Giuseppe De Michele

16.6k total citations · 1 hit paper
208 papers, 6.8k citations indexed

About

Giuseppe De Michele is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Giuseppe De Michele has authored 208 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 134 papers in Cellular and Molecular Neuroscience, 107 papers in Neurology and 78 papers in Molecular Biology. Recurrent topics in Giuseppe De Michele's work include Genetic Neurodegenerative Diseases (110 papers), Parkinson's Disease Mechanisms and Treatments (70 papers) and Mitochondrial Function and Pathology (62 papers). Giuseppe De Michele is often cited by papers focused on Genetic Neurodegenerative Diseases (110 papers), Parkinson's Disease Mechanisms and Treatments (70 papers) and Mitochondrial Function and Pathology (62 papers). Giuseppe De Michele collaborates with scholars based in Italy, United Kingdom and France. Giuseppe De Michele's co-authors include Alessandro Filla, Sergio Cocozza, G Campanella, Paolo Barone, Anna De Rosa, Francesca Cavalcanti, Antonella Monticelli, Elena Salvatore, Maria Teresa Pellecchia and Lucio Santoro and has published in prestigious journals such as Cell, PLoS ONE and NeuroImage.

In The Last Decade

Giuseppe De Michele

207 papers receiving 6.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease

1998 586 citations Giuseppe De Michele, Alessandro Filla et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Giuseppe De Michele Italy	43	3.9k	3.2k	3.0k	1.2k	537	208	6.8k
Alessandro Filla Italy	37	3.7k 1.0×	2.2k 0.7×	3.2k 1.1×	1.1k 0.9×	471 0.9×	155	5.7k
Ferdinando Squitieri Italy	49	6.4k 1.7×	5.4k 1.7×	5.7k 1.9×	1.0k 0.8×	549 1.0×	177	10.2k
Susanne A. Schneider Germany	47	2.4k 0.6×	3.9k 1.2×	2.0k 0.7×	2.2k 1.7×	380 0.7×	164	7.0k
Yaping Chu United States	39	4.1k 1.1×	4.1k 1.3×	2.8k 0.9×	1.2k 1.0×	440 0.8×	70	8.2k
Jean‐Christophe Corvol France	43	2.6k 0.7×	2.6k 0.8×	2.2k 0.7×	692 0.6×	381 0.7×	161	6.5k
Jochen H. Weishaupt Germany	48	1.8k 0.5×	3.2k 1.0×	3.0k 1.0×	1.4k 1.1×	449 0.8×	146	6.9k
Ralph W. Kuncl United States	37	5.7k 1.5×	3.8k 1.2×	3.9k 1.3×	1.5k 1.2×	347 0.6×	83	10.4k
Georg Auburger Germany	53	6.1k 1.6×	4.4k 1.4×	6.5k 2.2×	1.0k 0.8×	707 1.3×	194	11.1k
Edward J. Wild United Kingdom	39	4.4k 1.1×	2.5k 0.8×	3.8k 1.3×	465 0.4×	300 0.6×	111	6.3k
Sheng‐Han Kuo United States	37	2.3k 0.6×	2.6k 0.8×	1.6k 0.5×	653 0.5×	560 1.0×	163	5.4k

Countries citing papers authored by Giuseppe De Michele

Since Specialization

Citations

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

Fields of papers citing papers by Giuseppe De Michele

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Giuseppe De Michele. 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 Giuseppe De Michele. The network helps show where Giuseppe De Michele may publish in the future.

Co-authorship network of co-authors of Giuseppe De Michele

This figure shows the co-authorship network connecting the top 25 collaborators of Giuseppe De Michele. A scholar is included among the top collaborators of Giuseppe De Michele 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 Giuseppe De Michele. Giuseppe De Michele 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

Michele, Giovanna De, Luigi Maione, Sirio Cocozza, et al.. (2023). Ataxia and Hypogonadism: a Review of the Associated Genes and Syndromes. The Cerebellum. 23(2). 688–701. 1 indexed citations

Torella, Annalaura, Ivana Ricca, Giulio Piluso, et al.. (2023). A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A. Journal of Neurology. 270(10). 5057–5063. 4 indexed citations

Dubbioso, Raffaele, Vincenzo Provitera, Annamaria Stancanelli, et al.. (2021). Cutaneous sensory and autonomic denervation in progressive supranuclear palsy. Neuropathology and Applied Neurobiology. 47(5). 653–663. 13 indexed citations

Petracca, Martina, Anna Rita Bentivoglio, Serenella Servidei, et al.. (2021). Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement. Genes. 12(3). 344–344. 7 indexed citations

Assante, Roberta, Elena Salvatore, Carmela Nappi, et al.. (2020). Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington’s disease. Journal of Nuclear Cardiology. 29(2). 642–648. 7 indexed citations

Michele, Giovanna De, Giovanna De Michele, Maria Lieto, et al.. (2019). Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families. Parkinsonism & Related Disorders. 65. 91–96. 38 indexed citations

Severino, Mariasavina, Susanna Lualdi, Chiara Fiorillo, et al.. (2018). Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations. Journal of Neurology. 265(6). 1419–1425. 8 indexed citations

Salvatore, Elena, Alessandro Filla, Sirio Cocozza, et al.. (2016). Functional MRI signal fluctuations highlight altered resting brain activity in Huntington’s disease. Brain Imaging and Behavior. 11(5). 1459–1469. 13 indexed citations

Saccà, Francesco, Angela Marsili, Giorgia Puorro, et al.. (2012). Clinical use of frataxin measurement in a patient with a novel deletion in the FXN gene. Journal of Neurology. 260(4). 1116–1121. 24 indexed citations

10.

Pappatà, Sabina, Gabriella Santangelo, Dag Aarsland, et al.. (2011). Mild cognitive impairment in drug-naive patients with PD is associated with cerebral hypometabolism. Neurology. 77(14). 1357–1362. 71 indexed citations

11.

Saccà, Francesco, Giuseppe De Michele, Fabio Acquaviva, et al.. (2010). Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit. Movement Disorders. 26(4). 739–742. 38 indexed citations

12.

Ibáñez, Pablo, Suzanne Lesage, Ebba Lohmann, et al.. (2006). Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain. 129(3). 686–694. 123 indexed citations

13.

Patrono, Clarice, Valentina Scarano, Mariarosa Anna Beatrice Melone, et al.. (2005). Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis ofSPG4 reveals eleven novel mutations. Human Mutation. 25(5). 506–506. 30 indexed citations

14.

Coppola, Giovanni, Giuseppe De Michele, Francesca Cavalcanti, et al.. (1999). Why do some Friedreich's ataxia patients retain tendon reflexes?. Journal of Neurology. 246(5). 353–357. 24 indexed citations

15.

Farrer, Matthew J., et al.. (1999). Further evidence for a chromosome 4p haplotype segregating with Parkinson's disease in an independent Italian kindred.. UCL Discovery (University College London). 1 indexed citations

16.

Filla, Alessandro, Giuseppe De Michele, Lucio Santoro, et al.. (1999). Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families. Journal of Neurology. 246(6). 467–471. 48 indexed citations

17.

Michele, Giuseppe De, Pier Paolo Mainenti, Andrea Soricelli, et al.. (1998). Cerebral blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients. Journal of Neurology. 245(9). 603–608. 17 indexed citations

18.

Cocozza, Sergio, A. Antonelli, G Campanella, et al.. (1993). Evidence of a genetic marker associated with early onset in Friedreich's ataxia. Journal of Neurology. 240(4). 254–256. 2 indexed citations

19.

Sinisi, Leonardo, et al.. (1993). Hindbrain hernia headache and syncope in type I Arnold-Chiari malformation.. PubMed. 15(6). 457–61. 5 indexed citations

20.

Santoro, Lucio, A. Perretti, Alessandro Filla, et al.. (1992). Is early onset cerebellar ataxia with retained tendon reflexes identifiable by electrophysiologic and histologic profile?. Journal of the Neurological Sciences. 113(1). 43–49. 9 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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