|Avian influenza A (H9N2): computational molecular analysis and phylogenetic characterization of viral surface proteins isolated between 1997 and 2009 from the human population|
AM Butt, S Siddique, M Idrees, Y Tong
Virology journal 7 (1), 319, 2010
|Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability|
S Riazuddin, M Hussain, A Razzaq, Z Iqbal, M Shahzad, DL Polla, Y Song, ...
Molecular psychiatry 22 (11), 1604-1614, 2017
|Purification and medium optimization of α-amylase from Bacillus subtilis 168|
A Sumrin, W Ahmad, B Ijaz, MT Sarwar, S Gull, H Kausar, I Shahid, ...
African Journal of Biotechnology 10 (11), 2119-2129, 2011
|Variants in PUS7 cause intellectual disability with speech delay, microcephaly, short stature, and aggressive behavior|
APM De Brouwer, R Abou Jamra, N Körtel, C Soyris, DL Polla, M Safra, ...
The American Journal of Human Genetics 103 (6), 1045-1052, 2018
|Role of post translational modifications and novel crosstalk between phosphorylation and O-beta-GlcNAc modifications in human claudin-1, -3 and -4|
AM Butt, IB Khan, M Hussain, M Idress, J Lu, Y Tong
Molecular biology reports 39 (2), 1359-1369, 2012
|Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay|
M Ansar, S Riazuddin, MT Sarwar, P Makrythanasis, SA Paracha, Z Iqbal, ...
Genetics in Medicine 20 (7), 778-784, 2018
|Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss|
SR Kevin T Booth, Amama Ghaffar, Muhammad Rashid, Luke T Hovey, Mureed ...
Human Genetics, 2020
|Molecular and Genetic Basis of Intellectual Disability in Pakistani Population|
University of the Punjab, Lahore, 2018