Elena Manara

1.7k total citations
65 papers, 1.1k citations indexed

About

Elena Manara is a scholar working on Molecular Biology, Oncology and Hematology. According to data from OpenAlex, Elena Manara has authored 65 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 16 papers in Oncology and 13 papers in Hematology. Recurrent topics in Elena Manara's work include Acute Myeloid Leukemia Research (13 papers), Lymphatic System and Diseases (8 papers) and Genomics and Rare Diseases (5 papers). Elena Manara is often cited by papers focused on Acute Myeloid Leukemia Research (13 papers), Lymphatic System and Diseases (8 papers) and Genomics and Rare Diseases (5 papers). Elena Manara collaborates with scholars based in Italy, United States and Cyprus. Elena Manara's co-authors include Martina Pigazzi, Giuseppe Basso, Matteo Bertelli, Emma Baron, Stefano Paolacci, Sandro Michelini, Tommaso Beccari, Riccardo Masetti, K Dhuli and Franco Locatelli and has published in prestigious journals such as Blood, Cancer Research and Scientific Reports.

In The Last Decade

Elena Manara

59 papers receiving 1.1k citations

Peers

Elena Manara
Elena Manara
Citations per year, relative to Elena Manara Elena Manara (= 1×) peers Sébastien Chateauvieux

Countries citing papers authored by Elena Manara

Since Specialization
Citations

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

Fields of papers citing papers by Elena Manara

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Manara

This figure shows the co-authorship network connecting the top 25 collaborators of Elena Manara. A scholar is included among the top collaborators of Elena Manara 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 Manara. Elena Manara 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.
Michelini, Sandro, Karen L. Herbst, Vincenza Precone, et al.. (2022). A Multi-Gene Panel to Identify Lipedema-Predisposing Genetic Variants by a Next-Generation Sequencing Strategy. Journal of Personalized Medicine. 12(2). 268–268. 16 indexed citations
2.
Michelini, Sandro, Bruno Amato, Stefano Gentileschi, et al.. (2021). CDH5 , a Possible New Candidate Gene for Genetic Testing of Lymphedema. Lymphatic Research and Biology. 20(5). 496–506. 2 indexed citations
3.
Ceccarini, Maria Rachele, Vincenza Precone, Elena Manara, et al.. (2021). A next generation sequencing gene panel for use in the diagnosis of anorexia nervosa. Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity. 27(5). 1869–1880. 12 indexed citations
4.
Cannarella, Rossella, Vincenza Precone, Giulia Guerri, et al.. (2020). Clinical Evaluation of a Custom Gene Panel as a Tool for Precision Male Infertility Diagnosis by Next-Generation Sequencing. Life. 10(10). 242–242. 8 indexed citations
5.
Temel, Şehime Gülsün, Mahmut Çerkez Ergören, Elena Manara, et al.. (2020). Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann–Rautenstrauch syndrome. European Journal of Human Genetics. 28(12). 1675–1680. 7 indexed citations
6.
Michelini, Sandro, Bruno Amato, Elena Manara, et al.. (2020). Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema. Genes. 11(11). 1361–1361. 4 indexed citations
7.
Paolacci, Stefano, Raúl Mattassi, Giuseppe Marceddu, et al.. (2020). Somatic Variant Analysis Identifies Targets for Tailored Therapies in Patients with Vascular Malformations. Journal of Clinical Medicine. 9(11). 3387–3387. 7 indexed citations
8.
Iarossi, Giancarlo, Valerio Marino, Paolo Enrico Maltese, et al.. (2020). Expanding the Clinical and Genetic Spectrum of RAB28-Related Cone-Rod Dystrophy: Pathogenicity of Novel Variants in Italian Families. International Journal of Molecular Sciences. 22(1). 381–381. 8 indexed citations
9.
Manara, Elena, Natale Capodicasa, Paolo Enrico Maltese, et al.. (2020). Early-onset of Frontotemporal Dementia and Amyotrophic Lateral Sclerosis in an Albanian Patient with a c.1319C>T Variant in the UBQLN2 Gene. 7(1). 25–31. 1 indexed citations
10.
Severino, Mariasavina, Kerem Teralı, Elena Manara, et al.. (2020). Adult-onset glutaric aciduria type I: rare presentation of a treatable disorder. Neurogenetics. 21(3). 179–186. 14 indexed citations
11.
Bertelli, Matteo, Aysha Karim Kiani, Stefano Paolacci, et al.. (2019). Hydroxytyrosol: A natural compound with promising pharmacological activities. Journal of Biotechnology. 309. 29–33. 187 indexed citations
12.
Martelli, Francesco, et al.. (2019). Electrical Stimulation in the Treatment of Lymphedema and Associated Skin Ulcers. Lymphatic Research and Biology. 18(3). 270–276. 7 indexed citations
13.
Bertelli, Matteo, Aysha Karim Kiani, Stefano Paolacci, et al.. (2019). Molecular pathways involved in lymphedema: Hydroxytyrosol as a candidate natural compound for treating the effects of lymph accumulation. Journal of Biotechnology. 308. 82–86. 11 indexed citations
14.
Marino, Valerio, Elisa Oppici, Paolo Enrico Maltese, et al.. (2018). A novel p.(Glu111Val) missense mutation in GUCA1A associated with cone-rod dystrophy leads to impaired calcium sensing and perturbed second messenger homeostasis in photoreceptors. Human Molecular Genetics. 27(24). 4204–4217. 27 indexed citations
15.
Zampini, Matteo, Claudia Tregnago, Valéria Bisio, et al.. (2018). Epigenetic heterogeneity affects the risk of relapse in children with t(8;21)RUNX1-RUNX1T1-rearranged AML. Leukemia. 32(5). 1124–1134. 17 indexed citations
16.
Mattassi, Raúl, Elena Manara, Piergiuseppe Colombo, et al.. (2017). Variant discovery in patients with Mendelian vascular anomalies by next-generation sequencing and their use in patient clinical management. Journal of Vascular Surgery. 67(3). 922–932.e11. 16 indexed citations
17.
Tregnago, Claudia, Elena Manara, Matteo Zampini, et al.. (2016). CREB engages C/EBPδ to initiate leukemogenesis. Leukemia. 30(9). 1887–1896. 27 indexed citations
18.
Manara, Elena, Giuseppe Basso, Matteo Zampini, et al.. (2016). Characterization of children with FLT3-ITD acute myeloid leukemia: a report from the AIEOP AML-2002 study group. Leukemia. 31(1). 18–25. 27 indexed citations
20.
Pigazzi, Martina, Elena Manara, Silvia Bresolin, et al.. (2012). MicroRNA-34b promoter hypermethylation induces CREB overexpression and contributes to myeloid transformation. Haematologica. 98(4). 602–610. 36 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026