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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 Athar1,2, Faisal Amhed Al-Allaf1,3, Fahad Alnouri4 , Mohiuddin Mohammed Taher1,2, Abdellatif Bouazzaoui1,2, Neda Mustafa Bogari1, Wafa Mohammed Elbjeirami3, Hani Saleh Faidah5 , Zainularifeen Abduljaleel1,2,* 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 FA1, Abduljaleel Z1, Bogari NM2, Owaidah TMA3, Taher MM1, Athar M1, Elsendiony A4, Abalkhail H3, Abdellatif A5, Elbjeirami W6, Bouazzaoui A1.

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 Bogari1, Amr Ahmed Amin2,3, Ashwag Aljohani1, Ghida Dairi4, Mahmoud Zaki El-Readi2,5, Anas Dannoun1, Udaya Raja6, Mohammad Adil6, Nermeen Qutub7,8, Suhair Alhelfawi7,9, Amal Alobaidi8, Derar Alqudah7, Hussain Banni1, Safaa Yehia Eid2, Huda Balto10, Faisal Al-Allaf1, Mohiuddin Taher1,11, Hiba Saed Al-Amoodi2, Ahmed Fawzy12

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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