Follow
Dr. Muhammad Ajmal
Dr. Muhammad Ajmal
COMSATS University Islamabad
Verified email at comsats.edu.pk
Title
Cited by
Cited by
Year
Molecular Mechanism of Quorum-Sensing in Enterococcus faecalis: Its Role in Virulence and Therapeutic Approaches
L Ali, MU Goraya, Y Arafat, M Ajmal, JL Chen, D Yu
International journal of molecular sciences 18 (5), 960, 2017
1562017
In Silico Functional Meta‐Analysis of 5,962 ABCA4 Variants in 3,928 Retinal Dystrophy Cases
SS Cornelis, NM Bax, J Zernant, R Allikmets, LG Fritsche, JT den Dunnen, ...
Human mutation 38 (4), 400-408, 2017
1452017
Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts
H Ayub, MI Khan, S Micheal, F Akhtar, M Ajmal, S Shafique, SHB Ali, ...
Molecular vision 16, 18, 2010
952010
Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark
GDN Astuti, M Bertelsen, MN Preising, M Ajmal, B Lorenz, SMH Faradz, ...
European Journal of Human Genetics 24 (7), 1071-1079, 2016
842016
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
672014
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
622014
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
512013
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
342015
Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosa
M Ajmal, MI Khan, S Micheal, W Ahmed, A Shah, H Venselaar, H Bokhari, ...
Molecular Vision 18, 1226, 2012
342012
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
332016
Nutrient-induced antibiotic resistance in Enterococcus faecalis in the eutrophic environment
L Ali, YQ Wang, J Zhang, M Ajmal, Z Xiao, J Wu, JL Chen, D Yu
Journal of Global Antimicrobial Resistance 7, 78-83, 2016
312016
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
302011
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
292009
Implementation of public health genomics in Pakistan
M Riaz, J Tiller, M Ajmal, M Azam, R Qamar, P Lacaze
European Journal of Human Genetics 27 (10), 1485-1492, 2019
262019
Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosa
M Azam, RWJ Collin, A Malik, MI Khan, STA Shah, AA Shah, A Hussain, ...
Archives of Ophthalmology 129 (10), 1377-1378, 2011
262011
The molecular basis of retinal dystrophies in Pakistan
MI Khan, M Azam, M Ajmal, RWJ Collin, AI Den Hollander, FPM Cremers, ...
Genes 5 (1), 176-195, 2014
232014
Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani families
M Ajmal, MI Khan, K Neveling, YM Khan, SHB Ali, W Ahmed, MS Iqbal, ...
Molecular Vision 18, 1558, 2012
222012
The genetic spectrum of familial hypercholesterolemia in Pakistan
W Ahmed, R Whittall, M Riaz, M Ajmal, A Sadeque, H Ayub, R Qamar, ...
Clinica Chimica Acta 421, 219-225, 2013
212013
Association of IGF1 and VEGFA polymorphisms with diabetic retinopathy in Pakistani population
N Khan, AD Paterson, D Roshandel, A Raza, M Ajmal, NK Waheed, ...
Acta Diabetologica 57, 237-245, 2020
172020
Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia
M Ajmal, W Ahmed, A Sadeque, SHB Ali, SH Bokhari, N Ahmed, R Qamar
Molecular biology reports 37, 3869-3875, 2010
172010
The system can't perform the operation now. Try again later.
Articles 1–20