|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
|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
|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
|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
|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), 2014
|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
|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
|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
|The Origins of Pakistani Populations|
SQ Mehdi, R Qamar, Q Ayub, S Khaliq, A Mansoor, M Ismail, MF Hammer, ...
Genomic Diversity, 83-90, 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
|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
|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
|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
|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
|VNTR polymorphism of the DRD4 locus in different Pakistani ethnic groups|
A Mansoor, K Mazhar, R Qamar
Genetic testing 12 (2), 299-304, 2008
|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
|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), 14, 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
|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), 2015
|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), 2014