Author

Nesrine El-Gharbawi

Observed names: N. El-Gharbawi, Nesrine El Gharbawi, Nesrine M. El-Gharbawy, Nesrine Mohamed El Gharbawi, Nesrine Mohamed El-Gharbawi, Nesrine Mohamed Elgharabawi

Institution: Cairo University

Observed institutions: Cairo University, Cairo University hospitals

ORCID: 0009-0006-5800-5631

Observed ORCID: 0009-0006-5800-5631

OpenAlex ID: A5026850338

Chondrogenic differentiation of human umbilical cord blood‐derived mesenchymal stem cells in vitro

2015 · Azza Mostafa Ibrahim, Nesrine Mohamed Elgharabawi, et al. · Microscopy Research and Technique · 18

Incidence and Association of 563 C/T Mediterranean and the Silent 1311C/T G6PD Mutations in G6PD-deficient Egyptian Children

2011 · Hanaa H. Arnaout, Nesrine M. El-Gharbawy, et al. · Laboratory Medicine · 12

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Impact of Cytochromes P450 3A4 and 2B6 gene polymorphisms on predisposition and prognosis of acute myeloid leukemia: an Egyptian case-control study

2021 · Shahira Kamal Anis Botros, Nesrine El Gharbawi, et al. · Egyptian Journal of Medical Human Genetics · 11

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Genetic Variations of ferroportin-1(FPN1-8CG), TMPRSS6 (rs855791) and Hemojuvelin (I222N and G320V) Among a Cohort of Egyptian β-Thalassemia Major Patients

2022 · Nesrine El-Gharbawi, Iman Shaheen, et al. · Indian Journal of Hematology and Blood Transfusion · 4

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Combined tumor necrosis factor-α (−308 G/A) and tumor necrosis factor-β (+ 252 A/G) nucleotide polymorphisms and chronicity in Egyptian children with immune thrombocytopenia

2023 · Mona El-Ghamrawy, Nesrine El-Gharbawi, et al. · International Journal of Hematology · 2

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Association of hereditary antithrombin deficiency with intrauterine growth restriction

2018 · Hala Mufeed Said, Nesrine Mohamed El-Gharbawi, et al. · Blood Coagulation & Fibrinolysis · 2

Association of FOXO3a (rs4946936) genetic variant with chronic myeloid leukemia susceptibility and imatinib response in a cohort of Egyptian patients

2026 · Nesrine El-Gharbawi, Hend N. Ellithy, et al. · The Egyptian Journal of Haematology

Association of mannose-binding lectin promoter gene polymorphism with frequency of vaso-occlusive events in sickle cell disease patients: a single-center Egyptian study

2025 · Mona El-Ghamrawy, Nesrine El-Gharbawi, et al. · The Egyptian Journal of Haematology

5588568 Association of Mannose-binding Lectin Serum Level and Promoter Gene Variants Rs7096206 and Rs10031251 With Frequency of Vaso-occlusive Events in Sickle Cell Disease Patients; an Egyptian Cross-sectional Study

2023 · M. El-Ghamrawy, N. El-Gharbawi, et al. · HemaSphere

Low absolute neutrophilic and lymphocytic counts in children with CMV reactivation following HSCT

2022 · Khaled Mohamed Salama, Marwa Abd Elhady, et al. · International Journal of Health Sciences

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Works count: 10

Citation count: 49

H-index: 4

I10-index: 3