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Haplotype Diversity and Linkage Disequilibrium at Human G6PD: Recent Origin of Alleles That Confer Malarial Resistance

Science (American Association for the Advancement of Science), 2001-07, Vol.293 (5529), p.455-462

2001

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Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians

Cellular physiology and biochemistry, 2021-03, Vol.55 (1), p.117-129

2021

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Downregulation of miR-451 in Tunisian chronic myeloid leukemia patients: potential implication in imatinib resistance

Hematology, 2017-04, Vol.22 (4), p.201-207

2017

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The prevalence and prognostic significance of KRAS mutation in bladder cancer, chronic myeloid leukemia and colorectal cancer

Molecular biology reports, 2013-06, Vol.40 (6), p.4109-4114

2013

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Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency

Cellular physiology and biochemistry, 2021-12, Vol.55 (6), p.761-772

2021

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Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients

Biomedical papers of the Medical Faculty of the University Palacký, Olomouc, Czechoslovakia, 2015-03, Vol.159 (1), p.145-149

2015

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Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients

Tunisie Medicale, 2015-04, Vol.93 (4), p.237-241

2015

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Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia

Polish journal of pathology, 2013, Vol.64 (2), p.84-89

2013

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EZH2, new diagnosis and prognosis marker in acute myeloid leukemia patients

Advances in medical sciences, 2019-09, Vol.64 (2), p.395-401

2019

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First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby

Journal of pediatric hematology/oncology, 2021-11, Vol.43 (8), p.e1055-e1058

2021

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New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level

Journal of pediatric hematology/oncology, 2020-01, Vol.42 (1), p.20-22

2020

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Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia

Blood cells, molecules, & diseases, 2013-02, Vol.50 (2), p.110-114

2013

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hOCT1 gene expression predict for optimal response to Imatinib in Tunisian patients with chronic myeloid leukemia

Cancer chemotherapy and pharmacology, 2017-04, Vol.79 (4), p.737-745

2017

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Molecular study of ABCB1 gene and its correlation with imatinib response in chronic myeloid leukemia

Cancer chemotherapy and pharmacology, 2017-10, Vol.80 (4), p.829-839

2017

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Contribution to the Description of the β-Thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity

Hemoglobin, 2004-01, Vol.28 (3), p.189-195

2004

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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Hematology, 2016-08, Vol.21 (7), p.425-429

2016

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Genetic polymorphisms of NQO1, CYP1A1 and TPMT and susceptibility to acute lymphoblastic leukemia in a Tunisian population

Molecular biology reports, 2013-02, Vol.40 (2), p.1307-1314

2013

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Association of genetic variation in IKZF1, ARID5B, CDKN2A, and CEBPE with the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence

Pediatric hematology and oncology, 2016-04, Vol.33 (3), p.157-167

2016

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The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients

Hematology, 2017-03, Vol.22 (3), p.178-182

2017

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Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome

Hemoglobin, 2017-03, Vol.41 (2), p.147-150

2017

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A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]

Hemoglobin, 2014, Vol.38 (2), p.88-90

2014

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Early Complication in Sickle Cell Anemia Children due to A(TA)nTAA Polymorphism at the Promoter of UGT1A1 Gene

Disease markers, 2013, Vol.2013 (2013), p.1-6

2013

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Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1

Hematology, 2016-03, Vol.21 (2), p.121-125

2016

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Restriction mapping of βS locus among tunisian sickle-cell patients

American journal of human biology, 2011-11, Vol.23 (6), p.815-819

2011

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KIT mutation detection in Tunisian patients with newly diagnosed myelogenous leukemia: prevalence and prognostic significance

Cancer genetics, 2012-09, Vol.205 (9), p.436-441

2012

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Haplotype Diversity and Linkage Disequilibrium at Human G6PD: Recent Origin of Alleles That Confer Malarial Resistance

Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians

Downregulation of miR-451 in Tunisian chronic myeloid leukemia patients: potential implication in imatinib resistance

The prevalence and prognostic significance of KRAS mutation in bladder cancer, chronic myeloid leukemia and colorectal cancer

Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency

Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients

Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients

Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia

EZH2, new diagnosis and prognosis marker in acute myeloid leukemia patients

First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby

New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level

Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia

hOCT1 gene expression predict for optimal response to Imatinib in Tunisian patients with chronic myeloid leukemia

Molecular study of ABCB1 gene and its correlation with imatinib response in chronic myeloid leukemia

Contribution to the Description of the β-Thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Genetic polymorphisms of NQO1, CYP1A1 and TPMT and susceptibility to acute lymphoblastic leukemia in a Tunisian population

Association of genetic variation in IKZF1, ARID5B, CDKN2A, and CEBPE with the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence

The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients

Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome

A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]

Early Complication in Sickle Cell Anemia Children due to A(TA)nTAA Polymorphism at the Promoter of UGT1A1 Gene

Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1

Restriction mapping of βS locus among tunisian sickle-cell patients

KIT mutation detection in Tunisian patients with newly diagnosed myelogenous leukemia: prevalence and prognostic significance

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