Elena Marasco

2.2k total citations
37 papers, 1.2k citations indexed

About

Elena Marasco is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Elena Marasco has authored 37 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Elena Marasco's work include Epigenetics and DNA Methylation (11 papers), Acute Lymphoblastic Leukemia research (5 papers) and MicroRNA in disease regulation (4 papers). Elena Marasco is often cited by papers focused on Epigenetics and DNA Methylation (11 papers), Acute Lymphoblastic Leukemia research (5 papers) and MicroRNA in disease regulation (4 papers). Elena Marasco collaborates with scholars based in Italy, United States and Sweden. Elena Marasco's co-authors include Paolo Garagnani, Vilma Mantovani, Claudio Franceschi, Maria Giulia Bacalini, Chiara Pirazzini, Cristina Giuliani, Davide Gentilini, Giuseppe Passarino, Diego Centonze and Giorgio Bernardi and has published in prestigious journals such as Journal of Neuroscience, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Elena Marasco

35 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elena Marasco Italy	19	750	303	154	150	127	37	1.2k
Michael A. Nalls United States	14	940 1.3×	394 1.3×	276 1.8×	268 1.8×	76 0.6×	19	1.5k
Emanuela Mensa’ Italy	18	526 0.7×	284 0.9×	228 1.5×	47 0.3×	48 0.4×	32	1.0k
Michelle Moh United States	6	587 0.8×	96 0.3×	312 2.0×	153 1.0×	57 0.4×	14	1.1k
David A. Buchner United States	25	725 1.0×	137 0.5×	273 1.8×	240 1.6×	108 0.9×	44	1.4k
Dandan Zong China	18	489 0.7×	204 0.7×	219 1.4×	48 0.3×	53 0.4×	46	1.1k
Lars R. Ingerslev Denmark	16	974 1.3×	171 0.6×	404 2.6×	206 1.4×	368 2.9×	27	1.6k
Daniel R. Calnan United States	8	876 1.2×	102 0.3×	151 1.0×	49 0.3×	52 0.4×	20	1.4k
Rezvan Noroozi Iran	21	654 0.9×	435 1.4×	60 0.4×	257 1.7×	34 0.3×	77	1.3k
Constance Chen United States	13	530 0.7×	98 0.3×	142 0.9×	499 3.3×	68 0.5×	15	1.5k
Robert F. Hillary United Kingdom	16	517 0.7×	55 0.2×	134 0.9×	171 1.1×	155 1.2×	29	972

Countries citing papers authored by Elena Marasco

Since Specialization

Citations

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

Fields of papers citing papers by Elena Marasco

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Marasco

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

All Works

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20 of 20 papers shown

Mancardi, Maria Margherita, et al.. (2024). A de novo frameshift variant in MED13 gene in a patient with autism spectrum disorder and magnetic resonance imaging abnormalities mimicking tuberous sclerosis. American Journal of Medical Genetics Part A. 194(8). e63611–e63611.

Marini, Francesca, Elena Marasco, Luciano Xumerle, et al.. (2023). High frequency of heterozygous rare variants of the SLC34A1 and SLC9A3R1 genes in patients with atypical femur fracture. European Journal of Endocrinology. 188(1). 176–188. 3 indexed citations

Gensous, Noémie, Claudia Sala, Chiara Pirazzini, et al.. (2022). A Targeted Epigenetic Clock for the Prediction of Biological Age. Cells. 11(24). 4044–4044. 24 indexed citations

Storci, Gianluca, Sabrina De Carolis, Alessio Papi, et al.. (2019). Genomic stability, anti-inflammatory phenotype, and up-regulation of the RNAseH2 in cells from centenarians. Cell Death and Differentiation. 26(9). 1845–1858. 45 indexed citations

Montesanto, Alberto, Anna Rita Bonfigli, María De Luca, et al.. (2019). Erythropoietin (EPO) haplotype associated with all-cause mortality in a cohort of Italian patients with Type-2 Diabetes. Scientific Reports. 9(1). 10395–10395. 11 indexed citations

Giuliani, Cristina, David Biggs, Elena Marasco, et al.. (2018). First evidence of association between past environmental exposure to dioxin and DNA methylation of CYP1A1 and IGF2 genes in present day Vietnamese population. Environmental Pollution. 242(Pt A). 976–985. 8 indexed citations

Montesanto, Alberto, Anna Rita Bonfigli, Paolina Crocco, et al.. (2018). Genes associated with Type 2 Diabetes and vascular complications. Aging. 10(2). 178–196. 36 indexed citations

Gensous, Noémie, Maria Giulia Bacalini, Chiara Pirazzini, et al.. (2017). The epigenetic landscape of age-related diseases: the geroscience perspective. Biogerontology. 18(4). 549–559. 52 indexed citations

Bacalini, Maria Giulia, Patrizia D’Aquila, Elena Marasco, et al.. (2017). The methylation of nuclear and mitochondrial DNA in ageing phenotypes and longevity. Mechanisms of Ageing and Development. 165(Pt B). 156–161. 29 indexed citations

10.

Cricca, Monica, Elena Marasco, Federica Alessandrini, et al.. (2015). High-throughput genotyping of high-risk Human Papillomavirus by MALDI-TOF Mass Spectrometry-based method.. PubMed. 38(2). 211–23. 17 indexed citations

11.

Bonifazi, Francesca, Gianluca Storci, Giuseppe Bandini, et al.. (2013). Glutathione transferase-A2 S112T polymorphism predicts survival, transplant-related mortality, busulfan and bilirubin blood levels after allogeneic stem cell transplantation. Haematologica. 99(1). 172–179. 21 indexed citations

12.

Mori, Francesco, Michele Ribolsi, Hajime Kusayanagi, et al.. (2012). TRPV1 Channels Regulate Cortical Excitability in Humans. Journal of Neuroscience. 32(3). 873–879. 70 indexed citations

13.

Fornari, Francesca, Maddalena Milazzo, Pasquale Chieco, et al.. (2012). In hepatocellular carcinoma miR‐519d is up‐regulated by p53 and DNA hypomethylation and targets CDKN1A/p21, PTEN, AKT3 and TIMP2. The Journal of Pathology. 227(3). 275–285. 164 indexed citations

14.

Ferrari, Anna, Ilaria Iacobucci, Marco Sazzini, et al.. (2011). Abstract 3811: A germline polymorphism in the ANRIL (CDKN2BAS) locus is associated with susceptibility to Philadelphia-positive acute lymphoblastic leukemia (ALL). Cancer Research. 71(8_Supplement). 3811–3811. 1 indexed citations

15.

Hasan, Syed K., Fabio Buttari, Tiziana Ottone, et al.. (2011). Risk of acute promyelocytic leukemia in multiple sclerosis. Neurology. 76(12). 1059–1065. 28 indexed citations

16.

Vinci, Angela Di, Ida Casciano, Elena Marasco, et al.. (2011). Quantitative methylation analysis of HOXA3, 7, 9, and 10 genes in glioma: association with tumor WHO grade and clinical outcome. Journal of Cancer Research and Clinical Oncology. 138(1). 35–47. 37 indexed citations

17.

Mori, Francesco, Michele Ribolsi, Hajime Kusayanagi, et al.. (2011). Genetic variants of the NMDA receptor influence cortical excitability and plasticity in humans. Journal of Neurophysiology. 106(4). 1637–1643. 52 indexed citations

18.

Iacobucci, Ilaria, Marco Sazzini, Anna Ferrari, et al.. (2010). Susceptibility to Philadelphia-Positive acute Lymphoblastic Leukemia (ALL) Is Associated with a Germline Polymorphism In the ANRIL (CDKN2BAS) Locus.. Blood. 116(21). 1670–1670. 1 indexed citations

19.

Forlani, Gabriele, Stefano Zucchini, Antonio Rocco, et al.. (2010). Double Heterozygous Mutations Involving Both HNF1A/MODY3 and HNF4A/MODY1 Genes. Diabetes Care. 33(11). 2336–2338. 18 indexed citations

20.

Cozzolino, F, et al.. (1981). Report on two cases of aneurysmal bone cyst of the pelvis treated by selective arterial embolization.. PubMed. 7(3). 345–52. 1 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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