Alessandro Malandrini

1.2k total citations
48 papers, 734 citations indexed

About

Alessandro Malandrini is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Alessandro Malandrini has authored 48 papers receiving a total of 734 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 19 papers in Cellular and Molecular Neuroscience and 10 papers in Cell Biology. Recurrent topics in Alessandro Malandrini's work include Hereditary Neurological Disorders (14 papers), Mitochondrial Function and Pathology (10 papers) and Neurological diseases and metabolism (8 papers). Alessandro Malandrini is often cited by papers focused on Hereditary Neurological Disorders (14 papers), Mitochondrial Function and Pathology (10 papers) and Neurological diseases and metabolism (8 papers). Alessandro Malandrini collaborates with scholars based in Italy, Belgium and United States. Alessandro Malandrini's co-authors include Antonio Federico, Marcello Villanova, Silvia Palmeri, Gianna Berti, Maria Teresa Dotti, Filippo M. Santorelli, Enrico Bertini, Alessandra Renieri, Carla Battisti and Fiorella Piemonte and has published in prestigious journals such as Neurology, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Alessandro Malandrini

46 papers receiving 717 citations

Peers

Alessandro Malandrini
Sonia Ciarmatori Germany
Ginat Narkis Israel
Laura Davis Keppen United States
Hanna Mierzewska Poland
Xinghua Luan China
Kenji Nanao Japan
Sebahattin Çırak Germany
Stephan Niemann Germany
Tada-aki Hori Japan
Chiara Aiello Italy
Sonia Ciarmatori Germany
Alessandro Malandrini
Citations per year, relative to Alessandro Malandrini Alessandro Malandrini (= 1×) peers Sonia Ciarmatori

Countries citing papers authored by Alessandro Malandrini

Since Specialization
Citations

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

Fields of papers citing papers by Alessandro Malandrini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessandro Malandrini

This figure shows the co-authorship network connecting the top 25 collaborators of Alessandro Malandrini. A scholar is included among the top collaborators of Alessandro Malandrini 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 Alessandro Malandrini. Alessandro Malandrini 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.
Lopergolo, Diego, Gian Nicola Gallus, Giuseppe Pieraccini, et al.. (2024). CCDC78: Unveiling the Function of a Novel Gene Associated with Hereditary Myopathy. Cells. 13(17). 1504–1504. 1 indexed citations
2.
Gallus, Gian Nicola, Silvia Bianchi, Simona Salvatore, et al.. (2024). Novel Biomarkers for Limb Girdle Muscular Dystrophy (LGMD). Cells. 13(4). 329–329. 2 indexed citations
3.
Lopergolo, Diego, Gianna Berti, Francesca Mari, et al.. (2022). A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis. Neurological Sciences. 43(4). 2849–2852.
4.
Malfatti, Edoardo, Elena Cardaioli, Carla Battisti, et al.. (2010). A novel point mutation in the mitochondrial tRNA(Trp) gene produces late-onset encephalomyopathy, plus additional features. Journal of the Neurological Sciences. 297(1-2). 105–108. 9 indexed citations
5.
Cardaioli, Elena, Paola Da Pozzo, Edoardo Malfatti, et al.. (2010). A second MNGIE patient without typical mitochondrial skeletal muscle involvement. Neurological Sciences. 31(4). 491–494. 16 indexed citations
6.
Dotti, Maria Teresa, et al.. (2006). A new missense mutation in caveolin-3 gene causes rippling muscle disease. Journal of the Neurological Sciences. 243(1-2). 61–64. 6 indexed citations
7.
Cardaioli, Elena, Paola Da Pozzo, Alfonso Cerase, et al.. (2005). Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNAser(UCN) gene. Neuromuscular Disorders. 16(1). 26–31. 14 indexed citations
8.
Malandrini, Alessandro, et al.. (2004). A syndrome of bilateral hemorrhage of the thalamus and myocarditis with fatal course. Journal of Clinical Forensic Medicine. 11(4). 208–210. 2 indexed citations
9.
Gambelli, S., Alessandro Malandrini, Federica Ginanneschi, et al.. (2004). Mitochondrial Abnormalities in Genetically Assessed Oculopharyngeal Muscular Dystrophy. European Neurology. 51(3). 144–147. 15 indexed citations
10.
Gambelli, S., Federica Ginanneschi, Alessandro Malandrini, et al.. (2004). Antibodies to dorsal root ganglia and olfactory cells in a patient with chronic sensory neuropathy and anosmia. Journal of the Neurological Sciences. 221(1-2). 105–108. 1 indexed citations
11.
Verhoeven, Kristien, Marcello Villanova, Alessandro Rossi, et al.. (2001). Localization of the Gene for the Intermediate Form of Charcot-Marie-Tooth to Chromosome 10q24.1-q25.1. The American Journal of Human Genetics. 69(4). 889–894. 42 indexed citations
12.
Santoro, Lucio, Rosalba Carrozzo, Alessandro Malandrini, et al.. (2000). A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency. Neuromuscular Disorders. 10(6). 450–453. 33 indexed citations
13.
14.
Malandrini, Alessandro, Marcello Villanova, Sergio Tripodi, et al.. (1998). Neuronal intranuclear inclusion disease: neuropathologic study of a case. Brain and Development. 20(5). 290–294. 11 indexed citations
15.
Malandrini, Alessandro, Lucia Galli, Marcello Villanova, et al.. (1998). CAG Repeat Expansion in an Italian Family with Spinocerebellar Ataxia Type 2 (SCA2): A Clinical and Genetic Study. European Neurology. 40(3). 164–168. 14 indexed citations
16.
17.
Malandrini, Alessandro, Maria Teresa Dotti, & Antonio Federico. (1997). Selective ipsilateral neuromuscular involvement in a case of facial and somatic hemiatrophy. Muscle & Nerve. 20(7). 890–892. 13 indexed citations
18.
Squarzoni, Stefano, Marcello Villanova, Patrizia Sabatelli, et al.. (1997). Intracellular detection of laminin α2 chain in skin by electron microscopy immunocytochemistry: Comparison between normal and laminin α2 chain deficient subjects. Neuromuscular Disorders. 7(2). 91–98. 12 indexed citations
19.
Palmeri, Silvia, Alessandro Malandrini, G. Ciacci, et al.. (1994). Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: A variant of Kohlschütter‐Tönz syndrome?. American Journal of Medical Genetics. 50(1). 79–83. 10 indexed citations
20.
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

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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