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Sara Salime

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability
2015 · Majida Charif, Agathe Roubertie, et al. · Frontiers in Genetics · 49
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Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss
2016 · Amina Bakhchane, Amale Bousfiha, et al. · European Journal of Medical Genetics · 26
Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees
2015 · Amina Bakhchane, Majida Charif, et al. · PLoS ONE · 25
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Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families
2017 · Sara Salime, Majida Charif, et al. · International Journal of Pediatric Otorhinolaryngology · 20
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family
2020 · Soukaina Elrharchi, Zied Riahi, et al. · Human Heredity · 8
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family
2018 · Sara Salime, Zied Riahi, et al. · Gene · 7
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome
2018 · Soukaina Elrharchi, Zied Riahi, 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
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Works count: 9
Citation count: 142
H-index: 6
I10-index: 4
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