Author

Rob P. Igo

Case Western Reserve University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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 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

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

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