Luigi Serlenga

1.4k total citations
37 papers, 1.0k citations indexed

About

Luigi Serlenga is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Luigi Serlenga has authored 37 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Neurology, 15 papers in Molecular Biology and 13 papers in Cellular and Molecular Neuroscience. Recurrent topics in Luigi Serlenga's work include Genetic Neurodegenerative Diseases (13 papers), Amyotrophic Lateral Sclerosis Research (13 papers) and Neurogenetic and Muscular Disorders Research (11 papers). Luigi Serlenga is often cited by papers focused on Genetic Neurodegenerative Diseases (13 papers), Amyotrophic Lateral Sclerosis Research (13 papers) and Neurogenetic and Muscular Disorders Research (11 papers). Luigi Serlenga collaborates with scholars based in Italy, United States and France. Luigi Serlenga's co-authors include Giancarlo Logroscino, Stefano Zoccolella, Vito Samarelli, Ettore Beghi, Angela Fraddosio, Vito Lepore, Paolo Lamberti, Isabella Laura Simone, Vito Guerra and Giovanni Iliceto and has published in prestigious journals such as Neurology, FEBS Letters and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Luigi Serlenga

37 papers receiving 1.0k 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 Serlenga Italy 18 709 356 291 211 115 37 1.0k
Claudia Caponnetto Italy 17 633 0.9× 345 1.0× 253 0.9× 167 0.8× 224 1.9× 49 999
Kiyokazu Kawabe Japan 15 457 0.6× 125 0.4× 172 0.6× 127 0.6× 116 1.0× 48 804
Michael Rentzos Greece 22 719 1.0× 147 0.4× 271 0.9× 201 1.0× 406 3.5× 45 1.4k
Giuseppe Piscosquito Italy 20 558 0.8× 99 0.3× 371 1.3× 641 3.0× 233 2.0× 55 1.2k
Tomoya Kon Japan 15 554 0.8× 63 0.2× 226 0.8× 257 1.2× 126 1.1× 76 854
Luca Leonardi Italy 17 253 0.4× 57 0.2× 365 1.3× 346 1.6× 51 0.4× 63 764
Jung‐Joon Sung South Korea 20 670 0.9× 248 0.7× 263 0.9× 141 0.7× 109 0.9× 76 1.1k
Dongchao Shen China 15 420 0.6× 216 0.6× 142 0.5× 81 0.4× 74 0.6× 61 591
David Hutchinson New Zealand 16 484 0.7× 73 0.2× 534 1.8× 196 0.9× 37 0.3× 38 1.0k
Orna O’Toole Ireland 13 687 1.0× 153 0.4× 176 0.6× 119 0.6× 126 1.1× 28 959

Countries citing papers authored by Luigi Serlenga

Since Specialization
Citations

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

Fields of papers citing papers by Luigi Serlenga

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luigi Serlenga

This figure shows the co-authorship network connecting the top 25 collaborators of Luigi Serlenga. A scholar is included among the top collaborators of Luigi Serlenga 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 Serlenga. Luigi Serlenga 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.
Giannini, Margherita, Francesco Girolamo, Clélia Akiko Hiruma-Lima, et al.. (2018). FRI0397 Peculiar expression of autophagy biomarkers in necrotizing autoimmune myopathy muscle. Annals of the Rheumatic Diseases. 77. 731–731. 2 indexed citations
2.
Artuso, Lucia, Stefano Zoccolella, Rosa Capozzo, et al.. (2012). Mitochondrial genome aberrations in skeletal muscle of patients with motor neuron disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 14(4). 261–266. 15 indexed citations
3.
Manganelli, Fiore, Raffaele Dubbioso, Maria Nolano, et al.. (2011). Autoimmune Autonomic Ganglionopathy. Archives of Neurology. 68(4). 504–504. 12 indexed citations
4.
Musumeci, Olimpia, Claudio Bruno, Tiziana Mongini, et al.. (2011). Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII). Neuromuscular Disorders. 22(4). 325–330. 36 indexed citations
5.
Bisceglia, Luigi, Alessandra Torraco, Maria Rosaria Piemontese, et al.. (2010). A new locus on 3p23–p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H. European Journal of Human Genetics. 18(6). 636–641. 17 indexed citations
6.
Negro, Roberto, Lucia Artuso, Luigi Bisceglia, et al.. (2009). Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegia. Neuromuscular Disorders. 19(6). 423–426. 7 indexed citations
7.
Zoccolella, Stefano, Gabriele Masi, Domenico Maria Mezzapesa, et al.. (2008). Motoneuron disease after electric injury: a case report. Neurological Sciences. 29(1). 47–49. 10 indexed citations
8.
Zoccolella, Stefano, Ettore Beghi, Angela Fraddosio, et al.. (2007). ALS multidisciplinary clinic and survival. Journal of Neurology. 254(8). 1107–1112. 52 indexed citations
9.
Zoccolella, Stefano, Ettore Beghi, Angela Fraddosio, et al.. (2007). Riluzole and amyotrophic lateral sclerosis survival: a population‐based study in southern Italy. European Journal of Neurology. 14(3). 262–268. 86 indexed citations
10.
Zoccolella, Stefano, Ettore Beghi, Angela Fraddosio, et al.. (2007). Analysis of survival and prognostic factors in amyotrophic lateral sclerosis: a population based study. Journal of Neurology Neurosurgery & Psychiatry. 79(1). 33–37. 114 indexed citations
11.
Zoccolella, Stefano, Ettore Beghi, Angela Fraddosio, et al.. (2006). Signs and symptoms at diagnosis of amyotrophic lateral sclerosis: a population‐based study in southern Italy. European Journal of Neurology. 13(7). 789–792. 35 indexed citations
12.
Zoccolella, Stefano, Ettore Beghi, Luigi Serlenga, & Giancarlo Logroscino. (2005). Classification of amyotrophic lateral sclerosis cases at presentation in epidemiological studies. Neurological Sciences. 26(5). 330–333. 6 indexed citations
13.
Corrado, Addolorata, et al.. (2002). Mitochondrial Disease Mimicking Polymyositis: A Case Report. Clinical Rheumatology. 21(5). 411–414. 4 indexed citations
14.
Filla, Alessandro, Giuseppe De Michele, Lucio Santoro, et al.. (1999). Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families. Journal of Neurology. 246(6). 467–471. 48 indexed citations
15.
Lamberti, Paolo, et al.. (1997). Freezing Gait in Parkinson's Disease. European Neurology. 38(4). 297–301. 106 indexed citations
16.
Filla, Alessandro, Giuseppe De Michele, G Campanella, et al.. (1996). Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes. Journal of the Neurological Sciences. 142(1-2). 140–147. 28 indexed citations
17.
Lamberti, Paolo, et al.. (1993). Effect of L‐dopa on oculogyric crises in a case of dopa‐responsive dystonia. Movement Disorders. 8(2). 236–237. 5 indexed citations
18.
Papadia, Francesco, et al.. (1987). Progressive form of multiple pterygium syndrome in association with nemalin‐myopathy: Report of a female followed for twelve years. American Journal of Medical Genetics. 26(1). 73–83. 8 indexed citations
19.
Serlenga, Luigi, et al.. (1985). Centronuclear myopathy. Report of a sporadic case.. PubMed. 7(5). 416–24. 2 indexed citations
20.
Trizio, Michele, et al.. (1984). [Lecithin therapy of hereditary ataxia].. PubMed. 104(2). 49–59. 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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