Carlo Fusco

3.0k total citations
118 papers, 1.8k citations indexed

About

Carlo Fusco is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Carlo Fusco has authored 118 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 32 papers in Genetics and 30 papers in Cellular and Molecular Neuroscience. Recurrent topics in Carlo Fusco's work include Genetics and Neurodevelopmental Disorders (20 papers), Hereditary Neurological Disorders (19 papers) and Neurological diseases and metabolism (14 papers). Carlo Fusco is often cited by papers focused on Genetics and Neurodevelopmental Disorders (20 papers), Hereditary Neurological Disorders (19 papers) and Neurological diseases and metabolism (14 papers). Carlo Fusco collaborates with scholars based in Italy, United States and United Kingdom. Carlo Fusco's co-authors include Francesco Pisani, Antonis S. Zervos, Daniele Frattini, Carlotta Spagnoli, Stefano Négrini, Salvatore Atanasio, Fabio Zaina, Michele Romano, Stefano Martinotti and Caterina Cerminara and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Carlo Fusco

107 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Carlo Fusco Italy	21	565	353	323	296	276	118	1.8k
Uluç Yiş Türkiye	21	553 1.0×	271 0.8×	150 0.5×	351 1.2×	242 0.9×	172	1.6k
John H. Livingston United Kingdom	23	735 1.3×	249 0.7×	127 0.4×	322 1.1×	278 1.0×	56	1.8k
Francesco Nicita Italy	23	412 0.7×	288 0.8×	115 0.4×	188 0.6×	244 0.9×	94	1.3k
Brahim Tabarki Saudi Arabia	24	567 1.0×	168 0.5×	112 0.3×	456 1.5×	155 0.6×	89	1.8k
Kazuhiro Haginoya Japan	28	1.2k 2.2×	660 1.9×	152 0.5×	453 1.5×	352 1.3×	159	2.7k
Tsunekazu Yamano Japan	22	525 0.9×	159 0.5×	244 0.8×	448 1.5×	274 1.0×	120	1.8k
Byung Chan Lim South Korea	23	750 1.3×	481 1.4×	87 0.3×	375 1.3×	244 0.9×	165	1.8k
Maja von der Hagen Germany	22	651 1.2×	101 0.3×	175 0.5×	155 0.5×	249 0.9×	80	1.5k
Zühal Yapıcı Türkiye	20	523 0.9×	318 0.9×	61 0.2×	266 0.9×	253 0.9×	104	2.3k
Laura Papetti Italy	21	269 0.5×	720 2.0×	155 0.5×	160 0.5×	197 0.7×	106	1.6k

Countries citing papers authored by Carlo Fusco

Since Specialization

Citations

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

Fields of papers citing papers by Carlo Fusco

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carlo Fusco

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Spagnoli, Carlotta, A Cavalli, Stefano Giuseppe Caraffi, et al.. (2025). Myoclonic reflex and non‐reflex seizures in a female child with Coffin–Lowry syndrome: Clinical vignette. Epileptic Disorders. 27(2). 299–303. 1 indexed citations

Spagnoli, Carlotta, Stefano Giuseppe Caraffi, Manuela Napoli, et al.. (2024). Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literature. American Journal of Medical Genetics Part A. 197(1). e63848–e63848.

Spagnoli, Carlotta, et al.. (2024). Guillain-Barrè Syndrome—Retrospective Analysis of Data from a Cohort of Patients Referred to a Tertiary Care Pediatric Neuromuscular Center from 2000 to 2017: Electrophysiological Findings, Outcomes, and a Brief Literature Review. Medicina. 60(9). 1490–1490. 1 indexed citations

Spagnoli, Carlotta, Stefano Giuseppe Caraffi, A Cavalli, et al.. (2024). Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study. International Journal of Molecular Sciences. 25(2). 1248–1248. 9 indexed citations

Spagnoli, Carlotta, Stefano Giuseppe Caraffi, Daniele Frattini, et al.. (2024). Early-onset dysphagia and severe neurodevelopmental disorder as early signs in a patient with two novel variants in NARS1: a case report and brief review of the literature. Neurogenetics. 25(3). 287–291. 2 indexed citations

Spagnoli, Carlotta, et al.. (2023). A Novel Family with Demyelinating Charcot–Marie–Tooth Disease Caused by a Mutation in the PMP2 Gene: A Case Series of Nine Patients and a Brief Review of the Literature. Children. 10(5). 901–901.

Ivanovski, Ivan, Stefano Giuseppe Caraffi, Carlotta Spagnoli, et al.. (2023). Novel Insights from Clinical Practice: Xia-Gibbs Syndrome with Pes Cavus, Conjunctival Melanosis, and Eye Asymmetry due to a de novo AHDC1 Gene Variant – A Case Report and a Brief Review of the Literature. Molecular Syndromology. 15(1). 63–70. 2 indexed citations

Spagnoli, Carlotta, et al.. (2023). Pediatric-Onset Epilepsy and Developmental Epileptic Encephalopathies Followed by Early-Onset Parkinsonism. International Journal of Molecular Sciences. 24(4). 3796–3796. 3 indexed citations

Caraffi, Stefano Giuseppe, et al.. (2023). Severe Neurodevelopmental Disorder in Autosomal Recessive Spinocerebellar Ataxia 13 (SCAR13) Caused by Two Novel Frameshift Variants in GRM1. The Cerebellum. 23(5). 1768–1771. 2 indexed citations

10.

Pollazzon, Marzia, Cecilia Mancini, Simone Pizzi, et al.. (2023). Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures. Frontiers in Neurology. 14. 1207176–1207176. 3 indexed citations

11.

Spagnoli, Carlotta, Melissa Bellini, Emanuela Claudia Turco, et al.. (2023). Aromatic L-Amino-Acid Decarboxylase Deficiency Screening by Analysis of 3-O-Methyldopa in Dried Blood Spots: Results of a Multicentric Study in Neurodevelopmental Disorders. Genes. 14(9). 1828–1828.

12.

Caraffi, Stefano Giuseppe, Francesca Clementina Radio, Sabina Barresi, et al.. (2021). Adducted Thumb and Peripheral Polyneuropathy: Diagnostic Supports in Suspecting White–Sutton Syndrome: Case Report and Review of the Literature. Genes. 12(7). 950–950. 3 indexed citations

13.

Spagnoli, Carlotta, et al.. (2021). Further delineation of PIGB-related early infantile epileptic encephalopathy. European Journal of Medical Genetics. 64(10). 104268–104268. 2 indexed citations

14.

Spagnoli, Carlotta, et al.. (2020). Early-onset Dopamine Transporter Deficiency Syndrome: Long-term Follow-up. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 48(2). 285–286. 3 indexed citations

15.

Spagnoli, Carlotta, Francesco Pisani, Di Mario F, et al.. (2018). Peripheral neuropathy and gastroenterologic disorders: an overview on an underrecognized association.. PubMed. 89(9-S). 22–32. 8 indexed citations

16.

Carecchio, Miryam, Niccolò E. Mencacci, Alessandro Iodice, et al.. (2017). ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients. Parkinsonism & Related Disorders. 41. 37–43. 56 indexed citations

17.

Manara, Renzo, Raffaella Cusmai, Elena Freri, et al.. (2017). Neuroimaging Changes in Menkes Disease, Part 2. American Journal of Neuroradiology. 38(10). 1858–1865. 21 indexed citations

18.

Fusco, Carlo, Daniele Frattini, Enrico Farnetti, et al.. (2009). Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation. Brain and Development. 32(7). 592–594. 23 indexed citations

19.

Fusco, Carlo, et al.. (1999). Anomalie del corpo calloso: Polimorfismo neuroradiologico e difficoltà diagnostiche. Rivista di Neuroradiologia. 12(1). 45–48.

20.

Germani, Alfredo, Carlo Fusco, Stefano Martinotti, et al.. (1994). TPA-Induced Differentiation of Human Rhabdomyosarcoma Cells Involves Dephosphorylation and Nuclear Accumulation of Mutant p53. Biochemical and Biophysical Research Communications. 202(1). 17–24. 12 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.

Explore authors with similar magnitude of impact