Ghlana Meiloud

E23K variant in KCNJ11 gene is associated with susceptibility to type 2 diabetes in the Mauritanian population

Isselmou Abdelhamid, Khaled Lasram, Ghlana Meiloud et al. · Primary care diabetes · 2013 · 33 citations

Kcnj11 Gene, Diabetes Epidemiology, Genetic Determinant +9

Etiology and associated GJB2 mutations in Mauritanian children with non-syndromic hearing loss

Ely Cheikh Mohamed Moctar, Zied Riahi, Hala El Hachmi et al. · European Archives of Oto-Rhino-Laryngology · 2016 · 21 citations

Non-syndromic Hearing Loss, Pediatric Otolaryngology, Genetic Disorder +12

Type 2 diabetes in Mauritania: Prevalence of the undiagnosed diabetes, influence of family history and maternal effect

Ghlana Meiloud, Imen Arfa, Rym Kéfi et al. · Primary care diabetes · 2013 · 17 citations

Metabolic Syndrome, Family Medicine, Diabetes Epidemiology +12

Hb S [β6(A3)Glu→Val, G<i>A</i>G&gt;G<i>T</i>G] and β-Globin Gene Cluster Haplotype Distribution in Mauritania

Fatimetou Veten, Isselmou Abdelhamid, Ghlana Meiloud et al. · Hemoglobin · 2012 · 12 citations

Immunohematology, Ethnic Heterogeneity, Genetics +26

HLA class I (-A, -B, -C) and class II (-DR, -DQ) polymorphism in the Mauritanian population

Cheikh Tijani Hamed, Ghlana Meiloud, Fatimetou Veten et al. · BMC Medical Genetics · 2018 · 12 citations · Full text