Author

Tyler G. Kinzy

East Carolina UniversityORCID 0000-0002-4314-9791Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Assay:CITE-seq· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Jessica N. Cooke BaileyiD· 3 shared Dana C. CrawfordiD· 2 shared Jonathan L. HainesiD· 2 shared Margaret Ann Pericak‐VanceiD· 2 shared Alan J. Lerner· 1 shared Alan M. Kwong· 1 shared Alexander J. Brucker· 1 shared Alexis Boleda· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Jessica N. Cooke BaileyORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicineAnnals of Human GeneticsPeer-reviewedOct 18, 2026

Evidence for reduced somatic T-cell receptor sequence diversity profiles among Midwestern Amish in an aging cohort study

Lauren A. Cruz, Shiying Liu, Kristy L. S. Miskimen…·Dana C. Crawford

The paper examines T-cell receptor sequence diversity and HLA alleles in Midwestern Amish participants to explore associations with Alzheimer's disease and cognitive status.

DOI 10.1111/ahg.70063

humanCITE-seq

𝕏 PostBluesky

Genetic & Genomic MedicineNature GeneticsPeer-reviewedDec 1, 2024

Distinctive cross-ancestry genetic architecture for age-related macular degeneration

Bryan R. Gorman, Georgios Voloudakis, Robert P. Igo…·Srinivas V. Goverdhan

This study identifies 63 AMD risk loci across multiple ancestries, highlighting ancestry-dependent genetic heterogeneity and potential therapeutic targets.

58 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintAug 5, 2021

Distribution of rare LOXL1 missense alleles, haplotypes and diplotypes suggests association with reduced risk of glaucoma-related exfoliation syndrome.

Inas F. Aboobakar, Rob P. Igo, Tyler G. Kinzy…·Janey L. Wiggs

The paper identifies rare protective LOXL1 missense variants and shows their haplotypes and diplotypes are associated with reduced risk of exfoliation syndrome and glaucoma.

DOI 10.1101/2021.08.05.21261676

humanwhole-exome sequencing

𝕏 PostBluesky