Author

Jessica P. Roberts

Washington University in St. LouisPrimary ORCID profile (0009-0001-4103-9222 · 6 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Jessica P. RobertsiD6 papers · Colorado State University

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 B. Carman· 1 shared CRIS M. BROWN· 1 shared Daniela Soto HernándeziD· 1 shared Fumihiko UranoiD· 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

Genetic & Genomic MedicineOrphanet Journal of Rare DiseasesPeer-reviewedApr 18, 2026

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…·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.

1 citation

humanstatistical model

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