Caterina Mariotti

16.4k citations
158 papers · 6.3k indexed · 1 hit paper · h-index 45
Topics
Genetic Neurodegenerative Diseases (109 papers)Mitochondrial Function and Pathology (86 papers)Neurological disorders and treatments (35 papers)

In The Last Decade

Caterina Mariotti

152 papers receiving 6.2k citations

Hit Papers

Spinocerebellar ataxia20192026202120232019100200300

Peers

Caterina Mariotti
Comparison fields: 5 of 126
  • Molecular Biology 4.4k
  • Cellular and Molecular Neuroscience 3.7k
  • Neurology 1.8k
  • Clinical Biochemistry 766
  • Neurology 642
Replace Stefan M. Pulst with:
Stefan M. Pulst United States
Evelyn Jaros United Kingdom
Giuseppe De Michele Italy
S. H. Subramony United States
Paola Giunti United Kingdom
Thomas D. Bird United States
Susan Perlman United States
Dagmar Galter Sweden
Takeshi Ikeuchi Japan
Robert H. Baloh United States
Caterina Mariotti relative to Stefan M. Pulst United States Stefan M. Pulst's profile →
Citations per field
00.5×3.5×
Stefan M. Pulst · 1×
Citations per year

Countries citing papers authored by Caterina Mariotti

Since Specialization
Citations

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

Fields of papers citing papers by Caterina Mariotti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caterina Mariotti

This figure shows the co-authorship network connecting the top 25 collaborators of Caterina Mariotti. A scholar is included among the top collaborators of Caterina Mariotti 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 Caterina Mariotti. Caterina Mariotti 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
#WorkIndexed citations
1 0
2 0
3 0
4 24
5 10
6 55
7 13
8 23
9 23
10 177
11 2
12
Spinocerebellar ataxiabreakdown →
399
13 22
14 11
15 24
16 109
17 47
18 5
19 109
20
Autosomal dominant cerebellar ataxias: Genotype frequency and clinical/molecular correlations
1

About Caterina Mariotti

Caterina Mariotti is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 158 papers that have together received 6.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (109 papers), Mitochondrial Function and Pathology (86 papers) and Neurological disorders and treatments (35 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (3.7k citations), Neurology (1.8k citations) and Clinical Biochemistry (766 citations). Caterina Mariotti has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Thomas Klockgether, Cinzia Gellera, Stefano Di Donato, Henry L. Paulson, Massimo Zeviani, Franco Taroni, Sylvia Boesch, Paola Giunti, Elena Cattaneo and Davide Pareyson. Their work appears in journals such as The Lancet, Journal of Clinical Investigation and Nature Genetics.

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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