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Genetic construction between polycystic ovarian syndrome and type 2 diabetes

Saudi journal of biological sciences, 2020-10, Vol.27 (10), p.2539-2543

Bogari, Neda M.

2020

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

Journal of stroke and cerebrovascular diseases, 2024-08, Vol.33 (8), p.107824, Article 107824

2024

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

Pharmaceutics, 2021-01, Vol.13 (2), p.140

2021

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Novel LDLR Variant in Familial Hypercholesterolemia: NGS-Based Identification, In Silico Characterization, and Pharmacogenetic Insights

Life (Basel, Switzerland), 2023-07, Vol.13 (7), p.1542

2023

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Compound A Increases Cell Infiltration in Target Organs of Acute Graft-versus-Host Disease (aGVHD) in a Mouse Model

Molecules (Basel, Switzerland), 2021-07, Vol.26 (14), p.4237

2021

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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

Saudi pharmaceutical journal, 2021-12, Vol.29 (12), p.1458-1465

2021

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

Disease markers, 2024, Vol.2024 (1), p.8278727

2024

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

Clinica chimica acta, 2021-08, Vol.519, p.247-254

2021

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

Disease markers, 2021, Vol.2021, p.5522539-8

2021

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

Saudi journal of biological sciences, 2020-08, Vol.27 (8), p.2018-2024

2020

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

Frontiers in genetics, 2020-12, Vol.11, p.548559-548559

2020

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EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma

Oncology letters, 2020-12, Vol.20 (6), p.1-1

2020

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

Disease markers, 2021, Vol.2021, p.8884229-10

2021

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

Heliyon, 2023-03, Vol.9 (3), p.e13876-e13876, Article e13876

2023

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Next generation sequencing (NGS) in glucose-6-phosphate dehydrogenase (G6PD) deficiency studies

Bioinformation, 2016-01, Vol.12 (2), p.41-43

Bogari, Neda M

2016

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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

BMC cardiovascular disorders, 2019-01, Vol.19 (1), p.2-2, Article 2

2019

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

Journal of infection and public health, 2020-01, Vol.13 (1), p.27-33

2020

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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

Viruses, 2019-11, Vol.11 (11), p.1063

2019

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

Acta biochimica Polonica, 2019-02, Vol.66 (1), p.23

2019

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Corrigendum to “Anti- E. coli immunoglobulin yolk (IgY): Reduction of pathogen receptors and inflammation factors could be caused by decrease in E. coli load” [Heliyon 9(3) (February 21, 2023) e13876]

Heliyon, 2023-06, Vol.9 (6), p.e16582-e16582, Article e16582

2023

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A novel SNP in 3′ UTR of INS gene: A case report of neonatal diabetes mellitus

Diabetes research and clinical practice, 2015-09, Vol.109 (3), p.e14-e17

2015

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No association of apolipoprotein B gene polymorphism and blood lipids in obese Egyptian subjects

Journal of negative results in biomedicine, 2015-03, Vol.14 (1), p.7-7, Article 7

2015

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Pattern of Thyroid Lesions in Western Region of Saudi Arabia: A Retrospective Analysis and Literature Review

Journal of clinical medicine research, 2018-02, Vol.10 (2), p.106-116

2018

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Molecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics Studies

Journal of clinical medicine research, 2017-04, Vol.9 (4), p.317-331

2017

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Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients

Human molecular genetics, 2007-06, Vol.16 (12), p.1412-1422

2007

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Genetic construction between polycystic ovarian syndrome and type 2 diabetes

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

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

Novel LDLR Variant in Familial Hypercholesterolemia: NGS-Based Identification, In Silico Characterization, and Pharmacogenetic Insights

Compound A Increases Cell Infiltration in Target Organs of Acute Graft-versus-Host Disease (aGVHD) in a Mouse Model

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

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

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

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

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

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

EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma

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

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

Next generation sequencing (NGS) in glucose-6-phosphate dehydrogenase (G6PD) deficiency studies

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

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

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

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

Corrigendum to “Anti- E. coli immunoglobulin yolk (IgY): Reduction of pathogen receptors and inflammation factors could be caused by decrease in E. coli load” [Heliyon 9(3) (February 21, 2023) e13876]

A novel SNP in 3′ UTR of INS gene: A case report of neonatal diabetes mellitus

No association of apolipoprotein B gene polymorphism and blood lipids in obese Egyptian subjects

Pattern of Thyroid Lesions in Western Region of Saudi Arabia: A Retrospective Analysis and Literature Review

Molecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics Studies

Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients

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