Imen Amar

Affiliation : University of Sciences and Technology Houari Boumediene

1Publications (affiliation in Algeria)
1Total publications
46Citations
1h-index

Research profile

Imen Amar has 1 indexed publication (2010). Their work appears in “Genetic Testing and Molecular Biomarkers”. Their most cited article, “High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects” (2010), has been cited 46 times.

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Research areas

Genetic Associations and Epidemiology
Hearing, Cochlea, Tinnitus, Genetics
Congenital Ear and Nasal Anomalies

Publications (1)

High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects
2010 · Genetic Testing and Molecular Biomarkers · cited 46 times

Collaborations

Partner institutions : Centre of Biotechnology of Sfax

Co-authors’ countries : Tunisia

Bibliographic data from OpenAlex (open database).