Abdelhamid Barakat - Search Results

Year	Number of Results
2002	1
2004	1
2006	1
2007	4
2008	6
2010	3
2011	3
2012	8
2013	5
2014	8
2015	10
2016	4
2017	8
2018	9
2019	12
2020	9
2021	6
2022	11
2023	7
2024	1

1

A regionally based precision medicine implementation initiative in North Africa:The PerMediNA consortium.

Hamdi Y, Boujemaa M, Ben Aissa-Haj J, Radouani F, Khyatti M, Mighri N, Hannachi M, Ghedira K, Souiai O, Hkimi C, Kammoun MS, Mejri N, Bouaziz H, Beloufa MA, Charoute H, Barakat A, Najjar I, Taniguchi H, Pietrosemoli N; PerMediNA Consortium; Dellagi K, Abdelhak S, Boubaker MS, Chica C, Rouleau E. Hamdi Y, et al. Among authors: barakat a. Transl Oncol. 2024 Jun;44:101940. doi: 10.1016/j.tranon.2024.101940. Epub 2024 Mar 26. Transl Oncol. 2024. PMID: 38537326 Free article.

2

Novel pathogenic WHRN variant causing hearing loss in a moroccan family.

AitRaise I, Amalou G, Redouane S, Charoute H, Snoussi K, Abdelghaffar H, Bonnet C, Petit C, Barakat A. AitRaise I, et al. Among authors: barakat a. Mol Biol Rep. 2023 Dec;50(12):10663-10669. doi: 10.1007/s11033-023-08901-8. Epub 2023 Nov 4. Mol Biol Rep. 2023. PMID: 37924449

3

Molecular docking analysis of PPARγ with phytochemicals from Moroccan medicinal plants.

Elkhattabi L, Zouhdi S, Moussetad F, Kettani A, Barakat A, Saile R. Elkhattabi L, et al. Among authors: barakat a. Bioinformation. 2023 Jul 31;19(7):795-806. doi: 10.6026/97320630019795. eCollection 2023. Bioinformation. 2023. PMID: 37901293 Free PMC article.

4

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.

AitRaise I, Amalou G, Bakhchane A, Bousfiha A, Abdelghaffar H, Majida C, Bonnet C, Petit C, Barakat A. AitRaise I, et al. Among authors: barakat a. Biochem Genet. 2023 Oct 1. doi: 10.1007/s10528-023-10515-5. Online ahead of print. Biochem Genet. 2023. PMID: 37777971

5

Exploring the impact of CYP11A1's missense SNPs on the interaction between CYP11A1 and cholesterol: A comprehensive structural analysis and MD simulation study.

Redouane S, Harmak H, Elkarhat Z, Charoute H, Malki A, Barakat A, Rouba H. Redouane S, et al. Among authors: barakat a. Comput Biol Chem. 2023 Oct;106:107937. doi: 10.1016/j.compbiolchem.2023.107937. Epub 2023 Aug 2. Comput Biol Chem. 2023. PMID: 37552904

6

In silico exploration and molecular dynamics of deleterious SNPs on the human TERF1 protein triggering male infertility.

Harmak H, Redouane S, Charoute H, Aniq Filali O, Barakat A, Rouba H. Harmak H, et al. Among authors: barakat a. J Biomol Struct Dyn. 2023;41(24):14665-14688. doi: 10.1080/07391102.2023.2193995. Epub 2023 Mar 30. J Biomol Struct Dyn. 2023. PMID: 36995171

7

Genetic Association of LEP Gene Polymorphisms with Obesity in Moroccan Individuals: Case-Control Study and Updated Meta-analysis.

Bouafi H, Krami AM, Morjane I, Slaoui K, Harmak H, Charoute H, Saile R, Barakat A. Bouafi H, et al. Among authors: barakat a. Biochem Genet. 2023 Oct;61(5):1758-1774. doi: 10.1007/s10528-023-10342-8. Epub 2023 Feb 15. Biochem Genet. 2023. PMID: 36792840

8

Computational study of the potential impact of AURKC missense SNPs on AURKC-INCENP interaction and their correlation to macrozoospermia.

Redouane S, Charoute H, Harmak H, Malki A, Barakat A, Rouba H. Redouane S, et al. Among authors: barakat a. J Biomol Struct Dyn. 2023 Nov;41(19):9503-9522. doi: 10.1080/07391102.2022.2142846. Epub 2022 Nov 3. J Biomol Struct Dyn. 2023. PMID: 36326488

9

First characterization of LTBP3 variants in two Moroccan families with hypoplastic amelogenesis imperfecta.

Nouara F, Amalou G, Bouzidi A, Charif M, Charoute H, Lenaers G, El Arabi S, Bousfiha B, Barakat A. Nouara F, et al. Among authors: barakat a. Arch Oral Biol. 2022 Oct;142:105518. doi: 10.1016/j.archoralbio.2022.105518. Epub 2022 Aug 6. Arch Oral Biol. 2022. PMID: 35998423

10

Association between G2677T/A polymorphism in ABCB1 gene and the risk of drug resistance epilepsy: An updated systematic review and meta-analysis.

Krami AM, Ratib C, Charoute H, Rouba H, Roky R, Barakat A, Nahili H. Krami AM, et al. Among authors: barakat a. Epilepsy Res. 2022 Sep;185:106977. doi: 10.1016/j.eplepsyres.2022.106977. Epub 2022 Jul 8. Epilepsy Res. 2022. PMID: 35853334

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