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Ayda Bennour

Observed names: A. Bennour, Ayda BENNOUR
ORCID: 0000-0003-2256-1493
Observed ORCID: 0000-0003-2256-1493
OpenAlex ID: A5077880177
Chronic myeloid leukemia: Relevance of cytogenetic and molecular assays
2015 · Ayda Bennour, Ali Saad, et al. · Critical Reviews in Oncology/Hematology · 60
Analysis of the clinico-hematological relevance of the breakpoint location within M-BCR in chronic myeloid leukemia
2012 · Ayda Bennour, Ines Ouahchi, et al. · Medical Oncology · 35
Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9
2009 · Ayda Bennour, Halima Sennana, et al. · Cancer Genetics and Cytogenetics · 32
Comprehensive analysis of BCR/ABL variants in chronic myeloid leukemia patients using multiplex RT-PCR.
2012 · Ayda Bennour, Ines Ouahchi, et al. · PubMed · 21
Molecular cytogenetic characterization of Philadelphia-negative rearrangements in chronic myeloid leukemia patients
2011 · Ayda Bennour, Hatem Bellâaj, et al. · Journal of Cancer Research and Clinical Oncology · 18
E355G mutation appearing in a patient with e19a2 chronic myeloid leukaemia resistant to imatinib
2010 · Ayda Bennour, Nathalie Beaufils, et al. · Journal of Clinical Pathology · 18
Genome Tunisia Project: paving the way for precision medicine in North Africa
2024 · Yosr Hamdi, Mediha Trabelsi, et al. · Genome Medicine · 14
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A PML/RARA chimeric gene on chromosome 12 in a patient with acute promyelocytic leukemia (M4) associated with a new variant translocation: t(12;15;17)(q24;q24;q11)
2013 · Ayda Bennour, Ikram Tabka, et al. · Medical Oncology · 12
A masked BCR/ABL rearrangement in a case of chronic myeloid leukemia with translocation t(3;9)(p14;q34)
2008 · Ayda Bennour, Halima Sennana, et al. · Cancer Genetics and Cytogenetics · 7
A novel t(3;12)(q21;p13) translocation in a patient with accelerated chronic myeloid leukemia after imatinib and nilotinib therapy.
2013 · Ayda Bennour, Ikram Tabka, et al. · Europe PMC (PubMed Central) · 6
Honey-based therapeutics: a comprehensive review of anticancer, antioxidant, and prognostic impacts in breast cancer treatment
2024 · Walid Sabri Hamadou, Nouha Bouali, et al. · Journal of Cancer Prevention & Current Research · 4
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X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
2022 · Hamza Chouk, Sarra Saad, et al. · BMC Medical Genomics · 4
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Translocation t(X;10)(p10;p10): a rare chromosomal abnormality in a new born female with acute myeloid leukemia
2011 · Ayda Bennour, Halima Sennana, et al. · Medical Oncology · 3
Molecular cytogenetic study of derivative chromosome 9 deletion in chronic myeloid leukemia patients
2011 · Ayda Bennour, Ines Ouahchi, et al. · Medical Oncology · 2
Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach
2026 · Bochra Khadija, Hamza Hadj Abdallah, et al. · Frontiers in Genetics
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1st Congress of the Tunisian Society of Human Genomics October 17–18 & 19, 2024, Sousse, Tunisia Genomics for a sustainable healthcare system
2026 · Ayda Bennour, Haifa El Mabrouk, et al. · Journal of Community Genetics
Retrospective analysis of spinal muscular atrophy in tunisian population: phenotypic-genotypic associations and considerations for therapeutic advancement
2026 · Walid Sabri Hamadou, Abdelbasset Amara, et al. · Neurogenetics
Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights
2026 · Rim Khelifi, Houcemeddine Othmane, et al. · Molecular Cytogenetics
Molecular characterization of Tunisian B-acute lymphoblastic leukemia
2024 · Sawsen Besbes, Nouha Bouali, et al. · Journal of Cancer Prevention & Current Research
58P Molecular investigation using microarray-based comparative genomic hybridization in patients with myelodysplastic syndrome and normal karyotype
2023 · M.A.N. Ammar, A. Bennour, et al. · ESMO Open
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X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
2022 · Hamza CHOUK, Sarra SAAD, et al. · Research Square
X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
2022 · Hamza CHOUK, Sarra SAAD, et al. · Research Square
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Works count: 22
Citation count: 236
H-index: 8
I10-index: 8
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