Author

Paul T. Martin

Nationwide Children's HospitalORCID 0000-0002-0674-6191Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

Diane Marie Dunn· 2 shared John Burian· 2 shared Kevin M. FlaniganiD· 2 shared Lindsay N. AlfanoiD· 2 shared Megan A. WaldropiD· 2 shared Melissa Moore‐ClingenpeeliD· 2 shared Robert B. WeissiD· 2 shared Roxane Alles· 2 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Diane Marie Dunn

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2 papers

Recent·Most cited

Genetic & Genomic MedicineEuropean Journal of Human GeneticsPeer-reviewedMar 20, 2023

A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity

Kevin M. Flanigan, Megan A. Waldrop, Paul T. Martin…·Veronica J. Vieland

This paper conducts a genome-wide association study to identify genetic modifiers of disease severity in dystrophinopathy patients, finding multiple candidate loci associated with age at loss of ambulation.

12 citations

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintNov 3, 2021

Candidate gene modifiers of dystrophinopathy identified by the uniform application of genome-wide datasets to novel GWAS-identified loci

Kevin M. Flanigan, Megan A. Waldrop, Paul T. Martin…·Robert B. Weiss

The paper applies functional genomic datasets to six top GWAS loci to identify candidate gene modifiers of dystrophinopathy severity.

2 citations

humanGWAS summary statistics

𝕏 PostBluesky