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Saima Riazuddin

Affiliation : University of Maryland, Baltimore

2Publications (affiliation in the United States)
217Total publications
10104Citations
53h-index

Research profile

Saima Riazuddin has 2 indexed publications (2008–2026). Their work appears mainly in “Biomolecules” and “Nature Genetics”. Their most cited article, “Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans” (2008), has been cited 83 times. Their work is co-authored with at least 9 researchers, including institutions in Pakistan.

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Research areas

Hearing, Cochlea, Tinnitus, Genetics
Congenital Ear and Nasal Anomalies
Retinal Development and Disorders
Genomics and Rare Diseases
Hearing Loss and Rehabilitation

Publications (2)

Molecular Characterization of Syndromic Hearing Loss in North African Moroccan Families
2026 · Biomolecules
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans
2008 · Nature Genetics · cited 83 times

Publication venues

Biomolecules × 1
Nature Genetics × 1

Publications per year

20261
20081

Collaborations

Partner institutions : National Institute on Deafness and Other Communication Disorders · University of the Punjab · Centre of Excellence in Molecular Biology · University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center

Co-authors’ countries : Pakistan

Co-authors

Bibliographic data from OpenAlex (open database).