Athar M - Search Results

1

Mutation Profiling of Intracranial Myxopapillary Ependymoma by Next Generation DNA Sequencing.

Taher MM, Alhussini AA, Saeed M, Athar M, Bantan NAA, Jastania RA, Balkhoyour KB, Nageeti TH. Taher MM, et al. Among authors: athar m. Gulf J Oncolog. 2021 Sep;1(37):7-16. Gulf J Oncolog. 2021. PMID: 35152189

2

Next generation DNA sequencing of atypical choroid plexus papilloma of brain: Identification of novel mutations in a female patient by Ion Proton.

Taher MM, Hassan AA, Saeed M, Jastania RA, Nageeti TH, Alkhalidi H, Dairi G, Abduljaleel Z, Athar M, Bouazzaoui A, El-Bjeirami WM, Al-Allaf FA. Taher MM, et al. Among authors: athar m. Oncol Lett. 2019 Nov;18(5):5063-5076. doi: 10.3892/ol.2019.10882. Epub 2019 Sep 19. Oncol Lett. 2019. PMID: 31612017 Free PMC article.

3

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. Among authors: athar m. F1000Res. 2019 May 2;8:613. doi: 10.12688/f1000research.18721.2. eCollection 2019. F1000Res. 2019. PMID: 32612806 Free PMC article.

4

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: athar m. Acta Biochim Pol. 2019 Feb 22;66(1):23-31. doi: 10.18388/abp.2018_2339. Acta Biochim Pol. 2019. PMID: 30793713 Free article.

5

EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma.

Taher MM, Dairi G, Butt EM, Al-Quthami K, Al-Khalidi H, Jastania RA, Nageeti TH, Bogari NM, Athar M, Al-Allaf FA, Valerie K. Taher MM, et al. Among authors: athar m. Oncol Lett. 2020 Dec;20(6):384. doi: 10.3892/ol.2020.12247. Epub 2020 Oct 23. Oncol Lett. 2020. PMID: 33193845 Free PMC article.

6

Next generation sequencing to identify novel genetic variants causative of autosomal dominant familial hypercholesterolemia associated with increased risk of coronary heart disease.

Al-Allaf FA, Athar M, Abduljaleel Z, Taher MM, Khan W, Ba-Hammam FA, Abalkhail H, Alashwal A. Al-Allaf FA, et al. Among authors: athar m. Gene. 2015 Jul 1;565(1):76-84. doi: 10.1016/j.gene.2015.03.064. Epub 2015 Apr 1. Gene. 2015. PMID: 25839937

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: athar m. 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: athar m. 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

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: athar m. Atherosclerosis. 2018 Oct;277:425-433. doi: 10.1016/j.atherosclerosis.2018.06.878. Atherosclerosis. 2018. PMID: 30270081

10

DNA mismatch repair MSH2 gene-based SNP associated with different populations.

Abduljaleel Z, Al-Allaf FA, Khan W, Athar M, Shahzad N, Taher MM, Alanazi M, Elrobh M, Reddy NP. Abduljaleel Z, et al. Among authors: athar m. Mol Genet Genomics. 2014 Jun;289(3):469-87. doi: 10.1007/s00438-014-0826-4. Epub 2014 Feb 22. Mol Genet Genomics. 2014. PMID: 24562863

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