Patrizia Avoni

5.0k total citations
86 papers, 3.0k citations indexed

About

Patrizia Avoni is a scholar working on Neurology, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Patrizia Avoni has authored 86 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Neurology, 24 papers in Psychiatry and Mental health and 23 papers in Molecular Biology. Recurrent topics in Patrizia Avoni's work include Parkinson's Disease Mechanisms and Treatments (20 papers), Epilepsy research and treatment (15 papers) and Genetic Neurodegenerative Diseases (12 papers). Patrizia Avoni is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (20 papers), Epilepsy research and treatment (15 papers) and Genetic Neurodegenerative Diseases (12 papers). Patrizia Avoni collaborates with scholars based in Italy, United States and Switzerland. Patrizia Avoni's co-authors include Rocco Liguori, Agostino Baruzzi, Pietro Cortelli, Paolo Tinuper, E Lugaresi, Maria Pia Giannoccaro, Vincenzo Donadio, Alex Incensi, Sabina Capellari and Pierluigi Gambetti and has published in prestigious journals such as New England Journal of Medicine, The Lancet and PLoS ONE.

In The Last Decade

Patrizia Avoni

85 papers receiving 2.9k citations

Peers

Patrizia Avoni

NEURO

CMN

PMH

NEURO

Mustafa K. Başkaya United States

Girolama Alessandra Marfia Italy

Paolo Aridon Italy

Carlos Singer United States

Keisuke Suzuki Japan

Charles Murchison United States

Alban Latrémolière United States

Michael Karl Boettger Germany

Souhel Najjar United States

Yair Lampl Israel

Mustafa K. Başkaya United States

Patrizia Avoni

1.4k ×1.2

NEURO

717 ×0.7

733 ×1.2

CMN

204 ×0.3

PMH

448 ×0.8

NEURO

Citations per year, relative to Patrizia Avoni Patrizia Avoni (= 1×) peers Mustafa K. Başkaya

Countries citing papers authored by Patrizia Avoni

Since Specialization

Citations

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

Fields of papers citing papers by Patrizia Avoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrizia Avoni

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

All Works

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20 of 20 papers shown

Cirillo, Luigi, Patrizia Avoni, Vitantonio Di Stasi, et al.. (2023). Bibrachial amyotrophy as a rare manifestation of intraspinal fluid collection: a case report and systematic review. Neurological Sciences. 45(5). 2279–2288. 1 indexed citations

Pondrelli, Federica, Maria Pia Giannoccaro, Francesca Bisulli, et al.. (2022). Pilomotor seizures in autoimmune limbic encephalitis: description of two GAD65 antibodies- related cases and literature review. Seizure. 98. 71–78. 5 indexed citations

Giannoccaro, Maria Pia, Patrizia Avoni, & Rocco Liguori. (2021). Presynaptic Paraneoplastic Disorders of the Neuromuscular Junction: An Update. Brain Sciences. 11(8). 1035–1035. 7 indexed citations

Giannoccaro, Maria Pia, Matteo Paolucci, Corrado Zenesini, et al.. (2020). Comparison of ice pack test and single-fiber EMG diagnostic accuracy in patients referred for myasthenic ptosis. Neurology. 95(13). e1800–e1806. 15 indexed citations

Giannoccaro, Maria Pia, et al.. (2019). Sensitivity and specificity of single-fibre EMG in the diagnosis of ocular myasthenia varies accordingly to clinical presentation. Journal of Neurology. 267(3). 739–745. 14 indexed citations

Foschi, Matteo, Giovanni Rizzo, Rocco Liguori, et al.. (2019). Sleep-related disorders and their relationship with MRI findings in multiple sclerosis. Sleep Medicine. 56. 90–97. 54 indexed citations

Fileccia, Enrico, Vitantonio Di Stasi, Roberto Poda, et al.. (2019). Effects on cognition of 20-day anodal transcranial direct current stimulation over the left dorsolateral prefrontal cortex in patients affected by mild cognitive impairment: a case-control study. Neurological Sciences. 40(9). 1865–1872. 33 indexed citations

Giannoccaro, Maria Pia, Anna Bartoletti‐Stella, Annalisa Pession, et al.. (2017). Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature. Journal of Neurology. 264(7). 1426–1433. 28 indexed citations

Liguori, Rocco, Alex Incensi, Silvia De Pasqua, et al.. (2017). Skin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy. PLoS ONE. 12(7). e0180581–e0180581. 31 indexed citations

10.

Mainieri, Greta, Sabina Cevoli, Giulia Giannini, et al.. (2015). Headache in epilepsy: prevalence and clinical features. The Journal of Headache and Pain. 16(1). 556–556. 41 indexed citations

11.

Contardi, Sara, Fabio Pizza, Francesca Maria Antonella Falzone, et al.. (2011). Development of a disability scale for myotonic dystrophy type 1. Acta Neurologica Scandinavica. 125(6). 431–438. 11 indexed citations

12.

Donadio, Vincenzo, Pietro Cortelli, Mikael Elam, et al.. (2010). Autonomic innervation in multiple system atrophy and pure autonomic failure. Journal of Neurology Neurosurgery & Psychiatry. 81(12). 1327–1335. 62 indexed citations

13.

D’Aguanno, Simona, Alessandra Barassi, Piero Del Boccio, et al.. (2007). Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis. Journal of Neuroimmunology. 193(1-2). 156–160. 22 indexed citations

14.

Volta, Umberto, Roberto De Giorgio, Alessandro Granito, et al.. (2006). Anti-ganglioside antibodies in coeliac disease with neurological disorders. Digestive and Liver Disease. 38(3). 183–187. 52 indexed citations

15.

Bisulli, Francesca, Paolo Tinuper, Carla Marini, et al.. (2002). Partial epilepsy with prominent auditory symptoms not linked to chromosome 10q. Epileptic Disorders. 4(3). 183–188. 10 indexed citations

16.

Liguori, Rocco, Patrizia Avoni, Agostino Baruzzi, Vitantonio Di Stasi, & Pasquale Montagna. (2001). Familial continuous motor unit activity and epilepsy. Muscle & Nerve. 24(5). 630–633. 21 indexed citations

17.

Ferrillo, Franco, Giuseppe Plazzi, Lino Nobili, et al.. (2001). Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis study. Clinical Neurophysiology. 112(10). 1888–1892. 18 indexed citations

18.

Portaluppi, Francesco, Pietro Cortelli, Patrizia Avoni, et al.. (1995). Dissociated 24-Hour Patterns of Somatotropin and Prolactin in Fatal Familial Insomnia. Neuroendocrinology. 61(6). 731–737. 20 indexed citations

19.

Tinuper, Paolo, P. Montagna, Pietro Cortelli, et al.. (1992). Idiopathic recurring stupor: A case with possible involvement of the gamma–aminobutyric acid (GABA)ergic system. Annals of Neurology. 31(5). 503–506. 19 indexed citations

20.

Medori, Rossella, Valeria Manetto, H. Y. Chen, et al.. (1992). Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene. New England Journal of Medicine. 326(7). 444–449. 414 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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