CV | Amr Ahmed Amin Abd Elmottalib | Umm Al-Qura University

Qualifications

الدكتوراه

2008

العلوم الطبية الأساسية

جامعة الاسكندرية | جمهورية مصر

الماجستير

1999

العلوم الطبية الأساسية

جامعة عين شمس | جمهورية مصر

الماجستير

199

العلوم الطبية الأساسية

جامعة عين شمس | جمهورية مصر

البكالوريوس

1991

العلوم الطبية الأساسية

جامعة عين شمس | جمهورية مصر

Scientific Research

Infuence of matrix metalloproteinase 9 variant rs17576 on ischemic stroke risk and severity in acute coronary syndrome

2024

مقال في مجلة | Elsevier | journal of stroke and cerebrovascular diseases

Interleukin-10: Genetic and biochemical prediction of sepsis-induced acute kidney injury in critically ill patients in intensive care unit: A cross-sectional study

2024

مقال في مجلة | Wolters Kluwer | Journal of the chinese medical association

Integrated whole exome and transcriptome sequencing in cholesterol metabolism in melanoma: systemic review

2024

مقال في مجلة | KNE Publishing | sudan journal of medical sciences

Lipoprotein Lipase: Molecular structure, regulation, and risk with CVD

2023

مقال في مجلة | WILEY | European Chemical bulletin

Assessment of genetic polymorphism associated with ATP-binding cassette transporter A1 (ABCA1) gene and fluctuations in serum lipid profile levels in patients with coronary artery disease

2021

مقال في مجلة | ScienceDirect | Saudi Pharmaceutical Journal

Exome Sequencing Studies for Kids with Non-Familial Food Allergy

2019

مقال في مجلة | Fundacao de Pesquisas Cientificas de Ribeirao Preto. Brazil | Genetics and Molecular Research

Next Generation Exome Sequencing of paediatric Asthma Identifies Rare and Novel Variants in Candidate Genes

2021

مقال في مجلة | Hindaw | Disease Markers

Exome Sequencing Studies for Kids with Non-Familial Food Allergy

2019

مقال في مجلة | Fundacao de Pesquisas Cientificas de Ribeirao Preto. Brazil | Genetics and Molecular Research

Whole exome sequencing detects novel variants in Saudi children diagnosed with eczema

2019

مقال في مجلة | Elsevier BV Netherland | Journal of Infection and Public Health

A genetic variant c.553G > T (rs2075291) in the apolipoprotein A5 gene is associated with altered triglycerides levels in coronary artery disease (CAD) patients with lipid lowering drug

2019

مقال في مجلة | BioMed Central Ltd. UK | BMC Cardiovascular Disorders.

Exome Sequencing Studies for Kids with Non-Familial Food Allergy.

2019

مقال في مجلة | Fundacao de Pesquisas Cientificas de Ribeirao Preto. Brazil | Genetics and Molecular Research

Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population

2020

مقال في مجلة | King Saud University. KSA | Saudi J Biol Sci

لجنة مؤشرات الاداء

2022 – 2023

رئيس

لجنة اعداد التقرير السنوي للكلية

2022 – 2023

رئيس

وحدة ضمان الجودة

2024 – 2025

رئيس

متابعة تنفيذ الخطة الاستراتيجية - كلية الطب

2023 – 2024

عضو

لجنة مؤشرات الاداء

2025 – 2026

رئيس

وحدة ضمان الجودة

2025 – 2026

نائب رئيس

لجنة تحرير الاستبانات والتحليل وكتابة التقارير

2025 – 2026

رئيس

وحدة ضمان الجودة

2022 – 2023

رئيس

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CV

Qualifications

الدكتوراه

الماجستير

الماجستير

البكالوريوس

Scientific Research

Infuence of matrix metalloproteinase 9 variant rs17576 on ischemic stroke risk and severity in acute coronary syndrome

Interleukin-10: Genetic and biochemical prediction of sepsis-induced acute kidney injury in critically ill patients in intensive care unit: A cross-sectional study

Integrated whole exome and transcriptome sequencing in cholesterol metabolism in melanoma: systemic review

Lipoprotein Lipase: Molecular structure, regulation, and risk with CVD

Assessment of genetic polymorphism associated with ATP-binding cassette transporter A1 (ABCA1) gene and fluctuations in serum lipid profile levels in patients with coronary artery disease

Exome Sequencing Studies for Kids with Non-Familial Food Allergy

Next Generation Exome Sequencing of paediatric Asthma Identifies Rare and Novel Variants in Candidate Genes

Exome Sequencing Studies for Kids with Non-Familial Food Allergy

Whole exome sequencing detects novel variants in Saudi children diagnosed with eczema

A genetic variant c.553G > T (rs2075291) in the apolipoprotein A5 gene is associated with altered triglycerides levels in coronary artery disease (CAD) patients with lipid lowering drug

Exome Sequencing Studies for Kids with Non-Familial Food Allergy.

Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population

Committee

لجنة مؤشرات الاداء

لجنة اعداد التقرير السنوي للكلية

وحدة ضمان الجودة

متابعة تنفيذ الخطة الاستراتيجية - كلية الطب

لجنة مؤشرات الاداء

وحدة ضمان الجودة

لجنة تحرير الاستبانات والتحليل وكتابة التقارير

وحدة ضمان الجودة

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