Sous-spécialités
Génétique moléculaire, cytogénétique , Bio-informatique , Biostatistique
Domaines de compétences
*Analyse des prédispositions génétiques aux maladies multifactorielles : Diabète type 2, syndrome métabolique , Hypertension ..
*Diagnostic moléculaire des maladies Génétiques : surdités héréditaires , Infertilité masculine, Glioblastomes …
* Diagnostic moléculaire des infectieuse: Covid-19
*Mise en place et équipement de plateformes de Biologie Moléculaire.
Affiliation
Faculté de Médecine
| Date | Parcours |
|---|---|
| Depuis Décembre 2020 | Professeur Habilité en Génétique et Biologie Moléculaire. Faculté de Médecine, Université Mohammed VI des sciences de la santé, Casablanca. |
| Juin 2016- Décembre 2020 | Professeur-Assistant en Génétique et Biologie Moléculaire, Faculté de Médecine, Université Mohammed VI des sciences de la santé, Casablanca |
| Mai 2014 – mai 2016 | Support scientifique en Biologie Moléculaire à à Génome Biotechnologies |
| Décembre 2012 – Mai 2014 | Stage Postdoctoral: projet international « MEDGENE » pour l’étude du diabète de type 2 et syndrome métabolique chez la population marocaine.au Laboratoire de Génétique et Biologie Moléculaire à l’Institut Pasteur du Maroc, Casablanca. |
| 2012 | Doctorat en Biologie Spécialité : Biologie Moléculaire et Génétique Humaine. Faculté des Sciences Ain Chock, Université Hassan II Ain Chock, Casablanca. |
| 2008 | Diplôme des Etudes Supérieures Approfondies (DESA).Spécialité : Biotechnologie appliquée à l’industrie et à l’environnement.Faculté des Sciences Ain Chock, Université Hassan II Ain Chock, Casablanca. |
| 2006 | Licence en Biologie. Spécialité : Biologie Générale. Faculté des Sciences Ain Chock, Université Hassan II Ain Chock, Casablanca. |
| 2004 | Diplôme des Etudes Universitaires Générales (DEUG). Spécialité : Biologie- Géologie. Faculté des Sciences Ain Chock, Université Hassan II Ain Chock, Casablanca. |
Publications Article dans une revue indexée
| Type de publication | Intitulé | Lien |
|---|---|---|
| Review | A Review on Current Diagnostic Techniques for COVID-19 | https://pubmed.ncbi.nlm.nih.gov/33593219/ |
| Article | Large scale genomic analysis of 3067 SARS-CoV-2 genomes reveals a clonal geo-distribution and a rich genetic variations of hotspots mutations. | https://pubmed.ncbi.nlm.nih.gov/33170902/ |
| Article | Genomic Diversity and Hotspot Mutations in 30,983 SARS-CoV-2 Genomes: Moving Toward a Universal Vaccine for the « Confined Virus »? | https://pubmed.ncbi.nlm.nih.gov/33050463/ |
| Article | Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis | https://pubmed.ncbi.nlm.nih.gov/32832146/ |
| Article | Genome Sequences of Six SARS-CoV-2 Strains Isolated in Morocco, Obtained Using Oxford Nanopore MinION Technology | https://pubmed.ncbi.nlm.nih.gov/32763945/ |
| Article | Diagnosis of Coronavirus Disease 2019 (COVID-19): A laboratory based study of Casablanca Morocco. | https://www.publichealthinafrica.org/index.php/jphia/article/view/1458 |
| preprint | Do the Moroccan SARS-CoV-2 genetic diversity hamper the use of the developed universal vaccines in Morocco? | doi: https://doi.org/10.1101/2020.06.30.181123 |
| preprint | Epidemiological description and analysis of RdRp, E and N genes dynamic by RT-PCR of SARS-CoV-2 in Moroccan population: Experience of the National Reference Laboratory (LNR)-UM6SS | https://doi.org/10.1101/2020.06.18.20/135137. |
| preprint | Time to RNA negative conversion in Moroccan COVID-19 patients: A single-center experience. | DOI: 10.20944/preprints202006.0334.v1 |
| Article | Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patients. | https://pubmed.ncbi.nlm.nih.gov/32573970/ |
| Article | Association analysis of genetic variants with metabolic syndrome components in the Moroccan population. | https://pubmed.ncbi.nlm.nih.gov/28919193/ |
| Article | Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population. | https://pubmed.ncbi.nlm.nih.gov/27728995/ |
| Article | Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients. | https://pubmed.ncbi.nlm.nih.gov/26524954/ |
| Article | Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population. | https://pubmed.ncbi.nlm.nih.gov/26173767/ |
| Article | Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome. | https://pubmed.ncbi.nlm.nih.gov/25909077/ |
| Article | Evidence for association of the E23K variant of KCNJ11 gene with type 2 diabetes in Tunisian population: population-based study and meta-analysis. | https://pubmed.ncbi.nlm.nih.gov/25165692/ |
| Article | TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis. | https://pubmed.ncbi.nlm.nih.gov/24952604/ |
| Article | Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis. | https://pubmed.ncbi.nlm.nih.gov/24898818/ |
| Article | Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients. | https://pubmed.ncbi.nlm.nih.gov/24684850/ |
| Article | Contribution of CDKAL1 rs7756992 and IGF2BP2 rs4402960 polymorphisms in type 2 diabetes, diabetic complications, obesity risk and hypertension in the Tunisian population. | https://pubmed.ncbi.nlm.nih.gov/24636221/ |
| Article | Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss. | https://pubmed.ncbi.nlm.nih.gov/24339547/ |
| Article | Clinicopathological features and molecular analysis of primary glioblastomas in Moroccan patients. | https://pubmed.ncbi.nlm.nih.gov/22865003/ |
| Article | Association of the MTHFR A1298C variant with unexplained severe male infertility. | https://pubmed.ncbi.nlm.nih.gov/22457816/ |
| Article | Vitamin D Receptor Gene Polymorphisms and vitamin D status and susceptibility to Type 2 Diabetes Mellitus in Moroccans population. | http://www.ijsrp.org/research-paper-0814/ijsrp-p3221.pdf |
| Article | Relationship between Vitamin D Receptor (VDR) Gene Polymorphisms and susceptibility to Type 2 Diabetes Mellitus in Moroccans population. | http://www.ijias.issr-journals.org/abstract.php?article=IJIAS-14-214-01 |
| Article | Association between polymorphism in APOC3, and Metabolic Syndrome in the Moroccan Population. | http://www.ijsrp.org/research-paper-1014.php?rp=P343231 |
| Article | Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a Moroccan population. | https://pubmed.ncbi.nlm.nih.gov/22103601/ |
| Article | Maternal effect and familial aggregation in a type 2 diabetic Moroccan population. | https://pubmed.ncbi.nlm.nih.gov/21442339/ |
| Article | Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss. | https://pubmed.ncbi.nlm.nih.gov/20637512/ |
La FSTS adopte une gestion fondée sur l’écoute, la collégialité, la conviction, la confiance, la délégation et la communication.
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