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Ryan Webb

Affiliation : Broad Institute

• 1Publications (affiliation in the United States)
• 14Total publications
• 288Citations
• 5h-index

ORCIDOpenAlex

Research profile

Ryan Webb has 1 indexed publication (2025). Their work appears in “Genetics in Medicine”. Their most cited article, “ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time” (2025), has been cited 1 times. Their work is co-authored with at least 12 researchers.

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Research areas

• Genomics and Rare Diseases
• Genetic Associations and Epidemiology
• Biomedical Text Mining and Ontologies
• Semantic Web and Ontologies
• Systemic Lupus Erythematosus Research

Publications (1)

• ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time
  2025 · Genetics in Medicine · cited 1 times

Collaborations

Partner institutions : Mass General Brigham · National Institutes of Health · National Institute on Deafness and Other Communication Disorders · Boston Children's Hospital · University of Washington

Co-authors

• Enyonam Edoh
• Amal Aburyyan
• Vanessa N. Gitau
• Ellie Broeren
• Julie C. Ratliff
• Shelby E. Redfield
• Kezang C. Tshering
• Héla Azaiez
• Kevin T. A. Booth
• Sherin Shaaban
• Victoria Albano
• Hatice Duzkale

Bibliographic data from OpenAlex (open database).