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Molecular Neurobiology|July 15, 2017
Variants in the PRPF8 Gene are Associated with GlaucomaShazia Micheal, Barend F Hogewind, Muhammad Imran Khan, et al.
Molecular Biology Reports|February 8, 2012
Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patientsWaqas Ahmed, Muhammad Ajmal, Ahmed Sadeque, et al.
Investigative Ophthalmology & Visual Science|July 14, 2017
TNF-α Genetic Predisposition and Higher Expression of Inflammatory Pathway Components in KeratoconusMuneeza Arbab, Saira Tahir, Muhammad Khizar Niazi, et al.
Molecular Vision|April 6, 2013
Association of Pro12Ala polymorphism in peroxisome proliferator activated receptor gamma with proliferative diabetic retinopathyKhadija Tariq, Saira Bano Malik, Syeda Hafiza Benish Ali, et al.
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|December 10, 2014
Association of known common genetic variants with primary open angle, primary angle closure, and pseudoexfoliation glaucoma in Pakistani cohortsShazia Micheal, Humaira Ayub, Muhammad Imran Khan, 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.
Plos One|August 15, 2014
Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucomaHumaira Ayub, Shazia Micheal, Farah Akhtar, et al.
European Journal of Human Genetics : EJHG|December 3, 2015
Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in DenmarkGaluh D N Astuti, Mette Bertelsen, Markus N Preising, 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.
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