Saida Lahbib

Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients

Zied Riahi, Crystel Bonnet, Rim Zaïnine et al. · PLoS ONE · 2015 · 24 citations · Full text

Genetics, Genetic Epidemiology, Molecular Genetics +21

Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism

Rahma Mkaouar, Lamia Cherif Ben Abdallah, Chokri Naouali et al. · Frontiers in Genetics · 2021 · 24 citations · Full text

<b><i>TOP3B</i></b>: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?

Marwa Daghsni, Saida Lahbib, Mohamed Kacem Ben Fradj et al. · Cytogenetic and Genome Research · 2018 · 22 citations

Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology

Saida Lahbib, Claire S. Leblond, Meriem Hamza et al. · Journal of Applied Genetics · 2018 · 15 citations

Genetic Disorder, Genetics, Audiology +9

Identification of two variants in <i>AGRN</i> and <i>RPL3L</i> genes in a patient with catecholaminergic polymorphic ventricular tachycardia suggesting new candidate disease genes and digenic inheritance

Hager Jaouadi, Sonia Chabrak, Saida Lahbib et al. · Clinical Case Reports · 2022 · 13 citations · Full text