Author

Anthony D. Slonim

Renown HealthORCID 0000-0001-8437-4103Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:electronic health records· 2 Research Focus:fine-mapping· 2 Research Focus:GWAS / association mapping· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Gai ElhananiD· 3 shared Joseph J. GrzymskiiD· 3 shared Karen A. SchlauchiD· 3 shared Robert W. ReadiD· 3 shared William J. Metcalf· 3 shared Alexandre BolzeiD· 1 shared Bruce Lipp· 1 shared Chris J. Rowan· 1 shared

Activity by Year

2019-2019 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Gai ElhananORCID

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3 papers

Recent·Most cited

GeneticsG3 Genes Genomes GeneticsPeer-reviewedDec 30, 2019

A Comprehensive Genome-wide and Phenome-wide Examination of BMI and Obesity in a Northern Nevadan Cohort

Karen A. Schlauch, Robert W. Read, Vincent C. Lombardi…·Joseph J. Grzymski

This study uses EHR and genetics to perform GWAS and PheWAS on BMI and obesity, identifying known and novel variants and phenotypic associations.

38 citations

humanelectronic health records

𝕏 PostBluesky

GeneticsPLoS ONEPeer-reviewedJun 13, 2019

GWAS and PheWAS of Red Blood Cell Components in a Northern Nevadan Cohort

Karen A. Schlauch, Robert W. Read, Gai Elhanan…·Joseph J. Grzymski

This study performs GWAS and PheWAS on red blood cell components in a Northern Nevadan cohort, identifying genetic associations and linking SNPs to phenotypic diagnoses.

20 citations

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsbioRxivPreprintMay 27, 2019

Population Health Genetic Screening for Tier 1 Inherited Diseases in Northern Nevada: 90% of At-Risk Carriers are Missed

Joseph J. Grzymski, Gai Elhanan, E Smith…·James T. Lu

The paper finds that 90% of carriers of inherited disease variants are missed in current medical practice, highlighting the need for population-based genetic screening.

11 citations

humanwhole-exome sequencing

𝕏 PostBluesky