Valentina Sardone

1.8k total citations
14 papers, 1.2k citations indexed

About

Valentina Sardone is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Valentina Sardone has authored 14 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Neurology and 8 papers in Genetics. Recurrent topics in Valentina Sardone's work include Amyotrophic Lateral Sclerosis Research (9 papers), Neurogenetic and Muscular Disorders Research (8 papers) and RNA Research and Splicing (4 papers). Valentina Sardone is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (9 papers), Neurogenetic and Muscular Disorders Research (8 papers) and RNA Research and Splicing (4 papers). Valentina Sardone collaborates with scholars based in United Kingdom, Italy and Slovenia. Valentina Sardone's co-authors include Youn‐Bok Lee, Christopher E. Shaw, Emma L. Scotter, Agnes L. Nishimura, Boris Rogelj, Caroline Vance, Francesco Muntoni, Jean‐Marc Gallo, Bradley Smith and Han-Jou Chen and has published in prestigious journals such as PLoS ONE, Neurology and Journal of Cell Science.

In The Last Decade

Valentina Sardone

14 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valentina Sardone United Kingdom 13 850 552 439 161 126 14 1.2k
Tammy Reid United States 9 745 0.9× 714 1.3× 421 1.0× 425 2.6× 127 1.0× 10 1.2k
Jianwen Deng China 19 810 1.0× 651 1.2× 254 0.6× 395 2.5× 182 1.4× 85 1.4k
Mayana Zatz Brazil 6 504 0.6× 523 0.9× 334 0.8× 245 1.5× 101 0.8× 9 961
Takuto Hideyama Japan 13 644 0.8× 466 0.8× 223 0.5× 157 1.0× 70 0.6× 38 913
Kevin Drenner United States 9 514 0.6× 528 1.0× 345 0.8× 143 0.9× 87 0.7× 12 881
Basar Cenik United States 10 733 0.9× 930 1.7× 440 1.0× 115 0.7× 274 2.2× 13 1.4k
Jeffrey Rothstein United States 6 630 0.7× 394 0.7× 329 0.7× 159 1.0× 73 0.6× 9 987
Charlotte Ridler United States 9 536 0.6× 668 1.2× 424 1.0× 209 1.3× 171 1.4× 68 1.1k
Karthik Krishnamurthy United States 14 349 0.4× 492 0.9× 291 0.7× 164 1.0× 121 1.0× 44 899
Elisa Onesto Italy 17 819 1.0× 715 1.3× 411 0.9× 337 2.1× 161 1.3× 18 1.3k

Countries citing papers authored by Valentina Sardone

Since Specialization
Citations

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

Fields of papers citing papers by Valentina Sardone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valentina Sardone

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

All Works

14 of 14 papers shown
1.
Frank, Diane E., Frederick J. Schnell, Cody A. Desjardins, et al.. (2020). Increased dystrophin production with golodirsen in patients with Duchenne muscular dystrophy. Neurology. 94(21). e2270–e2282. 219 indexed citations
2.
Dell’Orco, Michela, Valentina Sardone, Amy S. Gardiner, et al.. (2020). HuD regulates SOD1 expression during oxidative stress in differentiated neuroblastoma cells and sporadic ALS motor cortex. Neurobiology of Disease. 148. 105211–105211. 20 indexed citations
3.
Sardone, Valentina, Matthew J. Ellis, Silvia Torelli, et al.. (2018). A novel high-throughput immunofluorescence analysis method for quantifying dystrophin intensity in entire transverse sections of Duchenne muscular dystrophy muscle biopsy samples. PLoS ONE. 13(3). e0194540–e0194540. 17 indexed citations
4.
Hiller, Monika, Maria Sofia Falzarano, Iker García, et al.. (2018). A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures. PLoS ONE. 13(10). e0204485–e0204485. 16 indexed citations
5.
Godfrey, Caroline, Lourdes R. Desviat, Bård Smedsrød, et al.. (2017). Delivery is key: lessons learnt from developing splice‐switching antisense therapies. EMBO Molecular Medicine. 9(5). 545–557. 116 indexed citations
6.
Sardone, Valentina, et al.. (2017). Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease. Molecules. 22(4). 563–563. 72 indexed citations
7.
Niblock, Michael, Bradley Smith, Youn‐Bok Lee, et al.. (2016). Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD. Acta Neuropathologica Communications. 4(1). 18–18. 45 indexed citations
8.
Dell’Orco, Michela, Pamela Milani, Laura Arrigoni, et al.. (2015). Hydrogen peroxide-mediated induction of SOD1 gene transcription is independent from Nrf2 in a cellular model of neurodegeneration. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1859(2). 315–323. 30 indexed citations
9.
Nishimura, Agnes L., Carole Shum, Emma L. Scotter, et al.. (2014). Allele-Specific Knockdown of ALS-Associated Mutant TDP-43 in Neural Stem Cells Derived from Induced Pluripotent Stem Cells. PLoS ONE. 9(3). e91269–e91269. 42 indexed citations
10.
Scotter, Emma L., Caroline Vance, Agnes L. Nishimura, et al.. (2014). Differential roles of the ubiquitin proteasome system (UPS) and autophagy in the clearance of soluble and aggregated TDP-43 species. Journal of Cell Science. 127(Pt 6). 1263–78. 211 indexed citations
11.
Milani, Pamela, Marialaura Amadio, Umberto Laforenza, et al.. (2013). Posttranscriptional regulation of SOD1 gene expression under oxidative stress: Potential role of ELAV proteins in sporadic ALS. Neurobiology of Disease. 60. 51–60. 38 indexed citations
12.
Lee, Youn‐Bok, Han-Jou Chen, João Peres, et al.. (2013). Expanded G4C2 repeats linked to C9ORF72ALS and FTD form length-dependent RNA foci, sequester RNA binding proteins and are neurotoxic. Molecular Neurodegeneration. 8(S1). 6 indexed citations
13.
Lee, Youn‐Bok, Han-Jou Chen, João Peres, et al.. (2013). Hexanucleotide Repeats in ALS/FTD Form Length-Dependent RNA Foci, Sequester RNA Binding Proteins, and Are Neurotoxic. Cell Reports. 5(5). 1178–1186. 365 indexed citations
14.
Gagliardi, Stella, Pamela Milani, Valentina Sardone, Orietta Pansarasa, & Cristina Cereda. (2012). From Transcriptome to Noncoding RNAs: Implications in ALS Mechanism. Neurology Research International. 2012. 1–7. 19 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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