| 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 | 802 | 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 | 345 | 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 | 279 | 2000 |
| 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 | 275 | 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 | 234 | 2016 |
| 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 | 214 | 2001 |
| 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 | 211 | 2018 |
| 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 | 211 | 2016 |
| 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 | 203 | 2018 |
| 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 Schlötzer-Schrehardt, G Thorleifsson, ... Nature genetics 49 (7), 993-1004, 2017 | 177 | 2017 |
| 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 | 126 | 2010 |
| Landslide dam and subsequent dam-break flood estimation using HEC-RAS model in Northern Pakistan MJ Butt, M Umar, R Qamar Natural Hazards, 241-254, 2013 | 117 | 2013 |
| 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 | 101 | 2010 |
| 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 | 96 | 2009 |
| 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, 1071-1079, 2016 | 95 | 2016 |
| 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 | 81 | 1997 |
| 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 | 75 | 2014 |
| CLRN1 mutations cause nonsyndromic retinitis pigmentosa MI Khan, FFJ Kersten, M Azam, RWJ Collin, A Hussain, STA Shah, ... Ophthalmology, 2011 | 75 | 2011 |
| 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 | 73 | 2014 |
| 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 | 71 | 2000 |
maleeha azamCOMSATS Institute of Information TechnologyVerified email at comsats.edu.pk
