CV | Neda Mustafa H Bogari | Umm Al-Qura University

Qualifications

الدكتوراه

2008

طب الوراثة

جامعة ساوثهمبتون ببرطانيا | بريطانيا

دبلوم عالي

1429

الطب الشرعي

University of the West of England | بريطانيا

البكالوريوس

2001

العلوم الطبية الأساسية

جامعة أم القرى

Scientific Research

Anti- E. coli Immunoglobulin Yolk (IgY): Reduction of pathogen receptors and inflammation factors could be caused by decrease in E. coli load

2023

مقال في مجلة | Elsevier | Heliyon

Role Of Single Nucleotide Polymorphism Rs On Coronary Artery Disease Risk Among Saudi Population Case Control Stud

2023

مقال في مجلة | Verduci Editore | European Review for Medical and Pharmacological Sciences

Identification of a Novel ATM Missense Mutation by Next Generation Sequencing in Choroid Plexus Papilloma

2018

ورقة مؤتمر | Association for Molecular Pathology | Association for Molecular Pathology

Next Generation Sequencing on Ion Proton for Mutation Detection in Brain Tumors: Development of Molecular Pathology Assays in the Kingdom of Saudi Arabia

2018

ورقة مؤتمر | Association for Molecular Pathology | AMP Europe Congress 2018

Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism

2020

مقال في مجلة | Elsevier | International journal of clinical chemistry

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

2020

مقال في مجلة | Saudi Pharmaceutical Society | Saudi pharmaceutical journal

Genetic construction between polycystic ovarian syndrome and type 2 diabetes

2019

مقال في مجلة | King Saud University | Saudi journal of biological sciences

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

2021

مقال في مجلة | Hindawi | Disease markers

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

2019

مقال في مجلة | King Saud University | Saudi journal of biological sciences

The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing

2020

مقال في مجلة | Frontiers | Frontiers in Genetics

Strategies for Vaccination: Conventional Vaccine Approaches Versus New-Generation Strategies in Combination with Adjuvants

2021

مقال في مجلة | MDPI | Pharmaceutics

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

2020

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

Exome Sequencing Studies for Kids with Non-Familial Food Allergy

2019

مقال في مجلة | GMR | Genetics and Molecular Research (GMR)

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 Centra | BMC cardiovascular disorders.

Genetic biomarkers predict susceptibility to autism spectrum disorder through interactive models of inheritance in a Saudi community

2019

مقال في مجلة | Taylor & Francis Group | Cogent Biology

EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma

2019

مقال في مجلة | Athens | Oncology letters

Identification of six novel factor VIII gene variants using next generation sequencing and molecular dynamics simulation

2019

مقال في مجلة | Warszawa | Acta biochimica Polonica

Molecular Dynamics Simulation Reveals Exposed Residues in the Ligand-Binding Domain of the Low-Density Lipoprotein Receptor that Interacts with Vesicular Stomatitis Virus-G Envelope

2018

مقال في مجلة | MDPI | Viruses-Basel

Whole Exome Sequencing Reveals Multiple Mutations in Uncommon Genes of Familial Hypercholesterolaemia

2019

مقال في مجلة | EManuscript Technologies | Journal of Cardiovascular Disease Research

The Genetic Variant c.553G>T in the Lipoprotein A5 Effects on Lipid Profile Parameters Levels

2019

مقال في مجلة | Scientific Research | World Journal of Cardiovascular Diseases

Whole Exome Sequencing: Novel Genetic Polymorphisms in Saudi Arabian Attention Deficit Hyperactivity Disorder (ADHD) Children

2019

مقال في مجلة | Scientific Research | Natural Science

Genetic Association of rs10757278 on Chromosome 9p21 and Coronary Artery Disease in a Saudi Population

2021

مقال في مجلة | dovepress | International Journal of General Medicine

Compound A increases cell infiltration in the target organs of acute graft-versus-host disease (aGVHD) in mouse model

2021

مقال في مجلة | MDPI | Molecules

Coronary Artery Disease: Association Study of 5 Loci with Angiographic Indices of Disease Severity

2021

مقال في مجلة | hindawi | Disease Markers

Genome Engineering

2016

Committee

لجنة البحث العلمي

2022 – 2023

عضو

لجنة البحث العلمي

2021 – 2022

عضو

Societies

Association for Clinical Genomic Science

2008 – 2037

https://www.acgs.uk.com/

British Society for Genetic Medicine

2008 – 2035

https://bsgm.org.uk/

Genetics Society

2018 – 2037

https://genetics.org.uk/

European Society of Human

2009 – 2038

https://www.eshg.org/home

European Society of Human

2009 – 2038

https://www.eshg.org/home

The American Society of Human Genetics

2008 – 2037

https://www.ashg.org/meetings/

Official government website of the Government of Kingdom of Saudi Arabia

Link to official Saudi websites end with edu.sa

Government websites use the HTTPS protocol for encryption and security.

CV

Qualifications

Scientific Research

Books

Committee

Societies