Author

F. Daniel Davis

Geisinger Health SystemORCID 0000-0002-5637-7806Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

David H. LedbetteriD· 3 shared David J. CareyiD· 3 shared Adam H. BuchananiD· 2 shared Adam J. Mansfield· 2 shared Amy Curry SturmiD· 2 shared Andrew Deubler· 2 shared Aris BarasiD· 2 shared Ayesha Rasool· 2 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

David H. LedbetterORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineCommunications BiologyPeer-reviewedJun 3, 2022

Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

Kavita Praveen, Lee Dobbyn, Lauren Gurski…·Joe Burns

This study identifies 53 genetic loci associated with hearing loss, including 15 novel ones, using genome-wide and exome-sequencing data from multiple cohorts.

36 citations

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsNature CommunicationsPeer-reviewedJul 27, 2021

GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms

Lucas D. Ward, Ho-Chou Tu, Chelsea B. Quenneville…·Paul Nioi

This study identifies a rare variant in SLC30A10 associated with elevated ALT/AST and hypermanganesemia symptoms, suggesting broader health impacts beyond diagnosed cases.

60 citationstop 4%

humanGWAS summary statistics

𝕏 PostBluesky

GenomicsThe American Journal of Human GeneticsPeer-reviewedAug 9, 2018

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort

Marci L.B. Schwartz, Cara Zayac McCormick, Amanda L. Lazzeri…·Michael F. Murray

The paper describes a model for returning secondary genomic findings to participants and healthcare providers in a large research cohort, with 93% successful contact rates and 222 providers notified.

182 citationstop 1%

humanwhole-exome sequencing

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