Mahmood A - Search Results

1

Homozygous missense variant in POPDC3 causes recessive limb-girdle muscular dystrophy type 26.

Ullah A, Lin Z, Younus M, Shafiq S, Khan S, Rasheed M, Mahmood A, Alqosaibi AI, Alshehri MA, Khan A, Umair M. Ullah A, et al. Among authors: mahmood a. J Gene Med. 2022 Apr;24(4):e3412. doi: 10.1002/jgm.3412. Epub 2022 Feb 7. J Gene Med. 2022. PMID: 35075722

2

Recalling the pathology of Parkinson's disease; lacking exact figure of prevalence and genetic evidence in Asia with an alarming outcome: A time to step-up.

Mahmood A, Shah AA, Umair M, Wu Y, Khan A. Mahmood A, et al. Clin Genet. 2021 Dec;100(6):659-677. doi: 10.1111/cge.14019. Epub 2021 Jul 11. Clin Genet. 2021. PMID: 34195994 Review.

3

A novel biallelic variant in the Popeye domain-containing protein 1 (POPDC1) underlies limb girdle muscle dystrophy type 25.

Mahmood A, Samad A, Shah AA, Wadood A, Alkathiri A, Alshehri MA, Alam MZ, Hussain T, He P, Umair M. Mahmood A, et al. Clin Genet. 2023 Feb;103(2):219-225. doi: 10.1111/cge.14238. Epub 2022 Oct 17. Clin Genet. 2023. PMID: 36155908

4

A novel de novo variant in the PHF21A causes craniofacial abnormalities, intellectual disability and skeletal manifestations.

Mustafa S, Abbas S, Mahmood A, Khan AZ, Zeb S, Khan A, Umair M. Mustafa S, et al. Among authors: mahmood a. Clin Genet. 2023 Jul;104(1):142-144. doi: 10.1111/cge.14317. Epub 2023 Mar 13. Clin Genet. 2023. PMID: 36843358

5

Identification of novel inhibitors for SARS-CoV-2 as therapeutic options using machine learning-based virtual screening, molecular docking and MD simulation.

Samad A, Ajmal A, Mahmood A, Khurshid B, Li P, Jan SM, Rehman AU, He P, Abdalla AN, Umair M, Hu J, Wadood A. Samad A, et al. Among authors: mahmood a. Front Mol Biosci. 2023 Mar 7;10:1060076. doi: 10.3389/fmolb.2023.1060076. eCollection 2023. Front Mol Biosci. 2023. PMID: 36959979 Free PMC article.

6

Integrative Genomic Analysis of m6a-SNPs Identifies Potential Functional Variants Associated with Alzheimer's Disease.

Jan SM, Fahira A, Shi Y, Khan MI, Jamal A, Mahmood A, Shams S, Parveen Z, Hu J, Umair M, Wadood A. Jan SM, et al. Among authors: mahmood a. ACS Omega. 2023 Mar 29;8(14):13332-13341. doi: 10.1021/acsomega.3c00696. eCollection 2023 Apr 11. ACS Omega. 2023. PMID: 37065064 Free PMC article.

7

Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.

Nawaz H, Mujahid, Khan SA, Bibi F, Waqas A, Bari A, Fardous, Khan N, Muhammad N, Khan A, Paracha SA, Alam Q, Kamal MA, Rafeeq MM, Muhammad N, Haq FU, Khan S, Mahmood A, Khan S, Umair M. Nawaz H, et al. Among authors: mahmood a. Genes (Basel). 2023 May 19;14(5):1113. doi: 10.3390/genes14051113. Genes (Basel). 2023. PMID: 37239474 Free PMC article.

8

Computer-assisted drug repurposing for thymidylate kinase drug target in monkeypox virus.

Ajmal A, Mahmood A, Hayat C, Hakami MA, Alotaibi BS, Umair M, Abdalla AN, Li P, He P, Wadood A, Hu J. Ajmal A, et al. Among authors: mahmood a. Front Cell Infect Microbiol. 2023 May 29;13:1159389. doi: 10.3389/fcimb.2023.1159389. eCollection 2023. Front Cell Infect Microbiol. 2023. PMID: 37313340 Free PMC article.

9

Structural and dynamics insights into the GBA variants associated with Parkinson's disease.

Mahmood A, Samad A, Bano S, Umair M, Ajmal A, Ilyas I, Shah AA, Li P, Hu J. Mahmood A, et al. J Biomol Struct Dyn. 2023 Jul 11:1-13. doi: 10.1080/07391102.2023.2233617. Online ahead of print. J Biomol Struct Dyn. 2023. PMID: 37434319

10

Truncated DNM1 variant underlines developmental delay and epileptic encephalopathy.

Afsar T, Huang X, Shah AA, Abbas S, Bano S, Mahmood A, Hu J, Razak S, Umair M. Afsar T, et al. Among authors: mahmood a. Front Pediatr. 2023 Oct 9;11:1266376. doi: 10.3389/fped.2023.1266376. eCollection 2023. Front Pediatr. 2023. PMID: 37900685 Free PMC article.

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