Erika Tenderini

850 total citations
13 papers, 353 citations indexed

About

Erika Tenderini is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Erika Tenderini has authored 13 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Cell Biology and 4 papers in Genetics. Recurrent topics in Erika Tenderini's work include Cellular transport and secretion (3 papers), RNA Research and Splicing (3 papers) and Virus-based gene therapy research (2 papers). Erika Tenderini is often cited by papers focused on Cellular transport and secretion (3 papers), RNA Research and Splicing (3 papers) and Virus-based gene therapy research (2 papers). Erika Tenderini collaborates with scholars based in Italy, United States and United Kingdom. Erika Tenderini's co-authors include Maria Teresa Bassi, Nereo Bresolin, Cinzia Baschirotto, Alessia Arnoldi, Andrea Martinuzzi, Claudia Crimella, Marina Scarlato, Elio Scarpini, Luciana Losito and Antonio Trabacca and has published in prestigious journals such as Bioinformatics, Neurology and Science Advances.

In The Last Decade

Erika Tenderini

12 papers receiving 347 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erika Tenderini Italy 11 180 102 87 84 60 13 353
Sımona Baldassari Italy 10 247 1.4× 94 0.9× 79 0.9× 91 1.1× 21 0.3× 22 399
Ryan W. O’Meara Canada 10 177 1.0× 99 1.0× 81 0.9× 53 0.6× 45 0.8× 11 354
Mireia Moreno‐Estellés Spain 8 301 1.7× 70 0.7× 39 0.4× 66 0.8× 39 0.7× 13 438
Souichi Oe Japan 9 389 2.2× 171 1.7× 47 0.5× 50 0.6× 29 0.5× 28 544
Samuele Negro Italy 14 185 1.0× 230 2.3× 31 0.4× 50 0.6× 27 0.5× 27 445
Estelle Arnaud Switzerland 7 227 1.3× 194 1.9× 73 0.8× 26 0.3× 63 1.1× 7 381
Alonso M. Higuero Spain 10 275 1.5× 117 1.1× 128 1.5× 27 0.3× 63 1.1× 13 427
Qihong Zhou United States 10 142 0.8× 77 0.8× 41 0.5× 30 0.4× 15 0.3× 10 355
Yan Hong United States 9 497 2.8× 290 2.8× 47 0.5× 75 0.9× 64 1.1× 10 616
T Miyake Japan 8 174 1.0× 108 1.1× 130 1.5× 22 0.3× 66 1.1× 13 369

Countries citing papers authored by Erika Tenderini

Since Specialization
Citations

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

Fields of papers citing papers by Erika Tenderini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erika Tenderini

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

All Works

13 of 13 papers shown
1.
Aprile, Davide, Reinald Shyti, Davide Castaldi, et al.. (2025). YY1 mutations disrupt corticogenesis through a cell type specific rewiring of cell-autonomous and non-cell-autonomous transcriptional programs. Molecular Psychiatry. 30(8). 3413–3429.
2.
Tobon, Alejandro, Reinald Shyti, Carlo Emanuele Villa, et al.. (2023). GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders. Science Advances. 9(48). eadh2726–eadh2726. 15 indexed citations
3.
Cheroni, Cristina, Sebastiano Trattaro, Nicolò Caporale, et al.. (2022). Benchmarking brain organoid recapitulation of fetal corticogenesis. Translational Psychiatry. 12(1). 520–520. 17 indexed citations
4.
Tobon, Alejandro, Carlo Emanuele Villa, Cristina Cheroni, et al.. (2019). Human Cortical Organoids Expose a Differential Function of GSK3 on Cortical Neurogenesis. Stem Cell Reports. 13(5). 847–861. 36 indexed citations
5.
Calabria, Andrea, Stefano Beretta, Ivan Merelli, et al.. (2019). γ-TRIS: a graph-algorithm for comprehensive identification of vector genomic insertion sites. Bioinformatics. 36(5). 1622–1624. 6 indexed citations
6.
Germain, Pierre‐Luc, Michael Zech, Sina Atashpaz, et al.. (2018). KMT2B Is Selectively Required for Neuronal Transdifferentiation, and Its Loss Exposes Dystonia Candidate Genes. Cell Reports. 25(4). 988–1001. 26 indexed citations
7.
Magnani, Chiara F., Fabrizio Benedicenti, Andrea Calabria, et al.. (2016). Immunotherapy of acute leukemia by chimeric antigen receptor-modified lymphocytes using an improved Sleeping Beauty transposon platform. Oncotarget. 7(32). 51581–51597. 42 indexed citations
8.
Calabria, Andrea, Giulio Spinozzi, Fabrizio Benedicenti, Erika Tenderini, & Eugenio Montini. (2015). adLIMS: a customized open source software that allows bridging clinical and basic molecular research studies. BMC Bioinformatics. 16(S9). S5–S5. 10 indexed citations
9.
Romaniello, Romina, Filippo Arrigoni, Anna Cavallini, et al.. (2014). Brain malformations and mutations in α‐ and β‐tubulin genes: a review of the literature and description of two new cases. Developmental Medicine & Child Neurology. 56(4). 354–360. 32 indexed citations
10.
Romaniello, Romina, Claudio Zucca, Erika Tenderini, et al.. (2013). A Novel Mutation in STXBP1 Gene in a Child With Epileptic Encephalopathy and an Atypical Electroclinical Pattern. Journal of Child Neurology. 29(2). 249–253. 14 indexed citations
11.
Ghezzi, Laura, Elio Scarpini, Mario Rango, et al.. (2012). A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation. Neurology. 79(20). 2077–2078. 14 indexed citations
12.
Arnoldi, Alessia, Claudia Crimella, Erika Tenderini, et al.. (2011). Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations. Clinical Genetics. 81(2). 150–157. 31 indexed citations
13.
Crimella, Claudia, Cinzia Baschirotto, Alessia Arnoldi, et al.. (2011). Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot–Marie–Tooth type 2. Clinical Genetics. 82(2). 157–164. 110 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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