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Redouane Boulouiz
Observed names:
Boulouiz, Redouane,
R., Boulouiz,
Redouan Boulouiz
Institution:
Mohamed I University
Observed institutions:
Mohammed V University,
Institut Pasteur,
Instituts Supérieurs des Professions Infirmières et Techniques de Santé,
Mohamed I University,
Chouaib Doukkali University,
Institut Pasteur du Maroc
show all 6
ORCID:
0000-0003-4430-3612
Observed ORCID:
0000-0003-4430-3612
OpenAlex ID:
A5085120958
A Mutation in PNPT1, Encoding Mitochondrial-RNA-Import Protein PNPase, Causes Hereditary Hearing Loss
2012
·
Simon von Ameln
, Geng Wang
, et al.
·
The American Journal of Human Genetics
·
99
PDF
Mutations in TPRN Cause a Progressive Form of Autosomal-Recessive Nonsyndromic Hearing Loss
2010
·
Yun Li
, Esther Pohl
, et al.
·
The American Journal of Human Genetics
·
59
PDF
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
Distribution and features of hematological malignancies in Eastern Morocco: a retrospective multicenter study over 5 years
2016
·
Mounia Elidrissi Errahhali
, Manal Elidrissi Errahhali
, et al.
·
BMC Cancer
·
42
PDF
Association Analysis of IGF2BP2, KCNJ11, and CDKAL1 Polymorphisms with Type 2 Diabetes Mellitus in a Moroccan Population: A Case–Control Study and Meta-analysis
2014
·
Houda Benrahma
, Hicham Charoute
, et al.
·
Biochemical Genetics
·
40
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
No Association between T222P/LGR8 Mutation and Cryptorchidism in the Moroccan Population
2008
·
Brahim El Houate
, Hassan Rouba
, et al.
·
Hormone Research in Paediatrics
·
28
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
Cancer incidence in eastern Morocco: cancer patterns and incidence trends, 2005–2012
2017
·
Manal Elidrissi Errahhali
, Mounia Elidrissi Errahhali
, et al.
·
BMC Cancer
·
26
PDF
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
Patients' Knowledge and Attitude Toward Biobanks in Eastern Morocco
2020
·
Saida Lhousni
, Fatiha Daoudi
, et al.
·
Biopreservation and Biobanking
·
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
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders
2023
·
Franziska Langhammer
, Reza Maroofian
, et al.
·
Genetics in Medicine
·
19
PDF
Morocco’s First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges
2020
·
Saida Lhousni
, Karam Yahya Belmokhtar
, et al.
·
BioMed Research International
·
18
PDF
Mutation rate at 17 Y-STR loci in “Father/Son” pairs from moroccan population
2013
·
Adil Laouina
, Sellama Nadifi
, et al.
·
Legal Medicine
·
18
Allele frequencies and population data for 17 Y-STR loci (The AmpFlSTR® Y-filer™) in Casablanca resident population
2010
·
Adil Laouina
, Brahim El Houate
, et al.
·
Forensic Science International Genetics
·
18
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
A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family
2008
·
Redouane Boulouiz
, Yun Li
, et al.
·
American Journal of Medical Genetics Part A
·
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
Assessment of Knowledge, Attitudes and Support of Health Professionals towards Biobanks in Eastern Morocco
2019
·
Saida Lhousni
, Redouane Boulouiz
, et al.
·
Open Journal of Epidemiology
·
13
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
Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss
2013
·
Majida Charif
, Amina Bakhchane
, et al.
·
Gene
·
10
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Works count:
54
Citation count:
766
H-index:
18
I10-index:
25
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