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Imen Darragi

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients
2015 · Leila Chaouch, Imen Moumni, et al. · Hematology · 24
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Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among Sickle Cell Aneamia patients
2013 · Leila Chaouch, Miniar Kalai, et al. · Biomedical Papers · 13
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The role of rs1984112_G atCD36gene in increasing reticulocyte level among sickle cell disease patients
2016 · Miniar Kalai, Marwa Dridi, et al. · Hematology · 10
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Molecular basis of pyruvate kinase deficiency among Tunisians: description of new mutations affecting coding and noncoding regions in the PKLR gene
2017 · M. Jaouani, L. Manco, et al. · International Journal of Laboratory Hematology · 8
Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia
2012 · Leila Chaouch, Yossra Said, et al. · Annales de biologie clinique · 8
New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level
2019 · Leila Chaouch, Houssem Sellami, et al. · Journal of Pediatric Hematology/Oncology · 5
Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome
2017 · Faten Haddad, Nawel Trabelsi, et al. · Hemoglobin · 5
Dynamics of SARS-CoV-2 antibodies after natural infection: insights from a study on Pasteur Institute of Tunis employees
2024 · Ines Cherif, Ghassen Kharroubi, et al. · Libyan Journal of Medicine · 3
Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians
2021 · Nawel Trabelsi, Ghada Bouguerra, et al. · Cellular Physiology and Biochemistry · 3
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Rapid and inexpensive detection of common HBB gene mutations in Tunisian population by high-resolution melting analysis: Implication for molecular diagnosis
2013 · Houyem Ouragini, Faten Haddad, et al. · Hematology · 3
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Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.
2016 · Leila Chaouch, Miniar Kalai1, et al. · PubMed · 2
Phenotypic and molecular genetic analysis of Pyruvate Kinase deficiency in a Tunisian family
2015 · Jaouani Mouna, Hamdi Nadia, et al. · Egyptian Journal of Medical Human Genetics · 2
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Implication of rs1026611 in the MCP-1 Gene and V64I of CCR2 in Stroke among SCA Tunisian Patients: A Brief Study
2022 · Leila Chaouch, Miniar Kalai, et al. · Book Publisher International (a part of SCIENCEDOMAIN International) · 1
Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia
2021 · Nawel Trabelsi, Leila Chaouch, et al. · European Journal of Medical Genetics · 1
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Hb Moscva [β24(B6)Gly→Asp (GGT>GAT), HBB: c.74G>A]: An Unstable Hemoglobin Newly Detected as a De Novo Mutation in a Mauritanian Patient
2018 · Sidi M. Ghaber, Nawel Trabelsi, et al. · Hemoglobin · 1
Association of rs1319868, rs1567811 and rs8041224 of IGF1R gene with infection among sickle cell anemia Tunisian patients
2016 · Mouna Ben Sassi, Leila Chaouch, et al. · Acta Haematologica Polonica · 1
P2-3 - Cinétique d'acquisition des anticorps du SARS-CoV-2 suite à une infection naturelle, Tunis, Tunisie
2024 · I. Cherif, G. Kharroubi, et al. · Journal of Epidemiology and Population Health
Works count: 17
Citation count: 90
H-index: 5
I10-index: 3
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