Lista de obras -

A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD.

artículo científico publicado en 2017

A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders

artículo científico publicado en 2017

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

artículo científico publicado en 2015

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

artículo científico publicado en 2007

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

artículo científico publicado en 2008

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

artículo científico publicado en 2013

Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.

artículo científico publicado en 2014

Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.

artículo científico publicado en 2014

Association of spermatogenic failure with the b2/b3 partial AZFc deletion

artículo científico publicado en 2012

Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a Moroccan population

artículo científico publicado en 2011

Association of the MTHFR A1298C variant with unexplained severe male infertility

artículo científico publicado en 2012

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

artículo científico publicado en 2008

Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco

artículo científico publicado en 2015

Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review

artículo científico publicado en 2018

Computational Analysis of the Potential Impact of MTC Complex Missenses SNPs Associated with Male Infertility

artículo científico publicado en 2022

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

artículo científico publicado en 2007

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

artículo científico publicado en 2013

Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome

artículo científico publicado en 2015

Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1

artículo científico publicado en 2010

Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.

artículo científico publicado en 2011

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population

artículo científico publicado en 2015

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

artículo científico publicado en 2012

Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma

artículo científico publicado en 2011

Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility

artículo científico publicado en 2009

Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.

artículo científico publicado en 2018

No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.

artículo científico publicado en 2017

Novel mutations involving the INSL3 gene associated with cryptorchidism

artículo científico publicado en 2007

Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population

artículo científico publicado en 2016

Phylogeography of E1b1b1b-M81 haplogroup and analysis of its subclades in Morocco

artículo científico publicado en 2014

Prevalence of the Aurora kinase C c.144delC mutation in infertile Moroccan men.

artículo científico publicado en 2014

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

artículo científico publicado en 2010

TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis

artículo científico publicado en 2014

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility

artículo científico publicado en 2013

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

artículo científico publicado en 2008

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

artículo científico publicado en 2012

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss

artículo científico publicado en 2016

Y-chromosomal STR haplotypes in Berber and Arabic-speaking populations from Morocco

artículo científico publicado en 2004

Y-chromosome AZFc structural architecture and relationship to male fertility

artículo científico publicado en 2008

Y-chromosome analysis in Egypt suggests a genetic regional continuity in Northeastern Africa

artículo científico publicado en 2002

Lista de obras de

A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD.

A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

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

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

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

Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.

Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.

Association of spermatogenic failure with the b2/b3 partial AZFc deletion

Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a Moroccan population

Association of the MTHFR A1298C variant with unexplained severe male infertility

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

Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco

Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review

Computational Analysis of the Potential Impact of MTC Complex Missenses SNPs Associated with Male Infertility

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

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

Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome

Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1

Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population

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

Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma

Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility

Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.

No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population

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

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.

Novel mutations involving the INSL3 gene associated with cryptorchidism

Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population

Phylogeography of E1b1b1b-M81 haplogroup and analysis of its subclades in Morocco

Prevalence of the Aurora kinase C c.144delC mutation in infertile Moroccan men.

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

TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility

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

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

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss

Y-chromosomal STR haplotypes in Berber and Arabic-speaking populations from Morocco

Y-chromosome AZFc structural architecture and relationship to male fertility

Y-chromosome analysis in Egypt suggests a genetic regional continuity in Northeastern Africa