Giulia Bisogni

2.1k total citations
37 papers, 742 citations indexed

About

Giulia Bisogni is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Giulia Bisogni has authored 37 papers receiving a total of 742 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Neurology, 18 papers in Molecular Biology and 14 papers in Genetics. Recurrent topics in Giulia Bisogni's work include Amyotrophic Lateral Sclerosis Research (16 papers), Peripheral Neuropathies and Disorders (12 papers) and Neurogenetic and Muscular Disorders Research (12 papers). Giulia Bisogni is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (16 papers), Peripheral Neuropathies and Disorders (12 papers) and Neurogenetic and Muscular Disorders Research (12 papers). Giulia Bisogni collaborates with scholars based in Italy, United States and Japan. Giulia Bisogni's co-authors include Mario Sabatelli, Marco Luigetti, Ângela Romano, Amelia Conte, Alessandra Del Grande, Marcella Zollino, Giuseppe Marangi, Serena Lattante, Paolo Maria Rossini and Andrea Di Paolantonio and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Human Molecular Genetics.

In The Last Decade

Giulia Bisogni

35 papers receiving 733 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giulia Bisogni Italy 15 481 372 304 135 122 37 742
Alessandra Del Grande Italy 17 678 1.4× 304 0.8× 310 1.0× 215 1.6× 150 1.2× 32 849
Paul R. Kasher United Kingdom 12 305 0.6× 384 1.0× 192 0.6× 178 1.3× 153 1.3× 29 847
NiCole A. Finch United States 12 680 1.4× 290 0.8× 241 0.8× 83 0.6× 221 1.8× 23 1.0k
Alexandra M. Nicholson United States 12 299 0.6× 255 0.7× 98 0.3× 88 0.7× 225 1.8× 17 710
Marcos Barbosa Portugal 13 169 0.4× 187 0.5× 232 0.8× 101 0.7× 58 0.5× 25 593
Francesca Boaretto Italy 12 136 0.3× 252 0.7× 74 0.2× 171 1.3× 84 0.7× 26 811
Yo‐Tsen Liu Taiwan 13 294 0.6× 315 0.8× 51 0.2× 392 2.9× 198 1.6× 30 792
Sonia Ciarmatori Germany 11 94 0.2× 629 1.7× 105 0.3× 312 2.3× 190 1.6× 11 1.0k
J. Blake United Kingdom 9 279 0.6× 250 0.7× 44 0.1× 468 3.5× 124 1.0× 10 681
Martine Therrien Canada 12 318 0.7× 355 1.0× 223 0.7× 184 1.4× 99 0.8× 17 808

Countries citing papers authored by Giulia Bisogni

Since Specialization
Citations

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

Fields of papers citing papers by Giulia Bisogni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giulia Bisogni

This figure shows the co-authorship network connecting the top 25 collaborators of Giulia Bisogni. A scholar is included among the top collaborators of Giulia Bisogni 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 Giulia Bisogni. Giulia Bisogni 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.
Romano, Ângela, Valeria Guglielmino, Giulia Bisogni, et al.. (2023). Early detection of nerve involvement in presymptomatic TTR mutation carriers: exploring potential markers of disease onset. Neurological Sciences. 45(4). 1675–1684. 5 indexed citations
4.
Romano, Ângela, Valeria Guglielmino, Andrea Di Paolantonio, et al.. (2022). Pupillometric findings in ATTRv patients and carriers: results from a single-centre experience. Amyloid. 29(4). 270–275. 4 indexed citations
5.
Luigetti, Marco, Valeria Guglielmino, Marina Romozzi, et al.. (2022). Nerve Conduction Studies of Dorsal Sural Nerve: Normative Data and Its Potential Application in ATTRv Pre-Symptomatic Subjects. Brain Sciences. 12(8). 1037–1037. 4 indexed citations
6.
Gentile, Luca, Massimo Russo, Marco Luigetti, et al.. (2021). Patisiran in hATTR Amyloidosis: Six-Month Latency Period before Efficacy. Brain Sciences. 11(4). 515–515. 9 indexed citations
7.
Romozzi, Marina, Giulia Bisogni, Mario Sabatelli, & Marco Luigetti. (2021). Reassessing IVIg therapy in chronic inflammatory demyelinating polyradiculoneuropathy during COVID-19: a chance to verify the need for chronic maintenance therapy. Neurological Sciences. 42(3). 787–789. 5 indexed citations
8.
Luigetti, Marco, et al.. (2020). Diagnosis and Treatment of Hereditary Transthyretin Amyloidosis (hATTR) Polyneuropathy: Current Perspectives on Improving Patient Care. SHILAP Revista de lepidopterología. 2 indexed citations
9.
Luigetti, Marco, Ângela Romano, Andrea Di Paolantonio, Giulia Bisogni, & Mario Sabatelli. (2020). <p>Diagnosis and Treatment of Hereditary Transthyretin Amyloidosis (hATTR) Polyneuropathy: Current Perspectives on Improving Patient Care</p>. Therapeutics and Clinical Risk Management. Volume 16. 109–123. 82 indexed citations
10.
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
11.
Luigetti, Marco, Silvia Giovannini, Ângela Romano, et al.. (2020). Small Fibre Involvement in Multifocal Motor Neuropathy Explored with Sudoscan: A Single-Centre Experience. Diagnostics. 10(10). 755–755. 2 indexed citations
12.
Luigetti, Marco, Annalisa Tortora, Ângela Romano, et al.. (2020). Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis: a Single-Centre Experience. Journal of Gastrointestinal and Liver Diseases. 29(3). 339–343. 14 indexed citations
13.
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
14.
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
15.
Luigetti, Marco, Giulia Bisogni, Ângela Romano, et al.. (2018). Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre. Amyloid. 25(4). 242–246. 27 indexed citations
16.
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
17.
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
18.
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
19.
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
20.
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

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

Breakdown of academic impact, for papers by Alessandra Del Grande Breakdown of academic impact, for papers by Paul R. Kasher Breakdown of academic impact, for papers by NiCole A. Finch Breakdown of academic impact, for papers by Alexandra M. Nicholson Breakdown of academic impact, for papers by Marcos Barbosa Breakdown of academic impact, for papers by Francesca Boaretto Breakdown of academic impact, for papers by Yo‐Tsen Liu Breakdown of academic impact, for papers by Sonia Ciarmatori Breakdown of academic impact, for papers by J. Blake Breakdown of academic impact, for papers by Martine Therrien
Rankless by CCL
2026