Daniela Bernardo

429 total citations
13 papers, 146 citations indexed

About

Daniela Bernardo is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Daniela Bernardo has authored 13 papers receiving a total of 146 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Neurology, 6 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Daniela Bernardo's work include Neurogenetic and Muscular Disorders Research (5 papers), Amyotrophic Lateral Sclerosis Research (5 papers) and Hereditary Neurological Disorders (4 papers). Daniela Bernardo is often cited by papers focused on Neurogenetic and Muscular Disorders Research (5 papers), Amyotrophic Lateral Sclerosis Research (5 papers) and Hereditary Neurological Disorders (4 papers). Daniela Bernardo collaborates with scholars based in Italy, Switzerland and Japan. Daniela Bernardo's co-authors include Donato Sauchelli, Guido Primiano, Serenella Servidei, Marco Luigetti, Giulia Bisogni, Giacomo Della Marca, Antonia Camporeale, Tommaso Sanna, Alessandro Cianfoni and Milena Leo and has published in prestigious journals such as Human Molecular Genetics, Neurobiology of Aging and Clinical Neurophysiology.

In The Last Decade

Daniela Bernardo

12 papers receiving 145 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniela Bernardo Italy 6 72 68 47 31 29 13 146
Fabrizia Stregapede Italy 9 83 1.2× 43 0.6× 90 1.9× 38 1.2× 41 1.4× 17 205
Zoltán Grosz Hungary 8 81 1.1× 33 0.5× 57 1.2× 50 1.6× 12 0.4× 20 170
Nicolas Chrestian Canada 10 195 2.7× 43 0.6× 142 3.0× 34 1.1× 17 0.6× 24 272
Anna Maija Saukkonen Finland 9 148 2.1× 83 1.2× 53 1.1× 72 2.3× 13 0.4× 12 250
A Barois France 7 81 1.1× 77 1.1× 45 1.0× 25 0.8× 29 1.0× 14 180
Catherine Antar France 9 194 2.7× 100 1.5× 26 0.6× 95 3.1× 26 0.9× 11 288
Liena E. O. Elsayed Sudan 6 40 0.6× 14 0.2× 53 1.1× 28 0.9× 13 0.4× 14 108
Marie‐France Rioux Canada 6 140 1.9× 22 0.3× 117 2.5× 32 1.0× 37 1.3× 8 270
Adriana Prundean France 5 76 1.1× 36 0.5× 76 1.6× 17 0.5× 24 0.8× 11 139
Fatima Jaffer United Kingdom 6 138 1.9× 55 0.8× 86 1.8× 17 0.5× 22 0.8× 12 264

Countries citing papers authored by Daniela Bernardo

Since Specialization
Citations

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

Fields of papers citing papers by Daniela Bernardo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Bernardo

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

All Works

13 of 13 papers shown
1.
Lattante, Serena, Daniela Bernardo, Agata Katia Patanella, et al.. (2025). Burden of pathogenetic and likely pathogenetic variants in SPG7, SPG11 and AP4 genes in Amyotrophic Lateral Sclerosis. A case-control study. Journal of Neurology. 272(7). 455–455.
2.
Lattante, Serena, Mario Sabatelli, Giulia Bisogni, et al.. (2023). Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis. European Journal of Neurology. 30(5). 1246–1255. 5 indexed citations
3.
Rollo, Eleonora, Marina Romozzi, Fedele Dono, et al.. (2023). Treatment of benzodiazepine-refractory status epilepticus: A retrospective, cohort study. Epilepsy & Behavior. 140. 109093–109093. 5 indexed citations
4.
Lattante, Serena, Amelia Conte, Giuseppe Marangi, et al.. (2021). Novel variants and cellular studies on patients’ primary fibroblasts support a role forNEK1missense variants in ALS pathogenesis. Human Molecular Genetics. 30(1). 65–71. 10 indexed citations
5.
Tasca, Giorgio, Serena Lattante, Giuseppe Marangi, et al.. (2020). SOD1 p.D12Y variant is associated with amyotrophic lateral sclerosis/distal myopathy spectrum. European Journal of Neurology. 27(7). 1304–1309. 4 indexed citations
6.
Lattante, Serena, Giuseppe Marangi, Amelia Conte, et al.. (2019). Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS. Neurobiology of Aging. 84. 239.e9–239.e14. 23 indexed citations
7.
Luigetti, Marco, Guido Primiano, Giulia Bisogni, et al.. (2018). Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy. Amyloid. 25(4). 261–262. 3 indexed citations
8.
Luigetti, Marco, Guido Primiano, Daniela Bernardo, et al.. (2018). Small fibre neuropathy in mitochondrial diseases explored with sudoscan. Clinical Neurophysiology. 129(8). 1618–1623. 11 indexed citations
9.
Servidei, Serenella, Guido Primiano, Valentina Muto, et al.. (2017). PLEC gene mutations cause familial disto-proximal myopathy and long QT syndrome mimicking mitochondrial disease. Neuromuscular Disorders. 27. S150–S151. 1 indexed citations
10.
Luigetti, Marco, Gian Maria Fabrizi, Giulia Bisogni, et al.. (2016). Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience. Clinical Neurology and Neurosurgery. 144. 67–71. 14 indexed citations
11.
Luigetti, Marco, Donato Sauchelli, Guido Primiano, et al.. (2016). Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single‐centre experience. European Journal of Neurology. 23(6). 1020–1027. 30 indexed citations
12.
Catteruccia, Michela, Donato Sauchelli, Giacomo Della Marca, et al.. (2015). “Myo-cardiomyopathy” is commonly associated with the A8344G “MERRF” mutation. Journal of Neurology. 262(3). 701–710. 39 indexed citations
13.
Luigetti, Marco, et al.. (2013). Subacute combined degeneration. Acta Neurologica Belgica. 114(3). 221–222. 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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2026