Ettore Salsano

3.0k total citations · 1 hit paper
72 papers, 1.6k citations indexed

About

Ettore Salsano is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Ettore Salsano has authored 72 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 18 papers in Neurology and 17 papers in Physiology. Recurrent topics in Ettore Salsano's work include RNA regulation and disease (17 papers), Hereditary Neurological Disorders (12 papers) and Mitochondrial Function and Pathology (10 papers). Ettore Salsano is often cited by papers focused on RNA regulation and disease (17 papers), Hereditary Neurological Disorders (12 papers) and Mitochondrial Function and Pathology (10 papers). Ettore Salsano collaborates with scholars based in Italy, United States and United Kingdom. Ettore Salsano's co-authors include Davide Pareyson, Letterio S. Politi, Marco Grimaldi, Giuseppe Piscosquito, Massimo Zeviani, Isabella Moroni, Bianca Pollo, Gaetano Finocchiaro, Eleonora Lamantea and Marica Eoli and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Ettore Salsano

67 papers receiving 1.5k 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.

Magnetic Resonance Imaging Alteration of the Brain in a Patient With Coronavirus Disease 2019 (COVID-19) and Anosmia

2020 280 citations Letterio S. Politi, Ettore Salsano et al. profile →

Peers

Ettore Salsano

NEURO

CMN

NEURO

GENET

Pedro Mancías United States

Teresa Sevilla Spain

Chen Zhang China

Alessandro Malandrini Italy

Arne Wrede Germany

Isabella Wimmer Austria

Keiko Kamakura Japan

Julia Wanschitz Austria

Juan J. Vílchez Spain

Yoshihisa Takiyama Japan

Pedro Mancías United States

Ettore Salsano

750 ×1.2

380 ×0.7

NEURO

809 ×1.9

CMN

280 ×0.9

NEURO

121 ×0.6

GENET

Citations per year, relative to Ettore Salsano Ettore Salsano (= 1×) peers Pedro Mancías

Countries citing papers authored by Ettore Salsano

Since Specialization

Citations

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

Fields of papers citing papers by Ettore Salsano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ettore Salsano

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Whitehead, Matthew T., Davide Tonduti, Laura Farina, et al.. (2024). Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. American Journal of Neuroradiology. 45(6). 769–772.

Grossi, Alice, et al.. (2024). A systematic review and meta-analysis of GFAP gene variants in Alexander disease. Scientific Reports. 14(1). 24341–24341. 2 indexed citations

Moscatelli, Marco, Fabio Martino Doniselli, Riccardo Pascuzzo, et al.. (2023). Interval between contrast administration and T1-weighted MRI for cerebral adrenoleukodystrophy: a single-case observation. European Radiology Experimental. 7(1). 57–57.

Brémovà-Ertl, Tatiana, Larry A. Abel, Mark Walterfang, et al.. (2021). A cross‐sectional, prospective ocular motor study in 72 patients with Niemann‐Pick disease type C. European Journal of Neurology. 28(9). 3040–3050. 9 indexed citations

Bachiocco, Valeria, Marco Cappa, A. Petroni, et al.. (2021). Pain Study in X-Linked Adrenoleukodystrophy in Males and Females. Pain and Therapy. 10(1). 505–523. 5 indexed citations

Moscatelli, Marco, et al.. (2021). Correction to: Metachromatic leukodystrophy with late adult-onset: diagnostic clues and differences from other genetic leukoencephalopathies with dementia. Journal of Neurology. 268(5). 1977–1979. 1 indexed citations

Nicita, Francesco, Silvia Masnada, Roberta Battini, et al.. (2021). Alexander disease evolution over time: data from an Italian cohort of pediatric-onset patients. Molecular Genetics and Metabolism. 134(4). 353–358. 6 indexed citations

Panteghini, Celeste, Chiara Reale, Alessia Nasca, et al.. (2021). Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson’s disease with brain iron accumulation through pseudo-exon activation. Neurogenetics. 22(4). 347–351. 4 indexed citations

Durães, João, Ettore Salsano, & Carmo Macário. (2020). Adult-Onset Krabbe Disease. Neurology Clinical Practice. 11(1). e15–e17. 4 indexed citations

10.

Marelli, Cécilia, Ettore Salsano, Letterio S. Politi, & Pierre Labauge. (2018). Spinal cord involvement in adult-onset metabolic and genetic diseases. Journal of Neurology Neurosurgery & Psychiatry. 90(2). 211–218. 16 indexed citations

11.

Agosta, Guillermo, William Benko, Jens C. Eickhoff, et al.. (2015). CSF and Blood Levels of GFAP in Alexander Disease. eNeuro. 2(5). ENEURO.0080–15.2015. 31 indexed citations

12.

Rossi, Giacomina, Antonio Bastone, Elena Piccoli, et al.. (2013). Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features. Neurobiology of Aging. 35(2). 408–417. 31 indexed citations

13.

Pareyson, Davide, Chiara Marchesi, & Ettore Salsano. (2013). Dominant Charcot–Marie–Tooth syndrome and cognate disorders. Handbook of clinical neurology. 115. 817–845. 3 indexed citations

14.

Salsano, Ettore, Gloria Bedini, Loris Bernard, et al.. (2013). An autoinflammatory neurological disease due to interleukin 6 hypersecretion. Journal of Neuroinflammation. 10(1). 29–29. 13 indexed citations

15.

Salsano, Ettore, Anna Rıta Gıovagnolı, Lucía Morandi, et al.. (2010). Mitochondrial dementia: A sporadic case of progressive cognitive and behavioral decline with hearing loss due to the rare m.3291T>C MELAS mutation. Journal of the Neurological Sciences. 300(1-2). 165–168. 22 indexed citations

16.

Pareyson, Davide, Chiara Marchesi, & Ettore Salsano. (2009). Hereditary predominantly motor neuropathies. Current Opinion in Neurology. 22(5). 451–459. 21 indexed citations

17.

Orthmann‐Murphy, Jennifer, Ettore Salsano, Charles K. Abrams, et al.. (2008). Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations. Brain. 132(2). 426–438. 105 indexed citations

18.

Salsano, Ettore, Laura Croci, Emanuela Maderna, et al.. (2007). Expression of the neurogenic basic helix-loop-helix transcription factor NEUROG1 identifies a subgroup of medulloblastomas not expressing ATOH1. Neuro-Oncology. 9(3). 298–307. 25 indexed citations

19.

Salsano, Ettore, Bianca Pollo, Marica Eoli, Maria Teresa Giordana, & Gaetano Finocchiaro. (2004). Expression of MATH1, a marker of cerebellar granule cell progenitors, identifies different medulloblastoma sub-types. Neuroscience Letters. 370(2-3). 180–185. 36 indexed citations

20.

Bissola, Lorena, Marica Eoli, Bianca Pollo, et al.. (2002). Association of chromosome 10 losses and negative prognosis in oligoastrocytomas. Annals of Neurology. 52(6). 842–845. 25 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