Marco Barberis

2.3k total citations
22 papers, 601 citations indexed

About

Marco Barberis is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Marco Barberis has authored 22 papers receiving a total of 601 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Neurology, 7 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Marco Barberis's work include Amyotrophic Lateral Sclerosis Research (16 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Parkinson's Disease Mechanisms and Treatments (5 papers). Marco Barberis is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (16 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Parkinson's Disease Mechanisms and Treatments (5 papers). Marco Barberis collaborates with scholars based in Italy, United States and United Kingdom. Marco Barberis's co-authors include Adriano Chiò, Cristina Moglia, Andrea Calvo, Maura Brunetti, Antonio Canosa, Gabriele Mora, Umberto Manera, Barbara Iazzolino, Rosario Vasta and Sandra D’Alfonso and has published in prestigious journals such as Neurology, American Journal of Respiratory and Critical Care Medicine and Neurobiology of Aging.

In The Last Decade

Marco Barberis

22 papers receiving 591 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marco Barberis Italy 12 389 228 167 155 109 22 601
Jay P. Ross Canada 15 241 0.6× 57 0.3× 226 1.4× 97 0.6× 74 0.7× 39 653
Francesco Limone United States 10 411 1.1× 255 1.1× 611 3.7× 87 0.6× 113 1.0× 13 886
J. Gavin Daigle United States 7 291 0.7× 186 0.8× 451 2.7× 62 0.4× 37 0.3× 9 670
Payal Ray United States 8 276 0.7× 137 0.6× 412 2.5× 87 0.6× 56 0.5× 12 643
Jennifer E. Stauffer United States 6 382 1.0× 218 1.0× 230 1.4× 83 0.5× 73 0.7× 7 537
Silvia Grifoni Italy 11 275 0.7× 155 0.7× 180 1.1× 92 0.6× 76 0.7× 14 453
Giulia Romano Italy 13 431 1.1× 319 1.4× 329 2.0× 62 0.4× 46 0.4× 20 662
Christopher P Webster United Kingdom 10 370 1.0× 162 0.7× 221 1.3× 108 0.7× 67 0.6× 12 579
Nandini Ramesh United States 13 332 0.9× 176 0.8× 352 2.1× 49 0.3× 42 0.4× 14 566
Erik Simons Netherlands 13 548 1.4× 50 0.2× 239 1.4× 157 1.0× 256 2.3× 17 786

Countries citing papers authored by Marco Barberis

Since Specialization
Citations

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

Fields of papers citing papers by Marco Barberis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Barberis

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Barberis. A scholar is included among the top collaborators of Marco Barberis 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 Marco Barberis. Marco Barberis 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
1.
Iazzolino, Barbara, Laura Peotta, Jean Pierre Zucchetti, et al.. (2020). Differential Neuropsychological Profile of Patients With Amyotrophic Lateral Sclerosis With and Without C9orf72 Mutation. Neurology. 96(1). e141–e152. 17 indexed citations
2.
Chiò, Adriano, Cristina Moglia, Antonio Canosa, et al.. (2020). ALS phenotype is influenced by age, sex, and genetics. Neurology. 94(8). e802–e810. 110 indexed citations
3.
Corrado, Lucia, Maura Brunetti, Marco Barberis, et al.. (2019). Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort. Neurological Sciences. 40(12). 2537–2540. 7 indexed citations
4.
Chiò, Adriano, Andrea Calvo, Letizia Mazzini, et al.. (2018). The influence of genetic mutations on the multistep process in ALS (S4.004). Neurology. 90(15_supplement). 1 indexed citations
5.
Canosa, Antonio, Giovanni De Marco, M. Rinaudo, et al.. (2018). A novel p.Ser108LeufsTer15 SOD1 mutation leading to the formation of a premature stop codon in an apparently sporadic ALS patient: insights into the underlying pathomechanisms. Neurobiology of Aging. 72. 189.e11–189.e17. 5 indexed citations
6.
Canosa, Antonio, Marco Pagani, Maura Brunetti, et al.. (2018). Correlation between Apolipoprotein E genotype and brain metabolism in amyotrophic lateral sclerosis. European Journal of Neurology. 26(2). 306–312. 8 indexed citations
7.
Capponi, Simona, Thomas Geuens, Alessandro Geroldi, et al.. (2016). Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1. Human Mutation. 37(11). 1202–1208. 39 indexed citations
8.
Chiò, Adriano, Maura Brunetti, Marco Barberis, et al.. (2016). C9ORF72 Is a Stronger Determinant Than APOE of Cognitive Impairment in ALS (S21.008). Neurology. 86(16_supplement). 1 indexed citations
9.
Chiò, Adriano, Maura Brunetti, Marco Barberis, et al.. (2016). The Role ofAPOEin the Occurrence of Frontotemporal Dementia in Amyotrophic Lateral Sclerosis. JAMA Neurology. 73(4). 425–425. 31 indexed citations
10.
Ekong, Rosemary, Mark Nellist, Marianne Hoogeveen‐Westerveld, et al.. (2015). Variants WithinTSC2Exons 25 and 31 Are Very Unlikely to Cause Clinically Diagnosable Tuberous Sclerosis. Human Mutation. 37(4). 364–370. 16 indexed citations
11.
Calvo, Andrea, Cristina Moglia, Antonio Canosa, et al.. (2014). A de novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis case. Neurobiology of Aging. 35(6). 1513.e7–1513.e11. 19 indexed citations
12.
Marrali, Giuseppe, Federico Casale, Paolina Salamone, et al.. (2014). NADPH oxidase (NOX2) activity is a modifier of survival in ALS. Journal of Neurology. 261(11). 2178–2183. 32 indexed citations
13.
Canosa, Antonio, Andrea Calvo, Cristina Moglia, et al.. (2014). A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year course. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 16(1-2). 127–128. 5 indexed citations
14.
Canosa, Antonio, Andrea Calvo, Marco Barberis, et al.. (2014). Amyotrophic lateral sclerosis onset after prolonged treatment with a VEGF receptors inhibitor. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 16(1-2). 129–130. 4 indexed citations
15.
Galbiati, Silvia, Stefania Stenirri, Luca Sbaiz, et al.. (2013). Identification of an 18 bp deletion in the TWIST1 gene by CO-amplification at lower denaturation temperature-PCR (COLD-PCR) for non-invasive prenatal diagnosis of craniosynostosis: first case report. Clinical Chemistry and Laboratory Medicine (CCLM). 52(4). 505–9. 8 indexed citations
16.
Borelli, I, Marco Barberis, Anna Allavena, et al.. (2012). A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian origin. European Journal of Human Genetics. 21(2). 154–161. 5 indexed citations
17.
Chiò, Adriano, Gabriele Mora, Gabriella Restagno, et al.. (2012). UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study. Neurobiology of Aging. 34(1). 357.e1–357.e5. 54 indexed citations
18.
Brussino, Alessandro, Sandra D’Alfonso, Cinzia Cagnoli, et al.. (2009). Mutations in the lamin B1 gene are not present in multiple sclerosis. European Journal of Neurology. 16(4). 544–546. 3 indexed citations
19.
Gambino, Giorgio, Irene Perrone, Andrea Carra, et al.. (2009). Transgene silencing in grapevines transformed with GFLV resistance genes: analysis of variable expression of transgene, siRNAs production and cytosine methylation. Transgenic Research. 19(1). 17–27. 32 indexed citations
20.
Schiavina, M, Valerio Di Scioscio, Paola Contini, et al.. (2007). Pulmonary Lymphangioleiomyomatosis in a Karyotypically Normal Man without Tuberous Sclerosis Complex. American Journal of Respiratory and Critical Care Medicine. 176(1). 96–98. 51 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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