Enrique Vidal
Impact in
- Molecular Biology top 5%
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- RNA modifications and cancer
- RNA Research and Splicing
- Cancer-related gene regulation
- Cancer Research top 10%
Papers in
-
- Genomics and Chromatin Dynamics 15
- Epigenetics and DNA Methylation 14
- RNA modifications and cancer 7
- RNA Research and Splicing 5
- Genomics and Phylogenetic Studies 4
- Cancer-related gene regulation 4
- Genetics 16
- Genetic Syndromes and Imprinting 4
- Genetics and Neurodevelopmental Disorders 4
- Co-authors
- Marina Pollán (12 shared papers)Manel Esteller (13 shared papers)Beatriz Pérez‐Gómez (11 shared papers)Núria Aragonés (11 shared papers)Gonzalo López‐Abente (11 shared papers)Javier García‐Pérez (8 shared papers)Holger Heyn (9 shared papers)Rebeca Ramis (6 shared papers)
- Journals
- Nucleic Acids Research (4 papers)BMC Cancer (4 papers)Nature Communications (3 papers)Nature Genetics (2 papers)PLoS Genetics (2 papers)
- Partner nations
- SpainUnited StatesSwitzerland
In The Last Decade
Enrique Vidal
51 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 148
- Molecular Biology 1.5k
- Cancer Research 289
- Genetics 499
- Health, Toxicology and Mutagenesis 146
- Transportation 65
Countries citing papers authored by Enrique Vidal
This map shows the geographic impact of Enrique Vidal'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 Enrique Vidal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Enrique Vidal more than expected).
Fields of papers citing papers by Enrique Vidal
This network shows the impact of papers produced by Enrique Vidal. 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 Enrique Vidal. The network helps show where Enrique Vidal may publish in the future.
Co-authors
The 25 scholars most cited alongside Enrique Vidal, 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 52 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 236 | |
| 2 | 2008 | 200 | |
| 3 | 2016 | 152 | |
| 4 | 2016 | 119 | |
| 5 | 2014 | 94 | |
| 6 | 2015 | 94 | |
| 7 | 2020 | 91 | |
| 8 | 2016 | 73 | |
| 9 | 2015 | 71 | |
| 10 | 2017 | 70 | |
| 11 | 2018 | 63 | |
| 12 | 2014 | 60 | |
| 13 | 2019 | 58 | |
| 14 | 2012 | 56 | |
| 15 | 2009 | 55 | |
| 16 | 2015 | 50 | |
| 17 | 2009 | 50 | |
| 18 | 2010 | 49 | |
| 19 | 2016 | 48 | |
| 20 | 2018 | 46 |
About Enrique Vidal
Enrique Vidal is a scholar working on Molecular Biology, Genetics, Oncology, Cancer Research and Surgery, having authored 52 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (15 papers), Epigenetics and DNA Methylation (14 papers), RNA modifications and cancer (7 papers), RNA Research and Splicing (5 papers), Genomics and Phylogenetic Studies (4 papers), Genetic Syndromes and Imprinting (4 papers), Cancer-related gene regulation (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Molecular Biology (1.5k citations), Cancer Research (289 citations), Genetics (499 citations), Health, Toxicology and Mutagenesis (146 citations) and Transportation (65 citations). Enrique Vidal has collaborated with scholars based in Spain, United States and Switzerland. Frequent co-authors include Marina Pollán, Manel Esteller, Beatriz Pérez‐Gómez, Núria Aragonés, Gonzalo López‐Abente, Javier García‐Pérez, Holger Heyn, Rebeca Ramis, Sebastián Morán and Elena Boldo. Their work appears in journals such as Nucleic Acids Research, BMC Cancer, Nature Communications, Nature Genetics and PLoS 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.