Redouane Boulouiz

发表

Morocco's First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges

Majida Charif, Y. Bentata, Saida Lhousni, 2020, BioMed research international.

Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness.

H. Rouba, A. Barakat, Redouane Boulouiz, 2008, International journal of pediatric otorhinolaryngology.

Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss.

B. Delprat, Majida Charif, G. Lenaers, 2012, Biochemical and biophysical research communications.

Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss

Majida Charif, G. Lenaers, H. Benrahma, 2013, Indian journal of human genetics.

Maternal Effect and Familial Aggregation in a Type 2 Diabetic Moroccan Population

Majida Charif, S. Abdelhak, H. Benrahma, 2011, Journal of Community Health.

Patients' Knowledge and Attitude Toward Biobanks in Eastern Morocco.

N. Abda, Saida Lhousni, K. Y. Belmokhtar, 2020, Biopreservation and biobanking.

Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco

Majida Charif, Saida Lhousni, Ihab Belmokhtar, 2022, Molecular genetics & genomic medicine.

Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C.

H. Bolz, Yun Li, B. Wollnik, 2007, Molecular vision.

No Association between T222P/LGR8 Mutation and Cryptorchidism in the Moroccan Population

H. Rouba, A. Barakat, K. McElreavey, 2008, Hormone Research in Paediatrics.

Association Analysis of IGF2BP2, KCNJ11, and CDKAL1 Polymorphisms with Type 2 Diabetes Mellitus in a Moroccan Population: A Case–Control Study and Meta-analysis

S. Abdelhak, H. Charoute, H. Benrahma, 2014, Biochemical Genetics.

AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.

H. Rouba, A. Barakat, K. McElreavey, 2007, Asian journal of andrology.

A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.

M. Teitell, R. Goodyear, G. Richardson, 2012, American journal of human genetics.

Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss

Majida Charif, G. Lenaers, H. Charoute, 2017, PloS one.

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

Majida Charif, G. Lenaers, A. Bakhchane, 2015, PloS one.

The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population

Majida Charif, H. Rouba, A. Barakat, 2012, Molecular Biology Reports.

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.

H. Rouba, A. Barakat, Redouane Boulouiz, 2007, International journal of pediatric otorhinolaryngology.

Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss.

J. Veltman, H. Kremer, Majida Charif, 2010, American journal of human genetics.

The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population.

H. Rouba, A. Barakat, Redouane Boulouiz, 2008, Biochemical and biophysical research communications.

Exploring the Antimicrobial Properties Against Human Pathogens and Mode of Action of Various Extracts from Fredolia aretioides, an Endemic Medicinal Plant of Morocco and Algeria

Redouane Boulouiz, M. Tajir, M. Ouarzane, 2019 .

Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family

C. Petit, H. Charoute, A. Barakat, 2021, Human Heredity.

A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family

G. Nürnberg, C. Becker, P. Nürnberg, 2008, American journal of medical genetics. Part A.

[Etiologic profile of severe and profound sensorineural hearing loss in children in the region of north-central Morocco].

Redouane Boulouiz, N. Benmansour, Z. Zaki, 2014, The Pan African medical journal.

Epidemiological , Clinical , Biological and Therapeutic Characteristics of Myeloproliferative Neoplasms in Eastern Morocco

Mohammed, Redouane Boulouiz, R. Seddik, 2016 .

Cancer incidence in eastern Morocco: cancer patterns and incidence trends, 2005–2012

Mounia Elidrissi Errahhali, Manal Elidrissi Errahhali, Redouane Boulouiz, 2017, BMC Cancer.

Distribution and features of hematological malignancies in Eastern Morocco: a retrospective multicenter study over 5 years

Mounia Elidrissi Errahhali, Manal Elidrissi Errahhali, Redouane Boulouiz, 2016, BMC Cancer.

[Lung cancer in Eastern Morocco: where do we stand?]

N. Abda, K. Y. Belmokhtar, Redouane Boulouiz, 2019, The Pan African Medical Journal.

Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.

H. Benrahma, H. Rouba, A. Barakat, 2010, International journal of pediatric otorhinolaryngology.

Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.

H. Rouba, A. Barakat, Redouane Boulouiz, 2008, Genetic testing.

Mutation rate at 17 Y-STR loci in "Father/Son" pairs from moroccan population.

Redouane Boulouiz, S. Nadifi, B. El houate, 2013, Legal medicine.

Assessment of Knowledge, Attitudes and Support of Health Professionals towards Biobanks in Eastern Morocco

N. Abda, Saida Lhousni, Redouane Boulouiz, 2019, Open Journal of Epidemiology.

A novel variant in BMPR1B causes acromesomelic dysplasia Grebe type in a consanguineous Moroccan family: Expanding the phenotypic and mutational spectrum of acromesomelic dysplasias.

G. Lenaers, Saida Lhousni, Redouane Boulouiz, 2023, Bone.

Cancer du poumon au Maroc Oriental: où en sommes-nous?

N. Abda, K. Y. Belmokhtar, Redouane Boulouiz, 2019, The Pan African medical journal.

Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.

G. Lenaers, A. Bakhchane, H. Rouba, 2013, Gene.

Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus–dystonia

H. Benrahma, Redouane Boulouiz, K. Ouldim, 2022, Clinical case reports.

Forensic Population Genetics—Short communication Allele frequencies and population data for 17 Y-STR loci (The AmpFlSTR 1 Y-filer TM ) in Casablanca resident population

Redouane Boulouiz, H. Azeddoug, B. E. Houate, 2011 .

Allele frequencies and population data for 17 Y-STR loci (The AmpFlSTR® Y-filer™) in Casablanca resident population.

Redouane Boulouiz, B. El houate, H. Azeddoug, 2011, Forensic science international. Genetics.

Teaching Pedigree Analysis and Risk Calculation for Diagnosis Purposes of Genetic Disease

Mostafa Azizi, Noureddine Kerzazi, Mohammed Bellaoui, 2020, WorldCIST.

The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population

H. Rouba, A. Barakat, Redouane Boulouiz, 2012, Molecular Biology Reports.

A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.

M. Teitell, R. Goodyear, G. Richardson, 2012, American journal of human genetics.

Cancer incidence in eastern Morocco: cancer patterns and incidence trends, 2005–2012

Mounia Elidrissi Errahhali, Manal Elidrissi Errahhali, Redouane Boulouiz, 2017, BMC Cancer.