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Neda Bogari
Neda Bogari
Professor of Genetics, Umm Al-Qura University
Verified email at uqu.edu.sa - Homepage
Title
Cited by
Cited by
Year
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
502007
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
402010
Strategies for vaccination: conventional vaccine approaches versus new-generation strategies in combination with adjuvants
A Bouazzaoui, AAH Abdellatif, FA Al-Allaf, NM Bogari, S Al-Dehlawi, ...
Pharmaceutics 13 (2), 140, 2021
362021
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
342018
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, 439-446, 2013
322013
Genetic construction between polycystic ovarian syndrome and type 2 diabetes
NM Bogari
Saudi Journal of Biological Sciences 27 (10), 2539-2543, 2020
182020
Human genome meeting 2016: houston, TX, USA. 28 February-2 March 2016
AK Srivastava, Y Wang, R Huang, C Skinner, T Thompson, L Pollard, ...
Human genomics 10, 1-40, 2016
172016
Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population
NM Bogari, A Aljohani, A Dannoun, O Elkhateeb, M Porqueddu, AA Amin, ...
Saudi Journal of Biological Sciences 27 (8), 2018-2024, 2020
122020
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 5 (1), 1606555, 2019
122019
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
122017
Impact of next generation sequencing in glucose-6- phosphate dehydrogenase deficiency studies
N Bogari
Bioinformation 12 (2), 41-43, 2016
12*2016
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
122014
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
122014
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, 1-6, 2019
112019
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, 1-6, 2015
102015
Next generation exome sequencing of pediatric asthma identifies rare and novel variants in candidate genes
NM Bogari, AA Amin, HH Rayes, A Abdelmotelb, MM Taher, FA Al-Allaf, ...
Disease markers 2021, 2021
82021
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
8*2014
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
82011
Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism
M Athar, IS Ghita, AA Albagenny, Z Abduljaleel, G Shadab, A Elsendiony, ...
Clinica Chimica Acta 519, 247-254, 2021
62021
The co-existence of ADHD with autism in Saudi children: an analysis using next-generation DNA sequencing
NM Bogari, FA Al-Allaf, A Aljohani, MM Taher, NA Qutub, S Alhelfawi, ...
Frontiers in Genetics 11, 548559, 2020
62020
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