Claudia Cagnoli

1.2k total citations
13 papers, 550 citations indexed

About

Claudia Cagnoli is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Claudia Cagnoli has authored 13 papers receiving a total of 550 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 2 papers in Neurology. Recurrent topics in Claudia Cagnoli's work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (8 papers) and Ubiquitin and proteasome pathways (4 papers). Claudia Cagnoli is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (8 papers) and Ubiquitin and proteasome pathways (4 papers). Claudia Cagnoli collaborates with scholars based in Italy, United States and France. Claudia Cagnoli's co-authors include Alfredo Brusco, Nicola Migone, Cinzia Gellera, Alessandro Brussino, Franco Taroni, Stefano Di Donato, Caterina Mariotti, Patrizia Pappi, Marco Seri and Daniela Di Bella and has published in prestigious journals such as Brain, Movement Disorders and Human Mutation.

In The Last Decade

Claudia Cagnoli

13 papers receiving 541 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Claudia Cagnoli Italy	11	464	394	122	114	56	13	550
Craig Bencsics United States	5	222 0.5×	326 0.8×	136 1.1×	129 1.1×	29 0.5×	6	472
Berry Kremer Netherlands	3	671 1.4×	719 1.8×	66 0.5×	376 3.3×	31 0.6×	5	872
Randall M. Thompson United States	7	354 0.8×	386 1.0×	26 0.2×	137 1.2×	69 1.2×	8	472
Zhe Long China	12	189 0.4×	141 0.4×	57 0.5×	88 0.8×	22 0.4×	34	336
Marzia Indrigo Italy	8	258 0.6×	179 0.5×	143 1.2×	134 1.2×	30 0.5×	12	452
Mohan K. Sapru United States	10	236 0.5×	210 0.5×	60 0.5×	148 1.3×	15 0.3×	12	450
Jayalakshmi Srinidhi Mysore United States	13	583 1.3×	594 1.5×	70 0.6×	227 2.0×	14 0.3×	17	704
Chiyomi Ito Japan	8	211 0.5×	168 0.4×	55 0.5×	173 1.5×	46 0.8×	9	362
Jayalakshmi Srinidhi United States	11	957 2.1×	1.0k 2.7×	96 0.8×	544 4.8×	30 0.5×	13	1.2k
Yongcheng Pan China	12	198 0.4×	156 0.4×	62 0.5×	38 0.3×	16 0.3×	22	305

Countries citing papers authored by Claudia Cagnoli

Since Specialization

Citations

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

Fields of papers citing papers by Claudia Cagnoli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudia Cagnoli

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

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Cagnoli, Claudia, Alessandro Brussino, Cecilia Mancini, et al.. (2018). Spinocerebellar Ataxia Tethering PCR. Journal of Molecular Diagnostics. 20(3). 289–297. 15 indexed citations

Sacco, Tiziana, Enrica Boda, Eriola Hoxha, et al.. (2010). Mouse brain expression patterns of Spg7, Afg3l1, and Afg3l2 transcripts, encoding for the mitochondrial m-AAA protease. BMC Neuroscience. 11(1). 55–55. 22 indexed citations

Gregorio, Eleonora Di, Laura Orsi, Giovanna Vaula, et al.. (2010). Two Italian Families with ITPR1 Gene Deletion Presenting a Broader Phenotype of SCA15. The Cerebellum. 9(1). 115–123. 32 indexed citations

Cagnoli, Claudia, Giovanni Stévanin, Alessandro Brussino, et al.. (2010). Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias. Human Mutation. 31(10). 1117–1124. 53 indexed citations

Stévanin, Giovanni, Sylvie Forlani, C. Cazeneuve, et al.. (2009). Conventional mutations are associated with a different phenotype than polyglutamine expansions in spinocerebellar ataxias. 16. 284–284. 5 indexed citations

Mariotti, Caterina, Alfredo Brusco, Daniela Di Bella, et al.. (2008). Spinocerebellar ataxia type 28: A novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. The Cerebellum. 7(2). 184–188. 36 indexed citations

Cagnoli, Claudia, Alessandro Brussino, Luca Sbaiz, et al.. (2008). A previously undiagnosed case of Gerstmann‐Sträussler‐Scheinker disease revealed by PRNP gene analysis in patients with adult‐onset ataxia. Movement Disorders. 23(10). 1468–1471. 9 indexed citations

Cagnoli, Claudia, Giovanni Stévanin, Alessandro Brussino, et al.. (2006). Large Pathogenic Expansions in the SCA2 and SCA7 Genes Can Be Detected by Fluorescent Repeat-Primed Polymerase Chain Reaction Assay. Journal of Molecular Diagnostics. 8(1). 128–132. 26 indexed citations

Brussino, Alessandro, Flora Tassone, Carlo Arduino, et al.. (2005). An Enhanced Polymerase Chain Reaction Assay to Detect Pre- and Full Mutation Alleles of the Fragile X Mental Retardation 1 Gene. Journal of Molecular Diagnostics. 7(5). 605–612. 89 indexed citations

10.

Cagnoli, Claudia, Caterina Mariotti, Franco Taroni, et al.. (2005). SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22–q11.2. Brain. 129(1). 235–242. 88 indexed citations

11.

Brusco, Alfredo, Cinzia Gellera, Claudia Cagnoli, et al.. (2004). Molecular Genetics of Hereditary Spinocerebellar Ataxia. Archives of Neurology. 61(5). 727–727. 109 indexed citations

12.

Cagnoli, Claudia, Tohru Matsuura, Tetsuo Ashizawa, et al.. (2004). Detection of Large Pathogenic Expansions in FRDA1, SCA10, and SCA12 Genes Using a Simple Fluorescent Repeat-Primed PCR Assay. Journal of Molecular Diagnostics. 6(2). 96–100. 43 indexed citations

13.

Brusco, Alfredo, Claudia Cagnoli, Alessandra Franco, et al.. (2002). Analysis of SCA8 and SCA12 loci in 134 Italian ataxic patients negative for SCA1-3, 6 and 7 CAG expansions. Journal of Neurology. 249(7). 923–929. 23 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.

Explore authors with similar magnitude of impact