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Molecular Vision|May 28, 2011
XRCC1 and XPD DNA repair gene polymorphisms: a potential risk factor for glaucoma in the Pakistani populationSajeela Yousaf, Muhammad Imran Khan, Shazia Micheal, 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.
Genome Research|November 23, 2017
ABCA4 midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt diseaseRiccardo Sangermano, Mubeen Khan, Stéphanie S Cornelis, 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.
Molecular Vision|June 6, 2012
Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosaMuhammad Ajmal, Muhammad Imran Khan, Shazia Micheal, et al.
Ophthalmology|February 12, 2011
CLRN1 mutations cause nonsyndromic retinitis pigmentosaMuhammad Imran Khan, Ferry F J Kersten, Maleeha Azam, et al.
Molecular Vision|June 28, 2012
Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani familiesMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
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