Publications by authors named "Imane Aitraise"

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Missense variants weakening a SOX9 phosphodegron linked to odontogenesis defects, scoliosis, and other skeletal features.
Imane Ettaki, Abdul Haseeb, Anirudha Karvande, Ghita Amalou, Asmae Saih, Imane AitRaise

HGG Adv· April 2025

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Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.
Imane AitRaise, Ghita Amalou, Amina Bakhchane, Amale Bousfiha, Houria Abdelghaffar

Biochem Genet· June 2024

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Novel pathogenic WHRN variant causing hearing loss in a moroccan family.
Imane AitRaise, Ghita Amalou, Salaheddine Redouane, Hicham Charoute, Khalid Snoussi

Mol Biol Rep· December 2023

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Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.
Imane AitRaise, Ghita Amalou, Amale Bousfiha, Hicham Charoute, Hassan Rouba

Mol Biol Rep· May 2022

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Virus-associated human cancers in Moroccan population: From epidemiology to prospective research.
Karima Abounouh, Imane Aitraise, Anas Benabou, Ikhlass Boussakri, Mohamed Amine Doumir

Infect Genet Evol· November 2019

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