Μάριος Πάνας

1.8k total citations
66 papers, 954 citations indexed

About

Μάριος Πάνας is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Μάριος Πάνας has authored 66 papers receiving a total of 954 indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Cellular and Molecular Neuroscience, 32 papers in Neurology and 26 papers in Molecular Biology. Recurrent topics in Μάριος Πάνας's work include Genetic Neurodegenerative Diseases (34 papers), Hereditary Neurological Disorders (20 papers) and Mitochondrial Function and Pathology (17 papers). Μάριος Πάνας is often cited by papers focused on Genetic Neurodegenerative Diseases (34 papers), Hereditary Neurological Disorders (20 papers) and Mitochondrial Function and Pathology (17 papers). Μάριος Πάνας collaborates with scholars based in Greece, United Kingdom and United States. Μάριος Πάνας's co-authors include Dimitrios Vassilopoulos, Georgia Karadima, Georgios Koutsis, Athina Kladi, Manolis Markianos, Nikolaos Kalfakis, Evangelos Vassos, Demetris Vassilopoulos, Henry Houlden and Charalampos Karadimas and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Annals of Neurology.

In The Last Decade

Μάριος Πάνας

65 papers receiving 923 citations

Peers

Μάριος Πάνας

CMN

NEURO

PHYSI

Georgia Karadima Greece

Kadiombo Bantubungi France

Wolfgang Nachbauer Austria

Dawei Zang China

Ilaria Guella Canada

Nicolas C. Royo United States

Xiaoli Si China

Hiroyuki Morino Japan

Lucie Guyant‐Maréchal France

Nadia Nabil Haj‐Yasein Norway

Georgia Karadima Greece

Μάριος Πάνας

381 ×0.6

CMN

329 ×0.8

240 ×0.6

NEURO

117 ×0.7

NEURO

72 ×0.9

PHYSI

Citations per year, relative to Μάριος Πάνας Μάριος Πάνας (= 1×) peers Georgia Karadima

Countries citing papers authored by Μάριος Πάνας

Since Specialization

Citations

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

Fields of papers citing papers by Μάριος Πάνας

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Μάριος Πάνας

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

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

Rentzos, Michail, Panagiotis Kokotis, Evangelos Anagnostou, et al.. (2023). Mutational screening of Greek patients with axonal Charcot‐Marie‐Tooth disease using targeted next‐generation sequencing: Clinical and molecular spectrum delineation. Journal of the Peripheral Nervous System. 28(4). 642–650. 1 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

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

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

Breza, Marianthi, et al.. (2019). Screening for spinocerebellar ataxia type 36 (SCA36) in the Greek population. Journal of the Neurological Sciences. 402. 131–132. 6 indexed citations

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

10.

Πάνας, Μάριος, et al.. (2012). The Byzantine Empress Zoe Porphyrogenita and the quest for eternal youth. Journal of Cosmetic Dermatology. 11(3). 245–248. 3 indexed citations

11.

Markianos, Manolis, et al.. (2008). Plasma Homovanillic Acid and Prolactin in Huntington’s Disease. Neurochemical Research. 34(5). 917–922. 17 indexed citations

12.

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

13.

Markianos, Manolis, et al.. (2005). Plasma testosterone in male patients with Huntington's disease: Relations to severity of illness and dementia. Annals of Neurology. 57(4). 520–525. 87 indexed citations

14.

Koutsis, Georgios, et al.. (2005). Acute Painful Sensory Neuropathy with Subclinical Autonomic Dysfunction as a Presenting Feature of Hodgkin’s Disease. European Neurology. 53(3). 157–159. 1 indexed citations

15.

Markianos, Manolis, Μάριος Πάνας, Nikolaos Kalfakis, & Dimitrios Vassilopoulos. (2004). Platelet monoamine oxidase activity in subjects tested for Huntington?s disease gene mutation. Journal of Neural Transmission. 111(4). 475–483. 12 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.

Spengos, Konstantinos, et al.. (2003). Crescendo Transient Ischemic Attacks due to Middle Cerebral Artery Stenosis. Cerebrovascular Diseases. 17(2-3). 266–268. 2 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, et al.. (1997). Apolipoprotein E polymorphism in the Greek population. Clinical Genetics. 52(4). 216–218. 38 indexed citations

20.

Kalfakis, Nikolaos, et al.. (1994). The risk of cancer in relatives of patients with brain neoplasm. Acta Neurochirurgica. 131(3-4). 226–228. 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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