Publications by authors named "Maleeha Azam"

43Publications

Association of IGF1 and VEGFA polymorphisms with diabetic retinopathy in Pakistani population.

Acta Diabetol 2020 Feb 31;57(2):237-245. Epub 2019 Aug 31.

Translational Genomics Laboratory, COMSATS University Islamabad, Park Road, Tarlai Kalan, Islamabad, 45600, Pakistan.

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http://dx.doi.org/10.1007/s00592-019-01407-5DOI Listing
February 2020

Molecular Mechanisms of Complement System Proteins and Matrix Metalloproteinases in the Pathogenesis of Age-Related Macular Degeneration.

Curr Mol Med 2019 ;19(10):705-718

Department of Biotechnology, COMSATS University Islamabad, Abbottabad Campus, 22060, Pakistan.

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http://dx.doi.org/10.2174/1566524019666190828150625DOI Listing
January 2019

Implementation of public health genomics in Pakistan.

Eur J Hum Genet 2019 10 17;27(10):1485-1492. Epub 2019 May 17.

Public Health Genomics, Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.

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http://dx.doi.org/10.1038/s41431-019-0428-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6777461PMC
October 2019

Prevalence of human T-lymphotropic virus 1/2 in Nigeria's capital territory and meta-analysis of Nigerian studies.

SAGE Open Med 2019 16;7:2050312119843706. Epub 2019 Apr 16.

Department of Veterinary Microbiology, Faculty of Veterinary Medicine and Public Health, Ahmadu Bello University, Zaria, Nigeria.

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http://dx.doi.org/10.1177/2050312119843706DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469272PMC
April 2019

Association of rs10490924 in ARMS2/HTRA1 with age-related macular degeneration in the Pakistani population.

Ann Hum Genet 2019 07 20;83(4):285-290. Epub 2019 Mar 20.

Transalational Genomics Laboratory, Department of Biosciences, COMSATS University Islamabad, Pakistan.

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http://dx.doi.org/10.1111/ahg.12311DOI Listing
July 2019

Role of Nitric Oxide in the Cardiovascular and Renal Systems.

Int J Mol Sci 2018 Sep 3;19(9). Epub 2018 Sep 3.

Department of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.

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http://dx.doi.org/10.3390/ijms19092605DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164974PMC
September 2018

CBS mutations and MTFHR SNPs causative of hyperhomocysteinemia in Pakistani children.

Mol Biol Rep 2018 Jun 29;45(3):353-360. Epub 2018 Mar 29.

COMSATS Institute of Information Technology, Park Road, Tarlai Kalan, Islamabad, 45600, Pakistan.

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http://dx.doi.org/10.1007/s11033-018-4169-9DOI Listing
June 2018

TNF-α Genetic Predisposition and Higher Expression of Inflammatory Pathway Components in Keratoconus.

Invest Ophthalmol Vis Sci 2017 07;58(9):3481-3487

Translational Genomics Laboratory, Department of Biosciences, COMSATS Institute of Information Technology, Islamabad, Pakistan.

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http://dx.doi.org/10.1167/iovs.16-21400DOI Listing
July 2017

Identification of novel potential genetic predictors of urothelial bladder carcinoma susceptibility in Pakistani population.

Fam Cancer 2017 Oct;16(4):577-594

Department of Biosciences, Faculty of Science, COMSATS Institute of Information Technology, Park Road, Tarlai Kalan, Islamabad, 45600, Pakistan.

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http://dx.doi.org/10.1007/s10689-017-9991-zDOI Listing
October 2017

Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.

PLoS One 2015 16;10(3):e0119806. Epub 2015 Mar 16.

Department of Biosciences, Commission on Science and Technology for Sustainable Development in the South Institute of Information Technology, Islamabad, Pakistan; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands; Radboud Institute for Molecular Life sciences, Radboud University Nijmegen, Nijmegen, the Netherlands.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0119806PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361598PMC
January 2016

Exome sequencing identifies three novel candidate genes implicated in intellectual disability.

PLoS One 2014 18;9(11):e112687. Epub 2014 Nov 18.

Department of Biosciences, Faculty of Science, COMSATS Institute of Information Technology, Islamabad, Pakistan; Department of Biochemistry, Al-Nafees Medical College & Hospital, Isra University, Islamabad, Pakistan.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0112687PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236113PMC
July 2015

A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma.

J Med Genet 2014 Jul 15;51(7):444-8. Epub 2014 Apr 15.

Faculty of Science, Department of Biosciences, COMSATS Institute of Information Technology, Islamabad, Pakistan Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1136/jmedgenet-2014-102316DOI Listing
July 2014

The molecular basis of retinal dystrophies in pakistan.

Genes (Basel) 2014 Mar 11;5(1):176-95. Epub 2014 Mar 11.

Department of Biosciences, Faculty of Science, COMSATS Institute of Information Technology, Islamabad 45600, Pakistan.

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http://dx.doi.org/10.3390/genes5010176DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978518PMC
March 2014

A complex microcephaly syndrome in a Pakistani family associated with a novel missense mutation in RBBP8 and a heterozygous deletion in NRXN1.

Gene 2014 Mar 16;538(1):30-5. Epub 2014 Jan 16.

Department of Human Genetics, Nijmegen Centre for Molecular Life Sciences, Radboud university medical center, Nijmegen, The Netherlands; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behavior, Nijmegen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2014.01.027DOI Listing
March 2014

A novel homozygous 10 nucleotide deletion in BBS10 causes Bardet-Biedl syndrome in a Pakistani family.

Gene 2013 Apr 9;519(1):177-81. Epub 2013 Feb 9.

Department of Biosciences, Faculty of Science, COMSATS Institute of Information Technology, Islamabad, Pakistan.

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http://dx.doi.org/10.1016/j.gene.2013.01.047DOI Listing
April 2013

A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease.

Mol Vis 2012 12;18:1253-9. Epub 2012 May 12.

Shifa College of Medicine, Islamabad, Pakistan.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365131PMC
December 2012

Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patients.

Mol Biol Rep 2012 Jul 7;39(7):7365-72. Epub 2012 Feb 7.

Department of Biosciences, Faculty of Science, COMSATS Institute of Information Technology, Park Road, Islamabad 45600, Pakistan.

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http://dx.doi.org/10.1007/s11033-012-1568-1DOI Listing
July 2012

CLRN1 mutations cause nonsyndromic retinitis pigmentosa.

Ophthalmology 2011 Jul 18;118(7):1444-8. Epub 2011 Feb 18.

Department of Biosciences, COMSATS Institute of Information Technology, Islamabad, Pakistan.

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http://dx.doi.org/10.1016/j.ophtha.2010.10.047DOI Listing
July 2011

Role of tissue plasminogen activator and plasminogen activator inhibitor polymorphism in myocardial infarction.

Mol Biol Rep 2011 Apr 17;38(4):2541-8. Epub 2010 Nov 17.

Department of Biosciences, COMSATS Institute of Information Technology, Park Road, Islamabad, 45600, Pakistan.

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http://dx.doi.org/10.1007/s11033-010-0392-8DOI Listing
April 2011