Rossella Tupler
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Molecular Biology top 5%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
Papers in
-
- Muscle Physiology and Disorders 37
- RNA Research and Splicing 10
- RNA modifications and cancer 8
- Genetics 22
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 7
- Co-authors
- Michael R. Green (6 shared papers)Davide Gabellini (6 shared papers)Giovanni Perini (3 shared papers)P Maraschio (18 shared papers)L. Tiepolo (9 shared papers)Giovanna Vaula (4 shared papers)Rudolph E. Tanzi (3 shared papers)Marzia Mortilla (4 shared papers)
- Journals
- Journal of Medical Genetics (7 papers)Human Genetics (6 papers)Neuromuscular Disorders (5 papers)Human Molecular Genetics (2 papers)Clinical Genetics (2 papers)
- Partner nations
- ItalyUnited StatesCanada
In The Last Decade
Rossella Tupler
74 papers receiving 2.3k citations
Peers
Comparison fields: 5 of 121
- Genetics 265
- Molecular Biology 1.7k
- Genetics 507
- Cellular and Molecular Neuroscience 262
- Physiology 346
Countries citing papers authored by Rossella Tupler
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
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-authors
The 25 scholars most cited alongside Rossella Tupler, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 80 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 311 | |
| 2 | 2001 | 296 | |
| 3 | 2005 | 170 | |
| 4 | Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease cases. | 1992 | 159 |
| 5 | 1996 | 101 | |
| 6 | 1992 | 100 | |
| 7 | 2003 | 71 | |
| 8 | 2020 | 61 | |
| 9 | 2010 | 49 | |
| 10 | 2006 | 49 | |
| 11 | 2004 | 48 | |
| 12 | 2012 | 44 | |
| 13 | 2017 | 41 | |
| 14 | 2017 | 40 | |
| 15 | 2011 | 35 | |
| 16 | 2007 | 33 | |
| 17 | 2009 | 33 | |
| 18 | 1996 | 33 | |
| 19 | 2021 | 32 | |
| 20 | 1999 | 32 |
About Rossella Tupler
Rossella Tupler is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Physiology and Cardiology and Cardiovascular Medicine, having authored 80 papers that have together received 2.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (37 papers), Genetic Neurodegenerative Diseases (11 papers), RNA Research and Splicing (10 papers), Genomic variations and chromosomal abnormalities (9 papers), RNA modifications and cancer (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Cardiomyopathy and Myosin Studies (7 papers) and Chromosomal and Genetic Variations (6 papers). The work is most often cited by research in Genetics (265 citations), Molecular Biology (1.7k citations), Genetics (507 citations), Cellular and Molecular Neuroscience (262 citations) and Physiology (346 citations). Rossella Tupler has collaborated with scholars based in Italy, United States and Canada. Frequent co-authors include Michael R. Green, Davide Gabellini, Giovanni Perini, P Maraschio, L. Tiepolo, Giovanna Vaula, Rudolph E. Tanzi, Marzia Mortilla, Jonathan L. Haines and Giuseppe D’Antona. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Neuromuscular Disorders, Human Molecular Genetics and Clinical Genetics.
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.