Carlo Casali

4.4k total citations
98 papers, 2.8k citations indexed

About

Carlo Casali is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Carlo Casali has authored 98 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 41 papers in Cellular and Molecular Neuroscience and 28 papers in Neurology. Recurrent topics in Carlo Casali's work include Mitochondrial Function and Pathology (37 papers), Genetic Neurodegenerative Diseases (31 papers) and Metabolism and Genetic Disorders (13 papers). Carlo Casali is often cited by papers focused on Mitochondrial Function and Pathology (37 papers), Genetic Neurodegenerative Diseases (31 papers) and Metabolism and Genetic Disorders (13 papers). Carlo Casali collaborates with scholars based in Italy, United States and United Kingdom. Carlo Casali's co-authors include Filippo M. Santorelli, Francesco Pierelli, Mariano Serrao, Alberto Ranavolo, Francesco Draicchio, S. DiMauro, Rosalba Carrozzo, Enrico Bertini, Michio Hirano and Christian Marcotulli and has published in prestigious journals such as Blood, Journal of the American College of Cardiology and PLoS ONE.

In The Last Decade

Carlo Casali

95 papers receiving 2.7k citations

Peers

Carlo Casali

CMN

NEURO

D J Dick United Kingdom

M. Ben Hamida Tunisia

Takao Yasuhara Japan

Alessandro Filla Italy

Yvonne Weber Germany

Sylvia Boesch Austria

S. H. Subramony United States

Graham Lennox United Kingdom

Hajime Tanaka Japan

Xinxiang Yan China

D J Dick United Kingdom

Carlo Casali

865 ×0.6

590 ×0.6

CMN

699 ×1.2

NEURO

210 ×0.4

131 ×0.3

NEURO

Citations per year, relative to Carlo Casali Carlo Casali (= 1×) peers D J Dick

Countries citing papers authored by Carlo Casali

Since Specialization

Citations

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

Fields of papers citing papers by Carlo Casali

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carlo Casali

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

Cioffi, Ettore, Alessandra Tessa, Antonio Petrucci, et al.. (2024). Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 variants in a series of Italian patients, shedding light upon genetic and phenotypic variability. Neurological Sciences. 45(8). 3845–3852.

Travaglini, Lorena, Vito Luigi Colona, Carlo Casali, et al.. (2024). De Novo GRID2 Variant as a Cause of Ataxia with Oculomotor Apraxia and Alpha-Fetoprotein Elevation. The Cerebellum. 23(6). 2408–2413.

Galatolo, Daniele, Rosanna Trovato, Salvatore Rossi, et al.. (2023). Power of NGS-based tests in HSP diagnosis: analysis of massively parallel sequencing in clinical practice. Neurogenetics. 24(3). 147–160. 3 indexed citations

Luigetti, Marco, Valeria Guglielmino, Giovanni Antonini, et al.. (2021). ATTRv in Lazio-Italy: A High-Prevalence Region in a Non-Endemic Country. Genes. 12(6). 829–829. 14 indexed citations

Marcotulli, Christian, et al.. (2019). 15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias. Journal of Neurology. 266(7). 1611–1622. 13 indexed citations

Vanacore, Nicola, Emanuele Rastelli, Giovanni Antonini, et al.. (2016). An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy. Neuroepidemiology. 46(3). 191–197. 32 indexed citations

Mignarri, Andrea, Alessandra Tessa, Alessandra Rufa, et al.. (2013). Cerebellum and neuropsychiatric disorders: insights from ARSACS. Neurological Sciences. 35(1). 95–97. 20 indexed citations

Serrao, Mariano, Francesco Pierelli, Alberto Ranavolo, et al.. (2011). Gait Pattern in Inherited Cerebellar Ataxias. The Cerebellum. 11(1). 194–211. 105 indexed citations

Fabio, Roberto Di, et al.. (2010). Hydroxyzine Hydrochloride in Familial Restless Legs Syndrome. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 37(3). 406–407. 2 indexed citations

10.

Guerini, Fabio, Ettore Beghi, Giulio Riboldazzi, et al.. (2009). BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson’s disease. European Journal of Neurology. 16(11). 1240–1245. 63 indexed citations

11.

Lorenzo, Cherubino Di, Giorgio Di Lorenzo, Grazia Sances, et al.. (2009). Drug consumption in medication overuse headache is influenced by brain-derived neurotrophic factor Val66Met polymorphism. The Journal of Headache and Pain. 10(5). 349–355. 51 indexed citations

12.

Santorelli, Filippo M., Roberto De Masi, Fabiana Fattori, et al.. (2009). Clinical and audiological follow up of a family with the 8363G > A mutation in the mitochondrial DNA. Neuromuscular Disorders. 19(4). 291–296. 2 indexed citations

13.

Campagna, Filomena, Luisa Nanni, Fabiana Quagliarini, et al.. (2008). Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathy. Biochemical and Biophysical Research Communications. 377(3). 843–846. 48 indexed citations

14.

Lorenzo, Cherubino Di, Chiara Rengo, Alessio Cardinale, et al.. (2007). Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I–II loop. Journal of the Neurological Sciences. 254(1-2). 69–71. 21 indexed citations

15.

Criscuolo, Chiara, Luchino Chessa, P Mancini, et al.. (2006). Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.. Neurourology and Urodynamics. 66(8). 1207–1210. 3 indexed citations

16.

Piemonte, Fiorella, Carlo Casali, Rosalba Carrozzo, et al.. (2001). Respiratory chain defects in hereditary spastic paraplegias. Neuromuscular Disorders. 11(6-7). 565–569. 15 indexed citations

17.

Vilà, Maya R., Josep Gámez, Abelardo Solano, et al.. (2000). Uncoupling Protein-1 mRNA Expression in Lipomas from Patients Bearing Pathogenic Mitochondrial DNA Mutations. Biochemical and Biophysical Research Communications. 278(3). 800–802. 26 indexed citations

18.

Casali, Carlo, Giancarlo Di Gennaro, Alfredo Costa, et al.. (1999). The mitochondrial A3243G mutation in maternally inherited migraine without aura.. UCL Discovery (University College London). 1 indexed citations

19.

Casali, Carlo, Giulia d’Amati, Luciano De Biase, et al.. (1999). Maternally inherited cardiomyopathy: clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid. Journal of the American College of Cardiology. 33(6). 1584–1589. 22 indexed citations

20.

Wuyts, Wim, Giancarlo Di Gennaro, Federico Bianco, et al.. (1999). Molecular and clinical examination of an Italian DEFECT 11 family. European Journal of Human Genetics. 7(5). 579–584. 22 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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