maleeha azam
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Role of nitric oxide in the cardiovascular and renal systems
A Ahmad, SK Dempsey, Z Daneva, M Azam, N Li, PL Li, JK Ritter
International journal of molecular sciences 19 (9), 2605, 2018
High-resolution homozygosity mapping is a powerful tool to detect novel mutations causative of autosomal recessive RP in the Dutch population
RWJ Collin, LI van den Born, BJ Klevering, M de Castro-Miró, KW Littink, ...
Investigative Ophthalmology & Visual Science 52 (5), 2227-2239, 2011
CLRN1 mutations cause nonsyndromic retinitis pigmentosa
MI Khan, FFJ Kersten, M Azam, RWJ Collin, A Hussain, STA Shah, ...
Ophthalmology 118 (7), 1444-1448, 2011
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families
S Shafique, S Siddiqi, M Schraders, J Oostrik, H Ayub, A Bilal, M Ajmal, ...
PloS one 9 (6), e100146, 2014
A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma
M Ajmal, MI Khan, K Neveling, YM Khan, M Azam, NK Waheed, ...
Journal of medical genetics 51 (7), 444-448, 2014
Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome
M Ajmal, MI Khan, K Neveling, A Tayyab, S Jaffar, A Sadeque, H Ayub, ...
Molecular vision 19, 644, 2013
Association of ANRIL polymorphism (rs1333049: C> G) with myocardial infarction and its pharmacogenomic role in hypercholesterolemia
W Ahmed, IS Ali, M Riaz, A Younas, A Sadeque, AK Niazi, SH Niazi, ...
Gene 515 (2), 416-420, 2013
Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype–Phenotype …
DS Mackay, AD Borman, R Sui, LI van den Born, EL Berson, LA Ocaka, ...
Human mutation 34 (11), 1537-1546, 2013
Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency
M Ansar, E Ranza, M Shetty, SA Paracha, M Azam, I Kern, J Iwaszkiewicz, ...
Human molecular genetics 29 (4), 618-623, 2020
Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan
M Maria, M Ajmal, M Azam, NK Waheed, SN Siddiqui, B Mustafa, H Ayub, ...
PLoS One 10 (3), e0119806, 2015
Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum
M Maria, IJC Lamers, M Schmidts, M Ajmal, S Jaffar, E Ullah, B Mustafa, ...
Scientific Reports 6 (1), 34764, 2016
Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells
CZ Seco, AP Giese, S Shafique, M Schraders, AMM Oonk, M Grossheim, ...
European Journal of Human Genetics 24 (4), 542-549, 2016
TNF-α genetic predisposition and higher expression of inflammatory pathway components in keratoconus
M Arbab, S Tahir, MK Niazi, M Ishaq, A Hussain, PM Siddique, S Saeed, ...
Investigative Ophthalmology & Visual Science 58 (9), 3481-3487, 2017
Exome sequencing identifies three novel candidate genes implicated in intellectual disability
Z Agha, Z Iqbal, M Azam, H Ayub, LELM Vissers, C Gilissen, SHB Ali, ...
PloS one 9 (11), e112687, 2014
Role of tissue plasminogen activator and plasminogen activator inhibitor polymorphism in myocardial infarction
W Ahmed, M Malik, I Saeed, AA Khan, A Sadeque, U Kaleem, N Ahmed, ...
Molecular biology reports 38, 2541-2548, 2011
Role of ACE and PAI-1 Polymorphisms in the Development and Progression of Diabetic Retinopathy
S Saleem, A Azam, SI Maqsood, I Muslim, S Bashir, N Fazal, M Riaz, ...
PloS one 10 (12), e0144557, 2015
Association of Pro12Ala polymorphism in peroxisome proliferator activated receptor gamma with proliferative diabetic retinopathy
K Tariq, SB Malik, SHB Ali, SE Maqsood, A Azam, I Muslim, MS Khan, ...
Molecular vision 19, 710, 2013
Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia
M Azam, RWJ Collin, STA Shah, AA Shah, MI Khan, A Hussain, ...
Molecular Vision 16, 774, 2010
A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family
M Azam, RWJ Collin, MI Khan, STA Shah, N Qureshi, M Ajmal, ...
Molecular vision 15, 1788, 2009
Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa
MI Khan, RWJ Collin, K Arimadyo, S Micheal, M Azam, N Qureshi, ...
Molecular Vision 16, 2753, 2010
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