Charalampos Karadimas

984 total citations
17 papers, 627 citations indexed

About

Charalampos Karadimas is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Charalampos Karadimas has authored 17 papers receiving a total of 627 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Clinical Biochemistry. Recurrent topics in Charalampos Karadimas's work include Mitochondrial Function and Pathology (6 papers), ATP Synthase and ATPases Research (5 papers) and Metabolism and Genetic Disorders (5 papers). Charalampos Karadimas is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), ATP Synthase and ATPases Research (5 papers) and Metabolism and Genetic Disorders (5 papers). Charalampos Karadimas collaborates with scholars based in Greece, United States and Netherlands. Charalampos Karadimas's co-authors include Sara Shanske, Kurenai Tanji, S. DiMauro, Michio Hirano, Carolyn M. Sue, E. Bonilla, Darryl C. De Vivo, Salvatore DiMauro, Nikolaos Kalfakis and Demetris Vassilopoulos and has published in prestigious journals such as Neurology, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Charalampos Karadimas

17 papers receiving 608 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Charalampos Karadimas Greece 14 473 245 135 101 55 17 627
Joan E. Pellegrino United States 11 256 0.5× 133 0.5× 215 1.6× 65 0.6× 31 0.6× 19 492
Veronika Karcagi Hungary 13 461 1.0× 100 0.4× 101 0.7× 79 0.8× 25 0.5× 32 616
Khalid Al‐Thihli Oman 13 219 0.5× 135 0.6× 116 0.9× 33 0.3× 50 0.9× 50 456
Nicole J. Lake United States 9 578 1.2× 314 1.3× 83 0.6× 52 0.5× 13 0.2× 17 668
Gert Van Goethem Belgium 12 1.0k 2.2× 649 2.6× 145 1.1× 230 2.3× 34 0.6× 13 1.2k
Daniel R. Carvalho Brazil 11 164 0.3× 92 0.4× 84 0.6× 57 0.6× 46 0.8× 31 343
Marwan Nashabat Saudi Arabia 13 229 0.5× 130 0.5× 105 0.8× 33 0.3× 66 1.2× 25 422
Anna Wedell Sweden 11 321 0.7× 220 0.9× 142 1.1× 30 0.3× 28 0.5× 28 498
Kathrin Jeltsch Germany 9 160 0.3× 198 0.8× 84 0.6× 98 1.0× 16 0.3× 18 387
Silvio Ferraris Italy 12 262 0.6× 198 0.8× 42 0.3× 34 0.3× 27 0.5× 12 370

Countries citing papers authored by Charalampos Karadimas

Since Specialization
Citations

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

Fields of papers citing papers by Charalampos Karadimas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charalampos Karadimas

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

All Works

17 of 17 papers shown
1.
Konstantinidou, Anastasia, Georgios Agrogiannis, Stavros Sifakis, et al.. (2009). Genetic skeletal disorders of the fetus and infant: Pathologic and molecular findings in a series of 41 cases. Birth Defects Research Part A Clinical and Molecular Teratology. 85(10). 811–821. 15 indexed citations
2.
Konstantinidou, Anastasia, Helen Fryssira, Stavros Sifakis, et al.. (2009). Cranioectodermal dysplasia: A probable ciliopathy. American Journal of Medical Genetics Part A. 149A(10). 2206–2211. 20 indexed citations
3.
Spinazzola, Antonella, René Santer, Xiaoqi Ding, et al.. (2008). Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome. Archives of Neurology. 65(8). 1108–13. 48 indexed citations
4.
Konstantinidou, Anastasia, Charalampos Karadimas, Hans R. Waterham, et al.. (2008). Pathologic, radiographic and molecular findings in three fetuses diagnosed with HEM/Greenberg skeletal dysplasia. Prenatal Diagnosis. 28(4). 309–312. 33 indexed citations
5.
Konstantinidou, A. E., Susanne Dertinger, M B Petersen, et al.. (2008). Placental Involvement in Glycogen Storage Disease Type IV. Placenta. 29(4). 378–381. 19 indexed citations
6.
Karadimas, Charalampos, et al.. (2006). Prenatal diagnosis of achondroplasia presenting with multiple‐suture synostosis: a novel association. Prenatal Diagnosis. 26(3). 258–261. 11 indexed citations
7.
Akman, Hasan O., Charalampos Karadimas, Yolanda Gyftodimou, et al.. (2006). Prenatal diagnosis of glycogen storage disease type IV. Prenatal Diagnosis. 26(10). 951–955. 21 indexed citations
8.
Karadimas, Charalampos, Tuan Vu, Catarina M. Quinzii, et al.. (2006). Navajo Neurohepatopathy Is Caused by a Mutation in the MPV17 Gene. The American Journal of Human Genetics. 79(3). 544–548. 112 indexed citations
9.
Karadimas, Charalampos, S. Sifakis, Voula Velissariou, et al.. (2006). Prenatal diagnosis of hypochondroplasia: Report of two cases. American Journal of Medical Genetics Part A. 140A(9). 998–1003. 11 indexed citations
10.
Velissariou, Voula, et al.. (2005). Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report. European Journal of Medical Genetics. 49(4). 331–337. 22 indexed citations
11.
Karadimas, Charalampos, Leonardo Salviati, Sabrina Sacconi, et al.. (2002). Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA. Neuromuscular Disorders. 12(9). 865–868. 30 indexed citations
12.
Gámez, Josep, Carmen Navarro, Antoni L. Andreu, et al.. (2001). Autosomal dominant limb-girdle muscular dystrophy. Neurology. 56(4). 450–454. 38 indexed citations
13.
Karadimas, Charalampos, Kurenai Tanji, Maciej Geremek, et al.. (2001). A5814G Mutation in Mitochondrial DNA Can Cause Mitochondrial Myopathy and Cardiomyopathy. Journal of Child Neurology. 16(7). 531–533. 14 indexed citations
14.
Πάνας, Μάριος, Nikolaos Kalfakis, Charalampos Karadimas, & Demetris Vassilopoulos. (2001). Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene. Neurology. 57(10). 1906–1908. 49 indexed citations
15.
Karadimas, Charalampos, Patricia Greenstein, Carolyn M. Sue, et al.. (2000). Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA. Neurology. 55(5). 644–649. 84 indexed citations
16.
Sue, Carolyn M., Charalampos Karadimas, Nicoletta Checcarelli, et al.. (2000). Differential features of patients with mutations in two COX assembly genes,SURF-1 andSCO2. Annals of Neurology. 47(5). 589–595. 99 indexed citations
17.
Sue, Carolyn M., Charalampos Karadimas, Nicoletta Checcarelli, et al.. (2000). Differential features of patients with mutations in two COX assembly genes, SURF1 and SCO2. Annals of Neurology. 47(5). 589–595. 1 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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