Anna Sagnelli

969 total citations
22 papers, 642 citations indexed

About

Anna Sagnelli is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Anna Sagnelli has authored 22 papers receiving a total of 642 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 9 papers in Molecular Biology and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in Anna Sagnelli's work include Genetic Neurodegenerative Diseases (8 papers), Amyotrophic Lateral Sclerosis Research (8 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Anna Sagnelli is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Amyotrophic Lateral Sclerosis Research (8 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Anna Sagnelli collaborates with scholars based in Italy, United Kingdom and United States. Anna Sagnelli's co-authors include Davide Pareyson, Paola Saveri, Giuseppe Piscosquito, Maria Rosaria Monsurrò, G. Tedeschi, Alberto Albanese, Antonio Emanuele Elia, Stefania Lalli, Alfonsa Claudia Taiello and Vincenzo La Bella and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neurology.

In The Last Decade

Anna Sagnelli

22 papers receiving 631 citations

Peers

Anna Sagnelli

NEURO

CMN

GENET

PHYSI

Jung‐Joon Sung South Korea

Orna O’Toole Ireland

Luigi Serlenga Italy

Eleonora Dalla Bella Italy

Katsuhisa Ogata Japan

Johannes Dorst Germany

Véronique Danel-Brunaud France

Eustachio D’Errico Italy

Stefano Tozza Italy

Madison T. Gray Canada

Jung‐Joon Sung South Korea

Anna Sagnelli

490 ×1.8

NEURO

176 ×0.8

113 ×0.6

CMN

165 ×1.3

GENET

80 ×0.9

PHYSI

Citations per year, relative to Anna Sagnelli Anna Sagnelli (= 1×) peers Jung‐Joon Sung

Countries citing papers authored by Anna Sagnelli

Since Specialization

Citations

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

Fields of papers citing papers by Anna Sagnelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Sagnelli

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Sagnelli. A scholar is included among the top collaborators of Anna Sagnelli 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 Anna Sagnelli. Anna Sagnelli 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

Scavone, Cristina, Maria Elena Di Battista, Simona Salvatore, et al.. (2021). Influenza Vaccine Hesitancy in Patients with Multiple Sclerosis: A Monocentric Observational Study. Brain Sciences. 11(7). 890–890. 14 indexed citations

Ranieri, Angelo, Massimo Napolitano, Katia Longo, et al.. (2020). One year experience with erenumab: real-life data in 30 consecutive patients. Neurological Sciences. 41(S2). 505–506. 11 indexed citations

Cortese, Andrea, Matilde Laurá, Carlo Casali, et al.. (2017). Altered TDP‐43‐dependent splicing in HSPB8‐related distal hereditary motor neuropathy and myofibrillar myopathy. European Journal of Neurology. 25(1). 154–163. 25 indexed citations

Pareyson, Davide, Pietro Fratta, Pierre-François Pradat, et al.. (2016). Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy. Journal of Molecular Neuroscience. 58(3). 394–400. 9 indexed citations

Sagnelli, Anna, Giuseppe Piscosquito, Daniela Di Bella, et al.. (2016). Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy. Journal of the Peripheral Nervous System. 22(1). 59–63. 1 indexed citations

Sagnelli, Anna, V. Scaioli, Giuseppe Piscosquito, et al.. (2015). Spinal and bulbar muscular atrophy and Charcot–Marie–Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patient. Neuromuscular Disorders. 25(10). 800–801. 1 indexed citations

Weydt, Patrick, Anna Sagnelli, Angela Rosenbohm, et al.. (2015). Clinical Trials in Spinal and Bulbar Muscular Atrophy—Past, Present, and Future. Journal of Molecular Neuroscience. 58(3). 379–387. 13 indexed citations

Pareyson, Davide, Paola Saveri, Anna Sagnelli, & Giuseppe Piscosquito. (2015). Mitochondrial dynamics and inherited peripheral nerve diseases. Neuroscience Letters. 596. 66–77. 89 indexed citations

Elia, Antonio Emanuele, Stefania Lalli, Maria Rosaria Monsurrò, et al.. (2015). Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis. European Journal of Neurology. 23(1). 45–52. 167 indexed citations

10.

Dossena, Marta, Gloria Bedini, P. Rusmini, et al.. (2014). Human Adipose-Derived Mesenchymal Stem Cells as a New Model of Spinal and Bulbar Muscular Atrophy. PLoS ONE. 9(11). e112746–e112746. 14 indexed citations

11.

Bella, Daniela Di, Davide Pareyson, M. Savoiardo, et al.. (2014). Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation. Neurology. 83(13). 1217–1218. 41 indexed citations

12.

Sagnelli, Anna, Giuseppe Piscosquito, Luisa Chiapparini, et al.. (2014). X‐linked Charcot‐Marie‐Tooth type 1: stroke‐like presentation of a novel GJB1 mutation. Journal of the Peripheral Nervous System. 19(2). 183–186. 18 indexed citations

13.

Sagnelli, Anna, M. Savoiardo, C. Marchesi, et al.. (2013). Adult polyglucosan body disease in a patient originally diagnosed with Fabry’s disease. Neuromuscular Disorders. 24(3). 272–276. 10 indexed citations

14.

Sagnelli, Anna, Giuseppe Piscosquito, & Davide Pareyson. (2013). Inherited neuropathies: an update. Journal of Neurology. 260(10). 2684–2690. 1 indexed citations

15.

Cirillo, Mario, Fabrizio Esposito, G Tedeschi, et al.. (2012). Widespread Microstructural White Matter Involvement in Amyotrophic Lateral Sclerosis: A Whole-Brain DTI Study. American Journal of Neuroradiology. 33(6). 1102–1108. 59 indexed citations

16.

Trojsi, Francesca, Anna Sagnelli, Giovanni Cirillo, et al.. (2012). Amyotrophic Lateral Sclerosis and Multiple Sclerosis Overlap: A Case Report. Case Reports in Medicine. 2012. 1–4. 13 indexed citations

17.

Trojsi, Francesca, Anna Sagnelli, Nicola Vanacore, et al.. (2012). Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database. SHILAP Revista de lepidopterología. 48(3). 287–291. 6 indexed citations

18.

Vecchio, Lucia Del, Alfonso Reginelli, Luigi Monaco, et al.. (2011). Search for compensation postures with videofluoromanometric investigation in dysphagic patients affected by amyotrophic lateral sclerosis. La radiologia medica. 116(7). 1083–1094. 23 indexed citations

19.

Tedeschi, Gioacchino, Francesca Trojsi, Alessandro Tessitore, et al.. (2010). Interaction between aging and neurodegeneration in amyotrophic lateral sclerosis. Neurobiology of Aging. 33(5). 886–898. 84 indexed citations

20.

Tamburrini, Stefania, et al.. (2010). Amyotrophic lateral sclerosis: sonographic evaluation of dysphagia. La radiologia medica. 115(5). 784–793. 36 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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