Enrico Bertini

55.7k total citations · 4 hit papers
637 papers, 22.6k citations indexed

About

Enrico Bertini is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Enrico Bertini has authored 637 papers receiving a total of 22.6k indexed citations (citations by other indexed papers that have themselves been cited), including 439 papers in Molecular Biology, 116 papers in Cellular and Molecular Neuroscience and 108 papers in Genetics. Recurrent topics in Enrico Bertini's work include Mitochondrial Function and Pathology (135 papers), Neurogenetic and Muscular Disorders Research (105 papers) and Muscle Physiology and Disorders (92 papers). Enrico Bertini is often cited by papers focused on Mitochondrial Function and Pathology (135 papers), Neurogenetic and Muscular Disorders Research (105 papers) and Muscle Physiology and Disorders (92 papers). Enrico Bertini collaborates with scholars based in Italy, United States and United Kingdom. Enrico Bertini's co-authors include Fiorella Piemonte, Adele D’Amico, Anna Pastore, Eugenio Mercuri, Giorgio Federici, Filippo M. Santorelli, Serenella Servidei, Carlo Dionisi‐Vici, Rosalba Carrozzo and Stefania Petrini and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Enrico Bertini

618 papers receiving 22.1k citations

Hit Papers

align trajectories

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.

Analysis of glutathione: implication in redox and detoxification

2003 937 citations Enrico Bertini, Fiorella Piemonte et al. profile →
Consensus Statement for Standard of Care in Spinal Muscular Atrophy

2007 615 citations Enrico Bertini et al. profile →
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1989 483 citations Enrico Bertini et al. profile →
Empirical Studies in Information Visualization: Seven Scenarios

2011 418 citations Enrico Bertini et al. IEEE Transactions on Visualization and Computer Graphics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Enrico Bertini Italy	71	14.3k	4.4k	3.2k	2.8k	2.7k	637	22.6k
Hanns Lochmüller Germany	68	11.7k 0.8×	3.0k 0.7×	2.8k 0.9×	1.0k 0.4×	2.8k 1.0×	534	17.6k
Heidi L. Rehm United States	53	13.8k 1.0×	1.8k 0.4×	1.5k 0.5×	1.2k 0.5×	14.5k 5.3×	186	31.4k
Wendy K. Chung United States	72	8.6k 0.6×	1.7k 0.4×	1.2k 0.4×	592 0.2×	7.3k 2.7×	567	22.7k
Thomas Meitinger Germany	69	11.2k 0.8×	481 0.1×	1.7k 0.5×	1.3k 0.5×	5.5k 2.0×	319	19.1k
Jeffery M. Vance United States	70	12.8k 0.9×	1.1k 0.2×	7.0k 2.2×	553 0.2×	4.4k 1.6×	298	29.0k
Eric P. Hoffman United States	92	28.1k 2.0×	3.9k 0.9×	5.1k 1.6×	344 0.1×	6.1k 2.3×	603	37.2k
Håkon Håkonarson United States	76	12.4k 0.9×	1.2k 0.3×	1.1k 0.3×	422 0.2×	11.6k 4.3×	587	34.7k
Jörg B. Schulz Germany	85	9.4k 0.7×	1.1k 0.2×	7.6k 2.4×	592 0.2×	755 0.3×	472	25.5k
Jürg Ott United States	74	10.6k 0.7×	1.1k 0.3×	2.6k 0.8×	253 0.1×	8.5k 3.1×	343	25.1k
Margaret A. Pericak‐Vance United States	63	7.0k 0.5×	1.1k 0.3×	2.4k 0.8×	319 0.1×	2.8k 1.0×	340	18.4k

Countries citing papers authored by Enrico Bertini

Since Specialization

Citations

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

Fields of papers citing papers by Enrico Bertini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Enrico Bertini

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

All Works

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20 of 20 papers shown

Petrini, Stefania, Alessia De Nisco, Anna Maria Giudetti, et al.. (2025). Altered dimerization of certain riboflavin transporter 2 mutants: a possible source of UPR, altered calcium signalling and mitochondrial derangements in RTD2. Archives of Biochemistry and Biophysics. 775. 110675–110675.

Bertini, Enrico, et al.. (2025). Stitching Meaning: Practices of Data Textile Creators. IEEE Transactions on Visualization and Computer Graphics. 32(1). 725–735.

Bertini, Enrico, et al.. (2024). Riboflavin supplementation in children with riboflavin transporter deficiency type 2 does not stop disease progression based on long‐term follow‐up. Developmental Medicine & Child Neurology. 67(3). 284–285.

Stregapede, Fabrizia, Vito Luigi Colona, Francesco Nicita, et al.. (2024). POLR3B de novo variants are a rare cause of infantile myoclonic epilepsy. Seizure. 121. 141–146.

Petrillo, Sara, Alessia Perna, Gabriella Silvestri, et al.. (2024). Differential Gene Expression in Late-Onset Friedreich Ataxia: A Comparative Transcriptomic Analysis Between Symptomatic and Asymptomatic Sisters. International Journal of Molecular Sciences. 25(21). 11615–11615. 1 indexed citations

Reinson, Karit, Marcello Bellusci, Julien H. Park, et al.. (2024). Current global vitamin and cofactor prescribing practices for primary mitochondrial diseases: Results of a European reference network survey. Journal of Inherited Metabolic Disease. 48(1). e12805–e12805. 2 indexed citations

Travaglini, Lorena, Marina Macchiaiolo, Giacomo Garone, et al.. (2024). Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe Forms. Genes. 15(4). 508–508.

Romaniello, Romina, Ludovica Pasca, Elena Panzeri, et al.. (2022). Superior Cerebellar Atrophy: An Imaging Clue to Diagnose ITPR1-Related Disorders. International Journal of Molecular Sciences. 23(12). 6723–6723. 5 indexed citations

Petrillo, Sara, Jessica D’Amico, Francesco Nicita, et al.. (2022). Antioxidant Response in Human X-Linked Adrenoleukodystrophy Fibroblasts. Antioxidants. 11(11). 2125–2125. 7 indexed citations

10.

Costanzo, Floriana, Ginevra Zanni, Elisa Fucà, et al.. (2022). Cerebellar Agenesis and Bilateral Polimicrogyria Associated with Rare Variants of CUB and Sushi Multiple Domains 1 Gene (CSMD1): A Longitudinal Neuropsychological and Neuroradiological Case Study. International Journal of Environmental Research and Public Health. 19(3). 1224–1224. 1 indexed citations

11.

Foppiani, Andrea, Ramona De Amicis, Alessandro Leone, et al.. (2021). Predictive fat mass equations for spinal muscular atrophy type I children: Development and internal validation. Clinical Nutrition. 40(4). 1578–1587. 3 indexed citations

12.

Nicita, Francesco, Chiara Aiello, Gessica Vasco, et al.. (2021). Expanding the Clinical and Mutational Spectrum of the PLP1-Related Hypomyelination of Early Myelinated Structures (HEMS). Brain Sciences. 11(1). 93–93. 6 indexed citations

13.

Sferra, Antonella, Francesco Nicita, & Enrico Bertini. (2020). Microtubule Dysfunction: A Common Feature of Neurodegenerative Diseases. International Journal of Molecular Sciences. 21(19). 7354–7354. 84 indexed citations

14.

Sferra, Antonella, Stefania Petrini, Emanuele Bellacchio, et al.. (2020). TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics. International Journal of Molecular Sciences. 21(4). 1385–1385. 26 indexed citations

15.

Nicita, Francesco, Emanuele Bellacchio, Paolo Alfieri, et al.. (2019). Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia. Clinical Genetics. 96(2). 169–175. 20 indexed citations

16.

Stregapede, Fabrizia, Lorena Travaglini, Adriana Rebelo, et al.. (2019). Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation. Clinical Genetics. 97(3). 521–526. 11 indexed citations

17.

Callea, Michele, Fabiana Fattori, Enrico Bertini, et al.. (2017). Estudio clínico y molecular en una familia con displasia cleidocraneal. Archivos Argentinos de Pediatria. 115(6). e440–e444. 3 indexed citations

18.

Rosa, Gabriella Di, Sonia Messina, Adele D’Amico, et al.. (2011). A new form of alpha‐dystroglycanopathy associated with severe drug‐resistant epilepsy and unusual EEG features. Epileptic Disorders. 13(3). 259–262. 7 indexed citations

19.

Sparaco, Marco, Laura Gaeta, Filippo M. Santorelli, et al.. (2009). Friedreich's ataxia: Oxidative stress and cytoskeletal abnormalities. Journal of the Neurological Sciences. 287(1-2). 111–118. 70 indexed citations

20.

Pepe, Guglielmina, Enrico Bertini, Paolo Bonaldo, et al.. (2002). Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC International Workshop, 23–24 November 2001, Naarden, The Netherlands. Neuromuscular Disorders. 12(10). 984–993. 67 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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