Almatrafi A - Search Results

1

Meta-analysis of clinical data using human meiotic genes identifies a novel cohort of highly restricted cancer-specific marker genes.

Feichtinger J, Aldeailej I, Anderson R, Almutairi M, Almatrafi A, Alsiwiehri N, Griffiths K, Stuart N, Wakeman JA, Larcombe L, McFarlane RJ. Feichtinger J, et al. Among authors: almatrafi a. Oncotarget. 2012 Aug;3(8):843-53. doi: 10.18632/oncotarget.580. Oncotarget. 2012. PMID: 22918178 Free PMC article.

2

Identification of a class of human cancer germline genes with transcriptional silencing refractory to the hypomethylating drug 5-aza-2'-deoxycytidine.

Almatrafi A, Feichtinger J, Vernon EG, Escobar NG, Wakeman JA, Larcombe LD, McFarlane RJ. Almatrafi A, et al. Oncoscience. 2014 Nov 10;1(11):745-50. doi: 10.18632/oncoscience.95. eCollection 2014. Oncoscience. 2014. PMID: 25594001 Free PMC article.

3

Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa.

Hashmi JA, Albarry MA, Almatrafi AM, Albalawi AM, Mahmood A, Basit S. Hashmi JA, et al. Among authors: almatrafi am. Congenit Anom (Kyoto). 2018 Jan;58(1):10-15. doi: 10.1111/cga.12225. Epub 2017 May 28. Congenit Anom (Kyoto). 2018. PMID: 28419563

4

Investigating the pathogenic SNPs in BLM helicase and their biological consequences by computational approach.

Alzahrani FA, Ahmed F, Sharma M, Rehan M, Mahfuz M, Baeshen MN, Hawsawi Y, Almatrafi A, Alsagaby SA, Kamal MA, Warsi MK, Choudhry H, Jamal MS. Alzahrani FA, et al. Among authors: almatrafi a. Sci Rep. 2020 Jul 23;10(1):12377. doi: 10.1038/s41598-020-69033-8. Sci Rep. 2020. PMID: 32704157 Free PMC article.

5

Homozygosity mapping and whole exome sequencing provide exact diagnosis of Cohen syndrome in a Saudi family.

Hashmi JA, Fadhli F, Almatrafi A, Afzal S, Ramzan K, Thiele H, Nürnberg P, Basit S. Hashmi JA, et al. Among authors: almatrafi a. Brain Dev. 2020 Sep;42(8):587-593. doi: 10.1016/j.braindev.2020.04.010. Epub 2020 May 10. Brain Dev. 2020. PMID: 32402540

6

KMT2C, a histone methyltransferase, is mutated in a family segregating non-syndromic primary failure of tooth eruption.

Assiry AA, Albalawi AM, Zafar MS, Khan SD, Ullah A, Almatrafi A, Ramzan K, Basit S. Assiry AA, et al. Among authors: almatrafi a. Sci Rep. 2019 Nov 11;9(1):16469. doi: 10.1038/s41598-019-52935-7. Sci Rep. 2019. PMID: 31712638 Free PMC article.

7

In silico drug repurposing using molecular docking and dynamics to target the protein interaction between the SARS-CoV-2 S-glycoprotein and the ACE2 receptor.

Hussein D, Almatrafi A, Gomaa M, Alhowsawi A, Almustafa S, Alsaihaty H, Alghamdi M. Hussein D, et al. Among authors: almatrafi a. F1000Res. 2024 Jul 26;12:1452. doi: 10.12688/f1000research.131508.2. eCollection 2023. F1000Res. 2024. PMID: 39474132 Free PMC article.

8

Comparing Selective Serotonin Reuptake Inhibitors (SSRIs) Alone and in Combination With Beta-Blockers for Treating Panic Disorders: A Prospective Cohort Study.

Bajabir D, Alsubhi A, Felimban SA, Alotaibi RZ, Almalki A, Allahyani NS, Yaseen RY, Kofiah FB, Almatrafi AA, Alzahrani SA. Bajabir D, et al. Among authors: almatrafi aa. Cureus. 2024 Sep 7;16(9):e68862. doi: 10.7759/cureus.68862. eCollection 2024 Sep. Cureus. 2024. PMID: 39376873 Free PMC article.

9

Public Awareness Regarding the Differences Between Ophthalmologists and Optometrists Among Adults Living in Makkah Province, Saudi Arabia.

Almatrafi AM, Almarzouki N, Almutairi MA, Ghandorah AM, Alqurashi BS, Tash RA, Aladni IS. Almatrafi AM, et al. Cureus. 2024 Sep 5;16(9):e68739. doi: 10.7759/cureus.68739. eCollection 2024 Sep. Cureus. 2024. PMID: 39371800 Free PMC article.

10

Mutations in the ciliary transport gene IFT140 cause syndromic congenital retinal dystrophy.

Danish E, Alhashem A, Naaman N, Almhmoudi F, Mushiba A, Almatrafi A, Raggam A, Bukhari R. Danish E, et al. Among authors: almatrafi a. J AAPOS. 2024 Oct;28(5):104007. doi: 10.1016/j.jaapos.2024.104007. Epub 2024 Sep 19. J AAPOS. 2024. PMID: 39304031

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