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List of works by Sellama Nadifi

A genetic overview of Atlantic coastal populations from Europe and North-West Africa based on a 17 X-STR panel

scientific article

A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report

scientific article published on 25 November 2015

A proteomic approach for the involvement of the GAPDH in Alzheimer disease in the blood of Moroccan FAD cases

scientific article

A rapid polymerase chain reaction-based test for screening Steinert's disease (DM1).

scientific article published on January 2010

A synergic effect between CYP2C19*2, CYP2C19*3 loss-of-function and CYP2C19*17 gain-of-function alleles is associated with Clopidogrel resistance among Moroccan Acute Coronary Syndromes patients

scientific article published on 18 January 2018

Absence of factor V Leiden mutation and low prothrombin G 20210 A mutation prevalence in a healthy Moroccan population

scientific article published on 01 December 2002

Aggressive and chronic periodontitis in a population of Moroccan school students

scientific article published on 31 May 2016

Allium sativum L. regulates in vitro IL-17 gene expression in human peripheral blood mononuclear cells

scientific article

Analysis of CYP1B1 Gene Mutations in Patients with Primary Congenital Glaucoma

scientific article published on 21 April 2017

Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population

scientific article

Anti-inflammatory potential of Capparis spinosa L. in vivo in mice through inhibition of cell infiltration and cytokine gene expression

scientific article (publication date: 31 January 2017)

Assessment of GAPDH expression by quantitative real time PCR in blood of Moroccan AD cases

scientific article published on 10 January 2017

Association between ABCB1 C3435T polymorphism and breast cancer risk: a Moroccan case-control study and meta-analysis

scientific article

Association of C677T MTHFR and G20210A FII prothrombin polymorphisms with susceptibility to myocardial infarction

scientific article published on 13 July 2016

Association of G894T eNOS, 4G/5G PAI and T1131C APOA5 polymorphisms with susceptibility to myocardial infarction in Morocco

scientific article published on 3 April 2016

Association of TP53 PIN3 polymorphism with breast cancer in Moroccan population

scientific article

Association of glutathione S-transferase (GSTM1 and GSTT1) genes with chronic myeloid leukemia

scientific article published on May 2015

Association of methylenetetrahydrofolate reductase gene (C677T) with the risk of hypertension in Morocco

scientific article published on 12 December 2015

Autosomal recessive and sporadic deafness in Morocco: high frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant

scientific article published on 21 October 2005

BRCA1 and BRCA2 germline mutations in Moroccan breast/ovarian cancer families: novel mutations and unclassified variants

scientific article published on 13 March 2012

Biomarkers for Alzheimer disease: Classical and novel candidates' review

scientific article

Clinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients

scientific article

Does i-T744C P2Y12 Polymorphism Modulate Clopidogrel Response among Moroccan Acute Coronary Syndromes Patients?

scientific article published on 05 February 2017

Duchenne and Becker muscular dystrophy: contribution of a molecular and immunohistochemical analysis in diagnosis in Morocco

scientific article published on 19 May 2009

Duchenne muscular dystrophy: Advances in molecular appraoch

scientific article published in January 2013

Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations

scientific article published on April 2013

Evolution of molecular diagnosis of Duchenne muscular dystrophy

scientific article published on 5 February 2013

First study of C2491T FV mutation with ischaemic stroke risk in Morocco

scientific article

Food hygiene assessment in catering establishments in Hay Hassani district-Casablanca

scientific article published on 30 August 2016

Functional polymorphism of CYP2B6 G15631T is associated with hematologic and cytogenetic response in chronic myeloid leukemia patients treated with imatinib

scientific article published on 29 November 2013

G2691A and C2491T mutations of factor V gene and pre-disposition to myocardial infarction in Morocco

scientific article published on 30 September 2016

Genetic Aspects of Myoclonus-Dystonia Syndrome (MDS).

scientific article

Genetic Polymorphisms of Multidrug Resistance Gene-1 (MDR1/ABCB1) and Glutathione S-Transferase Gene and the Risk of Inflammatory Bowel Disease among Moroccan Patients

scientific article published on 28 October 2015

Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile

scientific article published on 6 December 2017

Genetic polymorphisms of T-1131C APOA5 and ALOX5AP SG13S114 with the susceptibility of ischaemic stroke in Morocco

scientific article

Genetics of Glioblastoma in Moroccan population: Review of literature

article

Genotype variability and haplotype frequency of MDR1 (ABCB1) gene polymorphism in Morocco

scientific article published on 9 August 2013

Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels

scientific article published on April 2014

IL23R and ATG16L1 variants in Moroccan patients with inflammatory bowel disease

scientific article

Impact of I/D polymorphism of angiotensin-converting enzyme (ACE) gene on myocardial infarction susceptibility among young Moroccan patients

scientific article published on 21 December 2017

Influence of mutation of the HFE gene on the progression of chronic viral hepatitis B and C in Moroccan patients

scientific article published on December 2011

Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals

scientific article published on April 2013

Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals ⬇️

scientific article published on September 1, 2011

MTHFR C677T polymorphism and risk of nonsyndromic cleft lip with or without cleft palate in the Moroccan population

Methylenetetrahydrofolate reductase C677T variant in Moroccan patients with inflammatory bowel disease

scientific article

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

scientific article published on 25 April 2013

Myxovirus resistance 1 gene polymorphisms and outcomes of viral hepatitis B and C infections in Moroccan patients

scientific article published on 26 July 2016

NOD2/CARD15 gene influences disease behaviour but not IBD susceptibility in a Moroccan population

scientific article

Novel mutations in the amyloid precursor protein gene within Moroccan patients with Alzheimer's disease

scientific article

Peroxiredoxin-2 up-regulation in inflammatory bowel disease: Friend or foe?

scientific article

Polymorphisms in oxidative pathway related genes and susceptibility to inflammatory bowel disease

scientific article published on 21 December 2017

Polymorphisms in oxidative pathway related genes and susceptibility to inflammatory bowel disease

article

Population genetic data of eight tetrameric short tandem repeats (STRs) in Casablanca resident population to use in forensic casework ⬇️

scientific article published on March 12, 2003

Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first? ⬇️

scientific article published on September 1, 2010

Prenatal diagnosis of BMD in Morocco: evolution and limits

scientific article published on 8 September 2013

Prevalence of angiotensin-converting enzyme, methylenetetrahydrofolate reductase, Factor V Leiden, prothrombin and apolipoprotein E gene polymorphisms in Morocco

scientific article published on 5 August 2010

Prothrombin G20210A and Factor V Leiden Polymorphisms in Stroke ⬇️

scientific article published on June 24, 2011

Relationship between family history of breast cancer and clinicopathological features in Moroccan patients

scientific article published on July 2013

Risk of colorectal cancer and clotting factor gene polymorphisms in Moroccan Population

scientific article published in January 2017

Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients

scientific article

Sickle cell disease with double stroke in a Moroccan family

scientific article published on 23 January 2013

Stem cells in cerebrovascular diseases

scientific article

Synergistic effect of MTHFR C677T and F2 G20210A polymorphisms on ischemic stroke ⬇️

scientific article published on 16 October 2013

TP53 R72P Polymorphism and Susceptibility to Human Papillomavirus Infection Among Women With Human Immunodeficiency Virus in Morocco: A Case-control Study

scientific article published on 30 December 2017

Ten-year follow-up of a DOCK8-deficient child with features of systemic lupus erythematosus

scientific article published on November 2014

The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population

scientific article

The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population

scientific article

The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease

Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms: New data and a meta-analysis

scientific article

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

scientific article

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

scientific article

c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.

scientific article

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