Rossella Tupler

4.7k total citations
78 papers, 2.4k citations indexed

About

Rossella Tupler is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Rossella Tupler has authored 78 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 23 papers in Genetics and 17 papers in Cellular and Molecular Neuroscience. Recurrent topics in Rossella Tupler's work include Muscle Physiology and Disorders (37 papers), Genetic Neurodegenerative Diseases (16 papers) and Cardiomyopathy and Myosin Studies (12 papers). Rossella Tupler is often cited by papers focused on Muscle Physiology and Disorders (37 papers), Genetic Neurodegenerative Diseases (16 papers) and Cardiomyopathy and Myosin Studies (12 papers). Rossella Tupler collaborates with scholars based in Italy, United States and Canada. Rossella Tupler's co-authors include Michael R. Green, Davide Gabellini, Giovanni Perini, P Maraschio, L. Tiepolo, Marzia Mortilla, Giovanna Vaula, Rudolph E. Tanzi, Jonathan L. Haines and Maria Antonietta Pellegrino and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Rossella Tupler

72 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rossella Tupler Italy 26 1.7k 561 365 322 316 78 2.4k
Hasan O. Akman United States 29 1.3k 0.8× 596 1.1× 424 1.2× 198 0.6× 201 0.6× 71 2.5k
Alessandra Baumer Switzerland 27 1.7k 1.0× 1.3k 2.2× 286 0.8× 64 0.2× 239 0.8× 88 2.9k
Erik‐Jan Kamsteeg Netherlands 32 2.2k 1.3× 470 0.8× 343 0.9× 206 0.6× 704 2.2× 124 3.2k
Patrick Küry Germany 34 1.4k 0.8× 173 0.3× 181 0.5× 277 0.9× 717 2.3× 119 3.2k
Satoko Miyatake Japan 29 1.5k 0.9× 766 1.4× 142 0.4× 130 0.4× 508 1.6× 146 2.4k
Christian Windpassinger Austria 26 1.3k 0.8× 500 0.9× 192 0.5× 179 0.6× 451 1.4× 72 2.3k
Martin J. Somerville Canada 23 767 0.4× 640 1.1× 144 0.4× 192 0.6× 167 0.5× 45 1.8k
Salmo Raskin Brazil 28 1.5k 0.8× 578 1.0× 114 0.3× 196 0.6× 1.1k 3.4× 147 2.8k
Patrick A. Dreyfus France 26 1.1k 0.7× 157 0.3× 185 0.5× 322 1.0× 359 1.1× 49 2.0k
Hiroki Kato Japan 21 1.9k 1.1× 170 0.3× 379 1.0× 129 0.4× 410 1.3× 54 2.5k

Countries citing papers authored by Rossella Tupler

Since Specialization
Citations

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

Fields of papers citing papers by Rossella Tupler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rossella Tupler

This figure shows the co-authorship network connecting the top 25 collaborators of Rossella Tupler. A scholar is included among the top collaborators of Rossella Tupler 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 Rossella Tupler. Rossella Tupler 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.
Sozzi, Stefania, Massimo Negro, Rossella Tupler, et al.. (2025). Interplay between balance, gait kinematic and physical activity level in facioscapulohumeral muscular dystrophy. Scientific Reports. 15(1). 42973–42973.
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Tupler, Rossella, et al.. (2024). Bioimpedance analysis of fat free mass and its subcomponents and relative associations with maximal oxygen consumption in facioscapulohumeral dystrophy. European Journal of Applied Physiology. 125(1). 157–165. 5 indexed citations
6.
Beretta-Piccoli, Matteo, et al.. (2024). Maximal Oxygen Consumption Is Negatively Associated with Fat Mass in Facioscapulohumeral Dystrophy. International Journal of Environmental Research and Public Health. 21(8). 979–979. 6 indexed citations
7.
Salsi, Valentina, Gaetano Vattemi, & Rossella Tupler. (2023). The FSHD jigsaw: are we placing the tiles in the right position?. Current Opinion in Neurology. 36(5). 455–463. 8 indexed citations
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Pini, Sara, Enrico Tagliafico, Antonio La Marca, et al.. (2022). De novo variants and recombination at 4q35: Hints for preimplantation genetic testing in facioscapulohumeral muscular dystrophy. Clinical Genetics. 103(2). 242–246. 5 indexed citations
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Salsi, Valentina, et al.. (2021). The Italian National Registry for FSHD: an enhanced data integration and an analytics framework towards Smart Health Care and Precision Medicine for a rare disease. Orphanet Journal of Rare Diseases. 16(1). 470–470. 10 indexed citations
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Trevisan, Carlo P., Ebe Pastorello, Mario Ermani, et al.. (2007). Facioscapulohumeral Muscular Dystrophy: A Multicenter Study on Hearing Function. Audiology and Neurotology. 13(1). 1–6. 33 indexed citations
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Gabellini, Davide, Giuseppe D’Antona, Maurizio Moggio, et al.. (2005). Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1. Nature. 439(7079). 973–977. 170 indexed citations
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Gabellini, Davide, Michael R. Green, & Rossella Tupler. (2004). When enough is enough: genetic diseases associated with transcriptional derepression. Current Opinion in Genetics & Development. 14(3). 301–307. 16 indexed citations
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Soragna, D., Andrea Vettori, Gianni Carraro, et al.. (2003). A Locus for Migraine without Aura Maps on Chromosome 14q21.2-q22.3. The American Journal of Human Genetics. 72(1). 161–167. 70 indexed citations
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Maraschio, P, et al.. (1994). Molecular analysis of a human Y;1 translocation in an azoospermic male. Cytogenetic and Genome Research. 65(4). 256–260. 24 indexed citations
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Tupler, Rossella, Ekaterina Rogaeva, Giovanna Vaula, et al.. (1993). A highly informative microsatellite repeat polymorphism in intron 1 of the human amyloid precursor protein (APP) gene. Human Molecular Genetics. 2(5). 620–620. 4 indexed citations
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Vaula, Giovanna, Marzia Mortilla, Rossella Tupler, et al.. (1992). A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) gene. Neuroscience Letters. 144(1-2). 46–48. 9 indexed citations
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Zuffardi, Orsetta, P Maraschio, Rossella Tupler, et al.. (1989). Regional assignment of the loci for adenylate kinase to 9q32 and for ?1-acid glycoprotein to 9q31-q32. Human Genetics. 82(1). 17–19. 19 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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