Mario Saporta

3.2k total citations
46 papers, 1.0k citations indexed

About

Mario Saporta is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Mario Saporta has authored 46 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Cellular and Molecular Neuroscience, 19 papers in Molecular Biology and 12 papers in Neurology. Recurrent topics in Mario Saporta's work include Hereditary Neurological Disorders (27 papers), Genetic Neurodegenerative Diseases (10 papers) and Neurological diseases and metabolism (6 papers). Mario Saporta is often cited by papers focused on Hereditary Neurological Disorders (27 papers), Genetic Neurodegenerative Diseases (10 papers) and Neurological diseases and metabolism (6 papers). Mario Saporta collaborates with scholars based in United States, Brazil and France. Mario Saporta's co-authors include Michael E. Shy, István Katona, John T. Dimos, Manisha Juneja, Joshua Burns, Vincent Timmerman, Micheline Misrahi, Renata de Moraes Maciel, Yunhong Bai and Violaine Planté‐Bordeneuve and has published in prestigious journals such as Journal of Neuroscience, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Mario Saporta

44 papers receiving 996 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mario Saporta United States 18 604 430 247 212 178 46 1.0k
Federica Cerri Italy 15 359 0.6× 315 0.7× 228 0.9× 114 0.5× 90 0.5× 30 795
V. M.‐Y. Lee United States 10 279 0.5× 483 1.1× 264 1.1× 149 0.7× 126 0.7× 12 952
Rodolphe Perrot France 15 244 0.4× 331 0.8× 142 0.6× 234 1.1× 83 0.5× 27 892
Takao Omura Japan 19 595 1.0× 363 0.8× 174 0.7× 50 0.2× 82 0.5× 33 1.2k
Jens Reimann Germany 22 265 0.4× 845 2.0× 192 0.8× 296 1.4× 70 0.4× 55 1.3k
Takuji Kurimoto Japan 18 632 1.0× 533 1.2× 133 0.5× 42 0.2× 245 1.4× 65 1.3k
James Mull United States 14 595 1.0× 624 1.5× 89 0.4× 227 1.1× 141 0.8× 19 1.1k
Marija Cvetanović United States 20 495 0.8× 653 1.5× 153 0.6× 63 0.3× 159 0.9× 39 1.1k
Jose A. Gomez‐Sanchez Spain 14 581 1.0× 337 0.8× 104 0.4× 51 0.2× 60 0.3× 24 912
Eduardo Pérez-Torres Mexico 7 273 0.5× 426 1.0× 234 0.9× 108 0.5× 56 0.3× 23 747

Countries citing papers authored by Mario Saporta

Since Specialization
Citations

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

Fields of papers citing papers by Mario Saporta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mario Saporta

This figure shows the co-authorship network connecting the top 25 collaborators of Mario Saporta. A scholar is included among the top collaborators of Mario Saporta 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 Mario Saporta. Mario Saporta 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.
Lent, Jonas Van, Marina Kennerson, Tim Vangansewinkel, et al.. (2024). Advances and challenges in modeling inherited peripheral neuropathies using iPSCs. Experimental & Molecular Medicine. 56(6). 1348–1364. 10 indexed citations
3.
Rebelo, Adriana, Clemer Abad, Maike F. Dohrn, et al.. (2024). SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Brain. 147(9). 3131–3143. 5 indexed citations
4.
Zhu, Yi, Adriana Rebelo, Sheyum Syed, et al.. (2023). Sorbitol reduction via govorestat ameliorates synaptic dysfunction and neurodegeneration in sorbitol dehydrogenase deficiency. JCI Insight. 8(10). 11 indexed citations
5.
Narayanan, Ramesh K., Kaitao Lai, Melina Ellis, et al.. (2022). Novel gene–intergenic fusion involving ubiquitin E3 ligase UBE3C causes distal hereditary motor neuropathy. Brain. 146(3). 880–897. 9 indexed citations
6.
Desu, Haritha L., et al.. (2022). Transcriptional abnormalities in induced pluripotent stem cell-derived oligodendrocytes of individuals with primary progressive multiple sclerosis. Frontiers in Cellular Neuroscience. 16. 972144–972144. 5 indexed citations
7.
Wu, Kenneth, Hannah L. Watry, Gokul N. Ramadoss, et al.. (2021). Allele-Specific Gene Editing Rescues Pathology in a Human Model of Charcot-Marie-Tooth Disease Type 2E. Frontiers in Cell and Developmental Biology. 9. 723023–723023. 16 indexed citations
8.
Fridman, Vera & Mario Saporta. (2021). Mechanisms and Treatments in Demyelinating CMT. Neurotherapeutics. 18(4). 2236–2268. 28 indexed citations
9.
Bowles, Annie C., et al.. (2020). A Chemically Defined Common Medium for Culture of C2C12 Skeletal Muscle and Human Induced Pluripotent Stem Cell Derived Spinal Spheroids. Cellular and Molecular Bioengineering. 13(6). 605–619. 10 indexed citations
10.
Saporta, Mario & Renata de Moraes Maciel. (2018). Analysis of Myelinating Schwann Cells in Human Skin Biopsies. Methods in molecular biology. 1739. 359–369. 3 indexed citations
11.
Juneja, Manisha, Joshua Burns, Mario Saporta, & Vincent Timmerman. (2018). Challenges in modelling the Charcot-Marie-Tooth neuropathies for therapy development. Journal of Neurology Neurosurgery & Psychiatry. 90(1). 58–67. 63 indexed citations
12.
Saporta, Mario. (2015). Cellular reprogramming and inherited peripheral neuropathies: perspectives and challenges. SHILAP Revista de lepidopterología. 10(6). 894–894. 3 indexed citations
13.
Saporta, Mario, Vu Luan Dang, Dmitri Volfson, et al.. (2014). Axonal Charcot–Marie–Tooth disease patient-derived motor neurons demonstrate disease-specific phenotypes including abnormal electrophysiological properties. Experimental Neurology. 263. 190–199. 98 indexed citations
14.
Bai, Yunhong, Ágnes Patzkó, Xingyao Wu, et al.. (2013). Curcumin Derivatives Reduce Expression of Transcription Factors That Inhibit Myelination in R98C CMT1B Mouse (P05.066). Neurology. 80(7_supplement). 1 indexed citations
15.
Patzkó, Ágnes, Yunhong Bai, Mario Saporta, et al.. (2012). Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice. Brain. 135(12). 3551–3566. 88 indexed citations
16.
Saporta, Mario, Brian R. Shy, Ágnes Patzkó, et al.. (2012). MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot–Marie–Tooth disease type 1B. Brain. 135(7). 2032–2047. 54 indexed citations
17.
Saporta, Mario, István Katona, Xuebao Zhang, et al.. (2011). Neuropathy in a Human Without the PMP22 Gene. Archives of Neurology. 68(6). 814–21. 20 indexed citations
18.
Saporta, Mario, Marica Gršković, & John T. Dimos. (2011). Induced pluripotent stem cells in the study of neurological diseases. Stem Cell Research & Therapy. 2(5). 37–37. 32 indexed citations
19.
Bai, Yunhong, Xuebao Zhang, István Katona, et al.. (2010). Conduction Block in PMP22 Deficiency. Journal of Neuroscience. 30(2). 600–608. 51 indexed citations
20.
Saporta, Mario, et al.. (2009). Discordant expression of familial amyloid polyneuropathy in monozygotic Brazilian twins. Amyloid. 16(1). 38–41. 15 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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