Author

Fatima Ammar Khodja

Observed name: F. Ammar Khodja

Institution: University of Sciences and Technology Houari Boumediene

Observed institution: University of Sciences and Technology Houari Boumediene

OpenAlex ID: A5042640121

The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regions

2019 · Sonia Talbi, Crystel Bonnet, et al. · International Journal of Pediatric Otorhinolaryngology · 6

Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity

2025 · Zied Riahi, Sophie Boucher, et al. · Proceedings of the National Academy of Sciences · 1

Diversity of the genes involved in Algerian families with hearing loss identified by whole exome sequencing

2018 · M. Dahmani, F. Ammar Khodja, et al. · New Biotechnology

Works count: 3

Citation count: 7

H-index: 1

I10-index: