Author

Efren Sandoval

Helix (United States)ORCID 0000-0003-1314-3927Unclaimed ORCID profile · follow to get notified of new preprints

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Efren Sandoval1 paper

Biology Disciplines

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Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Donna M. Fath· 1 shared Elizabeth T. CirulliiD· 1 shared Francisco TanudjajaiD· 1 shared Gai ElhananiD· 1 shared James T. LuiD· 1 shared Joseph J. GrzymskiiD· 1 shared Karen A. SchlauchiD· 1 shared Magnus Isaksson· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Donna M. Fath

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1 paper

Recent·Most cited

GeneticsNature CommunicationsPeer-reviewedJan 28, 2020

Genome-wide rare variant analysis for thousands of phenotypes in 54,000 exomes

Elizabeth T. Cirulli, Simon White, Robert W. Read…·Nicole L. Washington

The paper analyzes rare variants in 54,000 exomes across 3,166 phenotypes, identifying 78 gene-based associations with significant effects on human traits.

139 citationstop 4%

humanwhole-exome sequencing

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