Elena Botta
Impact in
- Cancer Research top 5%
- Carcinogens and Genotoxicity Assessment
- Molecular Biology top 5%
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- RNA Research and Splicing
- RNA regulation and disease
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
Papers in
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- DNA Repair Mechanisms 17
- RNA regulation and disease 6
- CRISPR and Genetic Engineering 6
- RNA Research and Splicing 4
- Fungal and yeast genetics research 3
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- Carcinogens and Genotoxicity Assessment 6
- Co-authors
- Miria Stefanini (21 shared papers)Alan R. Lehmann (11 shared papers)Tiziana Nardò (12 shared papers)Donata Orioli (11 shared papers)Bernard C. Broughton (3 shared papers)Nicolaas G.J. Jaspers (4 shared papers)Heather Fawcett (5 shared papers)Alain Sarasin (4 shared papers)
- Journals
- Human Molecular Genetics (3 papers)Human Mutation (3 papers)Human Genetics (2 papers)Proceedings of the National Academy of Sciences (2 papers)Journal of Investigative Dermatology (2 papers)
- Partner nations
- ItalyUnited KingdomNetherlands
In The Last Decade
Elena Botta
30 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 67
- Cancer Research 318
- Molecular Biology 1.3k
- Genetics 254
- Aging 16
- Cell Biology 141
Countries citing papers authored by Elena Botta
This map shows the geographic impact of Elena Botta'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 Elena Botta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elena Botta more than expected).
Fields of papers citing papers by Elena Botta
This network shows the impact of papers produced by Elena Botta. 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 Elena Botta. The network helps show where Elena Botta may publish in the future.
Co-authors
The 25 scholars most cited alongside Elena Botta, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 254 | |
| 2 | 1997 | 213 | |
| 3 | 2002 | 100 | |
| 4 | Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome. | 1995 | 97 |
| 5 | 1998 | 91 | |
| 6 | 1993 | 87 | |
| 7 | 2009 | 83 | |
| 8 | 1996 | 58 | |
| 9 | 2018 | 50 | |
| 10 | 1996 | 45 | |
| 11 | 2019 | 44 | |
| 12 | 2019 | 44 | |
| 13 | 2015 | 41 | |
| 14 | 2005 | 41 | |
| 15 | 2021 | 31 | |
| 16 | Novel Chinese hamster ultraviolet-sensitive mutants for excision repair form complementation groups 9 and 10. | 1991 | 31 |
| 17 | 2006 | 28 | |
| 18 | 1996 | 28 | |
| 19 | 2005 | 25 | |
| 20 | Identification of the eleventh complementation group of UV-sensitive excision repair-defective rodent mutants. | 1992 | 24 |
About Elena Botta
Elena Botta is a scholar working on Molecular Biology, Cancer Research, Cell Biology, Genetics and Plant Science, having authored 30 papers that have together received 1.5k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (17 papers), Carcinogens and Genotoxicity Assessment (6 papers), RNA regulation and disease (6 papers), CRISPR and Genetic Engineering (6 papers), RNA Research and Splicing (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Fungal and yeast genetics research (3 papers) and Enzyme Structure and Function (3 papers). The work is most often cited by research in Cancer Research (318 citations), Molecular Biology (1.3k citations), Genetics (254 citations), Aging (16 citations) and Cell Biology (141 citations). Elena Botta has collaborated with scholars based in Italy, United Kingdom and Netherlands. Frequent co-authors include Miria Stefanini, Alan R. Lehmann, Tiziana Nardò, Donata Orioli, Bernard C. Broughton, Nicolaas G.J. Jaspers, Heather Fawcett, Alain Sarasin, Wim Vermeulen and Jan H.J. Hoeijmakers. Their work appears in journals such as Human Molecular Genetics, Human Mutation, Human Genetics, Proceedings of the National Academy of Sciences and Journal of Investigative Dermatology.
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.