Stefania Merella

1.8k total citations
9 papers, 734 citations indexed

About

Stefania Merella is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Stefania Merella has authored 9 papers receiving a total of 734 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Epidemiology. Recurrent topics in Stefania Merella's work include Virus-based gene therapy research (5 papers), CRISPR and Genetic Engineering (4 papers) and RNA Interference and Gene Delivery (4 papers). Stefania Merella is often cited by papers focused on Virus-based gene therapy research (5 papers), CRISPR and Genetic Engineering (4 papers) and RNA Interference and Gene Delivery (4 papers). Stefania Merella collaborates with scholars based in Italy, Germany and France. Stefania Merella's co-authors include Eugenio Montini, Luigi Naldini, Daniela Cesana, Fabrizio Benedicenti, Tiziana Plati, Alessia Capotondo, Alessandra Biffi, Manfred Schmidt, Marco Ranzani and Christof von Kalle and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Stefania Merella

9 papers receiving 727 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefania Merella Italy	8	484	399	163	95	89	9	734
Oumeya Adjali France	18	759 1.6×	581 1.5×	192 1.2×	104 1.1×	78 0.9×	53	1.1k
Stefan Michelfelder Germany	14	562 1.2×	444 1.1×	87 0.5×	128 1.3×	33 0.4×	21	828
Simona Cavalieri Italy	17	498 1.0×	329 0.8×	160 1.0×	95 1.0×	42 0.5×	25	740
Allison M. Keeler United States	16	618 1.3×	442 1.1×	181 1.1×	122 1.3×	169 1.9×	31	1.0k
Charles F. Towne United States	11	446 0.9×	305 0.8×	128 0.8×	168 1.8×	28 0.3×	11	903
Sanford L. Boye United States	11	625 1.3×	369 0.9×	84 0.5×	34 0.4×	42 0.5×	14	838
Lisa Woodworth United States	10	381 0.8×	277 0.7×	156 1.0×	284 3.0×	43 0.5×	13	711
Caroline Le Guiner France	20	1.3k 2.7×	657 1.6×	119 0.7×	81 0.9×	123 1.4×	47	1.6k
Colin L. Sweeney United States	15	752 1.6×	286 0.7×	207 1.3×	315 3.3×	103 1.2×	31	1.1k
Kelly M. Podetz-Pedersen United States	16	481 1.0×	322 0.8×	79 0.5×	90 0.9×	201 2.3×	30	810

Countries citing papers authored by Stefania Merella

Since Specialization

Citations

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

Fields of papers citing papers by Stefania Merella

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefania Merella

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

All Works

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9 of 9 papers shown

Resta, Chiara Di, Ivana Spiga, Stefania Merella, et al.. (2018). Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches.. PubMed. 29(1). 15–25. 6 indexed citations

Schaeffer, Céline, Stefania Merella, Elena Pasqualetto, Dejan Lazarević, & Luca Rampoldi. (2017). Mutant uromodulin expression leads to altered homeostasis of the endoplasmic reticulum and activates the unfolded protein response. PLoS ONE. 12(4). e0175970–e0175970. 31 indexed citations

Conte, Iván, Stefania Merella, José Manuel García-Manteiga, et al.. (2014). The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance. Nucleic Acids Research. 42(12). 7793–7806. 29 indexed citations

Calabria, Andrea, Simone Leo, Fabrizio Benedicenti, et al.. (2014). VISPA: a computational pipeline for the identification and analysis of genomic vector integration sites. Genome Medicine. 6(9). 67–67. 22 indexed citations

Cesana, Daniela, Marco Ranzani, Monica Volpin, et al.. (2014). Uncovering and Dissecting the Genotoxicity of Self-inactivating Lentiviral Vectors In Vivo. Molecular Therapy. 22(4). 774–785. 148 indexed citations

Ranzani, Marco, Daniela Cesana, Cynthia C. Bartholomae, et al.. (2013). Lentiviral vector–based insertional mutagenesis identifies genes associated with liver cancer. Nature Methods. 10(2). 155–161. 78 indexed citations

Cesana, Daniela, et al.. (2012). Whole transcriptome characterization of aberrant splicing events induced by lentiviral vector integrations. Journal of Clinical Investigation. 122(5). 1667–1676. 91 indexed citations

Capotondo, Alessia, Letterio S. Politi, Angelo Quattrini, et al.. (2012). Brain conditioning is instrumental for successful microglia reconstitution following hematopoietic stem cell transplantation. Proceedings of the National Academy of Sciences. 109(37). 15018–15023. 156 indexed citations

Biffi, Alessandra, Daniela Cesana, Nathalie Cartier, et al.. (2011). Lentiviral vector common integration sites in preclinical models and a clinical trial reflect a benign integration bias and not oncogenic selection. Blood. 117(20). 5332–5339. 173 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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