Milena Preti

784 total citations
8 papers, 576 citations indexed

About

Milena Preti is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Milena Preti has authored 8 papers receiving a total of 576 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 1 paper in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Milena Preti's work include RNA modifications and cancer (6 papers), RNA and protein synthesis mechanisms (4 papers) and RNA Research and Splicing (3 papers). Milena Preti is often cited by papers focused on RNA modifications and cancer (6 papers), RNA and protein synthesis mechanisms (4 papers) and RNA Research and Splicing (3 papers). Milena Preti collaborates with scholars based in Italy, France and Switzerland. Milena Preti's co-authors include Giorgio Dieci, Barbara Montanini, Pierre‐Emmanuel Gleizes, Marie-Françoise O’Donohue, Nathalie Montel-Lehry, Valérie Choesmel, Marie‐Line Bortolin‐Cavaillé, Michael Landowski, Christopher Buros and Félix Naef and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Molecular Cell.

In The Last Decade

Milena Preti

8 papers receiving 572 citations

Peers

Milena Preti

MB

CR

PHYSI

GENET

ONCOL

Hanna M. Petrykowska United States

Skye C McIver United States

Yebo Wang China

Yuliya Kremenska Japan

Hanqian L. Carlson United States

Nehal Gosalia United States

Kevin A. Hoegenauer United States

Zhigang Zhao China

Koen Theunis Belgium

Huiyan Jin United States

Hanna M. Petrykowska United States

Milena Preti

469 ×1.0

MB

114 ×0.8

CR

17 ×0.4

PHYSI

40 ×1.1

GENET

28 ×0.7

ONCOL

Citations per year, relative to Milena Preti Milena Preti (= 1×) peers Hanna M. Petrykowska

Countries citing papers authored by Milena Preti

Since Specialization

Citations

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

Fields of papers citing papers by Milena Preti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Milena Preti

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

All Works

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8 of 8 papers shown

1.

Bigot, Nicolas, Milena Preti, Séverine Loisel‐Meyer, et al.. (2015). Hypoxia Differentially Modulates the Genomic Stability of Clinical-Grade ADSCs and BM-MSCs in Long-Term Culture. Stem Cells. 33(12). 3608–3620. 35 indexed citations

2.

Preti, Milena, Marie-Françoise O’Donohue, Nathalie Montel-Lehry, et al.. (2013). Gradual processing of the ITS1 from the nucleolus to the cytoplasm during synthesis of the human 18S rRNA. Nucleic Acids Research. 41(8). 4709–4723. 70 indexed citations

3.

Gazda, Hanna T., Milena Preti, Mee Rie Sheen, et al.. (2012). Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia. Human Mutation. 33(7). 1037–1044. 109 indexed citations

4.

Dei, Alessandra, Valentina Spigoni, Laura Franzini, et al.. (2011). Lower endothelial progenitor cell number, family history of cardiovascular disease and reduced HDL-cholesterol levels are associated with shorter leukocyte telomere length in healthy young adults. Nutrition Metabolism and Cardiovascular Diseases. 23(3). 272–278. 34 indexed citations

5.

Preti, Milena, Cyril Ribeyre, Barbara Cortelazzi, et al.. (2010). The Telomere-Binding Protein Tbf1 Demarcates snoRNA Gene Promoters in Saccharomyces cerevisiae. Molecular Cell. 38(4). 614–620. 47 indexed citations

6.

Dieci, Giorgio, Milena Preti, & Barbara Montanini. (2009). Eukaryotic snoRNAs: A paradigm for gene expression flexibility. Genomics. 94(2). 83–88. 248 indexed citations

7.

Guffanti, Elisa, Roberto Ferrari, Milena Preti, et al.. (2006). A Minimal Promoter for TFIIIC-dependent in Vitro Transcription of snoRNA and tRNA Genes by RNA Polymerase III. Journal of Biological Chemistry. 281(33). 23945–23957. 27 indexed citations

8.

Preti, Milena, et al.. (2006). Assembly into snoRNP controls 5′-end maturation of a box C/D snoRNA in Saccharomyces cerevisiae. Biochemical and Biophysical Research Communications. 351(2). 468–473. 6 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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