Taïeb Messaoud

Gross genomic rearrangements involving deletions in the CFTR gene: characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and meta-analysis of the underlying mechanisms

Claude Férec, Teresa Casals, Nadia Chuzhanova et al. · European Journal of Human Genetics · 2006 · 93 citations · Full text

Genetic Disorder, Genetics, Pathology +7

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia

Chaîma Sahli, Amina Bibi, Faida Ouali et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 2013 · 45 citations

High APOE epsilon 4 allele frequencies associated with Alzheimer disease in a Tunisian population

Afef Achouri-Rassas, H. Khiari, S. Hadj Fredj et al. · Neurological Sciences · 2011 · 43 citations

Alzheimer's Disease, Aging, Dementia +9

Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci

Sylvia Quéméner, Jian‐Min Chen, Nadia Chuzhanova et al. · Human Mutation · 2010 · 33 citations · Full text

Distribution of CFTR Mutations inCystic Fibrosis Patients of TunisianOrigin: Identification of Two NovelMutations

Taïeb Messaoud, C. Verlingue, Érick Denamur et al. · European Journal of Human Genetics · 1996 · 33 citations