1. 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. (4th August 2020) Authors: Morjane, Imane; Charoute, Hicham; Ouatou, Sanaa; Elkhattabi, Lamiae; Benrahma, Houda; Saile, Rachid; Rouba, Hassan; Barakat, Abdelhamid Other Names: Chen Robert Academic Editor. Journal: Cardiology research and practice Issue: Volume 2020(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation. (3rd November 2019) Authors: Essadssi, Soukaina; Krami, Al Mehdi; Elkhattabi, Lamiae; Elkarhat, Zouhair; Amalou, Ghita; Abdelghaffar, Houria; Rouba, Hassan; Barakat, Abdelhamid Other Names: Petit Patrice Academic Editor. Journal: Journal of immunology research Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Computational Analysis of the Potential Impact of MTC Complex Missenses SNPs Associated with Male Infertility. (18th March 2022) Authors: Harmak, Houda; Charoute, Hicham; Redouane, Salaheddine; Filali, Ouafaa Aniq; Barakat, Abdelhamid; Rouba, Hassan Other Names: Harrison Paul Academic Editor. Journal: BioMed research international Issue: Volume 2022(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21‐year single‐center experience. Issue 8 (17th June 2019) Authors: Elkarhat, Zouhair; Belkady, Boutaina; Charoute, Hicham; Zarouf, Latifa; Razoki, Lunda; Aboulfaraj, Jamila; Nassereddine, Sanaa; Elbakay, Chadli; Nasser, Boubker; Barakat, Abdelhamid; Rouba, Hassan Journal: American journal of medical genetics Issue: Volume 179:Issue 8(2019) Page Start: 1516 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Identification of deleterious missense variants of human Piwi like RNA-mediated gene silencing 1 gene and their impact on PAZ domain structure, stability, flexibility and dimension: in silico analysis. Issue 15 (12th October 2020) Authors: Elkarhat, Zouhair; Elkhattabi, Lamiaa; Charoute, Hicham; Morjane, Imane; Errouagui, Abdellatif; Carey, Francis; Nasser, Boubker; Barakat, Abdelhamid; Rouba, Hassan Journal: Journal of biomolecular structure & dynamics Issue: Volume 38:Issue 15(2020) Page Start: 4600 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure. (20th May 2019) Authors: Elkhattabi, Lamiae; Morjane, Imane; Charoute, Hicham; Amghar, Soumaya; Bouafi, Hind; Elkarhat, Zouhair; Saile, Rachid; Rouba, Hassan; Barakat, Abdelhamid Other Names: Peterson Jonathan M. Academic Editor. Journal: Journal of diabetes research Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population. Issue 11 (30th July 2015) Authors: Charoute, Hicham; Bakhchane, Amina; Benrahma, Houda; Romdhane, Lilia; Gabi, Khalid; Rouba, Hassan; Fakiri, Malika; Abdelhak, Sonia; Lenaers, Guy; Barakat, Abdelhamid Journal: Human mutation Issue: Volume 36:Issue 11(2015:Nov.) Page Start: E2441 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies. (24th January 2018) Authors: Portnoi, Marie-France; Dumargne, Marie-Charlotte; Rojo, Sandra; Witchel, Selma F; Duncan, Andrew J; Eozenou, Caroline; Bignon-Topalovic, Joelle; Yatsenko, Svetlana A; Rajkovic, Aleksandar; Reyes-Mugica, Miguel; Almstrup, Kristian; Fusee, Leila; Srivastava, Yogesh; Chantot-Bastaraud, Sandra; Hyon,... Journal: Human molecular genetics Issue: Volume 27:Number 7(2018:Apr. 01) Page Start: 1228 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population. (2nd January 2018) Authors: Charoute, Hicham; Kefi, Rym; Bounaceur, Safaa; Benrahma, Houda; Reguig, Ahmed; Kandil, Mostafa; Rouba, Hassan; Bakhchane, Amina; Abdelhak, Sonia; Barakat, Abdelhamid Journal: Mitochondrial DNA Issue: Volume 29:Number 1(2018) Page Start: 9 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Potential inhibitors of SARS-cov-2 RNA dependent RNA polymerase protein: molecular docking, molecular dynamics simulations and MM-PBSA analyses. Issue 1 (2nd January 2022) Authors: Elkarhat, Zouhair; Charoute, Hicham; Elkhattabi, Lamiae; Barakat, Abdelhamid; Rouba, Hassan Journal: Journal of biomolecular structure & dynamics Issue: Volume 40:Issue 1(2022) Page Start: 361 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗