Elisa Adele Colombo
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Blood disorders and treatments
- Genetic and rare skin diseases.
- Hemoglobinopathies and Related Disorders
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 24
- Genomics and Rare Diseases 15
- Genetic and rare skin diseases. 14
- Blood disorders and treatments 7
- Glioma Diagnosis and Treatment 2
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- Genomics and Chromatin Dynamics 3
- Epigenetics and DNA Methylation 2
- DNA Repair Mechanisms 2
- Co-authors
- Lidia Larizza (22 shared papers)Cristina Gervasini (17 shared papers)Ludovica Volpi (5 shared papers)Gaia Roversi (4 shared papers)Daniela Concolino (4 shared papers)Elena Cassinerio (2 shared papers)Andrea Calabria (2 shared papers)Maria Domenica Cappellini (1 shared paper)
- Journals
- International Journal of Molecular Sciences (5 papers)Orphanet Journal of Rare Diseases (3 papers)European Journal of Human Genetics (3 papers)The American Journal of Human Genetics (2 papers)Human Genetics (2 papers)
- Partner nations
- ItalyUnited StatesTürkiye
In The Last Decade
Elisa Adele Colombo
34 papers receiving 574 citations
Peers
Comparison fields: 5 of 59
- Genetics 82
- Genetics 272
- Developmental Biology 11
- Cell Biology 45
- Immunology 48
Countries citing papers authored by Elisa Adele Colombo
This map shows the geographic impact of Elisa Adele Colombo'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 Elisa Adele Colombo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elisa Adele Colombo more than expected).
Fields of papers citing papers by Elisa Adele Colombo
This network shows the impact of papers produced by Elisa Adele Colombo. 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 Elisa Adele Colombo. The network helps show where Elisa Adele Colombo may publish in the future.
Co-authors
The 25 scholars most cited alongside Elisa Adele Colombo, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 127 | |
| 2 | 2008 | 78 | |
| 3 | 2022 | 45 | |
| 4 | 2012 | 43 | |
| 5 | 2019 | 31 | |
| 6 | 2010 | 30 | |
| 7 | 2011 | 24 | |
| 8 | 2016 | 23 | |
| 9 | 2018 | 22 | |
| 10 | 2020 | 22 | |
| 11 | 2020 | 18 | |
| 12 | 2014 | 12 | |
| 13 | 2015 | 12 | |
| 14 | 2021 | 12 | |
| 15 | 2017 | 11 | |
| 16 | 2018 | 8 | |
| 17 | 2018 | 8 | |
| 18 | 2022 | 8 | |
| 19 | 2013 | 7 | |
| 20 | 2015 | 7 |
About Elisa Adele Colombo
Elisa Adele Colombo is a scholar working on Genetics, Genetics, Molecular Biology, Cell Biology and Developmental Biology, having authored 38 papers that have together received 589 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (15 papers), Genetic and rare skin diseases. (14 papers), Blood disorders and treatments (7 papers), Genomics and Chromatin Dynamics (3 papers), Epigenetics and DNA Methylation (2 papers), Skin and Cellular Biology Research (2 papers), Glioma Diagnosis and Treatment (2 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Genetics (82 citations), Genetics (272 citations), Developmental Biology (11 citations), Cell Biology (45 citations) and Immunology (48 citations). Elisa Adele Colombo has collaborated with scholars based in Italy, United States and Türkiye. Frequent co-authors include Lidia Larizza, Cristina Gervasini, Ludovica Volpi, Gaia Roversi, Daniela Concolino, Elena Cassinerio, Andrea Calabria, Maria Domenica Cappellini, Eric Schoenmakers and Rolph Pfundt. Their work appears in journals such as International Journal of Molecular Sciences, Orphanet Journal of Rare Diseases, European Journal of Human Genetics, The American Journal of Human Genetics and Human 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.