|The genetic legacy of the Mongols|
T Zerjal, Y Xue, G Bertorelle, RS Wells, W Bao, S Zhu, R Qamar, Q Ayub, ...
The American Journal of Human Genetics 72 (3), 717-721, 2003
|Y-chromosomal DNA variation in Pakistan|
R Qamar, Q Ayub, A Mohyuddin, A Helgason, K Mazhar, A Mansoor, ...
The American Journal of Human Genetics 70 (5), 1107-1124, 2002
|Identification and characterisation of novel human Y-chromosomal microsatellites from sequence database information|
Q Ayub, A Mohyuddin, R Qamar, K Mazhar, T Zerjal, SQ Mehdi, ...
Nucleic acids research 28 (2), e8-e8, 2000
|Y-chromosome lineages trace diffusion of people and languages in southwestern Asia|
L Quintana-Murci, C Krausz, T Zerjal, SH Sayar, MF Hammer, SQ Mehdi, ...
The American Journal of Human Genetics 68 (2), 537-542, 2001
|Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements|
F Wang, H Wang, HF Tuan, DH Nguyen, V Sun, V Keser, SJ Bowne, ...
Human Genetics 133 (3), 331-345, 2014
|Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma|
CC Khor, T Do, H Jia, M Nakano, R George, K Abu-Amero, R Duvesh, ...
Nature genetics 48 (5), 556-562, 2016
|Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families|
R Harripaul, N Vasli, A Mikhailov, MA Rafiq, K Mittal, C Windpassinger, ...
Molecular psychiatry 23 (4), 973-984, 2018
|Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa|
D Bandah-Rozenfeld, RWJ Collin, E Banin, L Ingeborgh van den Born, ...
The American Journal of Human Genetics 87 (2), 199-208, 2010
|Evolution of codon usage in Zika virus genomes is host and vector specific|
AM Butt, I Nasrullah, R Qamar, Y Tong
Emerging microbes & infections 5 (1), 1-14, 2016
|MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma|
S Micheal, R Qamar, F Akhtar, MI Khan, WA Khan, A Ahmed
Molecular Vision 15, 2268, 2009
|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
|Differential structuring of human populations for homologous X and Y microsatellite loci|
R Scozzari, F Cruciani, P Malaspina, P Santolamazza, BM Ciminelli, ...
The American Journal of Human Genetics 61 (3), 719-733, 1997
|Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci|
T Aung, M Ozaki, MC Lee, U Schl÷tzer-Schrehardt, G Thorleifsson, ...
Nature genetics 49 (7), 993-1004, 2017
|Network analyses of Y-chromosomal types in Europe, northern Africa, and western Asia reveal specific patterns of geographic distribution|
P Malaspina, F Cruciani, BM Ciminelli, L Terrenato, P Santolamazza, ...
The American Journal of Human Genetics 63 (3), 847-860, 1998
|C677T polymorphism in the methylenetetrahydrofolate reductase gene is associated with primary closed angle glaucoma|
S Michael, R Qamar, F Akhtar, WA Khan, A Ahmed
Molecular Vision 14, 661, 2008
|P53 mutations, polymorphisms, and haplotypes in Pakistani ethnic groups and breast cancer patients|
S Khaliq, A Hameed, T Khaliq, Q Ayub, R Qamar, A Mohyuddin, K Mazhar, ...
Genetic testing 4 (1), 23-29, 2000
|ABCA4 midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease|
R Sangermano, M Khan, SS Cornelis, V Richelle, S Albert, A Garanto, ...
Genome research 28 (1), 100-110, 2018
|POLYAR, a new computer program for prediction of poly (A) sites in human sequences|
MN Akhtar, SA Bukhari, Z Fazal, R Qamar, IA Shahmuradov
BMC genomics 11 (1), 1-10, 2010
|A polymorphic L1 retroposon insertion in the centromere of the human Y chromosome|
FR Santos, A Pandya, M Kayser, RJ Mitchell, A Liu, L Singh, ...
Human molecular genetics 9 (3), 421-430, 2000
|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