Rafeeq MM - Search Results

1

A Novel Homozygous Missense Mutation in the Zinc Finger DNA Binding Domain of GLI1 Causes Recessive Post-Axial Polydactyly.

Umair M, Ahmad F, Ahmad S, Alam Q, Rehan M, Alqosaibi AI, Alnamshan MM, Rafeeq MM, Haque S, Sain ZM, Ismail M, Alfadhel M. Umair M, et al. Among authors: rafeeq mm. Front Genet. 2021 Oct 15;12:746949. doi: 10.3389/fgene.2021.746949. eCollection 2021. Front Genet. 2021. PMID: 34721536 Free PMC article.

2

Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type A.

Umair M, Palander O, Bilal M, Almuzzaini B, Alam Q, Ahmad F, Younus M, Khan A, Waqas A, Rafeeq MM, Alfadhel M. Umair M, et al. Among authors: rafeeq mm. Genomics. 2021 Jul;113(4):2495-2502. doi: 10.1016/j.ygeno.2021.05.015. Epub 2021 May 20. Genomics. 2021. PMID: 34022343 Free article.

3

Targeted exome sequencing identified a novel frameshift variant in the PGAM2 gene causing glycogen storage disease type X.

Nayab A, Alam Q, Alzahrani OR, Khan R, Sarfaraz S, Albaz AA, Rafeeq MM, Sain ZM, Waqas A, Umair M. Nayab A, et al. Among authors: rafeeq mm. Eur J Med Genet. 2021 Sep;64(9):104283. doi: 10.1016/j.ejmg.2021.104283. Epub 2021 Jul 5. Eur J Med Genet. 2021. PMID: 34237446

4

Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach.

Rahaman A, Almalki AA, Rafeeq MM, Akhtar O, Anjum F, Mashraqi MM, Sain ZM, Alzamami A, Ahmad V, Zeng XA, Jamal QMS. Rahaman A, et al. Among authors: rafeeq mm. Molecules. 2021 Oct 28;26(21):6517. doi: 10.3390/molecules26216517. Molecules. 2021. PMID: 34770925 Free PMC article.

5

Variants in the PNPLA1 Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance.

Ahmad F, Ahmed I, Alam Q, Ahmad T, Khan A, Ahmad I, Bilal M, Hayat A, Khan A, Waqas A, Rafeeq MM, Sain ZM, Umair M. Ahmad F, et al. Among authors: rafeeq mm. Mol Syndromol. 2021 Oct;12(6):351-361. doi: 10.1159/000516943. Epub 2021 Aug 24. Mol Syndromol. 2021. PMID: 34899144 Free PMC article.

6

Nanotechnology-based approaches in the fight against SARS-CoV-2.

Albaz AA, Rafeeq MM, Sain ZM, Almutairi WA, Alamri AS, Aloufi AH, Almalki WH, Tarique M. Albaz AA, et al. Among authors: rafeeq mm. AIMS Microbiol. 2021 Oct 12;7(4):368-398. doi: 10.3934/microbiol.2021023. eCollection 2021. AIMS Microbiol. 2021. PMID: 35071938 Free PMC article. Review.

7

Targeting Cytotoxin-Associated Antigen A, a Virulent Factor of Helicobacter pylori-Associated Gastric Cancer: Structure-Based In Silico Screening of Natural Compounds.

He S, Almalki AA, Rafeeq MM, Sain ZM, Alqosaibi AI, Alnamshan MM, Al-Dhuayan IS, Rahaman A, Zhang Y, Banjer HJ, Anjum F, Alzghaibi HAM, Alharbi AH, Jamal QMS. He S, et al. Among authors: rafeeq mm. Molecules. 2022 Jan 23;27(3):732. doi: 10.3390/molecules27030732. Molecules. 2022. PMID: 35164000 Free PMC article.

8

Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability.

Waqas A, Nayab A, Shaheen S, Abbas S, Latif M, Rafeeq MM, Al-Dhuayan IS, Alqosaibi AI, Alnamshan MM, Sain ZM, Habib AH, Alam Q, Umair M, Saqib MAN. Waqas A, et al. Among authors: rafeeq mm. Front Genet. 2022 Apr 28;13:878274. doi: 10.3389/fgene.2022.878274. eCollection 2022. Front Genet. 2022. PMID: 35571055 Free PMC article.

9

Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment.

Kakar MU, Akram M, Zubair Mehboob M, Younus M, Bilal M, Waqas A, Nazir A, Shafi M, Umair M, Ahmad S, Rafeeq MM. Kakar MU, et al. Among authors: rafeeq mm. PLoS One. 2022 Jun 16;17(6):e0268078. doi: 10.1371/journal.pone.0268078. eCollection 2022. PLoS One. 2022. PMID: 35709191 Free PMC article.

10

A novel biallelic variant further delineates PRDX3-related autosomal recessive cerebellar ataxia.

Rafeeq MM, Umair M, Bilal M, Habib AH, Waqas A, Sain ZM, Alam MZ, Ali RH. Rafeeq MM, et al. Neurogenetics. 2023 Jan;24(1):55-60. doi: 10.1007/s10048-022-00701-9. Epub 2022 Oct 3. Neurogenetics. 2023. PMID: 36190665

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