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Hatem Zayed
Hatem Zayed
Verified email at qu.edu.qa
Title
Cited by
Cited by
Year
Development of hyperactive sleeping beauty transposon vectors by mutational analysis
H Zayed, Z Izsvák, O Walisko, Z Ivics
Molecular Therapy 9 (2), 292-304, 2004
2952004
The DNA‐bending protein HMGB1 is a cellular cofactor of Sleeping Beauty transposition
H Zayed, Z Izsvák, D Khare, U Heinemann, Z Ivics
Nucleic acids research 31 (9), 2313-2322, 2003
1732003
The Sleeping Beauty transposable element: evolution, regulation and genetic applications
Z Ivics, CD Kaufman, H Zayed, C Miskey, O Walisko, Z Izsvák
Current issues in molecular biology 6 (1), 43-56, 2004
1182004
Enhanced identification of transcriptional enhancers provides mechanistic insights into diseases
Y Murakawa, M Yoshihara, H Kawaji, M Nishikawa, H Zayed, H Suzuki, ...
Trends in Genetics 32 (2), 76-88, 2016
1102016
Analysis of differentially expressed genes and molecular pathways in familial hypercholesterolemia involved in atherosclerosis: a systematic and bioinformatics approach
S Udhaya Kumar, D Thirumal Kumar, R Bithia, S Sankar, R Magesh, ...
Frontiers in Genetics 11, 734, 2020
982020
Role of non-coding RNA networks in leukemia progression, metastasis and drug resistance
AA Bhat, SN Younes, SS Raza, L Zarif, S Nisar, I Ahmed, R Mir, S Kumar, ...
Molecular cancer 19, 1-21, 2020
932020
A potential link between oxidative stress and endothelial-to-mesenchymal transition in systemic sclerosis
DTB Thuan, H Zayed, AH Eid, H Abou-Saleh, GK Nasrallah, AA Mangoni, ...
Frontiers in immunology 9, 385511, 2018
932018
Integrative bioinformatics approaches to map potential novel genes and pathways involved in ovarian cancer
SU Kumar, DT Kumar, R Siva, CGP Doss, H Zayed
Frontiers in bioengineering and biotechnology 7, 391, 2019
722019
Novel CD44-downstream signaling pathways mediating breast tumor invasion
A Ouhtit, B Rizeq, H Abou Saleh, MM Rahman, H Zayed
International journal of biological sciences 14 (13), 1782, 2018
712018
Genetic epidemiology of glucose-6-phosphate dehydrogenase deficiency in the Arab world
CGP Doss, DR Alasmar, RI Bux, P Sneha, FD Bakhsh, I Al-Azwani, ...
Scientific reports 6 (1), 37284, 2016
682016
A profound computational study to prioritize the disease-causing mutations in PRPS1 gene
AK Agrahari, P Sneha, C George Priya Doss, R Siva, H Zayed
Metabolic Brain Disease 33, 589-600, 2018
592018
Dysregulation of signaling pathways due to differentially expressed genes from the B-cell transcriptomes of systemic lupus erythematosus patients–a bioinformatics approach
S Udhaya Kumar, D Thirumal Kumar, R Siva, C George Priya Doss, ...
Frontiers in Bioengineering and Biotechnology 8, 276, 2020
572020
Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I
A Mosaeilhy, MM Mohamed, HSA El Abd, R Gamal, OK Zaki, H Zayed
Metabolic brain disease 32, 1417-1426, 2017
502017
Genetic epidemiology of type 1 diabetes in the 22 Arab countries
H Zayed
Current diabetes reports 16, 1-11, 2016
492016
The Arab genome: health and wealth
H Zayed
Gene 592 (2), 239-243, 2016
472016
Molecular dynamics-based analyses of the structural instability and secondary structure of the fibrinogen gamma chain protein with the D356V mutation
SK Ali, P Sneha, J Priyadharshini Christy, H Zayed, C George Priya Doss
Journal of Biomolecular Structure and Dynamics 35 (12), 2714-2724, 2017
462017
Epidemiology of diabetic ketoacidosis in Arab patients with type 1 diabetes: a systematic review
H Zayed
International journal of clinical practice 70 (3), 186-195, 2016
462016
Congenital diaphragmatic hernia and microtia in a newborn with mycophenolate mofetil (MMF) exposure: phenocopy for Fryns syndrome or broad spectrum of teratogenic effects?
MA Parisi, H Zayed, AM Slavotinek, JC Rutledge
American journal of medical genetics Part A 149 (6), 1237-1240, 2009
462009
Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach
P Sneha, R Siva, H Zayed
PLoS One 12 (4), e0174953, 2017
442017
Structural analysis of G1691S variant in the human Filamin B gene responsible for Larsen syndrome: a comparative computational approach
H Zayed
Journal of cellular biochemistry 118, 1900-1910, 2017
442017
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Articles 1–20