Caterina Mariotti

16.4k total citations · 1 hit paper
158 papers, 6.3k citations indexed

About

Caterina Mariotti is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Caterina Mariotti has authored 158 papers receiving a total of 6.3k indexed citations (citations by other indexed papers that have themselves been cited), including 114 papers in Cellular and Molecular Neuroscience, 105 papers in Molecular Biology and 67 papers in Neurology. Recurrent topics in Caterina Mariotti's work include Genetic Neurodegenerative Diseases (109 papers), Mitochondrial Function and Pathology (86 papers) and Neurological disorders and treatments (35 papers). Caterina Mariotti is often cited by papers focused on Genetic Neurodegenerative Diseases (109 papers), Mitochondrial Function and Pathology (86 papers) and Neurological disorders and treatments (35 papers). Caterina Mariotti collaborates with scholars based in Italy, United Kingdom and United States. Caterina Mariotti's 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 and has published in prestigious journals such as The Lancet, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Caterina Mariotti

152 papers receiving 6.2k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Spinocerebellar ataxia

2019 399 citations Thomas Klockgether, Caterina Mariotti et al. Nature Reviews Disease Primers profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Caterina Mariotti Italy	45	4.4k	3.7k	1.8k	766	642	158	6.3k
S. H. Subramony United States	34	4.5k 1.0×	4.6k 1.2×	2.4k 1.3×	233 0.3×	628 1.0×	123	6.5k
Susan Perlman United States	45	4.4k 1.0×	4.3k 1.1×	2.0k 1.1×	308 0.4×	527 0.8×	152	5.9k
Giuseppe De Michele Italy	43	3.0k 0.7×	3.9k 1.0×	3.2k 1.8×	266 0.3×	1.2k 1.9×	208	6.8k
G. Meola Italy	45	5.1k 1.1×	3.9k 1.0×	1.6k 0.9×	348 0.5×	194 0.3×	234	6.7k
Paola Giunti United Kingdom	40	3.7k 0.8×	3.7k 1.0×	1.7k 0.9×	209 0.3×	547 0.9×	138	5.2k
Stefan M. Pulst United States	44	4.1k 0.9×	3.3k 0.9×	2.3k 1.3×	220 0.3×	457 0.7×	157	6.2k
Thomas D. Bird United States	52	4.2k 0.9×	5.9k 1.6×	2.7k 1.5×	252 0.3×	1.8k 2.9×	170	8.6k
Evelyn Jaros United Kingdom	40	2.6k 0.6×	1.4k 0.4×	2.2k 1.2×	486 0.6×	901 1.4×	77	5.8k
Bing‐Wen Soong Taiwan	35	1.9k 0.4×	1.9k 0.5×	1.5k 0.8×	140 0.2×	569 0.9×	146	3.9k
Ferdinando Squitieri Italy	49	5.7k 1.3×	6.4k 1.7×	5.4k 3.0×	217 0.3×	1.0k 1.6×	177	10.2k

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

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

20 of 20 papers shown

Devita, Maria, Anna Panzeri, Anna Castaldo, et al.. (2025). The Italian Standardization of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale: Cognitive Profiling in a Healthy, Heterogeneous Population. The Cerebellum. 24(5). 138–138.

Graziola, Federica, Federica Rachele Danti, Marco Moscatelli, et al.. (2025). Preliminary observations of glucose metabolism dysregulation in pediatric Huntington’s disease. Frontiers in Neurology. 16. 1626275–1626275.

Grisoli, Marina, Anna Nigri, Sara Palermo, et al.. (2024). Tracking longitudinal thalamic volume changes during early stages of SCA1 and SCA2. La radiologia medica. 129(8). 1215–1223.

Lynch, David R., Angie Goldsberry, Christian Rummey, et al.. (2023). Propensity matched comparison of omaveloxolone treatment to Friedreich ataxia natural history data. Annals of Clinical and Translational Neurology. 11(1). 4–16. 24 indexed citations

Castaldo, Anna, Mariangela Farinotti, Mario Fichera, et al.. (2023). Italian cross-cultural adaptation of the patient-reported outcome measure of ataxia. Neurological Sciences. 44(8). 2773–2779. 2 indexed citations

Lynch, David R., Melanie Chin, Sylvia Boesch, et al.. (2022). Efficacy of Omaveloxolone in Friedreich's Ataxia: Delayed‐Start Analysis of the MOXIe Extension. Movement Disorders. 38(2). 313–320. 55 indexed citations

Migliore, Simone, Giulia D’Aurizio, Giovanni Ristori, et al.. (2021). Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional study. Brain and Behavior. 11(7). e02151–e02151. 13 indexed citations

Elia, Antonio Emanuele, Luigi Romito, Caterina Mariotti, et al.. (2021). Deep brain stimulation in Huntington’s disease: a literature review. Neurological Sciences. 42(11). 4447–4457. 23 indexed citations

Lynch, David R., Melanie Chin, Martin B. Delatycki, et al.. (2020). Safety and Efficacy of Omaveloxolone in Friedreich Ataxia (MOXIe Study). Annals of Neurology. 89(2). 212–225. 177 indexed citations

10.

Pozzi, Elisa, Elisa Giorgio, Cecilia Mancini, et al.. (2020). In vitro dexamethasone treatment does not induce alternative ATM transcripts in cells from Ataxia–Telangiectasia patients. Scientific Reports. 10(1). 20182–20182. 2 indexed citations

11.

Pensato, Viviana, Stefania Magri, Eleonora Dalla Bella, et al.. (2020). Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms. Journal of Clinical Medicine. 9(2). 412–412. 23 indexed citations

12.

Klockgether, Thomas, Caterina Mariotti, & Henry L. Paulson. (2019). Spinocerebellar ataxia. Nature Reviews Disease Primers. 5(1). 24–24. 399 indexed citations breakdown →

13.

Nanetti, Lorenzo, D. Alpini, Valentina Elisabetta Di Mattei, et al.. (2017). Stance instability in preclinical SCA1 mutation carriers: A 4-year prospective posturography study. Gait & Posture. 57. 11–14. 11 indexed citations

14.

Hirst, Jennifer, Marianna Madeo, Katrien Smets, et al.. (2016). Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48). Neurology Genetics. 2(5). e98–e98. 24 indexed citations

15.

Politi, Letterio S., Stefania Bianchi Marzoli, Claudia Godi, et al.. (2016). MRI Evidence of Cerebellar and Extraocular Muscle Atrophy Differently Contributing to Eye Movement Abnormalities in SCA2 and SCA28 Diseases. Investigative Ophthalmology & Visual Science. 57(6). 2714–2714. 8 indexed citations

16.

Reetz, Kathrin, Ana Sofia Costa, Shahram Mirzazade, et al.. (2013). Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6. Brain. 136(3). 905–917. 109 indexed citations

17.

Nanetti, Lorenzo, Silvia Baratta, Marta Panzeri, et al.. (2012). Novel and recurrent spastin mutations in a large series of SPG4 Italian families. Neuroscience Letters. 528(1). 42–45. 5 indexed citations

18.

Mariotti, Caterina, Roberto Fancellu, Lorenzo Nanetti, et al.. (2012). Erythropoietin in Friedreich ataxia: No effect on frataxin in a randomized controlled trial. Movement Disorders. 27(3). 446–449. 47 indexed citations

19.

Donato, Stefano Di, Cinzia Gellera, & Caterina Mariotti. (2001). The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias. Neurological Sciences. 22(3). 219–228. 51 indexed citations

20.

Pareyson, Davide, Cinzia Gellera, Barbara Castellotti, et al.. (1997). Autosomal dominant cerebellar ataxias: Genotype frequency and clinical/molecular correlations. The Italian Journal of Neurological Sciences. 18(4). 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.

Explore authors with similar magnitude of impact