Taher MM - Search Results

1

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

Bogari NM, Amin AA, Rayes HH, Abdelmotelb A, Taher MM, Al-Allaf FA, Bouazzaoui A, O'Gorman L, Holloway JW. Bogari NM, et al. Among authors: taher mm. Dis Markers. 2021 Feb 8;2021:8884229. doi: 10.1155/2021/8884229. eCollection 2021. Dis Markers. 2021. PMID: 33628342 Free PMC article.

2

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. Al-Allaf FA, et al. Among authors: taher mm. Acta Biochim Pol. 2019 Feb 22;66(1):23-31. doi: 10.18388/abp.2018_2339. Acta Biochim Pol. 2019. PMID: 30793713 Free article.

3

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

Bogari NM, Amin AA, Rayes HH, Abdelmotelb A, Al-Allaf FA, Dannoun A, Al-Amodi HS, Sedayo AA, Almalk H, Moulana A, Balkhair R, Jambi F, Madani F, Abutalib M, Taher MM, Bouazzaoui A, Aljohani A, Bogari MN, G K UR, Fawzy A, Alharbi KK, Ali Khan I. Bogari NM, et al. Among authors: taher mm. J Infect Public Health. 2020 Jan;13(1):27-33. doi: 10.1016/j.jiph.2019.05.020. Epub 2019 Jun 15. J Infect Public Health. 2020. PMID: 31213409 Free article.

4

Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencing.

Butt E, Alyami S, Nageeti T, Saeed M, AlQuthami K, Bouazzaoui A, Athar M, Abduljaleel Z, Al-Allaf F, Taher M. Butt E, et al. F1000Res. 2019 May 2;8:613. doi: 10.12688/f1000research.18721.2. eCollection 2019. F1000Res. 2019. PMID: 32612806 Free PMC article.

5

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

Bogari NM, Al-Allaf FA, Aljohani A, Taher MM, Qutub NA, Alhelfawi S, Alobaidi A, Alqudah DM, Banni H, Dairi G, Amin AA. Bogari NM, et al. Among authors: taher mm. Front Genet. 2020 Dec 15;11:548559. doi: 10.3389/fgene.2020.548559. eCollection 2020. Front Genet. 2020. PMID: 33384710 Free PMC article.

6

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. Bogari NM, et al. Among authors: taher mm. Diabetes Res Clin Pract. 2015 Sep;109(3):e14-7. doi: 10.1016/j.diabres.2015.06.002. Epub 2015 Jul 10. Diabetes Res Clin Pract. 2015. PMID: 26212367

7

Next-generation sequencing for molecular diagnosis of autosomal recessive polycystic kidney disease.

Edrees BM, Athar M, Al-Allaf FA, Taher MM, Khan W, Bouazzaoui A, Al-Harbi N, Safar R, Al-Edressi H, Alansary K, Anazi A, Altayeb N, Ahmed MA, Abduljaleel Z. Edrees BM, et al. Among authors: taher mm. Gene. 2016 Oct 10;591(1):214-226. doi: 10.1016/j.gene.2016.07.021. Epub 2016 Jul 9. Gene. 2016. PMID: 27401137

8

Compound heterozygous LDLR variant in severely affected familial hypercholesterolemia patient.

Al-Allaf FA, Alashwal A, Abduljaleel Z, Taher MM, Bouazzaoui A, Abalkhail H, Al-Allaf AF, Athar M. Al-Allaf FA, et al. Among authors: taher mm. Acta Biochim Pol. 2017;64(1):75-79. doi: 10.18388/abp.2016_1283. Epub 2016 Nov 23. Acta Biochim Pol. 2017. PMID: 27878139 Free article.

9

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

Al-Allaf FA, Taher MM, Abduljaleel Z, Bouazzaoui A, Athar M, Bogari NM, Abalkhail HA, Owaidah TM. Al-Allaf FA, et al. Among authors: taher mm. J Clin Med Res. 2017 Apr;9(4):317-331. doi: 10.14740/jocmr2876w. Epub 2017 Feb 21. J Clin Med Res. 2017. PMID: 28270892 Free PMC article.

10

Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia.

Alnouri F, Athar M, Al-Allaf FA, Abduljaleel Z, Taher MM, Bouazzaoui A, Al Ammari D, Karrar H, Albabtain M. Alnouri F, et al. Among authors: taher mm. Atherosclerosis. 2018 Oct;277:425-433. doi: 10.1016/j.atherosclerosis.2018.06.878. Atherosclerosis. 2018. PMID: 30270081

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