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Omar Askander
Affiliation : Université Mohammed VI des Sciences et de la Santé
- 10Publications (affiliation in Morocco)
- 20Total publications
- 247Citations
- 5h-index
Research profile
Omar Askander has 10 indexed publications (2021–2026). Their work appears mainly in “Epigenomes”, “Archives of Virology” and “Molecular Syndromology”. Their most cited article, “Identification of the novel SDR42E1 gene that affects steroid biosynthesis associated with the oculocutaneous genital syndrome” (2021), has been cited 11 times. 4 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- SARS-CoV-2 and COVID-19 Research
- COVID-19 Clinical Research Studies
- Genetic Associations and Epidemiology
Publications (10)
- Novel Perspectives on ATP8A2 Regulation: Evidence for Parental Imprinting and Chimeric Transcript Formation
- Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection
- A Novel Loss-of-Function Variant in COL4A3 in a Consanguineous Moroccan Family Displaying the Alport Syndrome with Variable Clinical Expression
- Atypical presentation of Dyggve-Melchior-Clausen disease in a Moroccan child without developmental delay and intellectual disabilities
- A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2
- Homozygous mutation in the ADH6 gene, involved in alcohol metabolism, associated with a multisystem disorder, analogous to the fetal alcohol syndrome
- Study of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans suggests a North African origin for Neanderthals
- Novel ITGB2 Mutation Is Responsible for a Severe Form of Leucocyte Adhesion Deficiency Type 1
- Coding-Complete Sequence of a SARS-CoV-2 Strain from an Omicron (B.1.1.529+BA.1) Variant Detected in Morocco
- Identification of the novel SDR42E1 gene that affects steroid biosynthesis associated with the oculocutaneous genital syndrome
Publication venues
- Epigenomes × 1
- Archives of Virology × 1
- Molecular Syndromology × 1
- Molecular Biology Reports × 1
- American Journal of Medical Genetics Part A × 1
- Journal of Clinical and Translational Endocrinology Case Reports × 1
Publications per year
- 20261
- 20243
- 20233
- 20222
- 20211
Collaborations
Partner institutions : Mohammed V University · Centre Hospitalier Universitaire Hassan II · Centre National pour la Recherche Scientifique et Technique (CNRST) · Université Internationale Abulcasis des Sciences de la Santé · Sidi Mohamed Ben Abdellah University
Co-authors
- Ahmed Bouhouche
- Elmostafa El Fahime
- Laila Bouguenouch
- Amine El Hassani
- Chaimae Nebhani
- Yasser Ali El Asri
- Abbas Ermilo Haroun
- Rédouane Abouqal
- Rachid Razıne
- Naima Erreimi
- Jihane Belayachi
- Karim Ouldim
Bibliographic data from OpenAlex (open database).
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