Charoute H - Search Results

1

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.

Bousfiha A, Riahi Z, Elkhattabi L, Bakhchane A, Charoute H, Snoussi K, Bonnet C, Petit C, Barakat A. Bousfiha A, et al. Among authors: charoute h. Hum Hered. 2019;84(3):109-116. doi: 10.1159/000503450. Epub 2019 Dec 4. Hum Hered. 2019. PMID: 31801140

2

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.

Charoute H, Nahili H, Abidi O, Gabi K, Rouba H, Fakiri M, Barakat A. Charoute H, et al. Eur J Hum Genet. 2014 Mar;22(3):322-6. doi: 10.1038/ejhg.2013.151. Epub 2013 Jul 17. Eur J Hum Genet. 2014. PMID: 23860041 Free PMC article.

3

Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.

Ouatou S, Ajjemami M, Charoute H, Sefri H, Ghalim N, Rhaissi H, Benrahma H, Barakat A, Rouba H. Ouatou S, et al. Among authors: charoute h. Lipids Health Dis. 2014 Apr 1;13:60. doi: 10.1186/1476-511X-13-60. Lipids Health Dis. 2014. PMID: 24684850 Free PMC article.

4

Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.

Benrahma H, Charoute H, Lasram K, Boulouiz R, Atig RK, Fakiri M, Rouba H, Abdelhak S, Barakat A. Benrahma H, et al. Among authors: charoute h. Biochem Genet. 2014 Oct;52(9-10):430-42. doi: 10.1007/s10528-014-9658-5. Epub 2014 Jun 5. Biochem Genet. 2014. PMID: 24898818

5

TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis.

Sefri H, Benrahma H, Charoute H, Lakbakbi el Yaagoubi F, Rouba H, Lyoussi B, Nourlil J, Abidi O, Barakat A. Sefri H, et al. Among authors: charoute h. Mol Biol Rep. 2014 Sep;41(9):5805-11. doi: 10.1007/s11033-014-3454-5. Epub 2014 Jun 22. Mol Biol Rep. 2014. PMID: 24952604

6

Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome.

Ajjemami M, Ouatou S, Charoute H, Fakiri M, Rhaissi H, Benrahma H, Rouba H, Barakat A. Ajjemami M, et al. Among authors: charoute h. J Diabetes Metab Disord. 2015 Apr 16;14:29. doi: 10.1186/s40200-015-0160-3. eCollection 2015. J Diabetes Metab Disord. 2015. PMID: 25909077 Free PMC article.

7

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.

Charoute H, Bakhchane A, Benrahma H, Romdhane L, Gabi K, Rouba H, Fakiri M, Abdelhak S, Lenaers G, Barakat A. Charoute H, et al. Hum Mutat. 2015 Nov;36(11):E2441-53. doi: 10.1002/humu.22835. Epub 2015 Jul 30. Hum Mutat. 2015. PMID: 26173767

8

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

Bakhchane A, Charoute H, Nahili H, Roky R, Rouba H, Charif M, Lenaers G, Barakat A. Bakhchane A, et al. Among authors: charoute h. Gene. 2015 Dec 10;574(1):28-33. doi: 10.1016/j.gene.2015.07.075. Epub 2015 Jul 28. Gene. 2015. PMID: 26226225

9

Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco.

Naasse Y, Charoute H, El Houate B, Elbekkay C, Razoki L, Malki A, Barakat A, Rouba H. Naasse Y, et al. Among authors: charoute h. BMC Urol. 2015 Sep 18;15:95. doi: 10.1186/s12894-015-0089-3. BMC Urol. 2015. PMID: 26385215 Free PMC article.

10

Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients.

Lakbakbi El Yaagoubi F, Charoute H, Bakhchane A, Ajjemami M, Benrahma H, Errouagui A, Kandil M, Rouba H, Barakat A. Lakbakbi El Yaagoubi F, et al. Among authors: charoute h. Pathol Biol (Paris). 2015 Dec;63(6):243-7. doi: 10.1016/j.patbio.2015.09.002. Pathol Biol (Paris). 2015. PMID: 26524954

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