| 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 | 273 | 2002 |
| 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 | 65 | 1997 |
| Reconstruction of human evolutionary tree using polymorphic autosomal microsatellites Q Ayub, A Mansoor, M Ismail, S Khaliq, A Mohyuddin, A Hameed, ... American Journal of Physical Anthropology: The Official Publication of the …, 2003 | 56 | 2003 |
| 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 | 53 | 2014 |
| HLA polymorphism in six ethnic groups from Pakistan A Mohyuddin, Q Ayub, S Khaliq, A Mansoor, K Mazhar, S Rehman, ... Tissue antigens 59 (6), 492-501, 2002 | 52 | 2002 |
| Patient HLA-DRB1* and-DQB1* allele and haplotype association with hepatitis C virus persistence and clearance L Ali, A Mansoor, N Ahmad, S Siddiqi, K Mazhar, AG Muazzam, R Qamar, ... Journal of General Virology 91 (8), 1931-1938, 2010 | 48 | 2010 |
| Investigation of the Greek ancestry of populations from northern Pakistan A Mansoor, K Mazhar, S Khaliq, A Hameed, S Rehman, S Siddiqi, ... Human genetics 114 (5), 484-490, 2004 | 41 | 2004 |
| African and Levantine Origins of Pakistani YAP⁺ Y Chromosomes R Qamar, Q Ayub, S Khaliq, A Mansoor, T Karafet, SQ Mehdi, MF Hammer Human biology, 745-755, 1999 | 32 | 1999 |
| Association of HLA-DRB1 and-DQB1alleles and haplotypes with rheumatoid arthritis in a Pakistani population AG Muazzam, A Mansoor, L Ali, S Siddiqi, A Hameed, M Ajmal, K Mazhar Arthritis Research & Therapy 15 (4), R95, 2013 | 19 | 2013 |
| The Origins of Pakistani Populations SQ Mehdi, R Qamar, Q Ayub, S Khaliq, A Mansoor, M Ismail, MF Hammer, ... Genomic Diversity, 83-90, 1999 | 17 | 1999 |
| Distribution of HLA‐A alleles in eight ethnic groups from Pakistan A Mohyuddin, F Williams, A Mansoor, SQ Mehdi, D Middleton Tissue antigens 61 (4), 286-291, 2003 | 14 | 2003 |
| Prevalence of the C677T single-nucleotide polymorphism in the methylenetetrahydrofolate reductase gene among Pakistani ethnic groups A Mansoor, K Mazhar, L Ali, AG Muazzam, S Siddiqi, S Usman Genetic Testing and Molecular Biomarkers 13 (4), 521-526, 2009 | 12 | 2009 |
| Genotype CC of rs12979860 is providing protection against infection rather than assisting in treatment response for HCV genotype 3a infection AH Hashmi, N Ahmad, S Riaz, L Ali, S Siddiqi, KM Khan, AR Shakoori, ... Genes & Immunity 15 (6), 430-432, 2014 | 10 | 2014 |
| VNTR polymorphism of the DRD4 locus in different Pakistani ethnic groups A Mansoor, K Mazhar, R Qamar Genetic testing 12 (2), 299-304, 2008 | 10 | 2008 |
| A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy CZ Seco, A Castells-Nobau, S Joo, M Schraders, JN Foo, M van der Voet, ... Disease models & mechanisms 10 (2), 105-118, 2017 | 9 | 2017 |
| Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome S Siddiqi, S Siddiq, A Mansoor, J Oostrik, N Ahmad, SAR Kazmi, ... Journal of human genetics 58 (12), 819-821, 2013 | 9 | 2013 |
| Molecular diagnosis of fragile X syndrome in subjects with intellectual disability of unknown origin: implications of its prevalence in regional Pakistan M Kanwal, S Alyas, M Afzal, A Mansoor, R Abbasi, F Tassone, S Malik, ... PLoS One 10 (4), e0122213, 2015 | 8 | 2015 |
| Occult HCV or delayed viral clearance from lymphocytes of Chronic HCV genotype 3 patients after interferon therapy AG Muazzam, S Qureshi, A Mansoor, L Ali, M Iqbal, S Siddiqi, KM Khan, ... Genetic vaccines and therapy 9 (1), 1-6, 2011 | 8 | 2011 |
| Frequency of CCR5 Gene 32-bp Deletion in Pakistani Ethnic Groups S Khaliq, A Hameed, Q Ayub, K Mazhar, A Mohyuddin, A Mansoor, ... Genetic Testing 6 (2), 123-127, 2002 | 8 | 2002 |
| A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias S Siddiqi, JN Foo, A Vu, S Azim, DL Silver, A Mansoor, SKH Tay, S Abbasi, ... PLoS One 9 (12), e113258, 2014 | 7 | 2014 |
