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List of works by Hatem Zayed

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Development of hyperactive sleeping beauty transposon vectors by mutational analysis

scientific article
The DNA-bending protein HMGB1 is a cellular cofactor of Sleeping Beauty transposition

scientific article
Enhanced Identification of Transcriptional Enhancers Provides Mechanistic Insights into Diseases

scientific article
A maternally inherited chromosome 18q22.1 deletion in a male with late-presenting diaphragmatic hernia and microphthalmia-evaluation of DSEL as a candidate gene for the diaphragmatic defect

scientific article published in April 2010
Congenital diaphragmatic hernia and microtia in a newborn with mycophenolate mofetil (MMF) exposure: phenocopy for Fryns syndrome or broad spectrum of teratogenic effects?

Genetic Epidemiology of Glucose-6-Dehydrogenase Deficiency in the Arab World

scientific article
Correction of DNA protein kinase deficiency by spliceosome-mediated RNA trans-splicing and sleeping beauty transposon delivery

scientific article published on 24 April 2007
Molecular dynamics-based analyses of the structural instability and secondary structure of the fibrinogen gamma chain protein with the D356V mutation

scientific article
Durable immunity to oncogenic human papillomaviruses elicited by adjuvanted recombinant Adeno-associated virus-like particle immunogen displaying L2 17-36 epitopes

scientific article
Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach

scientific article
Two patients with Canavan disease and structural modeling of a novel mutation

scientific article
Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I.

scientific article published on 07 April 2017
Structural Analysis of G1691S Variant in the Human Filamin B Gene Responsible for Larsen Syndrome: A Comparative Computational Approach.

scientific article
Genetic Epidemiology of Type 1 Diabetes in the 22 Arab Countries

scientific article published on May 1, 2016
In vitro functional correction of the mutation responsible for murine severe combined immune deficiency by small fragment homologous replacement

scientific article
Genotype-phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants

scientific article published on 23 May 2017
A profound computational study to prioritize the disease-causing mutations in PRPS1 gene

scientific article
The Arab genome: Health and wealth

scientific article
Substitution impact of highly conserved arginine residue at position 75 in GJB1 gene in association with X-linked Charcot-Marie-tooth disease: A computational study

scientific article published on 27 October 2017
Propionic acidemia in the Arab World

scientific article published on 09 April 2015
RPL13A and EEF1A1 Are Suitable Reference Genes for qPCR during Adipocyte Differentiation of Vascular Stromal Cells from Patients with Different BMI and HOMA-IR.

scientific article
Novel mutation in an Egyptian patient with infantile Canavan disease

scientific article published on 28 November 2015
Sanguinarine Induces Apoptosis Pathway in Multiple Myeloma Cell Lines via Inhibition of the JaK2/STAT3 Signaling

scientific article published on 17 April 2019
Structural Determination of the Broadly Reactive Anti-IGHV1-69 Anti-idiotypic Antibody G6 and Its Idiotope

scientific article published in December 2017
Protective Effect of Cyclically Pressurized Solid–Liquid Extraction Polyphenols from Cagnulari Grape Pomace on Oxidative Endothelial Cell Death

scientific article published on 21 August 2018
Novel CD44-downstream signaling pathways mediating breast tumor invasion

scholarly article by Allal Ouhtit published in October 2018
Computational approach to unravel the impact of missense mutations of proteins (D2HGDH and IDH2) causing D-2-hydroxyglutaric aciduria 2

Rapid generation of stable cell lines expressing high levels of erythropoietin, factor VIII, and an antihuman CD20 antibody using lentiviral vectors

scientific article published on August 2013
Corrigendum: Genetic Epidemiology of Glucose-6-Phosphate Dehydrogenase Deficiency in the Arab World

scientific article published on 3 January 2017
Computational modelling approaches as a potential platform to understand the molecular genetics association between Parkinson’s and Gaucher diseases

article
Canavan disease: An Arab scenario

scientific article published on February 7, 2015
Structural analysis of missense mutations in galactokinase 1 (GALK1) leading to galactosemia type-2

scientific article published on 12 June 2018
A Potential Link Between Oxidative Stress and Endothelial-to-Mesenchymal Transition in Systemic Sclerosis

scientific article published on 19 September 2018
Epidemiology of diabetic ketoacidosis in Arab patients with type 1 diabetes: a systematic review

scientific article published on February 4, 2016
Comparative computational assessment of the pathogenicity of mutations in the Aspartoacylase enzyme

scientific article
Myocardial Ischemic Subject's Thymus Fat: A Novel Source of Multipotent Stromal Cells

scientific article published on 10 December 2015
Spectrum of mutations of cystic fibrosis in the 22 Arab countries: A systematic review

scientific article published on 12 November 2018
Breast cancer in the GCC countries: A focus on BRCA1/2 and non-BRCA1/2 genes

Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene

scientific article published in August 2016
Computational insights of K1444N substitution in GAP-related domain of NF1 gene associated with neurofibromatosis type 1 disease: a molecular modeling and dynamics approach

article
An Arab Registry for Type 1 Diabetes: Global Benefits for Type 1 Diabetes Patients

scientific article published on 5 June 2016
A computational approach for investigating the mutational landscape of RAC-alpha serine/threonine-protein kinase (AKT1) and screening inhibitors against the oncogenic E17K mutation causing breast cancer

scientific article published on 21 October 2019
Integrative Bioinformatics Approaches to Map Potential Novel Genes and Pathways Involved in Ovarian Cancer

scientific article published on 17 December 2019
Molecular insights of the G2019S substitution in LRRK2 kinase domain associated with Parkinson's disease: A molecular dynamics simulation approach

scientific article published on 04 March 2019
Clinical Exome Sequencing unravels new disease-causing mutations in the myeloproliferative neoplasms: A pilot study in patients from the state of Qatar

scientific article published on 13 December 2018
Potential routes of spread of Zika virus to the Middle East, North Africa and Asia: action must be taken

article
Understanding the structure-function relationship of HPRT1 missense mutations in association with Lesch-Nyhan disease and HPRT1-related gout by in silico mutational analysis

scientific article published on 23 February 2019
Neuropathy of type 1 diabetes in the Arab world: A systematic review and meta-analysis

scientific article published on 22 March 2017
A comparative computational approach toward pharmacological chaperones (NN-DNJ and ambroxol) on N370S and L444P mutations causing Gaucher's disease

scientific article published on 01 December 2018
A computational method to characterize the missense mutations in the catalytic domain of GAA protein causing Pompe disease

scholarly article by D Thirumal Kumar published in October 2018

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