Accueil › Annuaire des chercheurs › Samia Menif
Samia Menif
Affiliation : Tunis University · Institut Pasteur de Tunis · Faculté de médecine de Tunis · Tunis El Manar University
- 62Publications (affiliation tunisienne)
- 76Publications au total
- 432Citations
- 13Indice h
Profil de recherche
Samia Menif compte 62 publications référencées (2006–2026). Ses travaux paraissent principalement dans « HemaSphere », « Molecular Biology Reports » et « PubMed ». Son article le plus cité, « Identification of genes and miRNA associated with idiopathic recurrent pregnancy loss: an exploratory data mining study » (2020), a été cité 37 fois. 13 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de Émirats arabes unis, États-Unis.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Hemoglobinopathies and Related Disorders
- Chronic Myeloid Leukemia Treatments
- Acute Myeloid Leukemia Research
- Acute Lymphoblastic Leukemia research
- Chronic Lymphocytic Leukemia Research
Publications (62)
- Health literacy and prenatal screening acceptability for hemoglobinopathies in Tunisia: a pilot mediation study
- Mutation Spectrum of Hemoglobinopathies in Tunisia
- Management of Philadelphia chromosome-positive B-acute lymphoblastic leukemia in Tunisia.
- Circulating Erythrocyte‐ and Endothelial‐Derived Microvesicles as Biomarkers of Hemolysis and Clinical Severity in Sickle Cell Disease
- Cord Blood-Based Neonatal Screening for Hemoglobinopathies in Northern Tunisia
- From misconceptions to empowerment: assessing health and genetic literacy on thalassemia among Tunisian secondary school students
- The role of IKZF1 rs4132601 and Δ4–7 somatic deletion in acute lymphoblastic leukemia: a bioinformatics and case-control study
- Hemoglobin Disorders Associated with Neurological Impairment: First Report of ATR-X Syndrome and Recessive Congenital Methemoglobinemia Type II in Tunisia
- Artificial intelligence and the challenge of genetic essentialism: interview with artificial intelligences on sickle-cell disease
- Integrating cancer education into Tunisian school curricula: A public health necessity
- Immunity in the Progeroid Model of Cockayne Syndrome: Biomarkers of Pathological Aging
- New Born Screening of Hemoglobinopathies in a Center Tunisian Population
- Epidemiological and biological characteristics of G6PD deficiency in women in Tunisia
- TP53 Gene 72 Arg/Pro (rs1042522) single nucleotide polymorphism increases the risk and the severity of chronic lymphocytic leukemia
- CHRONIC MYELOID LEUKEMIA IN CHILDREN AND YOUNG ADULTS IN TUNISIA
- PB1717: CD19-NEGATIVE B- ACUTE LYMPHOBLASTIC LEUKEMIA: WHAT CHALLENGES?
- PB1722: EARLY T-CELL PRECURSOR ACUTE LYMPHOBLASTIC LEUKEMIA: DIAGNOSIS AND TREATMENT CHALLENGES
- PB2526: UMBILICAL CORD BLOOD SCREENING FOR SICKLE CELL DISEASE: A PILOT STUDY IN THE NORTH OF TUNISIA
- PB2543: CIRCULATING MICROVESICLES AS POTENTIAL CELLULAR BIOMARKERS FOR THROMBOTIC RISKS IN BETA THALASSEMIA
- Identification of High-Risk Single Nucleotide Polymorphisms in the Human CYB5R3 Gene Responsible for Recessive Congenital Methemoglobinemia: A Computational Approach
- Tyrosol Derivatives, Bearing 3,5-Disubstituted Isoxazole and 1,4-Disubstituted Triazole, as Potential Antileukemia Agents by Promoting Apoptosis
- Emotional and behavioral attitudes of Tunisian youth towards childhood leukemia: health education and primary prevention in perspective
- Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn
- Hematological relevance of JAK2 V617F and calreticulin mutations in Tunisian patients with essential thrombocythemia
- Epidemiology of Chronic Myeloid Leukemia in Tunisia
- P105: BLOOD MICROVESICLES AS BIOMARKERS TO PREDICT VASO-OCCLUSIVE CRISIS IN SICKLE CELL ANEMIA
- P106: EARLY PREVENTIVE DIAGNOSIS OF HEMOLYTIC ANEMIA IN SICKLE CELL PATIENTS BY DETECTING THE TRIGGERING OF ERYPTOSIS.
- P1549: NOVEL SLC4A1 GENE MUTATIONS IN HEREDITARY SPHEROCYTOSIS BAND 3 PROTEIN-DEFICIENT TUNISIAN PATIENTS
- P-077: POTENTIAL BIOMARKERS IN THE PREVENTIVE DIAGNOSIS OF ACUTE COMPLICATIONS IN SICKLE CELL DISEASE
- Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family
- PB1843: ACUTE MYELOID LEUKEMIA WITH PHILADELPHIA CHROMOSOME: EXPERIENCE OF SFAX HEMATOLOGY DEPARTMENT
- Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency
- Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians
- JAK2 p.(V617F) mutation in Tunisian myeloproliferative neoplasms and its genotype-phenotype correlation.
- First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby
- Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia
- Identification of genes and miRNA associated with idiopathic recurrent pregnancy loss: an exploratory data mining study
- Eryptosis and circulating blood cells microparticules in sickle cell diseases
- Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions
- EZH2, new diagnosis and prognosis marker in acute myeloid leukemia patients
- In Ph+BCR-ABL1P210+ acute lymphoblastic leukemia the e13a2 (B2A2) transcript is prevalent
- Chronic myeloid leukemia patients in Tunisia: epidemiology and outcome in the imatinib era (a multicentric experience)
- 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
- Association of genetic variation inIKZF1, ARID5B, CDKN2A, andCEBPEwith the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence
- Downregulation of miR-451 in Tunisian chronic myeloid leukemia patients: potential implication in imatinib resistance
- Regulatory network analysis of microRNAs and genes in imatinib-resistant chronic myeloid leukemia
- Epidemiological Approach of Chronic Myeloid Leukemia. Algerian-Tunisian Study
- Polymorphisms in XPC, XPD and XPG DNA repair genes and leukemia risk in a Tunisian population
- The prevalence and prognostic significance of KRAS mutation in bladder cancer, chronic myeloid leukemia and colorectal cancer
- Chronic Myeloid Leukemia Patients In Tunisia: Epidemiology and Outcome In The Imatinib Era (A Multicentric Experience)
- Genetic polymorphisms of NQO1, CYP1A1 and TPMT and susceptibility to acute lymphoblastic leukemia in a Tunisian population
- KIT mutation detection in Tunisian patients with newly diagnosed myelogenous leukemia: prevalence and prognostic significance
- Influence of genetic polymorphisms of xenobiotic metabolizing enzymes on the risk of developing leukemia in a Tunisian population
- TREATMENT OF ACUTE PROMYELOCYTIC LEUKEMIA WITH AIDA BASED REGIMEN
- Treatment of acute promyelocytic leukemia with PETHEMA LPA 99 protocol: a Tunisian single center experience
- ATRA and anthracycline-based chemotherapy in the treatment of childhood acute promyelocytic leukemia (APL): A 10-year experience in Tunisia
- Recurrent differentiation syndrome or septic shock? Unresolved dilemma in a patient with acute promyelocytic leukemia
- Quantitative detection of bcr-abl transcripts in chronic myeloid leukemia
- Efficacité de l’imatinib dans les syndromes hyperéosinophiliques associés au transcrit FIP1L1–PDGFRA
- [RT-PCR use for the diagnostic of chronic myeloid leukaemia].
- FIP1L1–PDGFRA positive chronic eosinophilic leukemia in Tunisian patients
Revues de publication
- HemaSphere × 9
- Molecular Biology Reports × 3
- PubMed × 2
- BMC Public Health × 2
- Journal of Pediatric Hematology/Oncology × 2
- American Journal of Perinatology × 2
Publications par année
- 20263
- 20257
- 20243
- 20237
- 202211
- 20215
- 20203
- 20192
- 20181
- 20172
Collaborations
Établissements partenaires : Hôpital Farhat Hached · Hopital Universitaire Hedi Chaker · University of Monastir · Hôpital La Rabta · University of Sousse
Pays des co-auteurs : Émirats arabes unis · États-Unis
Co-auteurs
- Inès Safra
- Salem Abbès
- Imen Moumni
- Dorra Chaouachi
- Houyem Ouragini
- Ismael Soltani
- Khouloud Khalfaoui
- Dorra Chaouechi
- Hassiba Amouri
- Ahlem Farrah
- Slah Ouerhani
- Islem Ben Hassine
Données bibliographiques issues d’OpenAlex (base ouverte).
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