السيرة الذاتية

المؤهلات

الدكتوراه

2000

‏العلوم الطبية الأساسية

جامعة عين شمس | جمهورية مصر

الماجستير

1991

البرامج العامة والمؤهلات غير محددة أكثر

جامعة عين شمس | جمهورية مصر

البكالوريوس

1982

‏الكيمياء

جامعة القاهرة | جمهورية مصر

الأبحاث العلمية

KRASG12D/G13D-USP15 axis promotes TGF-β/SMAD signaling and glycolytic flux to accelerate NSCLC pathogenesis

2025

مقال في مجلة | Elsevier Scientific Publishers | Lung Cancer

أكثر

Harnessing biomarkers to guide immunotherapy in esophageal cancer: toward precision oncology

2025

مقال في مجلة | Springer Nature Link | Clinical and Translational Oncology

أكثر

Identification of adipose-proximal biomarkers in breast cancer using weighted gene co-expression network analysis

2025

مقال في مجلة | SpringerLink | Protoplasma

أكثر

Tracing the Molecular Landscape of Diabetic Nephropathy: Insights from Machine Learning and Experiment Verification

2025

مقال في مجلة | Asian Association for the Study of Diabetes and Blackwell Pub. Asia | Journal of Diabetes Investigation

أكثر

Descriptive epidemiology of female breast cancer around the world:incidence, mortality, and sociodemographic risks and disparities

2025

مقال في مجلة | Taylor & Francis | INTERNATIONAL JOURNAL OF ENVIRONMENTAL HEALTH RESEARCH

أكثر

Trimetazidine Alleviates Bleomycin-Induced Pulmonary Fibrosis by Targeting the Long Noncoding RNA CBR3-AS1-Mediated miRNA-29 and Resistin-Like Molecule alpha 1: Deciphering a Novel Trifecta Role of LncRNA CBR3-AS1/miRNA-29/FIZZ1 Axis in Lung Fibrosis

2024

مقال في مجلة | DOVE Press | Drug Design, Development and Therapy

أكثر

Clinical Epidemiology and APOE Gene Etiology: An Update on Alzheimer’s Disease

2024

مقال في مجلة | URF publishers | Medical & Clinical Case Reports Journal

أكثر

Deciphering the therapeutic potential of trimetazidine in rheumatoid arthritis via targeting mi-RNA128a, TLR4 signaling pathway, and adenosine-induced FADD-microvesicular shedding: In vivo and in silico study

2024

مقال في مجلة | Lausanne-Frontiers Media | Frontiers in Pharmacology

أكثر

Prospective Functions of miRNA Variants May Predict Breast Cancer Among Saudi Females

2023

مقال في مجلة | Palo Alto, CA : Cureus, Inc | Cureus

أكثر

Phenotypic variability to medication management: an update on fragile X syndrome

2023

مقال في مجلة | BMC-Springer Nature | Human Genomics

أكثر

Sequence Variants in PSMB8/PSMB9 Immunoproteasome Genes and Risk of Urothelial Bladder Carcinoma

2023

مقال في مجلة | Palo Alto, CA : Cureus, Inc | Cureus, Journal of Medical Science

أكثر

Variations in TAP1 and PSMB9 Genes Involved in Antigen Processing and Presentation Increase the Risk of Vitiligo in the Saudi Community

2021

مقال في مجلة | DovePress | International Journal of General Medicine

أكثر

Genetic etiology and clinical challenges of phenylketonuria

2022

مقال في مجلة | Springer Nature | Human Genomics

أكثر

NPHS1 and NPHS2 variants associated with early-onset frequently relapsing or steroid-dependent nephrotic syndrome in the Saudi community

2022

مقال في مجلة | IRIS Publishers | Annals of Urology and Nephrology

أكثر

Methylenetetrahydrofolate Reductase Gene and Potential Risk to Autism Spectrum Disorder

2022

مقال في مجلة | B P International | New Horizons in Medicine and Medical Research

أكثر

Variations in TAP1 and PSMB9 Genes Involved in Antigen Processing and Presentation Increase the Risk of Vitiligo in the Saudi Community

2021

مقال في مجلة | DOVE Medical Press Inc | International Journal of General Medicine

أكثر

Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population

2011

مقال في مجلة | Elsevier | Egyptian Journal of Medical Human Genetics

أكثر

Association between ANKK1 (rs1800497) and LTA (rs909253) Genetic Variants and Risk of Schizophrenia

2015

مقال في مجلة | Hindawi Pub. Co | BioMed Research International

أكثر

Risk of Colorectal Carcinoma May Predispose to the Genetic Variants of the GST, CYP450, and TP53 Genes among nonsmokers in the Saudi Community

2021

مقال في مجلة | DOVE Medical Press Inc | International Journal of General Medicine

أكثر

Transporter TAP1-637G and immunoproteasome PSMB9-60H variants influence the risk of developing vitiligo in the Saudi population

2014

مقال في مجلة | Hindawi Pub. Co | Disease Markers

أكثر

Common Tag STSs in the AZF Region Associated with Azoospermia and Severe Oligospermia in Infertile Egyptian Men

2010

مقال في مجلة | Benthamopen Inc | The Open Andrology Journal

أكثر

Azoospermia factor microdeletions: common tag STSs in infertile men with azoospermia and sever oligospermia from Egypt

2014

مقال في مجلة | BioMed Central | BMC Genomics

أكثر

TNF -238 polymorphism may predict bronchopulmonary dysplasia among preterm infants in the Egyptian population

2013

مقال في مجلة | Wiley | Pediatric Pulmonology

أكثر

Screening for six Mediterranean mutations in 90 Egyptian patients with phenylketonuria

2008

مقال في مجلة | SAP-Slovak Academic Press | Bratislav Medical Journal

أكثر

Molecular updating of beta-thalassemia mutations in Upper Egyptian population

2010

مقال في مجلة | Taylor and Francis online | Hemoglobin

أكثر

Association between beta+252 tumour necrosis factor polymorphism and asthma in western Saudi children

2011

مقال في مجلة | Elsevier | Saudi Journal of Biological Sciences

أكثر

Frameshift deletion mechanisms with Duchenne and Becker muscular dystrophy in Egyptian families

2004

مقال في مجلة | Korean Society for Molecular Biology | Molecules and Cells

أكثر

The impact of common tumor necrosis factor haplotypes on the development of asthma in children: an Egyptian model

2011

مقال في مجلة | Marry Ann Liebert Inc. Publisher | Genetic Testing and Molecular Biomarkers

أكثر

High precision DNA microsatellite genotyping in Duchenne muscular dystrophy families using ion-pair reversed-phase high performance liquid chromatography

2006

مقال في مجلة | ScienceDirect | Clinical Biochemistry

أكثر

Mutations in transglutaminase gene 1 in autosomal recessive congenital lamellar ichthyosis in Egyptian families

2005

مقال في مجلة | Chichester ; New York : Wiley | Disease Markers

أكثر

Polymorphisms of TAP1/LMP7 loci in Egyptian patients with vitiligo

2006

مقال في مجلة | Ain Shams University Press | Egyptian Journal of Medical Human Genetics

أكثر

The MTHFR 677T allele may influence the severity and biochemical risk factors of Alzheimer's disease in an Egyptian population

2013

مقال في مجلة | Hindawi Pub. Co | Disease Markers

أكثر

الكتب

New Horizons in Medicine and Medical Research

2022

موقع حكومي رسمي تابع لحكومة المملكة العربية السعودية

روابط المواقع الالكترونية الرسمية السعودية تنتهي بـ edu.sa

المواقع الالكترونية الحكومية تستخدم بروتوكول HTTPS للتشفير و الأمان.

المؤهلات

الأبحاث العلمية

الكتب