Efren Sandoval
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
Papers in
-
- Pluripotent Stem Cells Research 2
- Epigenetics and DNA Methylation 1
- Cancer-related gene regulation 1
- CRISPR and Genetic Engineering 1
- Genomics and Phylogenetic Studies 1
- Genetics 3
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 2
- Genetic Associations and Epidemiology 1
- Co-authors
- William Biggs (3 shared papers)Naisha Shah (1 shared paper)Chad Garner (1 shared paper)Ahmed Moustafa (1 shared paper)J. Craig Venter (1 shared paper)Suzanne Brewerton (1 shared paper)Amalio Telenti (1 shared paper)Martin M. Fabani (1 shared paper)
- Journals
- Cell stem cell (2 papers)Proceedings of the National Academy of Sciences (1 paper)Nature Communications (1 paper)
- Partner nations
- United States
In The Last Decade
Efren Sandoval
4 papers receiving 390 citations
Peers
Comparison fields: 5 of 80
- Genetics 183
- Aging 7
- Molecular Biology 258
- Cancer Research 47
- Health Informatics 2
Countries citing papers authored by Efren Sandoval
This map shows the geographic impact of Efren Sandoval'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 Efren Sandoval with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Efren Sandoval more than expected).
Fields of papers citing papers by Efren Sandoval
This network shows the impact of papers produced by Efren Sandoval. 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 Efren Sandoval. The network helps show where Efren Sandoval may publish in the future.
Co-authors
The 25 scholars most cited alongside Efren Sandoval, 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 | 2016 | 195 | |
| 2 | 2017 | 97 | |
| 3 | 2020 | 76 | |
| 4 | 2017 | 25 |
About Efren Sandoval
Efren Sandoval is a scholar working on Molecular Biology, Genetics, Infectious Diseases, Organic Chemistry and Surgery, having authored 4 papers that have together received 393 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers), Pluripotent Stem Cells Research (2 papers), Epigenetics and DNA Methylation (1 paper), Cancer-related gene regulation (1 paper), Genetic Associations and Epidemiology (1 paper), CRISPR and Genetic Engineering (1 paper) and Genomics and Phylogenetic Studies (1 paper). The work is most often cited by research in Genetics (183 citations), Aging (7 citations), Molecular Biology (258 citations), Cancer Research (47 citations) and Health Informatics (2 citations). Efren Sandoval has collaborated with scholars based in United States. Frequent co-authors include William Biggs, Naisha Shah, Chad Garner, Ahmed Moustafa, J. Craig Venter, Suzanne Brewerton, Amalio Telenti, Martin M. Fabani, Franz Josef Och and Julia di Iulio. Their work appears in journals such as Cell stem cell, Proceedings of the National Academy of Sciences and Nature Communications.
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.