Francesca Amati

2.4k total citations
58 papers, 1.8k citations indexed

About

Francesca Amati is a scholar working on Molecular Biology, Epidemiology and Immunology. According to data from OpenAlex, Francesca Amati has authored 58 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 12 papers in Epidemiology and 12 papers in Immunology. Recurrent topics in Francesca Amati's work include Congenital heart defects research (20 papers), Atherosclerosis and Cardiovascular Diseases (9 papers) and RNA modifications and cancer (9 papers). Francesca Amati is often cited by papers focused on Congenital heart defects research (20 papers), Atherosclerosis and Cardiovascular Diseases (9 papers) and RNA modifications and cancer (9 papers). Francesca Amati collaborates with scholars based in Italy, United States and United Kingdom. Francesca Amati's co-authors include Giuseppe Novelli, Bruno Dallapiccola, Renato Lauro, Rossella Menghini, Viviana Casagrande, Arnaldo Ippoliti, Alessandro Terrinoni, Massimo Federici, Eugenio Martelli and Gerry Melino and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and PLoS ONE.

In The Last Decade

Francesca Amati

58 papers receiving 1.8k citations

Peers

Francesca Amati

EPIDE

IMMUN

GENET

Mariusz Koda Poland

Oliver Tschopp Switzerland

Xueyuan Bai China

Edward Hsi Taiwan

Liv Thommesen Norway

Christos Adamopoulos Greece

Juan Carlos Calvo Argentina

Hyo Kyun Chung South Korea

Elisa Petrangeli Italy

Silvio Zaina Mexico

Mariusz Koda Poland

Francesca Amati

991 ×0.9

578 ×1.5

378 ×1.1

EPIDE

145 ×0.5

IMMUN

212 ×0.8

GENET

Citations per year, relative to Francesca Amati Francesca Amati (= 1×) peers Mariusz Koda

Countries citing papers authored by Francesca Amati

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Amati

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Amati

This figure shows the co-authorship network connecting the top 25 collaborators of Francesca Amati. A scholar is included among the top collaborators of Francesca Amati 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 Francesca Amati. Francesca Amati 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

Santobuono, Vincenzo Ezio, Marco Gentile, Francesca Amati, et al.. (2024). Bifocal coronary sinus pacing and transcatheter tricuspid valve-in-valve implantation: an innovative combined approach. Future Cardiology. 20(5-6). 281–286. 1 indexed citations

Morini, Elena, Francesca Romana Prandi, Francesco Barillà, et al.. (2023). Downregulation of Circulating Hsa-miR-200c-3p Correlates with Dyslipidemia in Patients with Stable Coronary Artery Disease. International Journal of Molecular Sciences. 24(2). 1112–1112. 4 indexed citations

Morini, Elena, et al.. (2021). Two RECK Splice Variants (Long and Short) Are Differentially Expressed in Patients with Stable and Unstable Coronary Artery Disease: A Pilot Study. Genes. 12(6). 939–939. 3 indexed citations

Amati, Francesca, Andrea Latini, Vito Luigi Colona, et al.. (2020). Expression profiles of the SARS-CoV-2 host invasion genes in nasopharyngeal and oropharyngeal swabs of COVID-19 patients. Heliyon. 6(10). e05143–e05143. 22 indexed citations

Morini, Elena, et al.. (2017). LOX-1 and Its Splice Variants: A New Challenge for Atherosclerosis and Cancer-Targeted Therapies. International Journal of Molecular Sciences. 18(2). 290–290. 38 indexed citations

Bruno, Valentina, Adalgisa Pietropolli, Renato Massoud, et al.. (2017). OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study. Genetic Testing and Molecular Biomarkers. 21(6). 363–372. 7 indexed citations

Morini, Elena, Federica Sangiuolo, Daniela Caporossi, Giuseppe Novelli, & Francesca Amati. (2015). Application of Next Generation Sequencing for personalized medicine for sudden cardiac death. Frontiers in Genetics. 6. 55–55. 19 indexed citations

Stocchi, Laura, Emanuela Polidori, Lucia Potenza, et al.. (2015). Mutational analysis of mitochondrial DNA in Brugada syndrome. Cardiovascular Pathology. 25(1). 47–54. 14 indexed citations

Valentini, Alessandra, Michela Biancolella, Francesca Amati, et al.. (2007). Valproic Acid Induces Neuroendocrine Differentiation and UGT2B7 Up-Regulation in Human Prostate Carcinoma Cell Line. Drug Metabolism and Disposition. 35(6). 968–972. 36 indexed citations

10.

Amati, Francesca, Rita Carsetti, Silvia Placidi, et al.. (2006). A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice. Cardiovascular Pathology. 15(4). 194–202. 26 indexed citations

11.

Botta, Annalisa, Fabrizio Rinaldi, E. Bonifazi, et al.. (2006). Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathway in DM1 and DM2. Gene Expression. 13(6). 339–351. 38 indexed citations

12.

Contino, Gianmarco, Francesca Amati, Sabina Pucci, et al.. (2004). Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. Gene. 328. 69–74. 22 indexed citations

13.

Giardina, Emiliano, Francesca Capon, Maria Rosaria D’Apice, et al.. (2002). Mutational analysis of Peroxiredoxin IV: exclusion of a positional candidate for multinodular goitre. BMC Medical Genetics. 3(1). 5–5. 9 indexed citations

14.

Luca, Alessandro De, Emanuela Conti, Francesca Amati, et al.. (2002). Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q‐rich‐associated protein) and schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 116B(1). 32–35. 16 indexed citations

15.

Ratti, Antonia, Francesca Amati, Maura Bozzali, et al.. (2001). Cloning and molecular characterization of three Ubiquitin Fusion Degradation 1 (Ufd1) ortholog genes from <i>Xenopus laevis, Gallus gallus</i> and<i>Drosophila melanogaster</i>. Cytogenetic and Genome Research. 92(3-4). 279–282. 6 indexed citations

16.

Pizzuti, Antonio, Giuseppe Novelli, Antonia Ratti, et al.. (1999). Isolation and Characterization of a Novel Transcript Embedded within HIRA, a Gene Deleted in DiGeorge Syndrome. Molecular Genetics and Metabolism. 67(3). 227–235. 16 indexed citations

17.

Novelli, Giuseppe, Francesca Amati, & Bruno Dallapiccola. (1999). UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?. Trends in Genetics. 15(7). 251–253. 14 indexed citations

18.

Digilio, M. Cristina, Bruno Marino, Rita Mingarelli, et al.. (1996). Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11?. Journal of the American College of Cardiology. 27(2). 93–93. 1 indexed citations

19.

Amati, Francesca, Aldo Mari, Rita Mingarelli, et al.. (1995). 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot. Human Genetics. 95(5). 479–82. 94 indexed citations

20.

Amati, Francesca, Aldo Mari, Rita Mingarelli, et al.. (1995). Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region on 8p. American Journal of Medical Genetics. 57(3). 483–488. 11 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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