Rossella Gulli

984 total citations
21 papers, 676 citations indexed

About

Rossella Gulli is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Rossella Gulli has authored 21 papers receiving a total of 676 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 7 papers in Neurology and 6 papers in Molecular Biology. Recurrent topics in Rossella Gulli's work include Hereditary Neurological Disorders (7 papers), Genetic Neurodegenerative Diseases (5 papers) and Botulinum Toxin and Related Neurological Disorders (4 papers). Rossella Gulli is often cited by papers focused on Hereditary Neurological Disorders (7 papers), Genetic Neurodegenerative Diseases (5 papers) and Botulinum Toxin and Related Neurological Disorders (4 papers). Rossella Gulli collaborates with scholars based in Italy, United States and Belarus. Rossella Gulli's co-authors include Francesco Puppo, Giuseppe Murdaca, Paola Mandich, Francesca Spanò, Paola Cagnati, Barbara Maria Colombo, Emilia Bellone, Paola Ciotti, Marina Grandis and Alessandro Geroldi and has published in prestigious journals such as The American Journal of Medicine, Journal of Investigative Dermatology and Movement Disorders.

In The Last Decade

Rossella Gulli

21 papers receiving 662 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rossella Gulli Italy 14 180 167 157 134 99 21 676
Daitaro Kurosaka Japan 16 202 1.1× 47 0.3× 173 1.1× 280 2.1× 90 0.9× 53 751
Tomonaga Matsushita Japan 12 270 1.5× 61 0.4× 138 0.9× 72 0.5× 29 0.3× 20 732
WILLIAM A. VALENTE United States 16 343 1.9× 84 0.5× 139 0.9× 56 0.4× 72 0.7× 23 1.3k
Carmen Capobianco Italy 13 282 1.6× 46 0.3× 202 1.3× 73 0.5× 134 1.4× 13 856
Jasmine Healy Canada 17 709 3.9× 119 0.7× 82 0.5× 71 0.5× 131 1.3× 31 1.0k
Elizabeth S. McDonald United States 14 202 1.1× 47 0.3× 184 1.2× 30 0.2× 328 3.3× 18 759
Siddharth Banka United Kingdom 18 339 1.9× 33 0.2× 125 0.8× 105 0.8× 55 0.6× 55 991
Jie Lin China 17 470 2.6× 95 0.6× 61 0.4× 52 0.4× 40 0.4× 66 827
Ruth Washington United States 10 165 0.9× 47 0.3× 181 1.2× 33 0.2× 70 0.7× 14 587
Beatrix Schäfer Germany 7 288 1.6× 57 0.3× 172 1.1× 41 0.3× 156 1.6× 7 636

Countries citing papers authored by Rossella Gulli

Since Specialization
Citations

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

Fields of papers citing papers by Rossella Gulli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rossella Gulli

This figure shows the co-authorship network connecting the top 25 collaborators of Rossella Gulli. A scholar is included among the top collaborators of Rossella Gulli 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 Rossella Gulli. Rossella Gulli 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.
Geroldi, Alessandro, Patrizia Lastella, Nicoletta Resta, et al.. (2017). Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance. Neuromuscular Disorders. 27(4). 377–381. 1 indexed citations
2.
Mandich, Paola, Rossella Gulli, Roberta Marchese, et al.. (2017). 1993-2014: two decades of predictive testing for Huntington's disease at the Medical Genetics Unit of the University of Genoa. Molecular Genetics & Genomic Medicine. 5(5). 473–480. 9 indexed citations
3.
Murdaca, Giuseppe, Simone Negrini, Ottavia Magnani, et al.. (2017). Update upon efficacy and safety of etanercept for the treatment of spondyloarthritis and juvenile idiopathic arthritis. Modern Rheumatology. 28(3). 417–431. 30 indexed citations
4.
Murdaca, Giuseppe, Miriam Contatore, Rossella Gulli, Paola Mandich, & Francesco Puppo. (2016). Genetic factors and systemic sclerosis. Autoimmunity Reviews. 15(5). 427–432. 49 indexed citations
5.
Pezzini, Ilaria, Alessandro Geroldi, Simona Capponi, et al.. (2015). GDAP1 mutations in Italian axonal Charcot–Marie–Tooth patients: Phenotypic features and clinical course. Neuromuscular Disorders. 26(1). 26–32. 17 indexed citations
6.
Murdaca, Giuseppe, Rossella Gulli, Francesca Spanò, et al.. (2014). TNF-α Gene Polymorphisms: Association with Disease Susceptibility and Response to Anti-TNF-α Treatment in Psoriatic Arthritis. Journal of Investigative Dermatology. 134(10). 2503–2509. 84 indexed citations
7.
Murdaca, Giuseppe, Rossella Gulli, Francesca Spanò, Paola Mandich, & Francesco Puppo. (2014). Pharmacogenetics and Future Therapeutic Scenarios: What Affects the Prediction of Response to Treatment with Etanercept?. Drug Development Research. 75(S1). S7–S10. 12 indexed citations
8.
Ciotti, Paola, Marco Luigetti, Alessandro Geroldi, et al.. (2014). A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot–Marie–Tooth disease. Journal of the Neurological Sciences. 343(1-2). 183–186. 15 indexed citations
9.
Murdaca, Giuseppe, Barbara Maria Colombo, Paola Cagnati, et al.. (2012). Endothelial dysfunction in rheumatic autoimmune diseases. Atherosclerosis. 224(2). 309–317. 163 indexed citations
10.
Murdaca, Giuseppe, Paola Cagnati, Rossella Gulli, et al.. (2012). Current Views on Diagnostic Approach and Treatment of Lymphedema. The American Journal of Medicine. 125(2). 134–140. 76 indexed citations
11.
Capponi, Simona, Alessandro Geroldi, Paola Fossa, et al.. (2011). HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients. Journal of the Peripheral Nervous System. 16(4). 287–294. 51 indexed citations
12.
Grandis, Marina, Rossella Gulli, Denise Cassandrini, et al.. (2010). The spectrum of GNE mutations: allelic heterogeneity for a common phenotype. Neurological Sciences. 31(3). 377–380. 14 indexed citations
13.
Mandich, Paola, Marina Grandis, Alessandro Geroldi, et al.. (2009). Severe Neuropathy After Diphtheria-Tetanus-Pertussis Vaccination in a Child Carrying a Novel Frame-Shift Mutation in the Small Heat-Shock Protein 27 Gene. Journal of Child Neurology. 25(1). 107–109. 25 indexed citations
14.
Ciotti, Paola, Anna Garuti, Rossella Gulli, et al.. (2009). Germline mutations in the von Hippel–Lindau gene in Italian patients. European Journal of Medical Genetics. 52(5). 311–314. 8 indexed citations
15.
Mandich, Paola, Paola Fossa, Simona Capponi, et al.. (2009). Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies. European Journal of Human Genetics. 17(9). 1129–1134. 31 indexed citations
16.
Bruno, Claudio, Marina Grandis, Denise Cassandrini, et al.. (2008). Gene symbol: CLN5. Disease: Neuronal Ceroid Lipofuscinosis, Finnish Variant.. PubMed. 123(5). 552–552. 6 indexed citations
17.
Vitale, Carmine, Rossella Gulli, Paola Ciotti, et al.. (2008). DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patients. European Journal of Neurology. 15(9). 985–987. 21 indexed citations
18.
Mandich, Paola, Marina Grandis, Alessandro Geroldi, et al.. (2008). Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease. Journal of Human Genetics. 53(6). 529–533. 13 indexed citations
19.
Maria, Emilio Di, Rossella Gulli, Alessandro De Luca, et al.. (2004). Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: A case‐control study. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 128B(1). 27–29. 30 indexed citations
20.
Maria, Emilio Di, Roberta Marchese, Emilia Bellone, et al.. (2003). Essential tremor is not associated with α‐synuclein gene haplotypes. Movement Disorders. 18(7). 823–826. 19 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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