Catia Andreassi
Impact in
- Genetics top 1%
- Neurogenetic and Muscular Disorders Research
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- Neuroscience and Neuropharmacology Research
- Nerve injury and regeneration
- Axon Guidance and Neuronal Signaling
Papers in
- Genetics 10
- Neurogenetic and Muscular Disorders Research 10
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- RNA Research and Splicing 4
- Epigenetics and DNA Methylation 1
- Co-authors
- Sibylle Jablonka (5 shared papers)Michael Sendtner (5 shared papers)Umrao R. Monani (5 shared papers)Kathrin N. Karle (2 shared papers)Wilfried Rossoll (3 shared papers)Adolfo Saiardi (3 shared papers)Christina Brahe (4 shared papers)Salvatore Fusco (1 shared paper)
- Journals
- Human Molecular Genetics (3 papers)The Journal of Cell Biology (2 papers)European Journal of Human Genetics (1 paper)Neurogenetics (1 paper)Clinical Rheumatology (1 paper)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Catia Andreassi
22 papers receiving 2k citations
Peers
Comparison fields: 5 of 76
- Genetics 886
- Cellular and Molecular Neuroscience 282
- Molecular Biology 669
- Orthodontics 58
- Neurology 95
Countries citing papers authored by Catia Andreassi
This map shows the geographic impact of Catia Andreassi'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 Catia Andreassi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Catia Andreassi more than expected).
Fields of papers citing papers by Catia Andreassi
This network shows the impact of papers produced by Catia Andreassi. 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 Catia Andreassi. The network helps show where Catia Andreassi may publish in the future.
Co-authors
The 25 scholars most cited alongside Catia Andreassi, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 544 | |
| 2 | 2009 | 271 | |
| 3 | 2003 | 221 | |
| 4 | 2001 | 192 | |
| 5 | 2010 | 155 | |
| 6 | 1999 | 139 | |
| 7 | 2003 | 127 | |
| 8 | 2003 | 80 | |
| 9 | 2006 | 73 | |
| 10 | 2013 | 60 | |
| 11 | 2019 | 31 | |
| 12 | 2021 | 25 | |
| 13 | 2018 | 22 | |
| 14 | 2018 | 21 | |
| 15 | 1998 | 17 | |
| 16 | 2002 | 17 | |
| 17 | 2023 | 12 | |
| 18 | 2007 | 9 | |
| 19 | 2001 | 8 | |
| 20 | Mitochondrial Dynamics, Biogenesis, and Function Are Coordinated with the Cell Cycle by APC/C-CDH1 (Retraction of vol 15, pg 466, 2012) | 2012 | 5 |
About Catia Andreassi
Catia Andreassi is a scholar working on Genetics, Molecular Biology, Rheumatology, Cellular and Molecular Neuroscience and Developmental Neuroscience, having authored 23 papers that have together received 2k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (10 papers), RNA Research and Splicing (4 papers), Nerve injury and regeneration (2 papers), Systemic Lupus Erythematosus Research (2 papers), Epigenetics and DNA Methylation (1 paper), Microtubule and mitosis dynamics (1 paper), Axon Guidance and Neuronal Signaling (1 paper) and Bone Tissue Engineering Materials (1 paper). The work is most often cited by research in Genetics (886 citations), Cellular and Molecular Neuroscience (282 citations), Molecular Biology (669 citations), Orthodontics (58 citations) and Neurology (95 citations). Catia Andreassi has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Sibylle Jablonka, Michael Sendtner, Umrao R. Monani, Kathrin N. Karle, Wilfried Rossoll, Adolfo Saiardi, Christina Brahe, Salvatore Fusco, Richard Mitter and Serena De Vita. Their work appears in journals such as Human Molecular Genetics, The Journal of Cell Biology, European Journal of Human Genetics, Neurogenetics and Clinical Rheumatology.
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.