Author

Asma Behlouli

Institution: University of Sciences and Technology Houari Boumediene

Observed institutions: University of Sciences and Technology Houari Boumediene, University of Algiers Benyoucef Benkhedda, Centre Hospitalo-Universitaire Bab El Oued

OpenAlex ID: A5080248257

EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness

2014 · Asma Behlouli, Crystel Bonnet, et al. · Orphanet Journal of Rare Diseases · 55

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

2016 · Samia Abdi, Amel Bahloul, et al. · PLoS ONE · 25

A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family

2016 · Asma Behlouli, Crystel Bonnet, et al. · International Journal of Pediatric Otorhinolaryngology · 15

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

Works count: 5

Citation count: 96

H-index: 3

I10-index: 3