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Rabia Faridi

Affiliation : National Institutes of Health · National Institute on Deafness and Other Communication Disorders

• 2Publications (affiliation in the United States)
• 25Total publications
• 667Citations
• 11h-index

ORCIDOpenAlex

Research profile

Rabia Faridi has 2 indexed publications (2021–2025). Their work appears mainly in “Genetics in Medicine” and “Human Mutation”. Their most cited article, “Variants of human CLDN9 cause mild to profound hearing loss” (2021), has been cited 6 times. Their work is co-authored with at least 12 researchers, including institutions in Pakistan.

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Research areas

• Hearing, Cochlea, Tinnitus, Genetics
• Congenital Ear and Nasal Anomalies
• Genomics and Rare Diseases
• Vestibular and auditory disorders
• Genetic and Kidney Cyst Diseases

Publications (2)

• ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time
  2025 · Genetics in Medicine · cited 1 times
• Variants of human CLDN9 cause mild to profound hearing loss
  2021 · Human Mutation · cited 6 times

Publication venues

• Genetics in Medicine × 1
• Human Mutation × 1

Publications per year

• 20251
• 20211

Collaborations

Partner institutions : Broad Institute · University of Iowa · Mass General Brigham · Johns Hopkins University · Boston Children's Hospital

Co-authors’ countries : Pakistan

Co-authors

• Enyonam Edoh
• Amal Aburyyan
• Vanessa N. Gitau
• Ryan Webb
• Ellie Broeren
• Julie C. Ratliff
• Shelby E. Redfield
• Kezang C. Tshering
• Héla Azaiez
• Kevin T. A. Booth
• Nara Lygia de Macena Sobreira
• Cristina Fenollar‐Ferrer

Bibliographic data from OpenAlex (open database).