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
- Genomics and Phylogenetic Studies 1
- Epigenetics and DNA Methylation 1
- Cancer-related gene regulation 1
- CRISPR and Genetic Engineering 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)B Perkins (1 shared paper)Ewen F. Kirkness (1 shared paper)Ahmed Moustafa (1 shared paper)Suzanne Brewerton (1 shared paper)Chad Garner (1 shared paper)Levi Pierce (1 shared paper)Chao Xie (1 shared paper)
- Journals
- Cell stem cell (2 papers)Nature Communications (1 paper)Proceedings of the National Academy of Sciences (1 paper)
- Partner nations
- United States
In The Last Decade
Efren Sandoval
4 papers receiving 394 citations
Peers
Comparison fields: 5 of 78
- Genetics 169
- Aging 7
- Molecular Biology 243
- Cancer Research 41
- 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 | 196 | |
| 2 | 2017 | 97 | |
| 3 | 2020 | 79 | |
| 4 | 2017 | 26 |
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 398 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), Genomics and Phylogenetic Studies (1 paper), Epigenetics and DNA Methylation (1 paper), Cancer-related gene regulation (1 paper), CRISPR and Genetic Engineering (1 paper) and Genetic Associations and Epidemiology (1 paper). The work is most often cited by research in Genetics (169 citations), Aging (7 citations), Molecular Biology (243 citations), Cancer Research (41 citations) and Health Informatics (2 citations). Efren Sandoval has collaborated with scholars based in United States. Frequent co-authors include William Biggs, B Perkins, Ewen F. Kirkness, Ahmed Moustafa, Suzanne Brewerton, Chad Garner, Levi Pierce, Chao Xie, J. Craig Venter and Franz Josef Och. Their work appears in journals such as Cell stem cell, Nature Communications and Proceedings of the National Academy of Sciences.
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.