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Compound A increases cell infiltration in the target organs of acute graft-versus-host disease (aGVHD) in mouse model. Abdellatif Bouazzaoui, Ahmed A. H. Abdellatif, Faisal A. Al-Allaf, Neda M. Bogari,Mohiuddin M. Taher, Mohammad Athar, Thomas Schubert, Turki M. Habeebullah and Sameer H. Qari . Molecules 2021, 26, 4237


Coronary Artery Disease: Association Study of 5 Loci with Angiographic Indices of Disease Severity. Neda M. Bogari , Reem M. Allam , Abdellatif Bouazzaoui  Osama Elkhateeb  Massimo Porqueddu , and Gualtiero I. Colombo Disease Marker 13 July 2021


Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism. Mohammad Athara, Ibrahim S. Ghita, Amani A. Albagenny, Zainularifeen Abduljaleel, Ghulam Shada , Ahmed Elsendion , Saeed H. Halawani , Mohammad M. Alkazmi, Khalid Alquthami, Mohammad M. Alkhuza, Abdulaziz A. Althebyani, Neda M. Bogari, Anas Dannoun , Faisal A. Al-Allaf


Genetic Association of rs10757278 on Chromosome 9p21 and Coronary Artery Disease in a Saudi Population. Neda Bogari, Anas Dannoun, Mohammad Athar, Osama Elkhateeb, Massimo Porqueddu, Reem Allam, and Francesco Alamanni


Next Generation Exome Sequencing of Pediatric Asthma Identifies Rare and Novel Variants in Candidate Genes. Neda M. Bogari, Amr A. Amin, Husni H. Rayes, Ahmed Abdelmotelb, Mohiuddin M. Taher, Faisal A. Al-Allaf, Abdellatif Bouazzaoui, Luke O’Gorman, and John W. Holloway DISEASE MARKERS Accepted for Publication 9/02/2021


Strategies for vaccination: Conventional vaccine approaches versus new-generation strategies in combination with adjuvants Abdellatif Bouazzaoui *, Ahmed A. H. Abdellatif, Faisal A. Al-Allaf, Neda M. Bogari, Saied Al-Dehlawi, Sameer. H. Qari Review, Pharmaceutics- Accepted for Publication 19/01/2021


The co-existence of ADHD with autism in Saudi children: An analysis using next-generation DNA sequencing. Neda M. Bogari, Faisal A. Al-Allaf, Ashwag Aljohani,   Mohiuddin M. Taher, Nermeen A. Qutub, Suhair H. Alhelfawi, Amal Alobaidi, Derar M. Alqudah, Hussain Banni, Ghida Dairi and Amr A. Amin   Frontiers in Genetics- Neurogenomics. 2020 Dec 15;11:548559



GFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma. Mohiuddin M. Taher Ghida Dairi Ejaz Muhammad Butt Khalid Al‑Quthami Hisham Al‑Khalidi Raid A. Jastania Tahani H. Nageeti Neda M. Bogari Mohammad Athar Faisal A. Al‑Allaf Kristoffer Valerie, ONCOLOGY LETTERS 20: 384, 2020, Received April 4, 2020; Accepted October 2, 2020


Correlation between rs320 variant in the lipoprotein lipase gene and presence of coronary artery disease and stroke among the Saudi population. Neda M. Bogari, Ashwag Aljohani, Anas Dannoun, Osama Elkhateeb, Masimo Porqueddu, Amr A. Amin, Dema N. Bogari, Mohiuddin M. Taher, Faruk Buba, Reem M. Allam, Mustafa N. Bogari, and Francesco Alamanni. Saudi J Biol Sci. 2020 Aug; 27(8): 2018–2024



Genetic construction between polycystic ovarian syndrome and Type 2 diabetes. Neda Bogari.Saudi J Biol Sci. 2020 Oct; 27(10): 2539–2543



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. Al-Allaf FA, Abduljaleel Z, Taher MM, Abdellatif AAH, Athar M, Bogari NM, Al-Ahdal MN, Al-Mohanna F, Al-Hassnan ZN, Alzabeedi KHY, Banssir TM, Bouazzaoui A. Viruses. 2019 Nov 15;11(11).


Whole exome sequencing detects novel variants in Saudi children diagnosed with eczema Neda M.Bogari,Amr A.Amin, Husni H.Rayes, AhmedAbdelmotelb,Faisal A.Al-Allaf, AnasDannoun, Hiba S.Al-Amodi, Anas A.Sedayo, HilalAlmalk, AmnaMoulana, RaniaBalkhair, FatmaJambi, FakhriahMadani, MwafaqAbutalib, Mohiuddin M.Taher, Abdellatif Bouazzaoui, AshwagAljohani, Mustafa N.Bogari, ImranAli Khan


Exome Sequencing Studies for Kids with Non-Familial Food Allergy Neda M Bogari, Amr A Amin, Husni H Rayes, Ahmed Abdelmotelb, Faisal A. Al- Allaf, Anas Dannoun, Mamdouh S Alhazmi, Saed A Basardah, Mohiuddin M Taher, Udaya Raja GK, Ashwag Aljohan, Soud Abdulraof A Khogeer, Mohamed Mahmoud Nour Eldein, Mohammad Adil, Mustafa Bogari, Imran Ali Khan, Khalid Khalaf Alharbi and Ahmed Fawzy Genet. Mol. Res. 18 (3)


Genetic biomarkers predict susceptibility to autism spectrum disorder through interactive models of inheritance in a Saudi community, Nasser A. Elhawary, Mohammed T. Tayeb, Ikhlas A. Sindi, Nermeen Qutub, Mona Rashad, Ahmad Muftia, Arwa H. Arab, Asim Khogeer, Ezzeldin N. Elhawary, Anas Dannoun and Neda Bogari, Cogent Biology, 16 April 2019


Whole Exome Sequencing Reveals Multiple Mutations in Uncommon Genes of Familial Hypercholesterolaemia Mohammad Athar, Faisal Amhed Al-Allaf, Fahad Alnouri, Mohiuddin Mohammed Taher, Abdellatif Bouazzaoui, Neda Mustafa Bogari, Wafa Mohammed Elbjeirami, Hani Saleh Faidah , Zainularifeen Abduljaleel, J Cardiovasc Disease Res., 2018; 9(4):x-x Acta Biochim Pol. 2019 Feb 22;66(1):23-31. doi: 10.18388/abp.2018_2339.


Identification of six novel factor viii gene variants using next generation sequencing and molecular dynamics simulation.  Al-Allaf FA, Abduljaleel Z, Bogari NM, Owaidah TMA, Taher MM, Athar M, Elsendiony A, Abalkhail H, Abdellatif A, Elbjeirami W, Bouazzaoui A.


The Genetic Variant c.553G>T in the Lipoprotein A5 Effects on Lipid Profile Parameters Levels  Neda M. Bogari, Ashwag Aljohani, Amr A. Amin, Faisal A. Al-Allaf, Anas Dannoun, Mohiuddin M. Taher, Atalla Elsayed, Dareen Ibrahim Rednah, Osama Elkhatee, Massimo Porqueddu, Francesco Alamanni, Ahmed Fawzy  World Journal of Cardiovascular Diseases Vol.9 No.2


Whole Exome Sequencing: Novel Genetic Polymorphisms in Saudi Arabian Attention Deficit Hyperactivity Disorder (ADHD) Children Neda Mostafa Bogari, Amr Ahmed Amin, Ashwag Aljohani, Ghida Dairi, Mahmoud Zaki El-Readi Anas Dannoun, Udaya Raja, Mohammad Adil, Nermeen Qutub, Suhair Alhelfawi, Amal Alobaidi, Derar Alqudah, Hussain Banni, Safaa Yehia Eid, Huda Balto, Faisal Al-Allaf, Mohiuddin Taher, Hiba Saed Al-Amoodi, Ahmed Fawzy


Identification of six novel factor viii gene variants using next generation sequencing and molecular dynamics simulation.Al-Allaf FA, Abduljaleel Z, Bogari NM, Owaidah TMA, Taher MM, Athar M, Elsendiony A, Abalkhail H, Abdellatif A, Elbjeirami W, Bouazzaoui A.


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. Bogari NM, Aljohani A, Amin AA, Al-Allaf FA, Dannoun A, Taher MM, Elsayed A, Rednah DI, Elkhatee O, Porqueddu M, Alamanni F, Khogeer SAA, Fawzy A. BMC Cardiovasc Disord. 2019 Jan 3;19(1):2. doi: 10.1186/s12872-018-0965-3.


Pattern of Thyroid Lesions in Western Region of Saudi Arabia: A Retrospective Analysis and Literature Review. Saeed MI, Hassan AA, Butt ME, Baniyaseen KA, Siddiqui MI, Bogari NM, Al-Allaf FA, Taher MM. J Clin Med Res. 2018 Feb;10(2):106-116


Next Generation Sequencing on Ion Proton for Mutation Detection in Brain Tumors: Development of Molecular Pathology Assays in the Kingdom of Saudi Arabia Poster: AMP Europe 2018, Rotterdam, April 30-2 May Faisal A. Al-Allaf, Mohiuddin M. Taher, Zainularifeen Abduljaleel, Abdellatif Bouazzaoui, Mohammed Athar, Neda M. Bogari, Halah A. Abalkhail Tarek MA. Owaida، Journal of Clinical Medicine Research،9,4, April 2017, 317-331


Obesity is associated with cardiac disease and the apolipoprotein A5 gene a genetic variant c.553G > T in is associated with an increased risk of coronary artery disease, Poster, Neda Bogari , Dareen Rednah, Osama Elkhateeb3, Anas I Dannoun, Amr Ahmed Amin  ,Massimo Porqueddu , Soud Khogeer  , Ahmed Fawzy Obesity and chronic diseases, 25-27 July 2016 las Vegas USA.


Impact of next generation sequencing in glucose-6-phosphate dehydrogenase deficiency studies. Neda Bogari. Bioinformation, 2016


VULNERABILITY OF GENETIC VARIANTS TO THE RISK OF AUTISM AMONG SAUDI CHILDREN, Tranlational Genomics Human Genome Meeting, Poster, N. Elhawary, M. Tayeb, N. Bogari, N. Qotb ,28 February-2 March 2016. Houston, USA


Molecular Genetic Diagnosis for a Family with Type I Spinal Muscular Atrophy (SMA) via analysis of Survival Motor Neuron (SMN) Gene. Neda M Bogari, Fareed R Bogari, Husni H Rayes, Noha M Alqassimi, Huda M Balto, Anas I Dannoun, Raneem H Abushanab, Amr Ahmed Amin, Soud Abdulraof A Khogeer, Rami Nassir, Azza M Abdel-Latif, Ahmed Fawzy.  Journal of Rare Disorders: Diagnosis & Therapy.  2015;1 3:21


A novel SNP in 3' UTR of INS gene: A case report of neonatal diabetes mellitus. Bogari NM, Rayes HH, Mostafa F, Abdel-Latif AM, Ramadan A, Al-Allaf FA, Taher MM, Fawzy A. Diabetes Res Clin Pract. 2015 Jul 10


No association of apolipoprotein B gene polymorphism and blood lipids in obese Egyptian subjects. Bogari NM, Abdel-Latif AM, Hassan MA, Ramadan A, Fawzy A. J Negat Results Biomed. 2015 Mar 18;14(1):7 PMID: 25889118


Apolipoprotein B (XbaI) allele frequencies in an Egyptian Population: impact onblood lipids. Neda M. Bogari , Azza M. Abdel-Latif and Maha A. Hassan , Ahmed Fawzy,  Int J Biol Med Res. 2014; 5(2): 3981-3987


Transporter TAP1-637G and Immunoproteasome PSMB9-60H Variants Influence the Risk of Developing Vitiligo in the Saudi Population Nasser Attia Elhawary, Neda Bogari, Essam Hussien Jiffri, Mona Rashad, Abdulhamid Fatani, Mohammed Tayeb Dis Markers. 2014; 2014: 260732. Published online 2014 December 7. doi: 10.1155/2014/260732 PMCID: PMC4273470


Genetic Polymorphisms of Glutathione S-Transferase Genes and Risk of Colorectal Cancer in the Saudi Population Mohammed T. Tayeb1, Ahmad O. Babalghith 1, Ahmed Fawzy2, Suleiman Jastaniah3, Neda M. Bogari UQU Med. J Vol. 4, No.2, pp. 61-71 (2013 )


The MTHFR 677T Allele May Influence the Severity and Biochemical Risk Factors of Alzheimer's Disease in an Egyptian Population. Elhawary NA, Hewedi D, Arab A, Teama S, Shaibah H, Tayeb MT, Bogari N.


Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population. Elhawary N, Bogari N, Rashad M, Tayeb M. The Egyptian journal of Medical Human Genetics 2011 ;12: 187-192.


Molecular updating of β-thalassemia mutations in the Upper Egyptian population. Jiffri EH, Bogari N, Zidan KH, Teama S, Elhawary NA. Hemoglobin. 2010;34(6):538-47.


Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients, Human molecular genetics, Kyriakou T1, Pontefract DE, Viturro E, Hodgkinson CP, Laxton RC, Bogari N, Cooper G, Davies M, Giblett J, Day IN, Simpson IA, Albrecht C, Ye S. 2007 Jun 15;16(12):1412-22 PMID: 17412755

 

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