Published in Genet Test Mol Biomarkers on November 21, 2011
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Methylenetetrahydrofolate reductase gene polymorphism and risk of type 2 diabetes mellitus. PLoS One (2013) 0.84
Association of tagging SNPs in the MTHFR gene with risk of type 2 diabetes mellitus and serum homocysteine levels in a Chinese population. Dis Markers (2014) 0.82
Additive Interaction of MTHFR C677T and MTRR A66G Polymorphisms with Being Overweight/Obesity on the Risk of Type 2 Diabetes. Int J Environ Res Public Health (2016) 0.75
Type II diabetes mellitus and hyperhomocysteinemia: a complex interaction. Diabetol Metab Syndr (2017) 0.75
Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1. Am J Hum Genet (2010) 1.35
Y-chromosome analysis in Egypt suggests a genetic regional continuity in Northeastern Africa. Hum Biol (2002) 1.31
Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss. Am J Hum Genet (2010) 1.23
AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men. Asian J Androl (2007) 0.95
GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation. Int J Pediatr Otorhinolaryngol (2007) 0.94
A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family. Am J Med Genet A (2008) 0.92
Homozygous deletion related to Alu repeats in RLBP1 causes retinitis punctata albescens. Invest Ophthalmol Vis Sci (2006) 0.92
Pharmacological potentiation of natriuretic peptide limits polymorphonuclear neutrophil-vascular cell interactions. Arterioscler Thromb Vasc Biol (2002) 0.92
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss. Am J Hum Genet (2012) 0.91
Association of spermatogenic failure with the b2/b3 partial AZFc deletion. PLoS One (2012) 0.89
Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss. Biochem Biophys Res Commun (2012) 0.88
Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss. Int J Pediatr Otorhinolaryngol (2010) 0.88
Y-chromosome AZFc structural architecture and relationship to male fertility. Fertil Steril (2008) 0.87
The prevalence of resistance-associated mutations to protease and reverse transcriptase inhibitors in treatment-naïve (HIV1)-infected individuals in Casablanca, Morocco. J Infect Dev Ctries (2009) 0.87
Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population. Genet Test (2008) 0.85
The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population. Biochem Biophys Res Commun (2008) 0.85
Association of the MTHFR A1298C variant with unexplained severe male infertility. PLoS One (2012) 0.85
Contribution of CDKAL1 rs7756992 and IGF2BP2 rs4402960 polymorphisms in type 2 diabetes, diabetic complications, obesity risk and hypertension in the Tunisian population. J Diabetes (2014) 0.85
The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population. Eur J Pediatr (2010) 0.85
Novel mutations involving the INSL3 gene associated with cryptorchidism. J Urol (2007) 0.84
Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility. Fertil Steril (2009) 0.84
SNPs in the TNF-α gene promoter associated with Behcet's disease in Moroccan patients. Rheumatology (Oxford) (2012) 0.83
The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population. Mol Biol Rep (2012) 0.82
Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients. Lipids Health Dis (2014) 0.82
Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma. Mol Vis (2011) 0.82
Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss. Gene (2013) 0.81
Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C. Mol Vis (2007) 0.80
Maternal effect and familial aggregation in a type 2 diabetic Moroccan population. J Community Health (2011) 0.80
No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population. Horm Res (2008) 0.79
Y-chromosomal STR haplotypes in Berber and Arabic-speaking populations from Morocco. Forensic Sci Int (2004) 0.79
HLA-A, -B, -DRB1 alleles and haplotypes frequencies in Moroccan patients with leukemia. Ann Biol Clin (Paris) (2010) 0.79
TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis. Mol Biol Rep (2014) 0.78
Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness. Int J Pediatr Otorhinolaryngol (2008) 0.78
HLA-B*27 allele associated to Behçet's disease and to anterior uveitis in Moroccan patients. Ann Biol Clin (Paris) (2011) 0.78
Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis. Biochem Genet (2014) 0.77
Three new BLM gene mutations associated with Bloom syndrome. Genet Test (2008) 0.77
Malignant insulinoma misdiagnosed and treated as epilepsy. Ann Endocrinol (Paris) (2013) 0.77
Interaction of CD154 with different receptors and its role in bidirectional signals. Eur J Immunol (2014) 0.76
Clinicopathological features and molecular analysis of primary glioblastomas in Moroccan patients. J Mol Neurosci (2012) 0.75
Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss. Indian J Hum Genet (2013) 0.75
Paraphenylene diamine exacerbates platelet aggregation and thrombus formation in response to a low dose of collagen. J Toxicol Sci (2016) 0.75
Ochratoxin A mediates MAPK activation, modulates IL-2 and TNF-α mRNA expression and induces apoptosis by mitochondria-dependent and mitochondria-independent pathways in human H9 T cells. J Toxicol Sci (2016) 0.75
Polymorphism of human leukocyte antigen-A, -B, and -DRB1 in a Moroccan population from Casablanca: study of the allelic and the haplotypic frequencies. Ann Biol Clin (Paris) (2011) 0.75
Prostate-Specific Antigen levels in Moroccan diabetic males: A cross-sectional study. Curr Diabetes Rev (2017) 0.75