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 | المملكة العربية السعودية

Scientific Research

IL-10 diplotype and septic shock: Genotype–Phenotype associations with hemodynamic dysfunction and IL-10 expression

2026

مقال في مجلة | Frontiers | Frontiers in Molecular Biosciences

Shifts in primary care utilization patterns following digital health implementation: an operational evaluation of the 2023–2024 Hajj mass gatherings

2026

مقال في مجلة | Frontiers | Frontiers in Public Health

Evaluating the Role of MIA3 Variant rs17465637 in Coronary Artery Disease: A Comprehensive Case–Control Analysis

2026

مقال في مجلة | MDPI | Diagnostics

Common molecular signatures: the role of BDNF, melatonin, and orexin in the ASD-schizophrenia continuum

2026

مقال في مجلة | Dordrecht, Boston, Reidel. | Molecular biology reports

Beyond categorical boundaries: Common molecular and cellular pathways in autism spectrum disorder and schizophrenia

2026

مقال في مجلة | Oxford ; New York : Pergamon Press | Progress in neuro-psychopharmacology & biological psychiatry.

Association of rs4977574 with Lipid Phenotypes, Smoking Status, and Statin Exposure in a Saudi Cardiovascular Cohort: A Sensitivity-Adjusted Genetic Association Study

2026

مقال في مجلة | MDPI | Journal of clinical medicine

Lymphocyte Subsets in Covid-19 Saudi Patients: Infection Caused Significant Reduction in Peripheral Blood Lymphocyte Subset

2025

مقال في مجلة | Heidelberg : Verlag Klinisches Labor | Clinical laboratory

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 | Taipei, Taiwan : Chinese Medical Association | Journal of the Chinese Medical Association

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

2024

مقال في مجلة | New York, NY : Demos Publications | Journal of stroke and cerebrovascular diseases

Impact of rs599839 Polymorphism on Coronary Artery Disease Risk in Saudi Diabetic Patients

2024

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

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

لجنة البحث العلمي

2022 – 2023

عضو

لجنة البحث العلمي

2021 – 2022

عضو

Societies

Association for Clinical Genomic Science

2008 – 2037

No | https://www.acgs.uk.com/

British Society for Genetic Medicine

2008 – 2035

No | https://bsgm.org.uk/

Genetics Society

2018 – 2037

No | https://genetics.org.uk/

European Society of Human

2009 – 2038

No | https://www.eshg.org/home

European Society of Human

2009 – 2038

no | https://www.eshg.org/home

The American Society of Human Genetics

2008 – 2037

no | 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

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CV

Qualifications

Scientific Research

Committee

Societies