Sahar Elouej

Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

Sahar Elouej, Karim Harhouri, Morgane Le Mao et al. · Nature Communications · 2020 · 60 citations · Full text

Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL)

Sahar Elouej, Ana Beleza‐Meireles, Richard Caswell et al. · Metabolism · 2017 · 49 citations · Full text

Mendelian Disorder, Genetic Disorder, Exome Sequencing Reveals +7

Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype

Meena Balasubramanian, Alexander J.M. Dingemans, Shadi Albaba et al. · European Journal of Human Genetics · 2021 · 32 citations · Full text

Association of rs9939609 Polymorphism with Metabolic Parameters and <i>FTO</i> Risk Haplotype Among Tunisian Metabolic Syndrome

Sahar Elouej, Hanen Belfki-Benali, Majdi Nagara et al. · Metabolic Syndrome and Related Disorders · 2016 · 29 citations

Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population

Sahar Elouej, Majdi Nagara, Redha Attaoua et al. · Journal of Diabetes and its Complications · 2015 · 28 citations

Obesity, Metabolic Syndrome, Genetic Determinant +10