Houyem Ouragini

High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis

Mariem Ben Rekaya, Olfa Messaoud, Faten Talmoudi et al. · Journal of Human Genetics · 2009 · 55 citations · Full text

Molecular Diagnosis, Molecular Diagnostic Techniques, Somatic Variant +13

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss

Zied Riahi, H. Hammami, Houyem Ouragini et al. · Gene · 2013 · 35 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +10

Differential impact of consanguineous marriages on autosomal recessive diseases in <scp>T</scp>unisia

Nizar Ben Halim, Sana Hsouna, Khaled Lasram et al. · American Journal of Human Biology · 2015 · 25 citations

Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity

Olfa Messaoud, Mariem Ben Rekaya, Houyem Ouragini et al. · Archives of Dermatological Research · 2011 · 25 citations

Allelic Variant, Mendelian Disorder, Genetic Disorder +10

rs11886868 and rs4671393 of <i>BCL11A</i> associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Leila Chaouch, Imen Moumni, Houyem Ouragini et al. · Hematology · 2016 · 19 citations · Full text