Marina Ferrone

563 total citations
16 papers, 413 citations indexed

About

Marina Ferrone is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Surgery. According to data from OpenAlex, Marina Ferrone has authored 16 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 3 papers in Surgery. Recurrent topics in Marina Ferrone's work include Mitochondrial Function and Pathology (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Muscle Physiology and Disorders (3 papers). Marina Ferrone is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Muscle Physiology and Disorders (3 papers). Marina Ferrone collaborates with scholars based in Italy, France and Japan. Marina Ferrone's co-authors include Lorenzo Silengo, Gabriella Restagno, Francesco Costanzo, Claudio Santoro, Riccardo Cortese, Carlo Minganti, Maria Marone, Innocenzo Rainero, Lorenzo Pinessi and Elisa Rubino and has published in prestigious journals such as Nucleic Acids Research, Neurology and Biochemical Journal.

In The Last Decade

Marina Ferrone

16 papers receiving 400 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marina Ferrone Italy	9	221	94	75	61	61	16	413
David Langer Germany	11	183 0.8×	114 1.2×	39 0.5×	56 0.9×	30 0.5×	12	469
Taiho Shibata Japan	8	163 0.7×	206 2.2×	23 0.3×	39 0.6×	24 0.4×	11	465
Filomena D’Amato Italy	14	169 0.8×	125 1.3×	26 0.3×	91 1.5×	51 0.8×	15	440
Federica La Russa United Kingdom	8	125 0.6×	179 1.9×	33 0.4×	183 3.0×	34 0.6×	11	469
Soraya Scuderi Italy	15	232 1.0×	217 2.3×	46 0.6×	58 1.0×	68 1.1×	21	508
Ali Lourhmati Germany	10	233 1.1×	162 1.7×	16 0.2×	80 1.3×	48 0.8×	11	592
Cecilia Dominguez Sweden	13	121 0.5×	212 2.3×	31 0.4×	130 2.1×	72 1.2×	25	649
Hideaki Ishiguro Japan	13	206 0.9×	155 1.6×	11 0.1×	62 1.0×	19 0.3×	34	538
S. Kashii Japan	10	217 1.0×	155 1.6×	18 0.2×	51 0.8×	13 0.2×	27	511
J. Schaller United States	11	128 0.6×	74 0.8×	30 0.4×	50 0.8×	24 0.4×	17	396

Countries citing papers authored by Marina Ferrone

Since Specialization

Citations

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

Fields of papers citing papers by Marina Ferrone

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Ferrone

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

All Works

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16 of 16 papers shown

Rubino, Elisa, Cecilia Mancini, Silvia Boschi, et al.. (2018). ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementia. Neurobiology of Aging. 73. 231.e7–231.e9. 21 indexed citations

Cagnoli, Claudia, Alessandro Brussino, Cecilia Mancini, et al.. (2018). Spinocerebellar Ataxia Tethering PCR. Journal of Molecular Diagnostics. 20(3). 289–297. 15 indexed citations

Brussino, Alessandro, Claudio Graziano, Marina Ferrone, et al.. (2010). Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia. Movement Disorders. 25(9). 1269–1273. 25 indexed citations

Rainero, Innocenzo, Salvatore Gallone, Walter Valfrè, et al.. (2004). A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache. Neurology. 63(7). 1286–1288. 90 indexed citations

Menegatti, Elisa, et al.. (2001). Molecular Genetic Analysis of von Hippel-Lindau Disease by Denaturing High-Performance Liquid Chromatography. Contributions to nephrology. 306–311. 1 indexed citations

Arduino, Carlo, Monica Gallo, Alfredo Brusco, et al.. (1999). Polyvariant mutant CFTR genes in patients with chronic pancreatitis. Clinical Genetics. 56(5). 401–405. 37 indexed citations

Arduino, Carlo, Marina Ferrone, Alfredo Brusco, et al.. (1998). Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene. Clinical Genetics. 53(3). 202–204. 4 indexed citations

Restagno, Gabriella, Norma B. Romero, Isabelle Richard, et al.. (1996). Prenatal diagnosis of limb-girdle muscular dystrophy type 2A. Neuromuscular Disorders. 6(3). 173–176. 7 indexed citations

Restagno, Gabriella, Marina Ferrone, C. Doriguzzi, et al.. (1995). Carrier detection of duchenne muscular dystrophy through analysis of dna from deciduous teeth of a dead affected child. Prenatal Diagnosis. 15(7). 672–674. 3 indexed citations

10.

Doriguzzi, C., et al.. (1993). Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy. Journal of Neurology. 240(5). 269–271. 31 indexed citations

11.

Restagno, Gabriella, et al.. (1993). A large deletion at the 3′ end of the rhodopsin gene in an Italian family with a diffuse form of autosomal dominant retinitis pigmentosa. Human Molecular Genetics. 2(2). 207–208. 41 indexed citations

12.

Daniele, Aurora, et al.. (1992). Mapping of Human Hexokinase 1 Gene to10q11→qter. Human Heredity. 42(2). 107–110. 2 indexed citations

13.

Restagno, Gabriella, et al.. (1992). Analysis of CA/GT microsatellite polymorphism in IVS8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a study of Italian CF families. Clinical Genetics. 42(6). 309–313. 1 indexed citations

14.

Magnani, Mauro, Marzia Bianchi, Anna Casabianca, et al.. (1992). A recombinant human ‘mini’-hexokinase is catalytically active and regulated by hexose 6-phosphates. Biochemical Journal. 285(1). 193–199. 38 indexed citations

15.

Daniele, Aurora, Fiorella Altruda, Marina Ferrone, et al.. (1991). Cloning and expression of a new human polypeptide which regulates protein phosphorylation in Escherichia coli. Molecular and Cellular Biochemistry. 107(2). 87–94. 1 indexed citations

16.

Santoro, Claudio, Maria Marone, Marina Ferrone, et al.. (1986). Cloning of the gene coding for human L apoferritin. Nucleic Acids Research. 14(7). 2863–2876. 96 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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