Abid A - Search Results

1

Association of specific single nucleotide variants (SNVs) in the promoter and 3'-Untranslated region of Vascular Endothelial growth factor (VEGF) gene with risk and higher tumour grade of head and neck cancers.

Ajaz S, Muneer R, Siddiqa A, Ali Memon M, Firasat S, Abid A, Khaliq S. Ajaz S, et al. Among authors: abid a. Oral Oncol. 2021 Nov;122:105519. doi: 10.1016/j.oraloncology.2021.105519. Epub 2021 Sep 9. Oral Oncol. 2021. PMID: 34509102

2

Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genes.

Ismail M, Abid A, Anwar K, Qasim Mehdi S, Khaliq S. Ismail M, et al. Among authors: abid a. J Hum Genet. 2006;51(9):827-831. doi: 10.1007/s10038-006-0028-y. Epub 2006 Aug 3. J Hum Genet. 2006. PMID: 16897189

3

Locus heterogeneity and Knobloch syndrome.

Joyce S, Tee L, Abid A, Khaliq S, Mehdi SQ, Maher ER. Joyce S, et al. Among authors: abid a. Am J Med Genet A. 2010 Nov;152A(11):2880-1. doi: 10.1002/ajmg.a.33619. Am J Med Genet A. 2010. PMID: 20979194 No abstract available.

4

Genetic heterogeneity for autosomal dominant familial hypertrophic cardiomyopathy in a Pakistani family.

Abid A, Akhtar N, Khaliq S, Mehdi SQ. Abid A, et al. J Coll Physicians Surg Pak. 2011 Apr;21(4):202-6. J Coll Physicians Surg Pak. 2011. PMID: 21453614

5

Association of a single-nucleotide polymorphism in the promoter region of the VEGF gene with the risk of renal cell carcinoma.

Ajaz S, Khaliq S, Abid A, Hassan AS, Hashmi A, Sultan G, Mohsin R, Mubarrak M, Naqvi SA, Rizvi SA, Mehdi SQ. Ajaz S, et al. Among authors: abid a. Genet Test Mol Biomarkers. 2011 Sep;15(9):653-7. doi: 10.1089/gtmb.2011.0029. Epub 2011 Apr 14. Genet Test Mol Biomarkers. 2011. PMID: 21491998

6

Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children.

Shahid S, Abid A, Mehdi SQ, Firasat S, Lanewala A, Naqvi SA, Rizvi SA, Khaliq S. Shahid S, et al. Among authors: abid a. Gene. 2012 Feb 1;493(1):165-8. doi: 10.1016/j.gene.2011.10.016. Epub 2011 Oct 15. Gene. 2012. PMID: 22033511

7

Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype.

Shah SH, Abid A, Shahid S, Khaliq S. Shah SH, et al. Among authors: abid a. J Pak Med Assoc. 2011 Nov;61(11):1060-4. J Pak Med Assoc. 2011. PMID: 22125978

8

A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.

Abid A, Khaliq S, Shahid S, Lanewala A, Mubarak M, Hashmi S, Kazi J, Masood T, Hafeez F, Naqvi SA, Rizvi SA, Mehdi SQ. Abid A, et al. Gene. 2012 Jul 10;502(2):133-7. doi: 10.1016/j.gene.2012.04.063. Epub 2012 Apr 28. Gene. 2012. PMID: 22565185

9

The effect of chemokine receptor gene polymorphisms (CCR2V64I, CCR5-59029G>A and CCR5Δ32) on renal allograft survival in Pakistani transplant patients.

Firasat S, Raza A, Abid A, Aziz T, Mubarak M, Naqvi SA, Rizvi SA, Mehdi SQ, Khaliq S. Firasat S, et al. Among authors: abid a. Gene. 2012 Dec 15;511(2):314-9. doi: 10.1016/j.gene.2012.09.099. Epub 2012 Oct 4. Gene. 2012. PMID: 23041556

10

HLA class I and II polymorphisms in the Gujjar population from Pakistan.

Raza A, Firasat S, Khaliq S, Abid A, Shah SS, Mehdi SQ, Mohyuddin A. Raza A, et al. Among authors: abid a. Immunol Invest. 2013;42(8):691-700. doi: 10.3109/08820139.2013.806541. Epub 2013 Jul 11. Immunol Invest. 2013. PMID: 23845092 Review.

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