Author

Liam Oiknine

Washington University in St. Louis

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

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Abby F. Tang· 2 shared Fumihiko UranoiD· 2 shared B. Carman· 1 shared CRIS M. BROWN· 1 shared Daniela Soto HernándeziD· 1 shared Evan M. LeeiD· 1 shared Jessica P. Roberts· 1 shared Kasra A. Vand· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 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

2 shared papersGenetic & Genomic Medicine

Abby F. Tang

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genotype-Based Severity Scoring System in Wolfram Syndrome: Correlation with Onset of Cardinal Symptoms and WFS1 Gene Variant Types

Liam Oiknine, Abby F. Tang, Evan M. Lee, Nila Palaniappan, Megha Verma, Kasra A. Vand, Sahiti Somalraju, Sarath Chandra Janga, Fumihiko Urano

Higher WFS1 genotype scores (variant frame, transmembrane location) tracked earlier diabetes mellitus and optic atrophy onset in 324 Wolfram patients, not hearing loss or diabetes insipidus.

Frontiers in Genetics · Jul 14, 2026Peer-reviewedGenetic & Genomic Medicine✦ In-depth digest

Natural history of patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy

Jessica P. Roberts, Abby F. Tang, Daniela Soto Hernández, B. Carman, Liam Oiknine, CRIS M. BROWN, Stacy Hurst, Yunshuo Tang, Fumihiko Urano

This study analyzes clinical data from 11 patients with autosomal dominant WFS1 variants to describe the natural history of optic atrophy and sensorineural hearing loss, identifying a novel variant and providing insights into disease progression.

Orphanet Journal of Rare Diseases · Apr 18, 2026Peer-reviewedGenetic & Genomic Medicine