Waqas A - Search Results

1

Exonuclease 5 is dispensable for meiotic progression and male fertility in mouse.

Zaman Q, Khan R, Hameed U, Shah W, Waqas A, Zubair M, Dil S, Zafar T, Ali A, Unar A, Shi Q. Zaman Q, et al. Among authors: waqas a. Gene. 2021 Feb 15;769:145254. doi: 10.1016/j.gene.2020.145254. Epub 2020 Oct 22. Gene. 2021. PMID: 33164760

2

Computational analysis of Cyclin D1 gene SNPs and association with breast cancer.

Aftab A, Khan R, Shah W, Azhar M, Unar A, Jafar Hussain HM, Waqas A. Aftab A, et al. Among authors: waqas a. Biosci Rep. 2021 Jan 29;41(1):BSR20202269. doi: 10.1042/BSR20202269. Biosci Rep. 2021. PMID: 33438725 Free PMC article.

3

CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family.

Ghouchanatigh MD, Khan R, Mojarrad M, Hameed U, Zubair M, Waqas A, Jalali M, Kalantari M, Shamsa A, Zhang H, Shi QH. Ghouchanatigh MD, et al. Among authors: waqas a. Asian J Androl. 2022 Jul-Aug;24(4):416-421. doi: 10.4103/aja202177. Asian J Androl. 2022. PMID: 34755701 Free PMC article.

4

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: waqas a. 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

5

Public stigma associated with mental illnesses in Pakistani university students: a cross sectional survey.

Waqas A, Zubair M, Ghulam H, Wajih Ullah M, Zubair Tariq M. Waqas A, et al. PeerJ. 2014 Dec 16;2:e698. doi: 10.7717/peerj.698. eCollection 2014. PeerJ. 2014. PMID: 25548734 Free PMC article.

6

Psychosocial predictors of antenatal stress in Pakistan: perspectives from a developing country.

Waqas A, Zubair M, Zia S, Meraj H, Aedma KK, Majeed MH, Naveed S. Waqas A, et al. BMC Res Notes. 2020 Mar 18;13(1):160. doi: 10.1186/s13104-020-05007-3. BMC Res Notes. 2020. PMID: 32188496 Free PMC article.

7

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. Front Genet. 2022 Apr 28;13:878274. doi: 10.3389/fgene.2022.878274. eCollection 2022. Front Genet. 2022. PMID: 35571055 Free PMC article.

8

Gain-of-function p.F28S variant in RAC3 disrupts neuronal differentiation, migration and axonogenesis during cortical development, leading to neurodevelopmental disorder.

Nishikawa M, Scala M, Umair M, Ito H, Waqas A, Striano P, Zara F, Costain G, Capra V, Nagata KI. Nishikawa M, et al. Among authors: waqas a. J Med Genet. 2023 Mar;60(3):223-232. doi: 10.1136/jmedgenet-2022-108483. Epub 2022 May 20. J Med Genet. 2023. PMID: 35595279

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: waqas a. 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. Among authors: waqas a. 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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