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Faiza Fakhfakh

Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis
2011 · Slaheddine Marrakchi, Philippe Guigue, et al. · New England Journal of Medicine · 992
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Effect of freezing–thawing process and quercetin on human sperm survival and DNA integrity
2012 · Nassira Zribi, Nozha Feki Chakroun, et al. · Cryobiology · 137
Sperm DNA fragmentation and oxidation are independent of malondialdheyde
2011 · Nassira Zribi, Nozha Chakroun, et al. · Reproductive Biology and Endocrinology · 100
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New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families
2004 · Chahnez Triki, Susana Quijano-Roy, et al. · Neurogenetics · 83
Association study of CARD8 (p.C10X) and NLRP3 (p.Q705K) variants with rheumatoid arthritis in French and Tunisian populations
2011 · M. Ben Hamad, F. Cornelis, et al. · International Journal of Immunogenetics · 51
Caffeic acid and quercetin protect erythrocytes against the oxidative stress and the genotoxic effects of lambda-cyhalothrin in vitro
2011 · F Ben Abdallah, H Fetoui, et al. · Human & Experimental Toxicology · 44
Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men
2013 · Siwar Baklouti-Gargouri, Myriam Ghorbel, et al. · Molecular Biology Reports · 38
The heteroplasmic m.14709T>C mutation in the tRNAGlu gene in two Tunisian families with mitochondrial diabetes
2010 · Najla Mezghani, Emna Mkaouar-Rebai, et al. · Journal of Diabetes and its Complications · 34
Molecular-Clinical Correlation in a Family With a Novel Heteroplasmic Leigh Syndrome Missense Mutation in the Mitochondrial Cytochrome c Oxidase III Gene
2010 · Emna Mkaouar-Rebai, Emna Ellouze, et al. · Journal of Child Neurology · 28
New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures
2010 · N. Fendri-Kriaa, F. Kammoun, et al. · European Journal of Neurology · 27
Association between Leptin gene polymorphisms and plasma leptin level in three consanguineous families with obesity
2013 · Mouna Fourati, Mouna Mnif, et al. · Gene · 26
The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy
2011 · Najla Mezghani, Mouna Mnif, et al. · Biochemical and Biophysical Research Communications · 26
Protective effects of pomegranate peel against hematotoxicity, chromosomal aberrations, and genotoxicity induced by barium chloride in adult rats
2016 · Awatef Elwej, Ghada Ben Salah, et al. · Pharmaceutical Biology · 25
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Identification of a novel m.9588G > A missense mutation in the mitochondrial COIII gene in asthenozoospermic Tunisian infertile men
2014 · Siwar Baklouti-Gargouri, Myriam Ghorbel, et al. · Journal of Assisted Reproduction and Genetics · 25
Polymorphisms of glutathione S-transferases M1, T1, P1 and A1 genes in the Tunisian population: An intra and interethnic comparative approach
2012 · Ghada Ben Salah, Fakhri Kallabi, et al. · Gene · 25
Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss
2006 · Emna Mkaouar-Rebai, Abdelaziz Tlili, et al. · Biochemical and Biophysical Research Communications · 25
Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases
2007 · Emna Mkaouar-Rebai, Abdelaziz Tlili, et al. · Biochemical and Biophysical Research Communications · 24
A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with sever nephropathy
2015 · Mouna Tabebi, Emna Mkaouar-Rebai, et al. · Biochemical and Biophysical Research Communications · 23
A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions
2013 · Najla Mezghani, Mouna Mnif, et al. · Biochemical and Biophysical Research Communications · 21
Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect
2009 · Nacim Louhichi, Moez Medhaffar, et al. · Annals of Hematology · 21
Biochemical analyses and molecular modeling explain the functional loss of 17β-hydroxysteroid dehydrogenase 3 mutant G133R in three Tunisian patients with 46, XY Disorders of Sex Development
2015 · Roger T. Engeli, Bochra Ben Rhouma, et al. · The Journal of Steroid Biochemistry and Molecular Biology · 20
A novel m.6307A>G mutation in the mitochondrialCOXIgene in asthenozoospermic infertile men
2013 · Siwar Baklouti-Gargouri, Myriam Ghorbel, et al. · Molecular Reproduction and Development · 20
A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNAIle m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss
2010 · Imen Chamkha, Emna Mkaouar-Rebai, et al. · Biochemical and Biophysical Research Communications · 20
Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation
2016 · Mouna Tabebi, Nadia Charfi, et al. · Journal of Diabetes and its Complications · 19
Pyridoxine-dependent epilepsy in Tunisia is caused by a founder missense mutation of the ALDH7A1 gene
2013 · Abdelaziz Tlili, Nadia Hamida Hentati, et al. · Gene · 19
Works count: 171
Citation count: 2,678
H-index: 20
I10-index: 58
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