Federica Taioli

1.1k total citations
43 papers, 749 citations indexed

About

Federica Taioli is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Federica Taioli has authored 43 papers receiving a total of 749 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Cellular and Molecular Neuroscience, 16 papers in Neurology and 14 papers in Molecular Biology. Recurrent topics in Federica Taioli's work include Hereditary Neurological Disorders (34 papers), Genetic Neurodegenerative Diseases (15 papers) and Neurological diseases and metabolism (10 papers). Federica Taioli is often cited by papers focused on Hereditary Neurological Disorders (34 papers), Genetic Neurodegenerative Diseases (15 papers) and Neurological diseases and metabolism (10 papers). Federica Taioli collaborates with scholars based in Italy, United States and Canada. Federica Taioli's co-authors include Tiziana Cavallaro, Gian Maria Fabrizi, Ilaria Cabrini, Moreno Ferrarini, N. Rizzuto, Laura Bertolasi, Alessandro Simonati, G Fabrizi, Chiara Angiari and N. Rizzuto and has published in prestigious journals such as Brain, Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Federica Taioli

43 papers receiving 732 citations

Peers

Countries citing papers authored by Federica Taioli

Since Specialization

Citations

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

Fields of papers citing papers by Federica Taioli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Federica Taioli

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

#	Work	Indexed citations
1	Rare among Rare: Phenotypes of Uncommon CMT Genotypes 2021 ·Brain Sciences ·Luca Gentile, Massimo Russo, Federica Taioli, Moreno Ferrarini, M. Aguennouz, Carmelo Rodolico, António Toscano, Gian Maria Fabrizi, Anna Mazzeo	1
2	Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: Pitfalls and red flags 2020 ·Journal of the Peripheral Nervous System ·Marta Campagnolo, Federica Taioli, Mario Cacciavillani, Marta Ruiz, Marco Luigetti, Alessandro Salvalaggio, Francesca Castellani, Silvia Testi, Moreno Ferrarini, Tiziana Cavallaro, Roberto Gasparotti, Gian Maria Fabrizi, Chiara Briani	14
3	Charcot-Marie-Tooth disease: experience from a large Italian tertiary neuromuscular center 2020 ·Neurological Sciences ·Luca Gentile, Massimo Russo, Gian Maria Fabrizi, Federica Taioli, Moreno Ferrarini, Silvia Testi, (unknown), M. Aguennouz, António Toscano, Giuseppe Vita, Anna Mazzeo	16
4	Inherited motor-sensory neuropathy with upper limb predominance associated with the tropomyosin-receptor kinase fused gene 2020 ·Neuromuscular Disorders ·Gian Maria Fabrizi, Helle Høyer, Federica Taioli, Tiziana Cavallaro, (unknown), Giovanna Squintani, Giampietro Zanette, Geir J. Braathen	2
5	TRPV4 related scapuloperoneal spinal muscular atrophy: Report of an Italian family and review of the literature 2016 ·Neuromuscular Disorders ·(unknown), Simona Portaro, Anna Mazzeo, Giuseppe Vita, Gian Maria Fabrizi, Federica Taioli, António Toscano, Carmelo Rodolico	14
6	Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience 2016 ·Clinical Neurology and Neurosurgery ·Marco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, Ângela Romano, Federica Taioli, Moreno Ferrarini, Daniela Bernardo, Paolo Maria Rossini, Mario Sabatelli	14
7	Charcot–Marie–Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family 2014 ·Neurological Sciences ·Claudia Stancanelli, Gian Maria Fabrizi, Moreno Ferrarini, Tiziana Cavallaro, Federica Taioli, Rita Di Leo, Massimo Russo, Luca Gentile, António Toscano, Giuseppe Vita, Anna Mazzeo	17
8	Autonomic nervous system involvement in a new CMT2B family 2012 ·Journal of the Peripheral Nervous System ·Fiore Manganelli, Chiara Pisciotta, Vincenzo Provitera, Federica Taioli, Rosa Iodice, (unknown), Gian Maria Fabrizi, Maria Nolano, Lucio Santoro	18
9	Variable presentations of TTR‐related familial amyloid polyneuropathy in seventeen patients 2011 ·Journal of the Peripheral Nervous System ·Manuel Cappellari, Tiziana Cavallaro, Moreno Ferrarini, Ilaria Cabrini, Federica Taioli, Sérgio Ferrari, Giampaolo Merlini, Laura Obici, Chiara Briani, Gian Maria Fabrizi	62
10	Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation 2011 ·Journal of the Neurological Sciences ·Marco Luigetti, Gian Maria Fabrizi, Federica Taioli, Amelia Conte, Alessandra Del Grande, Mario Sabatelli	8
11	Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity 2011 ·Clinical Neurology and Neurosurgery ·Marco Luigetti, Salvatore Maria Corsello, Serena Lattante, Pietro Locantore, (unknown), Gian Maria Fabrizi, Federica Taioli, Amelia Conte, Alessandra Del Grande, Mario Sabatelli	2
12	Déjerine‐Sottas syndrome with a silent nucleotide change of myelin protein zero gene 2011 ·Journal of the Peripheral Nervous System ·Federica Taioli, Ilaria Cabrini, Tiziana Cavallaro, Alessandro Simonati, Silvia Testi, Gian Maria Fabrizi	7
13	Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias 2010 ·Muscle & Nerve ·Chiara Briani, Gian Maria Fabrizi, Susanna Ruggero, Chiara Dalla Torre, Moreno Ferrarini, Marta Campagnolo, Tiziana Cavallaro, Sérgio Ferrari, Marina Scarlato, Federica Taioli, Fausto Adami	32
14	Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy and Right-to-Left Shunt: Lack of Evidence for an Association in a Prevalence Study 2008 ·European Neurology ·Sara Mazzucco, Gian Paolo Anzola, Moreno Ferrarini, Federica Taioli, (unknown), Alessandro P. Burlina, Gian Maria Fabrizi, N. Rizzuto	5
15	Early-onset Hereditary Neuropathy with Liability to Pressure Palsy 2007 ·Neuropediatrics ·Giovanni Antonini, Anna Luchetti, Mario Mastrangelo, (unknown), (unknown), Federica Taioli, Gian Maria Fabrizi, Paola Iannetti	12
16	Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1B 2006 ·Neuromuscular Disorders ·Gian Maria Fabrizi, Maria Pellegrini, Chiara Angiari, Tiziana Cavallaro, A Morini, Federica Taioli, Ilaria Cabrini, D. Orrico, Nicolo’ Rizzuto	17
17	Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton 2006 ·Brain ·G Fabrizi, Tiziana Cavallaro, Chiara Angiari, Ilaria Cabrini, Federica Taioli, Giovanni Malerba, Laura Bertolasi, N. Rizzuto	107
18	Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 2002 ·Journal of Neurology ·Alessandro Simonati, Gian Maria Fabrizi, Federica Taioli, Alberto Polo, R. Cerini, N. Rizzuto	11
19	Clinical and pathological correlations in charcot-marie-tooth neuropathy type 1A with the 17p11.2p12 duplication: A cross-sectional morphometric and immunohistochemical study in twenty cases 1998 ·Muscle & Nerve ·Gian Maria Fabrizi, Alessandro Simonati, Michela Morbin, Tiziana Cavallaro, Federica Taioli, Maria Donata Benedetti, Paolo Edomi, Nicolo’ Rizzuto	37
20	Expression and regulation of glial-cell-line-derived neurotrophic factor (GDNF) mRNA in human astrocytes in vitro 1996 ·Cell and Tissue Research ·Giuseppe Moretto, Douglas G. Walker, Paola Lanteri, Federica Taioli, Stefano Zaffagnini, Ren Xu, Nicolo’ Rizzuto	33

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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