M. T. Dotti

1.3k total citations
38 papers, 583 citations indexed

About

M. T. Dotti is a scholar working on Molecular Biology, Neurology and Rheumatology. According to data from OpenAlex, M. T. Dotti has authored 38 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Neurology and 9 papers in Rheumatology. Recurrent topics in M. T. Dotti's work include Mitochondrial Function and Pathology (8 papers), Cerebrovascular and genetic disorders (7 papers) and Metabolism and Genetic Disorders (6 papers). M. T. Dotti is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), Cerebrovascular and genetic disorders (7 papers) and Metabolism and Genetic Disorders (6 papers). M. T. Dotti collaborates with scholars based in Italy, United States and Canada. M. T. Dotti's co-authors include Antonio Federico, Silvia Bianchi, Alessandro Malandrini, G. C. Guazzi, Alessandra Rufa, Chiara Rengo, Maria Lucia Valentino, Anna Ghelli, Agostino Baruzzi and Alessandra Lugaresi and has published in prestigious journals such as Neurology, Annals of Neurology and Gut.

In The Last Decade

M. T. Dotti

36 papers receiving 562 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. T. Dotti Italy 13 309 153 123 82 80 38 583
Marwan Nashabat Saudi Arabia 13 229 0.7× 53 0.3× 130 1.1× 16 0.2× 66 0.8× 25 422
Cathy E. Woodward United Kingdom 13 420 1.4× 65 0.4× 259 2.1× 33 0.4× 20 0.3× 20 566
Bhim Singhal India 14 236 0.8× 147 1.0× 17 0.1× 42 0.5× 45 0.6× 21 506
M G Sweeney United Kingdom 18 1.0k 3.4× 128 0.8× 577 4.7× 68 0.8× 27 0.3× 21 1.2k
Gert Van Goethem Belgium 12 1.0k 3.3× 73 0.5× 649 5.3× 63 0.8× 34 0.4× 13 1.2k
Takashi Kurashige Japan 15 260 0.8× 194 1.3× 19 0.2× 63 0.8× 41 0.5× 58 593
Claudio Bruno Italy 20 833 2.7× 66 0.4× 314 2.6× 33 0.4× 246 3.1× 30 1.3k
Emanuela Bottani Italy 14 585 1.9× 43 0.3× 247 2.0× 25 0.3× 14 0.2× 25 810
Mahmoud Y. Issa Egypt 15 258 0.8× 28 0.2× 20 0.2× 19 0.2× 41 0.5× 45 482
Zhiying Xie China 14 282 0.9× 155 1.0× 22 0.2× 57 0.7× 23 0.3× 61 550

Countries citing papers authored by M. T. Dotti

Since Specialization
Citations

This map shows the geographic impact of M. T. Dotti'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 M. T. Dotti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. T. Dotti more than expected).

Fields of papers citing papers by M. T. Dotti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. T. Dotti. 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 M. T. Dotti. The network helps show where M. T. Dotti may publish in the future.

Co-authorship network of co-authors of M. T. Dotti

This figure shows the co-authorship network connecting the top 25 collaborators of M. T. Dotti. A scholar is included among the top collaborators of M. T. Dotti 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 M. T. Dotti. M. T. Dotti 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.
Donato, Ilaria Di, et al.. (2014). Adult-Onset Genetic Leukoencephalopathies. Focus on the More Recently Defined Forms. Current Molecular Medicine. 14(8). 944–958. 5 indexed citations
2.
Formichi, Patrizia, Lucilla Parnetti, Elena Radi, et al.. (2008). CSF levels of β‐amyloid 1‐42, tau and phosphorylated tau protein in CADASIL. European Journal of Neurology. 15(11). 1252–1255. 16 indexed citations
3.
Rufa, Alessandra, Alfonso Cerase, Lucia Monti, et al.. (2008). Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Journal of the Neurological Sciences. 271(1-2). 211–213. 9 indexed citations
4.
Gallus, Gian Nicola, Angelo Schenone, Alessandra Rufa, et al.. (2008). THE FIRST CEREBROTENDINOUS XANTHOMATOSIS FAMILY FROM ARGENTINA: A NEW MUTATION IN CYP27A1 GENE. Neurology. 70(5). 402–404. 12 indexed citations
5.
Battisti, Carla, Frank Forte, Silvia Funghini, et al.. (2007). A new case of short-chain acyl-CoA dehydrogenase deficiency: clinical, biochemical, genetic and 1H-NMR spectroscopic studies. Neurological Sciences. 28(6). 328–330. 6 indexed citations
6.
Pescini, Francesca, Cristina Sarti, Leonardo Pantoni, et al.. (2005). Cerebellar arteriovenous malformation and vertebral artery aneurysm in a CADASIL patient. Acta Neurologica Scandinavica. 113(1). 62–63. 6 indexed citations
7.
Rufa, Alessandra, et al.. (2005). Typical pathological changes of CADASIL in the optic nerve. Neurological Sciences. 26(4). 271–274. 15 indexed citations
8.
Federico, Antonio, Silvia Bianchi, & M. T. Dotti. (2005). The spectrum of mutations for CADASIL diagnosis. Neurological Sciences. 26(2). 117–124. 69 indexed citations
9.
Valentino, Maria Lucia, Piero Barboni, Anna Ghelli, et al.. (2004). The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy. Annals of Neurology. 56(5). 631–641. 93 indexed citations
10.
Pantoni, Leonardo, Cristina Sarti, Francesca Pescini, et al.. (2004). Thrombophilic risk factors and unusual clinical features in three Italian CADASIL patients. European Journal of Neurology. 11(11). 782–787. 15 indexed citations
11.
Bruno, Claudio, Enrico Bertini, Antonio Federico, et al.. (2004). Clinical and molecular findings in patients with giant axonal neuropathy (GAN). Neurology. 62(1). 13–16. 47 indexed citations
12.
Battisti, Carla, María Clara Bonaglia, Sabrina Giglio, et al.. (2003). De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalities. American Journal of Medical Genetics Part A. 117A(3). 207–211. 8 indexed citations
13.
Stefano, Nicola De, Sridar Narayanan, Paul M. Matthews, et al.. (2000). Proton MR spectroscopy to assess axonal damage in multiple sclerosis and other white matter disorders.. PubMed. 6 Suppl 2. S121–9. 17 indexed citations
14.
Battisti, Carla, Georgios Loudianos, Alessandra Rufa, et al.. (1999). Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency. American Journal of Medical Genetics. 85(2). 175–178. 2 indexed citations
15.
Villanova, Marcello, C. Ceuterick, M. T. Dotti, et al.. (1999). Detection of β-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren). Acta Neuropathologica. 98(1). 78–84. 3 indexed citations
16.
Macucci, Marco, M. T. Dotti, Stefania Battistini, et al.. (1994). Primary antiphospholipid syndrome: two case reports, one with histological examination of skin, peripheral nerve and muscle.. PubMed. 16(3). 87–96. 5 indexed citations
17.
Dotti, M. T., A. M. Bardelli, Nicola De Stefano, et al.. (1993). Optic Atrophy in Marinesco-Sjögren Syndrome: An Additional Ocular Feature: Report of three Cases in two Families. Ophthalmic Paediatrics and Genetics. 14(1). 5–7. 13 indexed citations
18.
Federico, Antonio, M. T. Dotti, Gian Maria Fabrizi, et al.. (1990). Congenital Lactic Acidosis due to a Defect of Pyruvate Dehydrogenase Complex (E<sub>1</sub>). European Neurology. 30(3). 123–127. 7 indexed citations
19.
Palmeri, Silvia, et al.. (1989). Macrosomia and mental retardation: Evidence of autosomal dominant inheritance in four generations. American Journal of Medical Genetics. 32(1). 67–71. 7 indexed citations
20.
Dotti, M. T., Alessandro Rossi, N. Rizzuto, et al.. (1985). Atypical Phenotype of Refsum’s Disease: Clinical, Biochemical, Neurophysiological and Pathological Study. European Neurology. 24(2). 85–93. 8 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

Breakdown of academic impact, for papers by Marwan Nashabat Breakdown of academic impact, for papers by Cathy E. Woodward Breakdown of academic impact, for papers by Bhim Singhal Breakdown of academic impact, for papers by M G Sweeney Breakdown of academic impact, for papers by Gert Van Goethem Breakdown of academic impact, for papers by Takashi Kurashige Breakdown of academic impact, for papers by Claudio Bruno Breakdown of academic impact, for papers by Emanuela Bottani Breakdown of academic impact, for papers by Mahmoud Y. Issa Breakdown of academic impact, for papers by Zhiying Xie
Rankless by CCL
2026