Alessandro Malandrini

4.1k total citations
95 papers, 2.2k citations indexed

About

Alessandro Malandrini is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Alessandro Malandrini has authored 95 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 24 papers in Cellular and Molecular Neuroscience and 23 papers in Neurology. Recurrent topics in Alessandro Malandrini's work include Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (13 papers) and Neurological diseases and metabolism (12 papers). Alessandro Malandrini is often cited by papers focused on Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (13 papers) and Neurological diseases and metabolism (12 papers). Alessandro Malandrini collaborates with scholars based in Italy, United States and United Kingdom. Alessandro Malandrini's co-authors include Antonio Federico, Maria Teresa Dotti, Marcello Villanova, Silvia Palmeri, Nicola De Stefano, Carla Battisti, Anthony P. Monaco, Justin P. Rubio, Adrian Danek and Elena Cardaioli and has published in prestigious journals such as Nature Genetics, Brain and Neurology.

In The Last Decade

Alessandro Malandrini

91 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alessandro Malandrini Italy 26 973 591 577 546 287 95 2.2k
Keisuke Mori Japan 35 1.6k 1.6× 282 0.5× 482 0.8× 151 0.3× 315 1.1× 133 3.8k
Eiichiro Uyama Japan 24 757 0.8× 366 0.6× 499 0.9× 139 0.3× 364 1.3× 85 1.8k
A E Harding United Kingdom 31 1.7k 1.7× 1.3k 2.2× 791 1.4× 468 0.9× 150 0.5× 61 3.1k
Gian Maria Fabrizi Italy 22 686 0.7× 891 1.5× 540 0.9× 313 0.6× 190 0.7× 88 1.6k
Julia Wanschitz Austria 26 741 0.8× 594 1.0× 715 1.2× 321 0.6× 204 0.7× 78 1.9k
Yoshihisa Takiyama Japan 30 1.7k 1.8× 1.6k 2.8× 693 1.2× 524 1.0× 98 0.3× 139 2.4k
Ettore Salsano Italy 22 638 0.7× 426 0.7× 535 0.9× 322 0.6× 187 0.7× 72 1.6k
E Satoyoshi Japan 27 1.0k 1.0× 896 1.5× 777 1.3× 141 0.3× 297 1.0× 104 2.6k
O. Dubourg France 33 985 1.0× 910 1.5× 668 1.2× 293 0.5× 411 1.4× 70 3.0k
Ayal Ben‐Zvi Israel 20 857 0.9× 388 0.7× 190 0.3× 879 1.6× 282 1.0× 31 2.2k

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.
2.
Castiglioni, Claudia, Fabiana Fattori, Bjarne Udd, et al.. (2018). Neuromyopathy with congenital cataracts and glaucoma: a distinct syndrome caused by POLG variants. European Journal of Human Genetics. 26(3). 367–373. 2 indexed citations
3.
Denora, Paola S., Katrien Smets, Carlo Casali, et al.. (2016). Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions. Brain. 139(Pt 6). aww061–aww061. 49 indexed citations
4.
Rubegni, Anna, Elena Cardaioli, Paola Da Pozzo, et al.. (2014). A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia. Journal of the Neurological Sciences. 338(1-2). 232–234. 3 indexed citations
5.
Vinciguerra, Claudia, Alessandra Rufa, Silvia Bianchi, et al.. (2013). Homozygosity and severity of phenotypic presentation in a CADASIL family. Neurological Sciences. 35(1). 91–93. 17 indexed citations
6.
Cardaioli, Elena, Edoardo Malfatti, Carla Battisti, et al.. (2012). Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutation. Journal of the Neurological Sciences. 321(1-2). 92–95. 5 indexed citations
7.
Kruer, Michael C., Allison Gregory, Alessandro Malandrini, et al.. (2011). Novel histopathologic findings in molecularly-confirmed pantothenate kinase-associated neurodegeneration. Brain. 134(4). 947–958. 99 indexed citations
8.
Malandrini, Alessandro, et al.. (2010). Transient “sicca syndrome” during phenobarbital treatment. Journal of the Neurological Sciences. 300(1-2). 164–164. 9 indexed citations
9.
Buccoliero, Rosaria, Silvia Palmeri, Alessandro Malandrini, Maria Teresa Dotti, & Antonio Federico. (2007). A case of dystonia with onset during pregnancy. Journal of the Neurological Sciences. 260(1-2). 265–266. 7 indexed citations
10.
Cardaioli, Elena, Paola Da Pozzo, Gian Nicola Gallus, et al.. (2007). A novel heteroplasmic tRNASer(UCN) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss. Neuromuscular Disorders. 17(9-10). 681–683. 16 indexed citations
11.
Buccoliero, Rosaria, S. Gambelli, Francesco Sicurelli, et al.. (2006). Leukoencephalopathy as a rare complication of hepatitis C infection. Neurological Sciences. 27(5). 360–363. 12 indexed citations
12.
Sicurelli, Francesco, Maria Teresa Dotti, Nicola De Stefano, et al.. (2005). Peripheral neuropathy in CADASIL. Journal of Neurology. 252(10). 1206–1209. 19 indexed citations
13.
Zannolli, Raffaella, Sabrina Buoni, Clelia Miracco, et al.. (2004). Hypertelorism, ptosis, and myopia associated with drug‐resistant epilepsy, mental delay, growth deficiency, ectodermal defects, and osteopenia. American Journal of Medical Genetics Part A. 127A(2). 212–216. 4 indexed citations
14.
Rampoldi, Luca, Carol Dobson‐Stone, Justin P. Rubio, et al.. (2001). A conserved sorting-associated protein is mutant in chorea-acanthocytosis. Nature Genetics. 28(2). 119–120. 223 indexed citations
15.
Battisti, Carla, et al.. (1998). Schnyder corneal crystalline dystrophy: Description of a new family with evidence of abnormal lipid storage in skin fibroblasts. American Journal of Medical Genetics. 75(1). 35–39. 36 indexed citations
16.
Villanova, Marcello, C. Sewry, Alessandro Malandrini, et al.. (1997). Immunolocalization of several laminin chains in the normal human central and peripheral nervous system.. PubMed. 29(3). 409–13. 13 indexed citations
17.
Navenot, Jean‐Marc, et al.. (1997). Expression of CD59, a regulator of the membrane attack complex of complement, on human skeletal muscle fibers. Muscle & Nerve. 20(1). 92–96. 28 indexed citations
18.
Villanova, Marcello, Alessandro Malandrini, Patrizia Sabatelli, et al.. (1997). Localization of laminin α2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study. Acta Neuropathologica. 94(6). 567–571. 31 indexed citations
19.
Rubio, Justin P., Adrian Danek, Caroline Stone, et al.. (1997). Chorea-Acanthocytosis: Genetic Linkage to Chromosome 9q21. The American Journal of Human Genetics. 61(4). 899–908. 54 indexed citations
20.
Malandrini, Alessandro, Silvia Palmeri, Gian Maria Fabrizi, et al.. (1996). Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities. Journal of the Neurological Sciences. 140(1-2). 129–131. 17 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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