Publications by authors named "Syed Qasim Mehdi"

17Publications

The association of urinary interferon-gamma inducible protein-10 (IP10/CXCL10) levels with kidney allograft rejection.

Inflamm Res 2017 May 28;66(5):425-432. Epub 2017 Feb 28.

Centre for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation (SIUT), Karachi, Pakistan.

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http://dx.doi.org/10.1007/s00011-017-1025-7DOI Listing
May 2017

Analysis of the glutathione S-transferase genes polymorphisms in the risk and prognosis of renal cell carcinomas. Case-control and meta-analysis.

Urol Oncol 2016 09 13;34(9):419.e1-419.e12. Epub 2016 May 13.

Centre for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation (SIUT), Karachi, Pakistan; Department of Human Genetics, University of Health Sciences (UHS), Lahore, Pakistan.

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http://dx.doi.org/10.1016/j.urolonc.2016.04.005DOI Listing
September 2016

Monoamine Oxidase A gene polymorphisms and self reported aggressive behaviour in a Pakistani ethnic group.

J Pak Med Assoc 2015 Aug;65(8):818-24

The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, United Kingdom.

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August 2015

The Kalash genetic isolate: ancient divergence, drift, and selection.

Am J Hum Genet 2015 May 30;96(5):775-83. Epub 2015 Apr 30.

Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK.

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http://dx.doi.org/10.1016/j.ajhg.2015.03.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570283PMC
May 2015

Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan.

Mutat Res 2014 May-Jun;763-764:45-52. Epub 2014 Apr 12.

Centre for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation (SIUT), Karachi, Pakistan. Electronic address:

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http://dx.doi.org/10.1016/j.mrfmmm.2014.03.008DOI Listing
May 2015

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

Immunol Invest 2013 11;42(8):691-700. Epub 2013 Jul 11.

Centre for Human Genetics and Molecular Medicine, Sindh Institute for Urology and Transplantation , Karachi , Pakistan .

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http://dx.doi.org/10.3109/08820139.2013.806541DOI Listing
July 2014

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

Gene 2012 Jul 28;502(2):133-7. Epub 2012 Apr 28.

Centre for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.

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http://dx.doi.org/10.1016/j.gene.2012.04.063DOI Listing
July 2012

Polymorphisms in the methylene tetrahydrofolate reductase gene and their unique combinations are associated with an increased susceptibility to the renal cancers.

Genet Test Mol Biomarkers 2012 May 22;16(5):346-52. Epub 2011 Nov 22.

Centre for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.

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http://dx.doi.org/10.1089/gtmb.2011.0206DOI Listing
May 2012

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

Gene 2012 Feb 15;493(1):165-8. Epub 2011 Oct 15.

Centre for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.

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http://dx.doi.org/10.1016/j.gene.2011.10.016DOI Listing
February 2012

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

Genet Test Mol Biomarkers 2011 Sep 14;15(9):653-7. Epub 2011 Apr 14.

Centre for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation (SIUT), Karachi, Pakistan.

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http://dx.doi.org/10.1089/gtmb.2011.0029DOI Listing
September 2011

Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2.

Am J Med Genet A 2007 Dec;143A(23):2768-74

Biomedical and Genetic Engineering Division, Dr. A. Q. Khan Research Laboratories, Islamabad, Pakistan.

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http://dx.doi.org/10.1002/ajmg.a.31739DOI Listing
December 2007

Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations.

Hum Genet 2005 Sep 16;117(5):452-9. Epub 2005 Jun 16.

Section of Medical and Molecular Genetics, Institute of Biomedical Research, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.

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http://link.springer.com/content/pdf/10.1007/s00439-005-1309
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http://dx.doi.org/10.1007/s00439-005-1309-9DOI Listing
September 2005