C. Doriguzzi

1.2k total citations
48 papers, 991 citations indexed

About

C. Doriguzzi is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, C. Doriguzzi has authored 48 papers receiving a total of 991 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 11 papers in Cardiology and Cardiovascular Medicine and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in C. Doriguzzi's work include Muscle Physiology and Disorders (23 papers), Cardiomyopathy and Myosin Studies (10 papers) and Glycogen Storage Diseases and Myoclonus (8 papers). C. Doriguzzi is often cited by papers focused on Muscle Physiology and Disorders (23 papers), Cardiomyopathy and Myosin Studies (10 papers) and Glycogen Storage Diseases and Myoclonus (8 papers). C. Doriguzzi collaborates with scholars based in Italy, United States and Norway. C. Doriguzzi's co-authors include L. Palmucci, Tiziana Mongini, Tiziana Mongini, Loredana Chiado'-Piat, Davide Schiffer, Tommie V. McCarthy, C. R. Müller, Fergus J. Couch, Helle Ørding and Katherine E. Keating and has published in prestigious journals such as Nature Genetics, Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

C. Doriguzzi

46 papers receiving 948 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. Doriguzzi Italy 16 821 326 201 122 118 48 991
L. Palmucci Italy 18 778 0.9× 357 1.1× 237 1.2× 125 1.0× 79 0.7× 74 1.1k
Nobuyoshi Fukuhara Japan 17 693 0.8× 126 0.4× 205 1.0× 120 1.0× 261 2.2× 35 1.1k
Tania Zaglia Italy 17 816 1.0× 412 1.3× 251 1.2× 172 1.4× 95 0.8× 47 1.3k
Elisabetta Tasca Italy 15 539 0.7× 76 0.2× 195 1.0× 165 1.4× 70 0.6× 23 761
Ann E. Rossi United States 13 861 1.0× 305 0.9× 257 1.3× 291 2.4× 26 0.2× 19 1.1k
Tiziana Mongini Italy 14 399 0.5× 117 0.4× 141 0.7× 111 0.9× 23 0.2× 46 595
M. Jenkison United Kingdom 11 501 0.6× 99 0.3× 243 1.2× 125 1.0× 87 0.7× 14 672
Z Kamieniecka Denmark 15 421 0.5× 77 0.2× 199 1.0× 80 0.7× 72 0.6× 30 747
J. Bethlem Netherlands 19 721 0.9× 270 0.8× 333 1.7× 99 0.8× 112 0.9× 35 1.4k
Enrico Bugiardini Italy 20 567 0.7× 139 0.4× 439 2.2× 151 1.2× 59 0.5× 44 932

Countries citing papers authored by C. Doriguzzi

Since Specialization
Citations

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

Fields of papers citing papers by C. Doriguzzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Doriguzzi

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

All Works

20 of 20 papers shown
1.
Pradotto, Luca, et al.. (2008). Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene. Journal of the Neurological Sciences. 271(1-2). 207–210. 11 indexed citations
2.
Mongini, Tiziana, et al.. (2002). Alpha-Sarcoglycan Deficiency Featuring Exercise Intolerance and Myoglobinuria. Neuropediatrics. 33(2). 109–111. 28 indexed citations
3.
Palmucci, L., C. Doriguzzi, Tiziana Mongini, Loredana Chiado'-Piat, & I. Ugo. (1999). Unusual Clinical Expression of Dystrophinopathy in a Female, Mimicking a Congenital Myopathy. European Neurology. 42(4). 221–224. 2 indexed citations
4.
Doriguzzi, C., L. Palmucci, Tiziana Mongini, et al.. (1999). Variable histological expression of dystrophinopathy in two females. Acta Neuropathologica. 97(6). 657–660. 4 indexed citations
5.
Migheli, Antonio, Tiziana Mongini, C. Doriguzzi, et al.. (1997). Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease. Neurogenetics. 1(2). 81–87. 45 indexed citations
6.
Doriguzzi, C., L. Palmucci, Tiziana Mongini, et al.. (1997). Systematic use of dystrophin testing in muscle biopsies: results in 201 cases. European Journal of Clinical Investigation. 27(4). 352–358. 9 indexed citations
7.
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
8.
Chiado'-Piat, Loredana, Tiziana Mongini, C. Doriguzzi, Mauro Maniscalco, & L. Palmucci. (1993). Clinical Spectrum of McArdle Disease: Three Cases with Unusual Expression. European Neurology. 33(3). 208–211. 8 indexed citations
9.
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
10.
Quane, Kathleen A., Jasmine Healy, Katherine E. Keating, et al.. (1993). Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia. Nature Genetics. 5(1). 51–55. 271 indexed citations
11.
Palmucci, L., C. Doriguzzi, Tiziana Mongini, et al.. (1992). Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy. Journal of the Neurological Sciences. 111(2). 218–221. 36 indexed citations
12.
Palmucci, L., et al.. (1991). Centronuclear myopathy: clinical, morphological and genetic characters a review of 288 cases. Journal of the Neurological Sciences. 103(1). 2–9. 26 indexed citations
13.
Palmucci, L., Tiziana Mongini, C. Doriguzzi, Mauro Maniscalco, & Davide Schiffer. (1991). Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophy.. Journal of Neurology Neurosurgery & Psychiatry. 54(1). 42–45. 3 indexed citations
14.
Mongini, Tiziana, et al.. (1991). Myoglobinuria and carnitine palmityl transferase deficiency in father and son. Journal of Neurology. 238(6). 323–324. 7 indexed citations
15.
Doriguzzi, C., L. Palmucci, Bianca Pollo, et al.. (1990). Cytochromec oxidase and coenzyme Q in neuromuscular diseases: a histochemical study. Acta Neuropathologica. 81(1). 25–29. 7 indexed citations
16.
Doriguzzi, C., L. Palmucci, Tiziana Mongini, et al.. (1989). Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.. Journal of Neurology Neurosurgery & Psychiatry. 52(1). 122–125. 12 indexed citations
17.
Doriguzzi, C., L. Palmucci, & W. Troni. (1982). Isolated accessory nerve palsy. Case report. Neurological Sciences. 3(2). 135–138. 2 indexed citations
18.
Palmucci, L., et al.. (1981). Myoglobinuria: presentation of personal cases and review of the literature. Neurological Sciences. 2(3). 275–281. 3 indexed citations
19.
Bertolotto, Antonio, Mario Marchi, C. Doriguzzi, et al.. (1981). Epidemiology of Duchenne muscular dystrophy in the province of Turin. The Italian Journal of Neurological Sciences. 2(1). 81–84. 7 indexed citations
20.
Palmucci, L., et al.. (1978). Fisher syndrome. Presentation of a clinical case.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 33(3). 270–2. 3 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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