Ahmed Bouhouche - Hôpital des Spécialités, CHU de Rabat-Salé Rabat Morocco

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论文共 86 篇作者统计合作学者相似作者

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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,Elmostafa El Fahime, Hakima Fares,Khalid Ennibi,Redouane Abouqal,Rachid Razine,Ahmed Bouhouche

Archives of Virology（2024）

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De Novo P.glu61ter Mutation in GCH1 in a Moroccan Patient with Dopa-Responsive Dystonia: a Case Report

Ahmed Bouhouche,Leila Tamaoui,Nazha Birouk

Pan African Medical Journal (2024)

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Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome

Ahmed Bouhouche, Sara Sefiani,Hicham Charoute,Tibar Houyam,Naima Bouslam, Fatima-Zahra El Yousfi, Wadi Bnouhana,Ali Benomar, Fatima-Zahra Ouadghiri,Wafaa Regragui

Genetic Testing and Molecular Biomarkersno. 6 (2024): 257-262

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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

Molecular Syndromologypp.1-6, (2024)

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Association of Renin–Angiotensin Pathway Gene Polymorphisms with COVID-19 Susceptibility and Severity in Moroccans: A Case–Control Study

Fatima-Zahra El Yousfi,Samia El Hilali,Jihane Belayachi,Khalid Ennibi,Rachid Razine,Redouane Abouqal,Ahmed Bouhouche

BIOCHEMICAL GENETICS (2024)

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Study of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans suggests a North African origin for Neanderthals

Fatima Zohra El Youssfi,Abbas Ermilo Haroun, Chaimae Nebhani,Jihane Belayachi,Omar Askander,Elmostafa El Fahime, Hakima Fares,Khalid Ennibi,Redouane Abouqal,Rachid Razine,Ahmed Bouhouche

medRxiv (Cold Spring Harbor Laboratory) (2023)

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Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson’s Disease in Sporadic Moroccan Patients

Imane Smaili,Houyam Tibar,Mounia Rahmani, Najlaa Machkour,Rachid Razine,Hajar Naciri Darai,Naima Bouslam,Ali Benomar,Wafa Regragui,Ahmed Bouhouche

Journal of Molecular Neuroscience（2023）

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Homozygous Mutation in the ADH6 Gene, Involved in Alcohol Metabolism, Associated with a Multisystem Disorder, Analogous to the Fetal Alcohol Syndrome

Ahmed Bouhouche,Omar Askander,Hicham Charoute,Mouna Sabib,Abdeljalil El Quessar,Amine El Hassani,Naima Erreimi

Journal of Clinical and Translational Endocrinology Case Reports (2023): 100144-100144

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Novel ITGB2 Mutation is Responsible for a Severe Form of Leucocyte Adhesion Deficiency Type 1

Ahmed Bouhouche, Yasmin Tabache,Omar Askander,Hicham Charoute, Nada Mesnaoui,Lamiae Belayachi,Naima El Hafidi, Houyam Hardizi,Elmostafa El Fahime,Naima Erreimi,Abdelhamid Barakat,Mohammed Khattab,Fouad Seghrouchni,Amine El Hassani

BioMed Research International（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,Amine El Hassani,Hinde Iraqi,Elmostafa El Fahime, Mohammed Belmekki

Experimental Eye Research (2021): 108671-108671

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