblings. Annals of Neurology. 41(1). 25–31. 8 indexed citations
15.
Papadimitriou, A., et al.. (1996). Myoglobinuria due to Quail Poisoning. European Neurology. 36(3). 142–145. 14 indexed citations
16.
Michelakakis, Helen, et al.. (1995). Plasma lysosomal enzyme levels in patients with motor neuron disease. Journal of Inherited Metabolic Disease. 18(1). 72–74. 4 indexed citations
17.
Checcarelli, Nicoletta, A. Prelle, Maurizio Moggio, et al.. (1994). Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy. Journal of the Neurological Sciences. 123(1-2). 74–79. 24 indexed citations
18.
Koutroumanidis, Michael, et al.. (1994). Temporal Distribution of Onset of Acute Ischemic Stroke in Athens, Greece: Role of Major Predisposing Factors and Association with Ambient Temperature. Cerebrovascular Diseases. 4(5). 359–364. 1 indexed citations
19.
Divry, P., C. Jakobs, Christine Vianey‐Saban, et al.. (1993). l‐2‐Hydroxyglutaric aciduria: Two further cases. Journal of Inherited Metabolic Disease. 16(3). 505–507. 27 indexed citations
20.
Papadimitriou, A., et al.. (1990). McArdle's disease: two clinical expressions in the same pedigree. Journal of Neurology. 237(4). 267–270. 19 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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