Amelia Conte

3.6k total citations
57 papers, 1.1k citations indexed

About

Amelia Conte is a scholar working on Neurology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Amelia Conte has authored 57 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Neurology, 22 papers in Genetics and 18 papers in Cellular and Molecular Neuroscience. Recurrent topics in Amelia Conte's work include Amyotrophic Lateral Sclerosis Research (28 papers), Neurogenetic and Muscular Disorders Research (21 papers) and Hereditary Neurological Disorders (15 papers). Amelia Conte is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (28 papers), Neurogenetic and Muscular Disorders Research (21 papers) and Hereditary Neurological Disorders (15 papers). Amelia Conte collaborates with scholars based in Italy, United States and Japan. Amelia Conte's co-authors include Mario Sabatelli, Marco Luigetti, Alessandra Del Grande, Marcella Zollino, Giuseppe Marangi, Serena Lattante, Giulia Bisogni, Francesca Madia, Ângela Romano and Paolo Maria Rossini and has published in prestigious journals such as Neurology, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Amelia Conte

52 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amelia Conte Italy 21 789 453 410 257 225 57 1.1k
Lindsey R. Fischer United States 7 1.1k 1.4× 694 1.5× 599 1.5× 443 1.7× 228 1.0× 9 1.6k
Hiroto Eguchi Japan 11 747 0.9× 329 0.7× 491 1.2× 136 0.5× 185 0.8× 21 1.1k
André Bento‐Abreu Belgium 12 372 0.5× 231 0.5× 383 0.9× 171 0.7× 144 0.6× 18 833
Nailah Siddique United States 14 525 0.7× 295 0.7× 383 0.9× 199 0.8× 216 1.0× 20 938
Yasumasa Kokubo Japan 18 702 0.9× 166 0.4× 196 0.5× 160 0.6× 212 0.9× 63 945
D. McKenna‐Yasek United States 15 1.1k 1.3× 656 1.4× 517 1.3× 199 0.8× 354 1.6× 19 1.4k
Alexander E. Volk Germany 19 761 1.0× 533 1.2× 563 1.4× 183 0.7× 238 1.1× 43 1.4k
Peggy Allred United States 12 663 0.8× 566 1.2× 694 1.7× 267 1.0× 343 1.5× 18 1.4k
Alessandra Del Grande Italy 17 678 0.9× 310 0.7× 304 0.7× 215 0.8× 150 0.7× 32 849
Giovanni Nardo Italy 19 587 0.7× 339 0.7× 365 0.9× 115 0.4× 169 0.8× 39 952

Countries citing papers authored by Amelia Conte

Since Specialization
Citations

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

Fields of papers citing papers by Amelia Conte

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amelia Conte

This figure shows the co-authorship network connecting the top 25 collaborators of Amelia Conte. A scholar is included among the top collaborators of Amelia Conte 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 Amelia Conte. Amelia Conte 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.
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.
Lattante, Serena, et al.. (2023). Characterization of SOD1-DT, a Divergent Long Non-Coding RNA in the Locus of the SOD1 Human Gene. Cells. 12(16). 2058–2058. 3 indexed citations
4.
Luigetti, Marco, Ângela Romano, Andrea Di Paolantonio, et al.. (2020). Pathological Findings in Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Single-Center Experience. Brain Sciences. 10(6). 383–383. 7 indexed citations
5.
Luigetti, Marco, Andrea Di Paolantonio, Giulia Bisogni, et al.. (2019). Sural nerve biopsy in peripheral neuropathies: 30-year experience from a single center. Neurological Sciences. 41(2). 341–346. 12 indexed citations
6.
Mandrioli, Jessica, Bernhard Michalke, Nikolay Solovyev, et al.. (2017). Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations. Neurodegenerative Diseases. 17(4-5). 171–180. 47 indexed citations
7.
Marangi, Giuseppe, Serena Lattante, Amelia Conte, et al.. (2016). Matrin 3 variants are frequent in Italian ALS patients. Neurobiology of Aging. 49. 218.e1–218.e7. 34 indexed citations
8.
Chiò, Adriano, Andrea Calvo, Cristina Moglia, et al.. (2015). ATXN2 PolyQ Intermediate Repeat Modifies ALS Phenotype and Survival (I8-3B). Neurology. 84(14_supplement). 1 indexed citations
9.
Luigetti, Marco, Alessandra Del Grande, Amelia Conte, et al.. (2014). Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience. Journal of the Neurological Sciences. 341(1-2). 46–50. 27 indexed citations
10.
Sabatelli, Mario, Alice Moncada, Amelia Conte, et al.. (2013). Mutations in the 3′ untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis. Human Molecular Genetics. 22(23). 4748–4755. 86 indexed citations
11.
Luigetti, Marco, Amelia Conte, Nicola Montano, et al.. (2012). Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy. Journal of the Neurological Sciences. 319(1-2). 75–80. 17 indexed citations
12.
Sabatelli, Mario, Marcella Zollino, Marco Luigetti, et al.. (2011). Uncovering amyotrophic lateral sclerosis phenotypes: Clinical features and long-term follow-up of upper motor neuron-dominant ALS. Amyotrophic Lateral Sclerosis. 12(4). 278–282. 31 indexed citations
13.
Luigetti, Marco, Gian Maria Fabrizi, Federica Taioli, et al.. (2011). Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation. Journal of the Neurological Sciences. 307(1-2). 168–170. 8 indexed citations
14.
Grande, Alessandra Del, Amelia Conte, Serena Lattante, et al.. (2011). D11Y SOD1 mutation and benign ALS: A consistent genotype-phenotype correlation. Journal of the Neurological Sciences. 309(1-2). 31–33. 7 indexed citations
15.
Grande, Alessandra Del, Marco Luigetti, Amelia Conte, et al.. (2011). A novel L67P SOD1 mutation in an Italian ALS patient. Amyotrophic Lateral Sclerosis. 12(2). 150–152. 11 indexed citations
16.
Luigetti, Marco, Serena Lattante, Marcella Zollino, et al.. (2011). SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant. Neurobiology of Aging. 32(10). 1924.e15–1924.e18. 30 indexed citations
17.
Luigetti, Marco, Salvatore Maria Corsello, Serena Lattante, et al.. (2011). Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity. Clinical Neurology and Neurosurgery. 114(6). 748–750. 2 indexed citations
18.
Luigetti, Marco, Antonio Pizzuti, Stefano Bartoletti, et al.. (2010). Triple A syndrome: A novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. Journal of the Neurological Sciences. 290(1-2). 150–152. 11 indexed citations
19.
Luigetti, Marco, Gian Maria Fabrizi, Francesca Madia, et al.. (2010). A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. Journal of the Neurological Sciences. 298(1-2). 114–117. 38 indexed citations
20.
Luigetti, Marco, Francesca Madia, Amelia Conte, et al.. (2009). SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis. 10(5-6). 479–482. 10 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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