Author

Arthur J. Sit

Mayo ClinicORCID 0000-0002-3904-2625Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Chiea Chuen KhoriD· 1 shared Inas F. Aboobakar· 1 shared Jae H. Kang· 1 shared Janey L. WiggsiD· 1 shared Jessica N. Cooke BaileyiD· 1 shared Jonathan L. HainesiD· 1 shared Louis Robert PasqualeiD· 1 shared Margaret Ann Pericak‐VanceiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Chiea Chuen KhorORCID

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1 paper

Recent·Most cited

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

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