Marilena Lepretti

1.1k total citations
32 papers, 876 citations indexed

About

Marilena Lepretti is a scholar working on Gastroenterology, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Marilena Lepretti has authored 32 papers receiving a total of 876 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Gastroenterology, 8 papers in Pulmonary and Respiratory Medicine and 6 papers in Molecular Biology. Recurrent topics in Marilena Lepretti's work include Celiac Disease Research and Management (10 papers), Blood properties and coagulation (8 papers) and Autoimmune Bullous Skin Diseases (4 papers). Marilena Lepretti is often cited by papers focused on Celiac Disease Research and Management (10 papers), Blood properties and coagulation (8 papers) and Autoimmune Bullous Skin Diseases (4 papers). Marilena Lepretti collaborates with scholars based in Italy, Brazil and Belgium. Marilena Lepretti's co-authors include Ivana Caputo, Lillà Lionetti, Stefania Martucciello, Mario Alberto Burgos-Aceves, Gaetana Paolella, Carla Esposito, Rosalba Putti, Maria Vittoria Barone, Caterina Faggio and Di Gregorio and has published in prestigious journals such as PLoS ONE, The Science of The Total Environment and Analytical Biochemistry.

In The Last Decade

Marilena Lepretti

31 papers receiving 857 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marilena Lepretti Italy 17 224 220 163 136 125 32 876
Gaetana Paolella Italy 17 117 0.5× 154 0.7× 76 0.5× 110 0.8× 170 1.4× 39 837
Hiroko Nakayama Japan 19 78 0.3× 57 0.3× 90 0.6× 58 0.4× 333 2.7× 47 915
G Morisi Italy 15 66 0.3× 180 0.8× 46 0.3× 66 0.5× 72 0.6× 56 621
Rui Huang China 15 66 0.3× 31 0.1× 39 0.2× 128 0.9× 216 1.7× 54 999
Knut-Jan Andersen Norway 17 45 0.2× 170 0.8× 31 0.2× 50 0.4× 191 1.5× 74 935
Yaofeng Jin China 15 39 0.2× 41 0.2× 150 0.9× 33 0.2× 386 3.1× 30 705
Ali Shawki United States 16 28 0.1× 399 1.8× 57 0.3× 58 0.4× 365 2.9× 37 1.5k
Fang China 17 18 0.1× 61 0.3× 92 0.6× 96 0.7× 455 3.6× 287 1.4k
R. A. Barter United States 18 28 0.1× 577 2.6× 95 0.6× 85 0.6× 220 1.8× 35 1.5k

Countries citing papers authored by Marilena Lepretti

Since Specialization
Citations

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

Fields of papers citing papers by Marilena Lepretti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marilena Lepretti

This figure shows the co-authorship network connecting the top 25 collaborators of Marilena Lepretti. A scholar is included among the top collaborators of Marilena Lepretti 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 Marilena Lepretti. Marilena Lepretti 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.
Burgos-Aceves, Mario Alberto, Vincenzo Migliaccio, Di Gregorio, et al.. (2021). 1,1,1-trichloro-2,2-bis (p-chlorophenyl)-ethane (DDT) and 1,1-Dichloro-2,2-bis (p, p’-chlorophenyl) ethylene (DDE) as endocrine disruptors in human and wildlife: A possible implication of mitochondria. Environmental Toxicology and Pharmacology. 87. 103684–103684. 50 indexed citations
2.
Burgos-Aceves, Mario Alberto, Vincenzo Migliaccio, Marilena Lepretti, et al.. (2021). Dose-Dependent Response to the Environmental Pollutant Dichlorodipheniletylhene (DDE) in HepG2 Cells: Focus on Cell Viability and Mitochondrial Fusion/Fission Proteins. Toxics. 9(11). 270–270. 18 indexed citations
3.
Gregorio, Di, Rosa Anna Busiello, Mario Alberto Burgos-Aceves, et al.. (2019). Environmental Pollutants Effect on Brown Adipose Tissue. Frontiers in Physiology. 9. 1891–1891. 30 indexed citations
4.
Lepretti, Marilena, Stefania Martucciello, Mario Alberto Burgos-Aceves, Rosalba Putti, & Lillà Lionetti. (2018). Omega-3 Fatty Acids and Insulin Resistance: Focus on the Regulation of Mitochondria and Endoplasmic Reticulum Stress. Nutrients. 10(3). 350–350. 167 indexed citations
5.
Capaldo, Anna, Flaminia Gay, Marilena Lepretti, et al.. (2018). Effects of environmental cocaine concentrations on the skeletal muscle of the European eel (Anguilla anguilla). The Science of The Total Environment. 640-641. 862–873. 33 indexed citations
6.
Martucciello, Stefania, Gaetana Paolella, Carla Esposito, Marilena Lepretti, & Ivana Caputo. (2018). Anti-type 2 transglutaminase antibodies as modulators of type 2 transglutaminase functions: a possible pathological role in celiac disease. Cellular and Molecular Life Sciences. 75(22). 4107–4124. 16 indexed citations
7.
Burgos-Aceves, Mario Alberto, Amit Cohen, Gaetana Paolella, et al.. (2018). Modulation of mitochondrial functions by xenobiotic-induced microRNA: From environmental sentinel organisms to mammals. The Science of The Total Environment. 645. 79–88. 86 indexed citations
8.
Capaldo, Anna, Flaminia Gay, Rosaria Scudiero, et al.. (2016). Histological changes, apoptosis and metallothionein levels in Triturus carnifex (Amphibia, Urodela) exposed to environmental cadmium concentrations. Aquatic Toxicology. 173. 63–73. 32 indexed citations
9.
Lepretti, Marilena, Luigi Rizzo, Ivana Caputo, et al.. (2016). Surface water disinfection by chlorination and advanced oxidation processes: Inactivation of an antibiotic resistant E. coli strain and cytotoxicity evaluation. The Science of The Total Environment. 554-555. 1–6. 62 indexed citations
10.
Lepretti, Marilena, Gaetana Paolella, Domenico Giordano, et al.. (2015). 4-Nonylphenol reduces cell viability and induces apoptosis and ER-stress in a human epithelial intestinal cell line. Toxicology in Vitro. 29(7). 1436–1444. 32 indexed citations
11.
Paolella, Gaetana, Ivana Caputo, Anna Marabotti, et al.. (2013). Celiac Anti-Type 2 Transglutaminase Antibodies Induce Phosphoproteome Modification in Intestinal Epithelial Caco-2 Cells. PLoS ONE. 8(12). e84403–e84403. 12 indexed citations
12.
Caputo, Ivana, Agnese Secondo, Marilena Lepretti, et al.. (2012). Gliadin Peptides Induce Tissue Transglutaminase Activation and ER-Stress through Ca2+ Mobilization in Caco-2 Cells. PLoS ONE. 7(9). e45209–e45209. 45 indexed citations
13.
Caputo, Ivana, Marilena Lepretti, Agnese Secondo, et al.. (2011). Anti-tissue transglutaminase antibodies activate intracellular tissue transglutaminase by modulating cytosolic Ca2+ homeostasis. Amino Acids. 44(1). 251–260. 20 indexed citations
14.
Caputo, Ivana, Maria Vittoria Barone, Marilena Lepretti, et al.. (2010). Celiac anti-tissue transglutaminase antibodies interfere with the uptake of alpha gliadin peptide 31–43 but not of peptide 57–68 by epithelial cells. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802(9). 717–727. 31 indexed citations
15.
Caputo, Ivana, Maria Vittoria Barone, Stefania Martucciello, Marilena Lepretti, & Carla Esposito. (2008). Tissue transglutaminase in celiac disease: role of autoantibodies. Amino Acids. 36(4). 693–699. 31 indexed citations
16.
Metafora, Salvatore, Carla Esposito, Ivana Caputo, et al.. (2007). Seminal Vesicle Protein IV and Its Derived Active Peptides: A Possible Physiological Role in Seminal Clotting. Seminars in Thrombosis and Hemostasis. 33(1). 53–59. 6 indexed citations
17.
Maria, S. De, Salvatore Metafora, Maria Cartenı̀, et al.. (2007). Effect of positive charge in VIP 16γ‐glutamyl diamino derivatives on hVPAC1 and hVPAC2 receptor function. Journal of Peptide Science. 14(1). 102–109. 1 indexed citations
18.
Micco, B. Di, et al.. (2007). SV-IV Peptide1–16 reduces coagulant power in normal Factor V and Factor V Leiden. Journal of Translational Medicine. 5(1). 69–69.
19.
Caraglia, Michele, Alessandra Dicitore, G. Giuberti, et al.. (2006). Effects of VIP and VIP–DAP on Proliferation and Lipid Peroxidation Metabolism in Human KB Cells. Annals of the New York Academy of Sciences. 1070(1). 167–172. 3 indexed citations
20.
Stiuso, Paola, Anna Marabotti, Angelo Facchiano, et al.. (2005). Assessment of the conformational features of vasoactive intestinal peptide in solution by limited proteolysis experiments. Biopolymers. 81(2). 110–119. 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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