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Majdi Nagara

Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia
2005 · G. Zanni, Y. Saillour, et al. · Neurology · 110
Cytolytic activity correlates with the mutational burden and deregulated expression of immune checkpoints in colorectal cancer
2019 · Apostolos Zaravinos, Constantinos Roufas, et al. · Journal of Experimental & Clinical Cancer Research · 97
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Abnormal function of the UBA5 protein in a case of early developmental and epileptic encephalopathy with suppression-burst
2018 · Cécile Mignon-Ravix, Mathieu Milh, et al. · Human Mutation · 46
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Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia
2015 · Nizar Ben Halim, Sana Hsouna, et al. · American Journal of Human Biology · 33
Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome
2016 · Sahar Elouej, Hanen Belfki-Benali, et al. · Metabolic Syndrome and Related Disorders · 30
Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia
2015 · M. Jerbi, M. Ben Rekaya, et al. · British Journal of Dermatology · 27
Specific Aspects of Consanguinity: Some Examples from the Tunisian Population
2014 · Lilia Romdhane, Nizar Ben Halim, et al. · Human Heredity · 27
Gender-specific associations of genetic variants with metabolic syndrome components in the Tunisian population
2016 · Sahar Elouej, Insaf Rejeb, et al. · Endocrine Research · 24
Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population
2015 · Sahar Elouej, Majdi Nagara, et al. · Journal of Diabetes and its Complications · 24
Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity
2015 · Nizar Ben Halim, Majdi Nagara, et al. · Annals of Human Genetics · 23
Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: Implication for diagnosis in North Africa
2013 · Majdi Nagara, Afaf Tiar, et al. · Gene · 22
A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci
2018 · Yosr Hamdi, Mariem Ben Rekaya, et al. · BMC Cancer · 20
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Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis
2017 · Mariem Ben Rekaya, Chokri Naouali, et al. · Journal of Dermatological Science · 18
Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population
2017 · Rym Kefi, Meriem Hechmi, et al. · Annales d Endocrinologie · 16
Molecular Investigation of Distal Renal Tubular Acidosis in Tunisia, Evidence for Founder Mutations
2014 · Majdi Nagara, Konstantinos Voskarides, et al. · Genetic Testing and Molecular Biomarkers · 16
Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations
2017 · Yosra Ben Halima, Rym Kefi, et al. · Genes & Nutrition · 14
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Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population
2015 · Nizar Ben Halim, Imen Dorboz, et al. · Neurological Sciences · 13
A Tunisian Patient with Two Rare Syndromes: Triple A Syndrome and Congenital Hypogonadotropic Hypogonadism
2014 · Lamia Cherif Ben Abdallah, Youssef Lakhoua, et al. · Hormone Research in Paediatrics · 13
Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young
2020 · Hager Jaouadi, Yosra Bouyacoub, et al. · Herz · 12
Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance
2017 · Majdi Nagara, Gregory Papagregoriou, et al. · European Journal of Medical Genetics · 9
Adult gaucher disease in southern Tunisia: report of three cases
2012 · Faten Ben Rhouma, Faten Kallel, et al. · Diagnostic Pathology · 8
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History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation
2015 · Faten Ben Rhouma, Habib Messai, et al. · Mitochondrial DNA Part A · 5
A novel splice-site mutation in ATP6V0A4 gene in two brothers with distal renal tubular acidosis from a consanguineous Tunisian family
2014 · MAJDI NAGARA, KONSTANTINOS VOSKARIDES, et al. · Journal of Genetics · 4
A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families
2013 · Zied Riahi, Houda Chahed, et al. · International Journal of Pediatric Otorhinolaryngology · 3
Biotinidase deficiency: Novel mutations in Algerian patients
2013 · A. Tiar, A. Mekki, et al. · Gene · 3
Works count: 61
Citation count: 622
H-index: 15
I10-index: 19
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