Davide Bondavalli

764 total citations
7 papers, 33 citations indexed

About

Davide Bondavalli is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Davide Bondavalli has authored 7 papers receiving a total of 33 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Cardiology and Cardiovascular Medicine and 2 papers in Genetics. Recurrent topics in Davide Bondavalli's work include Cardiomyopathy and Myosin Studies (2 papers), Cardiovascular Effects of Exercise (2 papers) and Viral Infections and Immunology Research (1 paper). Davide Bondavalli is often cited by papers focused on Cardiomyopathy and Myosin Studies (2 papers), Cardiovascular Effects of Exercise (2 papers) and Viral Infections and Immunology Research (1 paper). Davide Bondavalli collaborates with scholars based in Italy, Australia and United States. Davide Bondavalli's co-authors include Ingrid Winship, Elisa Giacomini, L Bonelli, Irène Feroce, Aline Martayan, Francesca Malvestiti, Alessandra Viel, Filomena Mazzei, Jessica Taylor and Maria Teresa Ricci and has published in prestigious journals such as American Journal of Medical Genetics Part A, Journal of Human Genetics and Australasian Journal of Dermatology.

In The Last Decade

Davide Bondavalli

6 papers receiving 33 citations

Peers

Davide Bondavalli
Tatyana Der United States
Paul Hale United States
Kendra Engleman United States
Davide Bondavalli
Citations per year, relative to Davide Bondavalli Davide Bondavalli (= 1×) peers Erh‐Chan Yeh

Countries citing papers authored by Davide Bondavalli

Since Specialization
Citations

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

Fields of papers citing papers by Davide Bondavalli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Davide Bondavalli

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

All Works

7 of 7 papers shown
1.
Urtis, Mario, et al.. (2025). The contemporary role of genetics in cardiovascular medicine: from phenotypes to precision diagnoses. European Heart Journal Supplements. 27(Supplement_1). i67–i72.
2.
Grasso, Maurizia, Davide Bondavalli, Alessandro Di Toro, et al.. (2024). The new 2023 ESC guidelines for the management of cardiomyopathies: a guiding path for cardiologist decisions. European Heart Journal Supplements. 26(Supplement_1). i1–i5. 5 indexed citations
3.
Bondavalli, Davide, et al.. (2022). Movement of the Tongue During Target Reaching on a 2-Dimensional Surface. 2022 44th Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC). 2022. 4278–4281. 2 indexed citations
4.
Bondavalli, Davide, et al.. (2017). BRCA1 homozygous unclassified variant in a patient with non‑Fanconi anemia: A case report. Oncology Letters. 15(3). 3329–3332. 3 indexed citations
5.
Ricci, Maria Teresa, Sara Miccoli, Daniela Turchetti, et al.. (2016). Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study. Journal of Human Genetics. 62(2). 309–315. 12 indexed citations
6.
Bondavalli, Davide, Susan M. White, Andrew C. Steer, Andreas Pflaumer, & Ingrid Winship. (2015). Is cardiac rhabdomyoma a feature of Birt Hogg Dubé syndrome?. American Journal of Medical Genetics Part A. 167(4). 802–804. 7 indexed citations
7.
Taylor, Jessica, et al.. (2014). Mal de Meleda in Indonesia: Mutations in the SLURP1 gene appear to be ubiquitous. Australasian Journal of Dermatology. 57(1). e11–3. 4 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