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Gene|February 19, 2020
Effect of gasotransmitters treatment on expression of hypertension, vascular and cardiac remodeling and hypertensive nephropathy genes in left ventricular hypertrophyAshfaq Ahmad, Zainab Riaz, Munavvar Abdul Sattar, et al.
Molecular Vision|September 16, 2009
A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani familyMaleeha Azam, Rob W J Collin, Muhammad Imran Khan, et al.
Microbial Pathogenesis|September 20, 2023
Identification of contributing factors, microorganisms and antimicrobial resistance involved in the complication of diabetic foot ulcer treatmentMuhammad Shakil Khan, Maleeha Azam, Muhammad Nadeem Khan, et al.
Molecular Vision|December 24, 2010
Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosaMuhammad Imran Khan, Rob W J Collin, Kentar Arimadyo, et al.
Familial Cancer|April 8, 2017
Identification of novel potential genetic predictors of urothelial bladder carcinoma susceptibility in Pakistani populationSyeda Hafiza Benish Ali, Kashif Sardar Bangash, Abdur Rauf, et al.
Plos One|November 19, 2014
Exome sequencing identifies three novel candidate genes implicated in intellectual disabilityZehra Agha, Zafar Iqbal, Maleeha Azam, et al.
Plos One|December 15, 2015
Role of ACE and PAI-1 Polymorphisms in the Development and Progression of Diabetic RetinopathySaba Saleem, Aisha Azam, Sundus Ijaz Maqsood, et al.
Annals of Human Genetics|March 22, 2019
Association of rs10490924 in ARMS2/HTRA1 with age-related macular degeneration in the Pakistani populationHumaira Ayub, Sobia Shafique, Aisha Azam, et al.
Annals of Human Genetics|November 16, 2017
A 3' untranslated region polymorphism rs2304277 in the DNA repair pathway gene OGG1 is a novel risk modulator for urothelial bladder carcinomaTayyaba Ahmed, Saira Nawaz, Rabia Noreen, et al.
Ophthalmology|February 12, 2011
CLRN1 mutations cause nonsyndromic retinitis pigmentosaMuhammad Imran Khan, Ferry F J Kersten, Maleeha Azam, et al.
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