Author

Inas F. Aboobakar

Massachusetts Eye and Ear InfirmaryPrimary ORCID profile (0000-0002-4556-8818 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Inas F. AboobakariD1 paper · Duke Medical Center

Biology Disciplines

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Genetic & Genomic Medicine· 1

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

Arthur J. SitiD· 1 shared Chiea Chuen KhoriD· 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

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Arthur J. SitORCID

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1 paper

Recent·Most cited

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, Jessica N. Cooke Bailey, Chiea Chuen Khor, Tin Aung, Robert Ritch, Arthur J. Sit, Richard K. Lee, Margaret Ann Pericak‐Vance, Jae H. Kang, Jonathan L. Haines, Louis Robert Pasquale, 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.

medRxiv · Aug 5, 2021 · PreprintGenetic & Genomic Medicine