Panos Ioannou

811 total citations
26 papers, 632 citations indexed

About

Panos Ioannou is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Panos Ioannou has authored 26 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in Panos Ioannou's work include Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (8 papers) and DNA Repair Mechanisms (5 papers). Panos Ioannou is often cited by papers focused on Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (8 papers) and DNA Repair Mechanisms (5 papers). Panos Ioannou collaborates with scholars based in Australia, Cyprus and France. Panos Ioannou's co-authors include Joseph P. Sarsero, Martin B. Delatycki, Lingli Li, Robert Williamson, Samuel McLenachan, Lucille Voullaire, Hady Wardan, Aaron G. Smith, Edmund Ui‐Hang Sim and Melissa H. Little and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Neurology.

In The Last Decade

Panos Ioannou

26 papers receiving 617 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Panos Ioannou Australia 15 478 239 123 115 73 26 632
Sabrina A. Volpi United States 8 389 0.8× 167 0.7× 48 0.4× 33 0.3× 15 0.2× 9 667
Shehla Mohammed United Kingdom 12 497 1.0× 61 0.3× 248 2.0× 55 0.5× 17 0.2× 25 680
Yasuhide Hayashi Japan 9 374 0.8× 288 1.2× 47 0.4× 68 0.6× 73 1.0× 9 741
Paola Prandini Italy 11 799 1.7× 152 0.6× 212 1.7× 71 0.6× 14 0.2× 15 1.0k
T O'Brien United Kingdom 8 382 0.8× 115 0.5× 147 1.2× 73 0.6× 12 0.2× 11 483
Andrew G. L. Douglas United Kingdom 12 498 1.0× 87 0.4× 145 1.2× 163 1.4× 15 0.2× 31 739
Antonino Cascino Italy 14 402 0.8× 104 0.4× 106 0.9× 131 1.1× 11 0.2× 24 678
Sergio Arias Venezuela 11 229 0.5× 94 0.4× 107 0.9× 27 0.2× 24 0.3× 33 414
Alphonse Chu Canada 13 545 1.1× 47 0.2× 66 0.5× 54 0.5× 26 0.4× 14 707
N. Ravisé France 14 298 0.6× 345 1.4× 111 0.9× 29 0.3× 7 0.1× 30 585

Countries citing papers authored by Panos Ioannou

Since Specialization
Citations

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

Fields of papers citing papers by Panos Ioannou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Panos Ioannou

This figure shows the co-authorship network connecting the top 25 collaborators of Panos Ioannou. A scholar is included among the top collaborators of Panos Ioannou 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 Panos Ioannou. Panos Ioannou 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.
Li, Lingli, Lucille Voullaire, Chiranjeevi Sandi, et al.. (2013). Pharmacological Screening Using an FXN-EGFP Cellular Genomic Reporter Assay for the Therapy of Friedreich Ataxia. PLoS ONE. 8(2). e55940–e55940. 35 indexed citations
2.
Rowley, Simone M., Lavinia Gordon, Paul J. Lockhart, et al.. (2011). Long Range Regulation of Human FXN Gene Expression. PLoS ONE. 6(7). e22001–e22001. 9 indexed citations
3.
Khaniani, Mahmoud Shekari, Hady Wardan, Jean‐François Benoist, et al.. (2009). Gene induction for the treatment of methylmalonic aciduria. The Journal of Gene Medicine. 11(4). 361–369. 5 indexed citations
4.
McLenachan, Samuel, Yona Goldshmit, Kerry J. Fowler, et al.. (2008). Transgenic mice expressing the Peripherin-EGFP genomic reporter display intrinsic peripheral nervous system fluorescence. Transgenic Research. 17(6). 1103–1116. 13 indexed citations
5.
McLenachan, Samuel, Joseph P. Sarsero, & Panos Ioannou. (2007). Flow-cytometric analysis of mouse embryonic stem cell lipofection using small and large DNA constructs. Genomics. 89(6). 708–720. 32 indexed citations
6.
Sarsero, Joseph P., Timothy P. Holloway, Lingli Li, et al.. (2005). Evaluation of an FRDA–EGFP genomic reporter assay in transgenic mice. Mammalian Genome. 16(4). 228–241. 11 indexed citations
7.
Vadolas, Jim, Hady Wardan, Duangporn Jamsai, et al.. (2005). Transgene copy number-dependent rescue of murine β-globin knockout mice carrying a 183 kb human β-globin BAC genomic fragment. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1728(3). 150–162. 17 indexed citations
8.
Delatycki, Martin B., Panos Ioannou, & Andrew Churchyard. (2005). Friedreich ataxia: from genes to therapies?. The Medical Journal of Australia. 182(9). 439–439. 3 indexed citations
9.
Sarsero, Joseph P., Lingli Li, Timothy P. Holloway, et al.. (2004). Human BAC-mediated rescue of the Friedreich ataxia knockout mutation in transgenic mice. Mammalian Genome. 15(5). 370–382. 38 indexed citations
10.
Ioannou, Panos, et al.. (2004). Friedreich ataxia?update on pathogenesis and possible therapies. Neurogenetics. 5(1). 1–8. 53 indexed citations
11.
Sturm, Brigitte, Matthias Schranzhofer, Joseph P. Sarsero, et al.. (2004). Friedreich's Ataxia, No Changes in Mitochondrial Labile Iron in Human Lymphoblasts and Fibroblasts. Journal of Biological Chemistry. 280(8). 6701–6708. 64 indexed citations
12.
Jamsai, Duangporn, Mikhail Nefedov, Kumaran Narayanan, et al.. (2003). Insertion of common mutations into the human β-globin locus using GET Recombination and an EcoRI endonuclease counterselection cassette. Journal of Biotechnology. 101(1). 1–9. 14 indexed citations
13.
Sim, Edmund Ui‐Hang, et al.. (2002). Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1. Oncogene. 21(19). 2948–2960. 73 indexed citations
14.
Sarsero, Joseph P., et al.. (2002). Upregulation of expression from the FRDA genomic locus for the therapy of Friedreich ataxia. The Journal of Gene Medicine. 5(1). 72–81. 56 indexed citations
15.
16.
Christodoulou, Kyproula, Feza Deymeer, Piraye Oflazer, et al.. (2001). Mapping of the second Friedreich's ataxia (FRDAff2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity. Neurogenetics. 3(3). 127–132. 22 indexed citations
17.
Puechberty, Jacques, Sylvie Gimenez, Alain Billault, et al.. (1999). Genetic and Physical Analyses of the Centromeric and Pericentromeric Regions of Human Chromosome 5: Recombination across 5cen. Genomics. 56(3). 274–287. 40 indexed citations
18.
Furihata, Kenichi, Anthi Drousiotou, George Christopoulos, et al.. (1999). Novel splice site mutation at IVS8 nt 5 of HEXB responsible for a Greek-Cypriot case of Sandhoff disease. Human Mutation. 13(1). 38–43. 6 indexed citations
19.
Ioannou, Panos, et al.. (1994). Mutation analysis of a Sandhoff disease patient in the Maronite community in Cyprus. Human Genetics. 94(2). 136–40. 8 indexed citations
20.
Deltas, Constantinos, et al.. (1992). ΔF508 cystic fibrosis mutation appears very infrequently in the Greek-Cypriot community of Cyprus. Human Mutation. 1(6). 503–505. 2 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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