Natàlia Padilla
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- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 4
- Genetic Associations and Epidemiology 3
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- Genomics and Phylogenetic Studies 5
- Epigenetics and DNA Methylation 3
- RNA and protein synthesis mechanisms 3
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- Cancer Genomics and Diagnostics 3
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- Attention Deficit Hyperactivity Disorder 2
- Co-authors
- Xavier de la CruzMarian A. Martínez‐BalbásPaul ZierepStefan GüntherMireia PagerolsVanesa RicharteIris Garcia‐MartínezAlejandro Arias Vásquez
- Journals
- International Journal of Molecular Sciences (2 papers)Human Mutation (2 papers)Familial Cancer (1 paper)
- Partner nations
- SpainGermanyNetherlands
In The Last Decade
Natàlia Padilla
14 papers receiving 189 citations
Peers
Comparison fields: 5 of 49
- Genetics 84
- Molecular Biology 124
- Biological Psychiatry 4
- Cancer Research 20
- Psychiatry and Mental health 19
Countries citing papers authored by Natàlia Padilla
This map shows the geographic impact of Natàlia Padilla'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 Natàlia Padilla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Natàlia Padilla more than expected).
Fields of papers citing papers by Natàlia Padilla
This network shows the impact of papers produced by Natàlia Padilla. 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 Natàlia Padilla. The network helps show where Natàlia Padilla may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Natàlia Padilla, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 3 | |
| 2 | 2024 | 0 | |
| 3 | 2023 | 0 | |
| 4 | 2023 | 3 | |
| 5 | 2021 | 7 | |
| 6 | 2021 | 14 | |
| 7 | 2021 | 0 | |
| 8 | 2020 | 3 | |
| 9 | 2019 | 1 | |
| 10 | 2019 | 42 | |
| 11 | 2019 | 8 | |
| 12 | 2018 | 29 | |
| 13 | 2017 | 21 | |
| 14 | 2017 | 3 | |
| 15 | 2017 | 12 | |
| 16 | 2016 | 7 | |
| 17 | 2016 | 37 |
About Natàlia Padilla
Natàlia Padilla is a scholar working on Genetics, Cancer Research and Hematology, having authored 17 papers that have together received 190 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Genomics and Phylogenetic Studies (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genetic Associations and Epidemiology (3 papers), Epigenetics and DNA Methylation (3 papers), Cancer Genomics and Diagnostics (3 papers), RNA and protein synthesis mechanisms (3 papers) and Attention Deficit Hyperactivity Disorder (2 papers). The work is most often cited by research in Genetics (84 citations), Molecular Biology (124 citations) and Biological Psychiatry (4 citations). Natàlia Padilla has collaborated with scholars based in Spain, Germany and Netherlands. Frequent co-authors include Xavier de la Cruz, Marian A. Martínez‐Balbás, Paul Zierep, Stefan Günther, Mireia Pagerols, Vanesa Richarte, Iris Garcia‐Martínez, Alejandro Arias Vásquez, María Soler Artigas and Miguel Casas. Their work appears in journals such as International Journal of Molecular Sciences, Human Mutation, Familial Cancer, Frontiers in Immunology 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.