Gamal Ebid - Concepedia

Author

Gamal Ebid

Also Known As

G. T. A. Ebid, Gamal T Ebid, Gamal Ebid, Gamal T Ebid, Gamal T. A. Ebid, Gamal T. Ebid, Gamal T.A. Ebid, Gamal TA Ebid, Gamal Thabet Aly Ebid

Publications

205

Citations

H-Index

Concepts

All Affiliations

Cairo University Fred Hutch Cancer Center

About

Gamal Ebid is an author at Cairo University specializing in cancer research, radiation oncology, and oncology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Health Sciences	1	1	17
2	Medicine	1	1	17
3	Genetics	1	1	17
4	Hematology	1	1	17
5	Cancer Research	1	1	17

Gamal Ebid

Publications

141

Citations

H-Index

Page 1

	Year	Citations
Synergistic effect of methyltetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphism as risk modifiers of pediatric acute lymphoblastic leukemia. Azza M. Kamel, Heba S. Moussa, Gamal Ebid, PubMed	2007	44
N-Acetyltransferase 2 (NAT2) polymorphism as a risk modifier of susceptibility to pediatric acute lymphoblastic leukemia Azza M. Kamel, Gamal Ebid, Heba S. Moussa Tumor Biology	2015	23
Clinical Effect of Combined Mutations in DNMT3A, FLT3-ITD, and NPM1 Among Egyptian Acute Myeloid Leukemia Patients Mosaad M. El Gammal, Gamal Ebid, Youssef Madney, Clinical Lymphoma Myeloma & Leukemia Combined MutationsHematological MalignancyMedicineGeneticsMixed-phenotype Acute Leukemia	2019	17
Coagulation Profile in COVID-19 Patients and its Relation to Disease Severity and Overall Survival: A Single-Center Study Amal Ezzat Abd El-Lateef, Saad Alghamdi, Gamal Ebid, British Journal of Biomedical Science	2022	17
MDM2 T309G has a Synergistic Effect with P21 ser31arg Single Nucleotide Polymorphisms on the Risk of Acute Myeloid Leukemia Gamal Ebid, I. Sedhom, Mosaad M. ElGammal, Asian Pacific Journal of Cancer Prevention	2012	16
Lack of association of CTLA-4 +49 A/G polymorphism with predisposition to type 1 diabetes in a cohort of Egyptian families Azza M. Kamel, Marwa Farouk Mira, Ghada I. Mossallam, Egyptian Journal of Medical Human Genetics	2013	13
Prevalence of the frequency of JAK2 (V617F) mutation in different myeloproliferative disorders in Egyptian patients. Gamal Ebid, Mohamed Ghareeb, Omina Salaheldin, PubMed	2015	11

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