Efren Sandoval

2.9k total citations
4 papers, 393 citations indexed

About

Efren Sandoval is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Efren Sandoval has authored 4 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 0 papers in Infectious Diseases. Recurrent topics in Efren Sandoval's work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Pluripotent Stem Cells Research (2 papers). Efren Sandoval is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Pluripotent Stem Cells Research (2 papers). Efren Sandoval collaborates with scholars based in United States. Efren Sandoval's co-authors include William Biggs, Ewen F. Kirkness, Chad Garner, Yaron Turpaz, Amalio Telenti, B Perkins, J. Craig Venter, Chao Xie, Martin M. Fabani and Franz Josef Och and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Cell stem cell.

In The Last Decade

Efren Sandoval

4 papers receiving 390 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Efren Sandoval United States	4	258	183	47	18	15	4	393
Cheng Cui United States	11	418 1.6×	166 0.9×	44 0.9×	28 1.6×	23 1.5×	19	518
Jason E. Miller United States	11	289 1.1×	64 0.3×	34 0.7×	7 0.4×	5 0.3×	26	379
Ligia Mateiu Belgium	12	285 1.1×	157 0.9×	46 1.0×	6 0.3×	30 2.0×	29	480
Denise E. Mauldin United States	7	177 0.7×	178 1.0×	39 0.8×	3 0.2×	11 0.7×	7	302
Alba Sanchis‐Juan United Kingdom	8	234 0.9×	224 1.2×	49 1.0×	7 0.4×	3 0.2×	15	431
George J. Kargul United States	6	331 1.3×	100 0.5×	43 0.9×	5 0.3×	10 0.7×	7	448
N. A. Skryabin Russia	10	184 0.7×	157 0.9×	35 0.7×	5 0.3×	12 0.8×	46	371
Nathan R. Zemke United States	9	210 0.8×	78 0.4×	24 0.5×	6 0.3×	10 0.7×	13	307
Aaron Hardin United States	6	220 0.9×	74 0.4×	26 0.6×	4 0.2×	10 0.7×	16	292

Countries citing papers authored by Efren Sandoval

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Efren Sandoval

This figure shows the co-authorship network connecting the top 25 collaborators of Efren Sandoval. A scholar is included among the top collaborators of Efren Sandoval based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Efren Sandoval. Efren Sandoval is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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4 of 4 papers shown

1.

Cirulli, Elizabeth T., Simon White, Robert W. Read, et al.. (2020). Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts. Nature Communications. 11(1). 542–542. 76 indexed citations

2.

DeBoever, Christopher, He Li, David Jakubosky, et al.. (2017). Large-Scale Profiling Reveals the Influence of Genetic Variation on Gene Expression in Human Induced Pluripotent Stem Cells. Cell stem cell. 20(4). 533–546.e7. 97 indexed citations

3.

Panopoulos, Athanasia D., Erin N. Smith, Angelo D. Arias, et al.. (2017). Aberrant DNA Methylation in Human iPSCs Associates with MYC-Binding Motifs in a Clone-Specific Manner Independent of Genetics. Cell stem cell. 20(4). 505–517.e6. 25 indexed citations

4.

Telenti, Amalio, Levi Pierce, William Biggs, et al.. (2016). Deep sequencing of 10,000 human genomes. Proceedings of the National Academy of Sciences. 113(42). 11901–11906. 195 indexed citations

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.

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