Neda Bogari
Neda Bogari
Assistant Professor of Genetics, Umm Al-Qura University
Verified email at uqu.edu.sa - Homepage
TitleCited byYear
Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients
T Kyriakou, DE Pontefract, E Viturro, CP Hodgkinson, RC Laxton, ...
Human molecular genetics 16 (12), 1412-1422, 2007
372007
Molecular updating of β-thalassemia mutations in the upper Egyptian population
EH Jiffri, N Bogari, KH Zidan, S Teama, NA Elhawary
Hemoglobin 34 (6), 538-547, 2010
272010
The MTHFR 677T allele may influence the severity and biochemical risk factors of Alzheimer’s disease in an Egyptian population
NA Elhawary, D Hewedi, A Arab, S Teama, H Shaibah, MT Tayeb, ...
Disease markers 35 (5), 439-446, 2013
212013
Transporter TAP1-637G and immunoproteasome PSMB9-60H variants influence the risk of developing vitiligo in the Saudi population
NA Elhawary, N Bogari, EH Jiffri, M Rashad, A Fatani, M Tayeb
Disease markers 2014, 2014
52014
Transporter TAP1-637G and immunoproteasome PSMB9-60H variants influence the risk of developing vitiligo in the Saudi population
NA Elhawary, N Bogari, EH Jiffri, M Rashad, A Fatani, M Tayeb
Disease markers 2014, 2014
52014
Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population
NA Elhawary, N Bogari, M Rashad, MT Tayeb
Egyptian Journal of Medical Human Genetics 12 (2), 187-192, 2011
52011
International journal of biological & medical research
A Batta
Int J Biol Med Res 6 (4), 5258-5266, 2015
4*2015
Pattern of Thyroid Lesions in Western Region of Saudi Arabia: A Retrospective Analysis and Literature Review
MI Saeed, AA Hassan, ME Butt, KA Baniyaseen, MI Siddiqui, NM Bogari, ...
Journal of clinical medicine research 10 (2), 106, 2018
32018
Impact of next generation sequencing in glucose-6- phosphate dehydrogenase deficiency studies
N Bogari
Bioinformation 12 (2), 41-43, 2016
3*2016
Apolipoprotein B (XbaI) allele frequencies in an Egyptian Population: impact onblood lipids
AF Neda M. Bogari , Azza M. Abdel-Latif and Maha A. Hassan
International Journal of Biological & Medical Research 5 (2), 3981-3987, 2014
3*2014
Molecular analysis of factor VIII and factor IX genes in hemophilia patients: identification of novel mutations and molecular dynamics studies
FA Al-Allaf, MM Taher, Z Abduljaleel, A Bouazzaoui, M Athar, NM Bogari, ...
Journal of clinical medicine research 9 (4), 317, 2017
22017
No association of apolipoprotein B gene polymorphism and blood lipids in obese Egyptian subjects
NM Bogari, AM Abdel-Latif, MA Hassan, A Ramadan, A Fawzy
Journal of negative results in biomedicine 14 (1), 7, 2015
22015
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 …
NM Bogari, A Aljohani, AA Amin, FA Al-Allaf, A Dannoun, MM Taher, ...
BMC cardiovascular disorders 19 (1), 2, 2019
12019
A novel SNP in 3′ UTR of INS gene: A case report of neonatal diabetes mellitus
NM Bogari, HH Rayes, F Mostafa, AM Abdel-Latif, A Ramadan, FA Al-Allaf, ...
Diabetes research and clinical practice 109 (3), e14-e17, 2015
12015
Genetic biomarkers predict susceptibility to autism spectrum disorder through interactive models of inheritance in a Saudi community
NA Elhawary, MT Tayeb, IA Sindi, N Qutub, M Rashad, A Mufti, AH Arab, ...
Cogent Biology, 1606555, 2019
2019
Identification of six novel factor VIII gene variants using next generation sequencing and molecular dynamics simulation
FA Al-Allaf, Z Abduljaleel, NM Bogari, TMA Owaidah, MM Taher, M Athar, ...
Acta Biochimica Polonica 66 (1), 23-31, 2019
2019
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 …
B N
BMC Cardiovasc Disord 19, 2, 2019
2019
The Genetic Variant c. 553G> T in the Lipoprotein A5 Effects on Lipid Profile Parameters Levels
NM Bogari, A Aljohani, AA Amin, FA Al-Allaf, A Dannoun, MM Taher, ...
World Journal of Cardiovascular Diseases 9, 122-131, 2019
2019
Whole Exome Sequencing Reveals Multiple Mutations in Uncommon Genes of Familial Hypercholesterolaemia
M Athar, FA Al-Allaf, F Alnouri, MM Taher, A Bouazzaoui, NM Bogari, ...
Journal of Cardiovascular Disease Research 10 (1), 2019
2019
Obesity is Associated with Cardiac Disease and the Apo Lipoprotein A5 Gene a Genetic Variant C.553g > T is Associated with an Increased Risk of Coronary Artery Disease
HBAF Neda Bogari, Dareen Rednah, Osama Elkhateeb, Anas I Dannoun, Amr Ahmed ...
International Conference on Obesity and Chronic Diseases (ICOCD-2016) hosted …, 2016
2016
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