Author

Connor W. Edsall

National Institutes of HealthORCID 0000-0001-6876-1496Unclaimed 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· 2 Approach:statistical model· 2 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Approach:machine learning (classical)· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Andrew SingletoniD· 2 shared Dena G. HernandeziD· 2 shared Jesse Raphael GibbsiD· 2 shared A RodrígueziD· 1 shared Adolfo López de MunaíniD· 1 shared Adolfo Mínguez‐CastellanosiD· 1 shared Adriano Jiménez‐EscrigiD· 1 shared Ana CámaraiD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersNeuroscience

Andrew SingletonORCID

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2 papers

Recent·Most cited

NeuroscienceMovement DisordersPeer-reviewedOct 29, 2019

The genetic architecture of Parkinson disease in Spain: characterizing population-specific risk, differential haplotype structures, and providing etiologic insight

Sara Bandrés‐Ciga, Sarah Ahmed, Marya S. Sabir…·Andrew Singleton

This study conducts a GWAS of Parkinson disease in Spain, identifies a novel population-specific signal at PARK2 associated with age-at-onset, and highlights genetic substructure for future fine-mapping.

67 citationstop 4%

humanwhole-genome sequencing

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GenomicsbioRxivPreprintFeb 23, 2018

A comprehensive assessment of benign genetic variability for neurodegenerative disorders

Rita João Guerreiro, Celeste Sassi, Jesse Raphael Gibbs…·José Brás

The paper assesses benign genetic variability in elderly individuals without neurodegenerative disease to aid in distinguishing pathogenic mutations.

19 citations

humanwhole-exome sequencing

𝕏 PostBluesky