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Mohamed Makrelouf

A Predominantly Neolithic Origin for Y-Chromosomal DNA Variation in North Africa
2004 · Barbara Arredi, Estella S. Poloni, et al. · The American Journal of Human Genetics · 194
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Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy
2002 · Ercan Demir, Patrizia Sabatelli, et al. · The American Journal of Human Genetics · 168
IFN-γ and TNF-α Are Involved During Alzheimer Disease Progression and Correlate with Nitric Oxide Production: A Study in Algerian Patients
2014 · Mourad Belkhelfa, Hayet Rafa, et al. · Journal of Interferon & Cytokine Research · 120
IL36RN Mutations Affect Protein Expression and Function: A Basis for Genotype-Phenotype Correlation in Pustular Diseases
2016 · Marie Tauber, Elodie Bal, et al. · Journal of Investigative Dermatology · 104
The CD2 isoform of protocadherin‐15 is an essential component of the tip‐link complex in mature auditory hair cells
2014 · Elise Pepermans, Vincent Michel, et al. · EMBO Molecular Medicine · 80
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EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness
2014 · Asma Behlouli, Crystel Bonnet, et al. · Orphanet Journal of Rare Diseases · 55
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Molecular screening of deafness in Algeria: High genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F
2009 · Fatima Ammar-Khodja, Valérie Faugère, et al. · European Journal of Medical Genetics · 30
Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome
2016 · Samia Abdi, Amel Bahloul, et al. · PLoS ONE · 25
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Validation of the neutrophil-to-lymphocyte ratio as a new simple biomarker of adult onset Still’s disease: A STROBE-Compliant prospective observational study
2022 · Karima Daghor Abbaci, Nadia Ait Hamadouche, et al. · Medicine · 18
A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family
2016 · Asma Behlouli, Crystel Bonnet, et al. · International Journal of Pediatric Otorhinolaryngology · 15
Proposal of a new diagnostic algorithm for adult-onset Still’s disease
2023 · Karima Daghor-Abbaci, Nadia Ait Hamadouche, et al. · Clinical Rheumatology · 12
Crucial Interactions between Altered Plasma Trace Elements and Fatty Acids Unbalance Ratio to Management of Systemic Arterial Hypertension in Diabetic Patients: Focus on Endothelial Dysfunction
2024 · Ines Gouaref, Mohamed Makrelouf, et al. · International Journal of Molecular Sciences · 10
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Primary evaluation of antioxidant status oligomineral patient with type 2 diabetes Algeria: special interest manganese and chromium
2012 · Hassiba Harani, Amel Otmane, et al. · Annales de biologie clinique · 10
Reconsidering vitamin D optimal values based on parathyroid hormone levels in a North Algerian cohort: stratification by gender and season
2022 · Salam Bennouar, Abdelghani Bachir Cherif, et al. · Archives of Osteoporosis · 6
Disease activity score for still’s disease
2024 · Karima Daghor-Abbaci, Nazim Laraba, et al. · Clinical Rheumatology · 5
Polymorphisms in NAT2 Gene and Atherosclerosis in an Algerian Population
2010 · Malika Khelil, Akila Zenati, et al. · Archives of Medical Research · 4
Frequency of the 35delG allele causing nonsyndromic recessive deafness in the Algerian patients.
2007 · F Ammar-Khodja, M Makrelouf, et al. · PubMed · 4
Plasma GLP-1 (Glucagon-like Peptide-1) Depletion Is Correlated with Dysregulation of Adipocytokine in Type 2 Diabetic Patients With or Without Metabolic-Associated Fatty Liver Disease (MAFLD): A Cross-Sectional Study Related to Gender-Sex Disparities
2026 · Houda Zoubiri, Wassila Saiah, et al. · International Journal of Molecular Sciences · 3
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Living donors kidney transplantation and oxidative stress: Nitric oxide as a predictive marker of graft function
2024 · Djamila Izemrane, Ali Benziane, et al. · PLoS ONE · 3
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Comparison of three indexes HOMA, QUICKI and TyG to evaluate insulin resistance in type 2 diabetic patients
2022 · Amel OTMANE, Sadjia ACID, et al. · Metabolism · 3
Dosage de l'homocystéine totale chez une cohorte de diabétiques de type 2
2007 · Amel Otmane, Mohamed Makrelouf, et al. · Revue Francophone des Laboratoires · 3
Paraben exposure profiles in pregnant women and association with changes in thyroid hormone levels
2025 · Abderrezak Khelfi, Asma Idjeraoui, et al. · Annales d Endocrinologie · 2
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity
2025 · Zied Riahi, Sophie Boucher, et al. · Proceedings of the National Academy of Sciences · 1
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Apo E Gene Polymorphism (c112r, R158c) and Lipid Profile in Hypertensive Patients
2022 · Amel Otmane, Mohamed Makrelouf, et al. · Journal of Hypertension · 1
Interaction between Metabolic syndrome, insulin resistance and oxidative stress in hypertensive patients
2022 · A. Otmane, F. Kasdi, et al. · Metabolism · 1
Works count: 56
Citation count: 879
H-index: 11
I10-index: 13
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