Publications by authors named "Omar Askander"

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Novel Variant in the NLRP12 Gene: Insights From a Case Report and Systematic Review.
Abdelhamid Bouramtane, Badreddine Elmakhzen, Hinde Elmouhi, Mohamed Ahakoud, Laila Bouguenouch, Omar Askander

Int J Immunogenet· November 2025

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Expanding the spectrum of ATP8A2 mutations: a new splicing variant and systematic review of CAMRQ4 syndrome.
Bouramtane Abdelhamid, Elmakhzen Badreddine, Ouskri Amal, Bouchikhi Rania, Yasser Ali El-Asri, Askander Omar

Mol Biol Rep· May 2025

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Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders.
Elisa Cali, Tania Quirin, Clarissa Rocca, Stephanie Efthymiou, Antonella Riva, Omar Askander

Genet Med· April 2025

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A Novel Loss-of-Function Variant in COL4A3 in a Consanguineous Moroccan Family Displaying the Alport Syndrome with Variable Clinical Expression.
Oumayma Taroua, Omar Askander, Hakima Rhou, Ahmed Bouhouche

Mol Syndromol· February 2025

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Atypical presentation of Dyggve-Melchior-Clausen disease in a Moroccan child without developmental delay and intellectual disabilities.
Badreddine Elmakhzen, Laila Bouguenouch, Kettani Oussama, Yasser Ali El Asri, Omar Askander

Mol Biol Rep· December 2024

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Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection.
Fatima Zahra El Yousfi, Abbas Ermilo Haroun, Chaimae Nebhani, Jihane Belayachi, Omar Askander

Arch Virol· April 2024

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Hypomorphic variants of SEL1L-HRD1 ER-associated degradation are associated with neurodevelopmental disorders.
Huilun H Wang, Liangguang L Lin, Zexin J Li, Xiaoqiong Wei, Omar Askander

J Clin Invest· January 2024

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A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2.
Khawla El Fizazi, Abdelhamid Bouramtane, Meriame Abbassi, Yasser Ali El Asri, Omar Askander

Am J Med Genet A· November 2023

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Genetic characterization of Schuurs-Hoeijmakers syndrome in a moroccan individual with heterozygote PACS1 mutation.
Meriame Abbassi, Abdelhamid Bourmtane, Hanane Sayel, Hinde El Mouhi, Meryem Jalte, Omar Askander

Mol Biol Rep· November 2023

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Coding-Complete Sequence of a SARS-CoV-2 Strain from an Omicron (B.1.1.529+BA.1) Variant Detected in Morocco.
Taha Chouati, Mouhssine Hemlali, Marouane Melloul, Sanaa Alaoui-Amine, Safae Rhoulam, Omar Askander

Microbiol Resour Announc· May 2022

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Novel Mutation Is Responsible for a Severe Form of Leucocyte Adhesion Deficiency Type 1.
Ahmed Bouhouche, Yasmin Tabache, Omar Askander, Hicham Charoute, Nada Mesnaoui

Biomed Res Int· April 2022

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Identification of the novel SDR42E1 gene that affects steroid biosynthesis associated with the oculocutaneous genital syndrome.
Ahmed Bouhouche, Nada Albaroudi, My Abdelaziz El Alaoui, Omar Askander, Zineb Habbadi

Exp Eye Res· August 2021

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