Author

B. Carman

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

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Abby F. Tang· 1 shared CRIS M. BROWN· 1 shared Daniela Soto HernándeziD· 1 shared Fumihiko UranoiD· 1 shared Jessica P. Roberts· 1 shared Liam Oiknine· 1 shared Stacy Hurst· 1 shared Yunshuo Tang· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abby F. Tang

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1 paper

Recent·Most cited

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