Emilia Bellone

2.8k total citations
100 papers, 1.8k citations indexed

About

Emilia Bellone is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Emilia Bellone has authored 100 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Cellular and Molecular Neuroscience, 39 papers in Neurology and 37 papers in Molecular Biology. Recurrent topics in Emilia Bellone's work include Hereditary Neurological Disorders (49 papers), Genetic Neurodegenerative Diseases (28 papers) and Neurological diseases and metabolism (19 papers). Emilia Bellone is often cited by papers focused on Hereditary Neurological Disorders (49 papers), Genetic Neurodegenerative Diseases (28 papers) and Neurological diseases and metabolism (19 papers). Emilia Bellone collaborates with scholars based in Italy, United States and Belgium. Emilia Bellone's co-authors include Paola Mandich, Emilio Di Maria, Franco Ajmar, Angelo Schenone, F. Ajmar, Gianluigi Mancardi, Alessandro Geroldi, Paola Ciotti, Marina Grandis and Roberta Marchese and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Annals of Neurology.

In The Last Decade

Emilia Bellone

100 papers receiving 1.8k citations

Peers

Countries citing papers authored by Emilia Bellone

Since Specialization

Citations

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

Fields of papers citing papers by Emilia Bellone

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emilia Bellone

This figure shows the co-authorship network connecting the top 25 collaborators of Emilia Bellone. A scholar is included among the top collaborators of Emilia Bellone 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 Emilia Bellone. Emilia Bellone 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	Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement 2024 ·Pediatric Neurology ·Alessandro Geroldi, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Paola Origone, (unknown), (unknown), (unknown), Chiara Gemelli, (unknown), Angelo Schenone, Paola Lanteri, Chiara Fiorillo, Marina Grandis, Paola Mandich, Emilia Bellone	1
2	People with Charcot-Marie-Tooth disease and COVID-19: Impaired physical conditions due to the lockdown. An International cross-sectional survey 2020 ·Annals of Physical and Rehabilitation Medicine ·Valeria Prada, (unknown), Filippo Genovese, (unknown), Luana Benedetti, Emilia Bellone, Marina Grandis, Paola Mandich, Angelo Schenone	3
3	Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA repeats carrier 2018 ·SHILAP Revista de lepidopterología ·Paola Origone, (unknown), (unknown), (unknown), Alessandro Geroldi, (unknown), (unknown), Federico Massa, (unknown), Matteo Bauckneht, Roberta Marchese, Giovanni Abbruzzese, Emilia Bellone, Paola Mandich	11
4	Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance 2017 ·Neuromuscular Disorders ·Alessandro Geroldi, Patrizia Lastella, (unknown), (unknown), Nicoletta Resta, Grazia Devigili, Carlo Sabbà, Rossella Gulli, (unknown), Paola Origone, Paola Mandich, Emilia Bellone	1
5	A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family 2012 ·Journal of the Peripheral Nervous System ·Fiore Manganelli, Chiara Pisciotta, Maria Nolano, Simona Capponi, Alessandro Geroldi, (unknown), Emilia Bellone, Arvid Suls, Paola Mandich, Lucio Santoro	11
6	Outcome Measures and Rehabilitation Treatment in Patients Affected by Charcot-Marie-Tooth Neuropathy 2011 ·American Journal of Physical Medicine & Rehabilitation ·Giovanni Maggi, Margherita Monti Bragadin, Luca Padua, (unknown), Emilia Bellone, Marina Grandis, Lizia Reni, (unknown), (unknown), (unknown), (unknown), Riccardo Zuccarino, Emanuele Crimi, Angelo Schenone	35
7	Currarino syndrome with pelvic neuroendocrine tumor diagnosed by post‐mortem genetic analysis of tissue specimens 2011 ·American Journal of Medical Genetics Part A ·Paola Ciotti, Paola Mandich, Emilia Bellone, Paola Ceppa, Marta Bovio, Pietro Ameri, Giancarlo Torre, Roberto Fiocca, Giovanni Murialdo	13
8	Quantitative Fluorescence-Polymerase Chain Reaction Assay for the Detection of the Duplication of the Charcot Marie Tooth Disease Type 1A Critical Region 2010 ·Genetic Testing and Molecular Biomarkers ·Simona De Toffol, Emilia Bellone, Francesca Dulcetti, Anna Ruggeri, (unknown), (unknown), Paola Mandich, Federico Maggi, Giuseppe Simoni, Francesca Romana Grati	1
9	Germline mutations in the von Hippel–Lindau gene in Italian patients 2009 ·European Journal of Medical Genetics ·Paola Ciotti, Anna Garuti, Rossella Gulli, Alberto Ballestrero, Emilia Bellone, Paola Mandich	8
10	Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies 2009 ·European Journal of Human Genetics ·Paola Mandich, Paola Fossa, Simona Capponi, Alessandro Geroldi, (unknown), Rossella Gulli, Paola Ciotti, Fiore Manganelli, Marina Grandis, Emilia Bellone	31
11	Multifocal bilateral renal cell carcinoma and retinal angiomas in a patient with de novo von Hippel-Lindau disease: Identification of a new germline mutation 2005 ·Journal of Nephrology ·Adalberto Sessa, Graziana Battini, Mietta Meroni, (unknown), Marco Righetti, Paola Ciotti, Emilio Di Maria, Emilia Bellone, Franco Ajmar, Paola Mandich	3
12	Does parkin play a role in the peripheral nervous system? A family report 2004 ·Movement Disorders ·Giovanni Abbruzzese, (unknown), Angelo Schenone, Emilia Bellone, Roberta Marchese, Emilio Di Maria, Luana Benedetti, Paola Ciotti, Lucilla Nobbio, Vincenzo Bonifati, Franco Ajmar, Paola Mandich	26
13	Different consequences of EGR2 mutants on the transactivation of human cx32 promoter 2003 ·Neurobiology of Disease ·Marco Musso, (unknown), Franco Taroni, Emilia Bellone, Paola Mandich	9
14	Essential tremor is not associated with α‐synuclein gene haplotypes 2003 ·Movement Disorders ·(unknown), Emilio Di Maria, Roberta Marchese, Emilia Bellone, Rossella Gulli, Cesa Scaglione, (unknown), Paolo Barone, Paolo Martinelli, Giovanni Abbruzzese, Franco Ajmar, Paola Mandich	19
15	Congenital hypomyelination due to myelin protein zero Q215X mutation 1999 ·Annals of Neurology ·Paola Mandich, Gianluigi Mancardi, (unknown), (unknown), Emilio Di Maria, Emilia Bellone, M. Bado, (unknown), Anthony J. Windebank, F. Ajmar, Angelo Schenone	35
16	Isolation and Characterization of a Novel Transcript Embedded within HIRA, a Gene Deleted in DiGeorge Syndrome 1999 ·Molecular Genetics and Metabolism ·Antonio Pizzuti, Giuseppe Novelli, Antonia Ratti, Francesca Amati, Roberta Bordoni, Paola Mandich, Emilia Bellone, Emanuela Conti, Mario Bengala, Aldo Mari, Vincenzo Silani, Bruno Dallapiccola	16
17	Molecular Analysis of the IT15 Gene in Patients with Apparently ‘Sporadic’ Huntington’s Disease 1996 ·European Neurology ·Paola Mandich, Emilio Di Maria, Emilia Bellone, F. Ajmar, Giovanni Abbruzzese	4
18	Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding 1995 ·Neuroscience Letters ·(unknown), Emilia Bellone, Eva Nelis, Paola Mandich, Angelo Schenone, Gianluigi Mancardi, Christine Van Broeckhoven, M. Abbruzzese, Franco Ajmar	3
19	17p11.2 Duplication Is a Common Finding in Sporadic Cases of Charcot-Marie-Tooth Type 1 1994 ·European Neurology ·Gianluigi Mancardi, Antonio Uccelli, Emilia Bellone, Angelo Sghirlanzoni, Paola Mandich, Davide Pareyson, Angelo Schenone, M. Abbruzzese, F. Ajmar	6
20	[Changes in blood gases in anxiety states of medium severity]. 1971 ·PubMed ·(unknown), (unknown), (unknown), Emilia Bellone, (unknown)	4

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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