Remo Sanges

3.9k total citations
79 papers, 2.1k citations indexed

About

Remo Sanges is a scholar working on Molecular Biology, Cancer Research and Plant Science. According to data from OpenAlex, Remo Sanges has authored 79 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 17 papers in Cancer Research and 15 papers in Plant Science. Recurrent topics in Remo Sanges's work include RNA Research and Splicing (15 papers), Cancer-related molecular mechanisms research (14 papers) and Chromosomal and Genetic Variations (14 papers). Remo Sanges is often cited by papers focused on RNA Research and Splicing (15 papers), Cancer-related molecular mechanisms research (14 papers) and Chromosomal and Genetic Variations (14 papers). Remo Sanges collaborates with scholars based in Italy, United Kingdom and United States. Remo Sanges's co-authors include Maria Immacolata Ferrante, Swaraj Basu, Raffaele Calogero, Francesco Musacchia, Elia Stupka, Stefano Gustincich, Francesca Cordero, Ferenc Müller, Giuseppe Petrosino and Marina Montresor and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Remo Sanges

79 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Remo Sanges Italy 26 1.4k 410 376 357 238 79 2.1k
Rhona Stuart United States 16 2.5k 1.8× 323 0.8× 293 0.8× 151 0.4× 398 1.7× 28 3.1k
Burkhard Becker Germany 29 1.6k 1.2× 495 1.2× 55 0.1× 396 1.1× 95 0.4× 74 2.8k
Ryo Koyanagi Japan 22 614 0.5× 776 1.9× 61 0.2× 338 0.9× 152 0.6× 61 2.2k
Alexander Ereskovsky France 31 806 0.6× 611 1.5× 83 0.2× 248 0.7× 214 0.9× 114 3.1k
James E. Cleaver United States 19 617 0.5× 161 0.4× 248 0.7× 279 0.8× 55 0.2× 32 1.4k
Eiichi Shoguchi Japan 28 1.3k 1.0× 1.0k 2.5× 42 0.1× 510 1.4× 317 1.3× 67 2.7k
Philippe Ganot Monaco 18 1.2k 0.9× 434 1.1× 173 0.5× 247 0.7× 68 0.3× 31 1.8k
Manabu Shirai Japan 21 1.1k 0.8× 180 0.4× 71 0.2× 173 0.5× 187 0.8× 50 1.6k
Robert Steen United States 13 1.2k 0.9× 565 1.4× 78 0.2× 164 0.5× 406 1.7× 19 2.3k
Marie Castets France 22 1.1k 0.8× 235 0.6× 84 0.2× 83 0.2× 321 1.3× 38 1.6k

Countries citing papers authored by Remo Sanges

Since Specialization
Citations

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

Fields of papers citing papers by Remo Sanges

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Remo Sanges

This figure shows the co-authorship network connecting the top 25 collaborators of Remo Sanges. A scholar is included among the top collaborators of Remo Sanges 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 Remo Sanges. Remo Sanges 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.
Sena-Tomás, Carmen de, Changshou Gao, Hieu T. Nim, et al.. (2025). Nkx2.7 is a conserved regulator of craniofacial development. Nature Communications. 16(1). 3802–3802. 1 indexed citations
2.
Murray, David, et al.. (2024). Paternal starvation affects metabolic gene expression during zebrafish offspring development and lifelong fitness. Molecular Ecology. 33(6). e17296–e17296. 4 indexed citations
3.
Mangoni, Damiano, Anna P. Mazzetti, Alessandro Simi, et al.. (2024). From the genome's perspective: Bearing somatic retrotransposition to leverage the regulatory potential of L1 RNAs. BioEssays. 47(2). e2400125–e2400125. 2 indexed citations
4.
Filosi, Michele, et al.. (2023). Exploratory analysis of L1 retrotransposons expression in autism. Molecular Autism. 14(1). 22–22. 6 indexed citations
5.
Van, Amanda Lo, Damiano Mangoni, Rosa Maria Cossu, et al.. (2022). Piwil2 (Mili) sustains neurogenesis and prevents cellular senescence in the postnatal hippocampus. EMBO Reports. 24(2). e53801–e53801. 17 indexed citations
6.
Annunziata, Rossella, Bruno Hay Mele, Pina Marotta, et al.. (2022). Trade-off between sex and growth in diatoms: Molecular mechanisms and demographic implications. Science Advances. 8(3). eabj9466–eabj9466. 14 indexed citations
7.
Pistollato, Francesca, Mauro Petrillo, Laure‐Alix Clerbaux, et al.. (2022). Effects of spike protein and toxin-like peptides found in COVID-19 patients on human 3D neuronal/glial model undergoing differentiation: Possible implications for SARS-CoV-2 impact on brain development. Reproductive Toxicology. 111. 34–48. 12 indexed citations
8.
Espinoza, Stefano, Paola Valentini, Devid Damiani, et al.. (2021). SINEUPs: a novel toolbox for RNA therapeutics. Essays in Biochemistry. 65(4). 775–789. 18 indexed citations
9.
Pisciotta, Livia, Margherita Squillario, Maria Teresa Divizia, et al.. (2021). Case Report: Whole Exome Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Autism Spectrum Disorder, Intellectual Disability, Hyperactivity, Sleep and Gastrointestinal Disturbances. Frontiers in Genetics. 12. 625564–625564. 9 indexed citations
10.
Amendola, Elena, Remo Sanges, Swaraj Basu, et al.. (2019). A ceRNA Circuitry Involving the Long Noncoding RNA Klhl14-AS, Pax8, and Bcl2 Drives Thyroid Carcinogenesis. Cancer Research. 79(22). 5746–5757. 23 indexed citations
11.
Vieira, Fabio Rocha Jimenez, Alberto Amato, Éric Pelletier, et al.. (2019). Meta-Omics Reveals Genetic Flexibility of Diatom Nitrogen Transporters in Response to Environmental Changes. Molecular Biology and Evolution. 36(11). 2522–2535. 27 indexed citations
12.
Amato, Alberto, Göran M. Nylund, Johanna Bergkvist, et al.. (2018). Grazer-induced transcriptomic and metabolomic response of the chain-forming diatom Skeletonema marinoi. The ISME Journal. 12(6). 1594–1604. 46 indexed citations
13.
Amato, Alberto, Francesco Musacchia, Rossella Annunziata, et al.. (2017). Marine diatoms change their gene expression profile when exposed to microscale turbulence under nutrient replete conditions. Scientific Reports. 7(1). 24 indexed citations
14.
Ruocco, Miriam, Francesco Musacchia, Irene Olivé, et al.. (2017). Genomewide transcriptional reprogramming in the seagrass Cymodocea nodosa under experimental ocean acidification. Molecular Ecology. 26(16). 4241–4259. 24 indexed citations
15.
Carotenuto, Ylenia, Emanuela Dattolo, Chiara Lauritano, et al.. (2013). Insights into the transcriptome of the marine copepod Calanus helgolandicus feeding on the oxylipin-producing diatom Skeletonema marinoi. Harmful Algae. 31. 153–162. 31 indexed citations
16.
Sanges, Remo, Yavor Hadzhiev, Agnès Roure, et al.. (2013). Highly conserved elements discovered in vertebrates are present in non-syntenic loci of tunicates, act as enhancers and can be transcribed during development. Nucleic Acids Research. 41(6). 3600–3618. 23 indexed citations
17.
Silberschmidt, Daniel, Alina Rodríguez-Mallón, Gaetano Calı̀, et al.. (2011). In vivo role of different domains and of phosphorylation in the transcription factor Nkx2-1. BMC Developmental Biology. 11(1). 9–9. 40 indexed citations
18.
Motti, Dario, Caroline Le Duigou, Emmanuel Eugène, et al.. (2010). Gene expression analysis of the emergence of epileptiform activity after focal injection of kainic acid into mouse hippocampus. European Journal of Neuroscience. 32(8). 1364–1379. 23 indexed citations
19.
Roma, Guglielmo, Marco Sardiello, Gilda Cobellis, et al.. (2007). The UniTrap resource: tools for the biologist enabling optimized use of gene trap clones. Nucleic Acids Research. 36(Database). D741–D746. 5 indexed citations
20.
Quaglino, Elena, Simona Rolla, Manuela Iezzi, et al.. (2004). Concordant morphologic and gene expression data show that a vaccine halts HER-2/neu preneoplastic lesions. Journal of Clinical Investigation. 113(5). 709–717. 7 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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