Author

Saida Lahbib

Institutions: Tunis University, Institut Pasteur de Tunis, Tunis El Manar University

Observed institutions: Tunis University, Institut Pasteur de Tunis, Tunis El Manar University

ORCID: 0000-0001-7652-8053

Observed ORCID: 0000-0001-7652-8053

OpenAlex ID: A5070032386

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

2015 · Zied Riahi, Crystel Bonnet, et al. · PLoS ONE · 28

TOP3B: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?

2018 · Marwa Daghsni, Saida Lahbib, et al. · Cytogenetic and Genome Research · 22

Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism

2021 · Rahma Mkaouar, Lamia Cherif Ben Abdallah, et al. · Frontiers in Genetics · 18

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

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

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

2022 · Hager Jaouadi, Sonia Chabrak, et al. · Clinical Case Reports · 11

Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family

2019 · Saida Lahbib, Mediha Trabelsi, et al. · Molecular Biology Reports · 6

Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health

2024 · Rahma Mkaouar, Zied Riahi, et al. · Frontiers in Genetics · 3

Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health

2024 · Rahma Mkaouar, Zied Riahi, et al. · Frontiers in Genetics · 1

Works count: 8

Citation count: 104

H-index: 6

I10-index: 5