الرئيسية › دليل الباحثين › Ayda Bennour

Ayda Bennour

الانتماء : Hôpital Farhat Hached · University of Sousse

• 22منشورات (انتماء تونسي)
• 22مجموع المنشورات
• 222الاستشهادات
• 8مؤشر h

ORCIDOpenAlex

مجالات البحث

• Genomic variations and chromosomal abnormalities
• Chronic Myeloid Leukemia Treatments
• Retinoids in leukemia and cellular processes
• Acute Myeloid Leukemia Research
• Genomics and Rare Diseases

المنشورات (22)

• Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights
  2026 · Molecular Cytogenetics
• Retrospective analysis of spinal muscular atrophy in tunisian population: phenotypic-genotypic associations and considerations for therapeutic advancement
  2026 · Neurogenetics
• 1st Congress of the Tunisian Society of Human Genomics October 17–18 & 19, 2024, Sousse, Tunisia Genomics for a sustainable healthcare system
  2026 · Journal of Community Genetics
• Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach
  2026 · Frontiers in Genetics
• Genome Tunisia Project: paving the way for precision medicine in North Africa
  2024 · Genome Medicine · استُشهد به 13 مرة
• Honey-based therapeutics: a comprehensive review of anticancer, antioxidant, and prognostic impacts in breast cancer treatment
  2024 · Journal of Cancer Prevention & Current Research · استُشهد به 4 مرة
• Molecular characterization of Tunisian B-acute lymphoblastic leukemia
  2024 · Journal of Cancer Prevention & Current Research
• 58P Molecular investigation using microarray-based comparative genomic hybridization in patients with myelodysplastic syndrome and normal karyotype
  2023 · ESMO Open
• X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
  2022 · BMC Medical Genomics · استُشهد به 4 مرة
• X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
  2022 · Research Square
• X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
  2022 · Research Square
• Chronic myeloid leukemia: Relevance of cytogenetic and molecular assays
  2015 · Critical Reviews in Oncology/Hematology · استُشهد به 53 مرة
• 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 · Medical Oncology · استُشهد به 12 مرة
• A novel t(3;12)(q21;p13) translocation in a patient with accelerated chronic myeloid leukemia after imatinib and nilotinib therapy.
  2013 · Europe PMC (PubMed Central) · استُشهد به 6 مرة
• Analysis of the clinico-hematological relevance of the breakpoint location within M-BCR in chronic myeloid leukemia
  2012 · Medical Oncology · استُشهد به 31 مرة
• Comprehensive analysis of BCR/ABL variants in chronic myeloid leukemia patients using multiplex RT-PCR.
  2012 · PubMed · استُشهد به 20 مرة
• Molecular cytogenetic characterization of Philadelphia-negative rearrangements in chronic myeloid leukemia patients
  2011 · Journal of Cancer Research and Clinical Oncology · استُشهد به 18 مرة
• Translocation t(X;10)(p10;p10): a rare chromosomal abnormality in a new born female with acute myeloid leukemia
  2011 · Medical Oncology · استُشهد به 3 مرة
• Molecular cytogenetic study of derivative chromosome 9 deletion in chronic myeloid leukemia patients
  2011 · Medical Oncology · استُشهد به 2 مرة
• E355G mutation appearing in a patient with e19a2 chronic myeloid leukaemia resistant to imatinib
  2010 · Journal of Clinical Pathology · استُشهد به 17 مرة
• Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9
  2009 · Cancer Genetics and Cytogenetics · استُشهد به 32 مرة
• A masked BCR/ABL rearrangement in a case of chronic myeloid leukemia with translocation t(3;9)(p14;q34)
  2008 · Cancer Genetics and Cytogenetics · استُشهد به 7 مرة

مجلات النشر

• Medical Oncology × 4
• Journal of Cancer Prevention & Current Research × 2
• Research Square × 2
• Cancer Genetics and Cytogenetics × 2
• Molecular Cytogenetics × 1
• Neurogenetics × 1

المنشورات حسب السنة

• 20264
• 20243
• 20231
• 20223
• 20151
• 20132
• 20122
• 20113
• 20101
• 20091

التعاون العلمي

المؤسسات الشريكة : Tunis University · Tunis El Manar University · Institut Pasteur de Tunis · University of Monastir · University of Sfax

المؤلفون المشاركون

• Halima Sennana
• Abderrahim Khélif
• Dorra Hmida
• Yosra Ben Youssef
• Hamza Chouk
• Haïfa El Mabrouk
• S. Dimassi
• Monia Zaier
• Ines Ouahchi
• Amira Benzarti
• Moez Elloumi
• Mohamed DENGUEZLI

البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).