A. Fayez

发表

Non-target Genes Regulate miRNAs-Mediated Migration Steering of Colorectal Carcinoma

S. Salem, Ahmed R. Hamed, A. Fayez, 2018, Pathology & Oncology Research.

Apoptosis, reactive oxygen species and DNA damage in Familial Mediterranean Fever patients

H. El-Bassyouni, S. M. Kassem, A. Fayez, 2019, Gene Reports.

miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients

Engy A. Ashaat, S. Salem, A. Fayez, 2022, The Egyptian Heart Journal.

The association of +1150A polymorphism with low GH level in isolated growth hormone deficiency (IGHD) patients

H. El-Bassyouni, Manal M. Thomas, S. Salem, 2019, Gene Reports.

Prediction of the functional consequences of a novel homozygous TBX 5 variant in isolated AVSD patient

Engy A. Ashaat, A. Kamel, A. Fayez, 2022 .

Detection of mutations in GATA4 and Nkx2.5 genes in patients with Fallot’s tetralogy

I. Hussein, M. El-Desouky, A. Fahmi, 2012 .

Molecular Characterization of Some Genetic Factors Controlling Spermatogenesis in Egyptian Patients with Male Infertility

A. El-Sayed, K. Rao, M. El-Desouky, 2012 .

Independent of DAZL-T54A variant and AZF microdeletion in a sample of Egyptian patients with idiopathic non-obstructed azoospermia

J. Sabry, A. Fayez, E. Behiry, 2018, The application of clinical genetics.

Screening of the most common MEFV mutations in a large cohort of Egyptian patients with Familial Mediterranean fever

H. El-Bassyouni, A. Fayez, Bardees M. Foda, 2018, Gene Reports.

A Novel Loss-of-Sclerostin Function Mutation in a First Egyptian Family with Sclerosteosis

M. Aglan, A. Fayez, M. E. El Ruby, 2015, BioMed research international.

An infertile azoospermic male with 45,X karyotype and a unique complex (Y;14); (Y;22) translocation: cytogenetic and molecular characterization

A. Mohamed, A. Kamel, M. Mekkawy, 2018, Journal of Assisted Reproduction and Genetics.

Using postgenome-wide association study analysis; Vars2-Pic3ca-AKT is novel putative interactive pathway associated with conotruncal heart defects

A. Fayez, 2018 .

Variable predicted pathogenic mechanisms for novel MECP2 variants in RTT patients

M. Zaki, M. Issa, A. Kilany, 2022, Journal of Genetic Engineering and Biotechnology.

Detection and putative effect of GATA4 gene variants in patients with congenital cardiac septal defects.

A. Fayez, E. Behiry, H. A. Issa, 2016, Cellular and molecular biology.

Nager acrofacial dysostosis with a novel mutation in SF3B4 and developmental retardation in an Egyptian child

S. Temtamy, M. Aglan, A. Fayez, 2017 .

DALIA- a comprehensive resource of Disease Alleles in Arab population.

Vandana Sharma, V. Scaria, S. Sivasubbu, 2021, PloS one.

The potential impact of COMT gene variants on dopamine regulation and phenotypic traits of ASD patients

M. Zaki, M. Issa, R. Mosaad, 2020, Behavioural Brain Research.

Association between

A. Fayez, M. E. El Ruby, Sonia A. Alsaiedi, 2023 .

New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects

A. Fayez, M. E. El Ruby, H. Raouf, 2023, Journal of Taibah University Medical Sciences.

Dynamic disequilibrium-based pathogenicity model in mutated pyrin’s B30.2 domain—Casp1/p20 complex

Khaled H. Hamed, H. El-Bassyouni, Maha M Kobesiy, 2022, Journal of Genetic Engineering and Biotechnology.

Novel gene-specific Bayesian Gaussian mixture model to predict the missense variants pathogenicity of Sanfilippo syndrome

E. Fateen, A. Fayez, Eman E A Mohammed, 2024, Scientific reports.

Immunological and molecular study in children with combined immunodeficiency.

A. Fayez, N. Kholoussi, Shams Kholoussi, 2023, European annals of allergy and clinical immunology.