Ahmed Bouhouche

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 17

Top Venues

Archives of virology

Genetic testing and molecular biomarkers

Case reports in genetics

BioMed research international

Université Mohammed V Agdal

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Université Mohammed V Agdal

Morocco

Professor :: Neurology - Neurogenetics

Publications

Ahmed Bouhouche, Sara Sefiani, Hicham Charoute, Tibar Houyam, Naima Bouslam, Fatima-Zahra El Yousfi, Wadi Bnouhana, Ali Benomar, Fatima-Zahra Ouadghiri, Wafaa Regragui
Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome. Genetic testing and molecular biomarkers (2024)
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
Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection. Archives of virology 169 (5) (2024)
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
Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection. Archives of virology 169 (5) (2024)
Ahmed Bouhouche, Sara Sefiani, Hicham Charoute, Tibar Houyam, Naima Bouslam, Fatima-Zahra El Yousfi, Wadi Bnouhana, Ali Benomar, Fatima-Zahra Ouadghiri, Wafaa Regragui
Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome. Genetic testing and molecular biomarkers 28 (6) (2024)
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
Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection. Archives of virology 169 (5) (2024)
Ahmed Bouhouche, Sara Sefiani, Hicham Charoute, Tibar Houyam, Naima Bouslam, Fatima-Zahra El Yousfi, Wadi Bnouhana, Ali Benomar, Fatima-Zahra Ouadghiri, Wafaa Regragui
Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome. Genetic testing and molecular biomarkers 28 (6) (2024)
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
Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection. Archives of virology 169 (5) (2024)
Fatima-Zahra El Yousfi, Samia El Hilali, Jihane Belayachi, Khalid Ennibi, Rachid Razine, Redouane Abouqal, Ahmed Bouhouche
Association of Renin-Angiotensin Pathway Gene Polymorphisms with COVID-19 Susceptibility and Severity in Moroccans: A Case-Control Study. Biochemical genetics (2024)
Imane Smaili, Houyam Tibar, Mounia Rahmani, Najlaa Machkour, Rachid Razine, Hajar Naciri Darai, Naima Bouslam, Ali Benomar, Wafa Regragui, Ahmed Bouhouche
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients. Journal of molecular neuroscience : MN (2023)
Ahmed Bouhouche, Yasmin Tabache, Omar Askander, Hicham Charoute, Nada Mesnaoui, Lamiae Belayachi, Naima El Hafidi, Houyam Hardizi, Elmostafa El Fahime, Naima Erreimi, Adbelhamid Barakat, Mohammed Khattab, Fouad Seghrouchni, Amine El Hassani
Novel ITGB2 Mutation Is Responsible for a Severe Form of Leucocyte Adhesion Deficiency Type 1. BioMed research international 2022 (2022)
Imane Smaili, Christelle Tesson, Wafa Regragui, Hélène Bertrand, Mounia Rahmani, Naima Bouslam, Ali Benomar, Alexis Brice, Suzanne Lesage, Ahmed Bouhouche
Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease. Journal of molecular neuroscience : MN 71 (1) (2020)
Imane Smaili, Imane Hajjaj, Rachid Razine, Houyam Tibar, Ayyoub Salmi, Naima Bouslam, Ahmed Moussa, Wafa Regragui, Ahmed Bouhouche
A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia. Case reports in genetics 2020 (2020)
Fatima Ouchkat, Wafaa Regragui, Imane Smaili, Hajar Naciri Darai, Naima Bouslam, Mounia Rahmani, Adyl Melhaoui, Yasser Arkha, Elmostafa El Fahime, Ahmed Bouhouche
Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report. BMC medical genetics 21 (1) (2020)
Ahmed Bouhouche, Houyam Tibar, Yamna Kriouale, Mohammed Jiddane, Imane Smaili, Naima Bouslam, Ali Benomar, Mohamed Yahyaoui, Elmostafa El Fahime
Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing. Case reports in genetics 2018 (2018)
Rafiqua Ben El Haj, Ayyoub Salmi, Wafa Regragui, Ahmed Moussa, Naima Bouslam, Houyam Tibar, Ali Benomar, Mohamed Yahyaoui, Ahmed Bouhouche
Evidence for prehistoric origins of the G2019S mutation in the North African Berber population. PloS one 12 (7) (2017)
Ahmed Bouhouche, Houyam Tibar, Rafiqua Ben El Haj, Khalil El Bayad, Rachid Razine, Sanaa Tazrout, Asmae Skalli, Naima Bouslam, Loubna Elouardi, Ali Benomar, Mohammed Yahyaoui, Wafa Regragui
LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease. Parkinson's disease 2017 (2017)
Rafiqua Ben El Haj, Wafaa Regragui, Rachid Tazi-Ahnini, Asmae Skalli, Naima Bouslam, Ali Benomar, Mohamed Yahyaoui, Ahmed Bouhouche
A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism. BioMed research international 2016 (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ahmed Bouhouche