Get started
Author

Halima Nahili

Observed names: H. Nahili, Nahili Halima
ORCID: 0000-0003-4872-5476
Observed ORCID: 0000-0003-4872-5476
OpenAlex ID: A5020741820
AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men
2007 · Laila Imken, Brahim El Houate, et al. · Asian Journal of Andrology · 56
GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation
2007 · Omar Abidi, Redouane Boulouiz, et al. · International Journal of Pediatric Otorhinolaryngology · 39
The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population
2012 · Majida Charif, Safaa Bounaceur, et al. · Molecular Biology Reports · 27
Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees
2015 · Amina Bakhchane, Majida Charif, et al. · PLoS ONE · 26
PDF
Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss
2010 · Halima Nahili, Majida Charif, et al. · International Journal of Pediatric Otorhinolaryngology · 23
The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility
2013 · Hicham Charoute, Halima Nahili, et al. · European Journal of Human Genetics · 22
PDF
A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
2015 · Amina Bakhchane, Hicham Charoute, et al. · Gene · 21
Maternal Effect and Familial Aggregation in a Type 2 Diabetic Moroccan Population
2011 · Houda Benrahma, Imen Arfa, et al. · Journal of Community Health · 21
Carrier Frequencies of Mutations/Polymorphisms in the Connexin 26 Gene ( GJB2 ) in the Moroccan Population
2008 · Omar Abidi, Redouane Boulouiz, et al. · Genetic Testing · 18
Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss
2012 · Majida Charif, Omar Abidi, et al. · Biochemical and Biophysical Research Communications · 16
The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population
2008 · Omar Abidi, Redouane Boulouiz, et al. · Biochemical and Biophysical Research Communications · 15
Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness
2008 · Halima Nahili, Mohamed Ridal, et al. · International Journal of Pediatric Otorhinolaryngology · 15
Molecular Modelling and Dynamics Study of nsSNP in STXBP1 Gene in Early Infantile Epileptic Encephalopathy Disease
2019 · Krami Al Mehdi, Benhnini Fouad, et al. · BioMed Research International · 14
PDF
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss
2017 · Amina Bakhchane, Majida Charif, et al. · PLoS ONE · 12
PDF
A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability
2022 · Al Mehdi Krami, Aymane Bouzidi, et al. · European Journal of Medical Genetics · 11
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome
2018 · Soukaina Elrharchi, Zied Riahi, et al. · International Journal of Pediatric Otorhinolaryngology · 9
Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study
2020 · Chaimaa Ait El Cadi, Al Mehdi Krami, et al. · BioMed Research International · 8
PDF
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family
2018 · Sara Salime, Zied Riahi, et al. · Gene · 8
Association between G2677T/A polymorphism in ABCB1 gene and the risk of drug resistance epilepsy: An updated systematic review and meta-analysis
2022 · Al Mehdi Krami, Chorouk Ratib, et al. · Epilepsy Research · 7
Methylenetetrahydrofolate Reductase Gene Polymorphisms (C677T and A1298C) and Hemorrhagic Stroke in Moroccan Patients
2018 · Omar Abidi, Mohammed Haissam, et al. · Journal of Stroke and Cerebrovascular Diseases · 7
Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss
2013 · Abdelhamid Barakat, Majida Charif, et al. · Indian journal of human genetics · 6
PDF
Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder
2021 · Khaoula Rochdi, Mathieu Cerino, et al. · Clinica Chimica Acta · 5
PDF
First characterization of congenital myasthenic syndrome type 5 in North Africa
2021 · Rochdi Khaoula, Mathieu Cerino, et al. · Molecular Biology Reports · 5
PDF
First characterization of LHON pedigrees in North Africa
2020 · Aymane Bouzidi, Nisrine Aboussair, et al. · Eye · 5
PDF
GNE Myopathy and Duchenne Muscular Dystrophy in Two Moroccans Families
2023 · Najat Sifeddine, Ghita Amalou, et al. · Muscles Ligaments and Tendons Journal · 1
PDF
Works count: 29
Citation count: 398
H-index: 13
I10-index: 15
Year
Topic
Type