Luigi Citrigno

632 total citations
31 papers, 356 citations indexed

About

Luigi Citrigno is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Luigi Citrigno has authored 31 papers receiving a total of 356 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 9 papers in Neurology. Recurrent topics in Luigi Citrigno's work include Hereditary Neurological Disorders (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Neurological diseases and metabolism (4 papers). Luigi Citrigno is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Neurological diseases and metabolism (4 papers). Luigi Citrigno collaborates with scholars based in Italy, United States and United Kingdom. Luigi Citrigno's co-authors include M. Muglia, F. L. Conforti, C Ungaro, Aldo Quattrone, R. Mazzei, A. Magariello, T. Sprovieri, Francesca Cavalcanti, Patrizia Spadafora and Antonio Cerasa and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Luigi Citrigno

26 papers receiving 351 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luigi Citrigno Italy 11 160 101 78 71 67 31 356
Tomokatsu Yoshida Japan 12 342 2.1× 140 1.4× 51 0.7× 57 0.8× 63 0.9× 54 546
Samantha L. Sison United States 9 272 1.7× 100 1.0× 109 1.4× 48 0.7× 85 1.3× 10 412
Uri Nimrod Ramírez-Jarquín Mexico 10 278 1.7× 146 1.4× 149 1.9× 39 0.5× 77 1.1× 14 480
Alberto Catanese Germany 11 129 0.8× 139 1.4× 98 1.3× 36 0.5× 66 1.0× 21 314
Kristina Gotovac Croatia 9 205 1.3× 114 1.1× 74 0.9× 32 0.5× 24 0.4× 25 382
Haruko Nakamura Japan 11 270 1.7× 70 0.7× 127 1.6× 43 0.6× 21 0.3× 24 455
Adam Dickinson United Kingdom 7 319 2.0× 54 0.5× 39 0.5× 34 0.5× 46 0.7× 9 465
Birgit Nimmervoll United States 9 151 0.9× 36 0.4× 83 1.1× 38 0.5× 66 1.0× 10 323
Marianthi Breza Greece 10 104 0.7× 134 1.3× 136 1.7× 82 1.2× 50 0.7× 32 337
Wotu Tian China 10 105 0.7× 68 0.7× 68 0.9× 47 0.7× 21 0.3× 39 280

Countries citing papers authored by Luigi Citrigno

Since Specialization
Citations

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

Fields of papers citing papers by Luigi Citrigno

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luigi Citrigno

This figure shows the co-authorship network connecting the top 25 collaborators of Luigi Citrigno. A scholar is included among the top collaborators of Luigi Citrigno 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 Luigi Citrigno. Luigi Citrigno 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.
Sire, Alessandro de, Elettra Mancuso, Nicola Marotta, et al.. (2025). Association between gut microbiota composition and physical functioning in patients with knee osteoarthritis: a machine learning study. Scientific Reports. 15(1). 40826–40826.
2.
Citrigno, Luigi, et al.. (2024). Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies. Journal of the Neurological Sciences. 457. 122869–122869.
3.
Citrigno, Luigi, Béatrice Gréco, Giuseppe Passarino, et al.. (2024). The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions. International Journal of Molecular Sciences. 25(11). 6062–6062. 6 indexed citations
4.
Bruno, Francesco, Paolo Abondio, Rossella Bruno, et al.. (2023). Alzheimer’s disease as a viral disease: Revisiting the infectious hypothesis. Ageing Research Reviews. 91. 102068–102068. 38 indexed citations
5.
Lagani, Vincenzo, Silvana Geracitano, Luigi Citrigno, et al.. (2023). An ELOVL2-Based Epigenetic Clock for Forensic Age Prediction: A Systematic Review. International Journal of Molecular Sciences. 24(3). 2254–2254. 14 indexed citations
6.
Geracitano, Silvana, Vincenzo Lagani, Patrizia D’Aquila, et al.. (2022). A Blood-Based Molecular Clock for Biological Age Estimation. Cells. 12(1). 32–32. 10 indexed citations
7.
Veredice, Chiara, Ilaria Contaldo, Michela Quintiliani, et al.. (2022). Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes. Pediatric Neurology. 132. 45–49. 5 indexed citations
8.
9.
Sprovieri, T., C Ungaro, Serena Sivo, et al.. (2019). Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report. BMC Medical Genetics. 20(1). 40–40. 7 indexed citations
10.
11.
Ungaro, C, Luigi Citrigno, Francesca Trojsi, et al.. (2018). ALS and CHARGE syndrome: a clinical and genetic study. Acta Neurologica Belgica. 118(4). 629–635. 3 indexed citations
12.
Muglia, M., Luigi Citrigno, Eustachio D’Errico, et al.. (2014). A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness. Journal of the Neurological Sciences. 343(1-2). 218–220. 8 indexed citations
13.
Patitucci, A., A. Magariello, C Ungaro, et al.. (2012). SMN1 gene copy number analyses for SMA healthy carriers in Italian population.. Europe PMC (PubMed Central). 1(2). 99–102.
14.
Pennisi, Manuela, Alberto Raggi, Rita Barone, et al.. (2012). Phenotypic heterogeneity in hereditary motor neuropathy type V: a new case report series. Acta Neurologica Belgica. 112(1). 57–64. 3 indexed citations
15.
McCorquodale, D. James, Uzoezi Ozomaro, Jiaqiang Huang, et al.. (2010). Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia. Clinical Genetics. 79(6). 523–530. 42 indexed citations
16.
Magariello, A., M. Muglia, A. Patitucci, et al.. (2009). Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia. Journal of the Neurological Sciences. 288(1-2). 96–100. 20 indexed citations
17.
Sprovieri, T., F. L. Conforti, Agata Fiumara, et al.. (2009). A novel mutation in the X‐linked cyclin‐dependent kinase‐like 5 (CDKL5) gene associated with a severe Rett phenotype. American Journal of Medical Genetics Part A. 149A(4). 722–725. 16 indexed citations
18.
Conforti, F. L., T. Sprovieri, R. Mazzei, et al.. (2008). Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy. Amyotrophic Lateral Sclerosis. 10(1). 58–60. 11 indexed citations
19.
Ungaro, C, F. L. Conforti, T. Sprovieri, et al.. (2008). Gene symbol: NOTCH3. Disease: CADASIL.. PubMed. 123(5). 554–554. 1 indexed citations
20.
Mazzei, R., Donata Guidetti, C Ungaro, et al.. (2007). First evidence of a pathogenic insertion in the NOTCH3 gene causing CADASIL. Journal of Neurology Neurosurgery & Psychiatry. 79(1). 108–110. 10 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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