| 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 |
| Genetics of vascular dementia–review from the ICVD working group MA Ikram, A Bersano, R Manso-Calderón, JP Jia, H Schmidt, L Middleton, ... BMC medicine 15 (1), 48, 2017 | 74 | 2017 |
| 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 | 64 | 2003 |
| Genetic instability in EBV-transformed lymphoblastoid cell lines A Mohyuddin, Q Ayub, S Siddiqi, DR Carvalho-Silva, K Mazhar, ... Biochimica et Biophysica Acta (BBA)-General Subjects 1670 (1), 81-83, 2004 | 58 | 2004 |
| 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 | 57 | 2004 |
| 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 | 53 | 2010 |
| Biallelic variants in four genes underlying recessive osteogenesis imperfecta A Hayat, S Hussain, M Bilal, M Kausar, B Almuzzaini, S Abbas, A Tanveer, ... European journal of medical genetics 63 (8), 103954, 2020 | 42 | 2020 |
| Molecular characterization of multidrug-resistant isolates of Mycobacterium tuberculosis from patients in Punjab, Pakistan SN Khan, S Niemann, M Gulfraz, M Qayyum, S Siddiqi, ZS Mirza, ... Pakistan Journal of Zoology 45 (1), 2013 | 36 | 2013 |
| A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy C Zazo Seco, A Castells-Nobau, S Joo, M Schraders, JN Foo, ... Disease models & mechanisms 10 (2), 105-118, 2017 | 32 | 2017 |
| 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 | 31 | 2013 |
| Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies A Lischka, K Eggermann, CJ Record, MF Dohrn, P Laššuthová, F Kraft, ... Brain 146 (12), 4880-4890, 2023 | 25 | 2023 |
| 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 | 25 | 2014 |
| 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 | 23 | 2013 |
| Genetic polymorphism of CYP2C19 in Pakistani population S Riaz, SM Din, MU Tareen, F Tariq, Y Latif, S Siddiqi, A Sultan, ... Iranian Journal of Pharmaceutical Research: IJPR 18 (2), 1097, 2019 | 20 | 2019 |
| Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta M Kausar, S Siddiqi, M Yaqoob, S Mansoor, O Makitie, A Mir, CC Khor, ... Journal of biomedical science 25 (1), 82, 2018 | 18 | 2018 |
| A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family M Kausar, EGY Chew, H Ullah, M Anees, CC Khor, JN Foo, O Makitie, ... Frontiers in Genetics 10, 144, 2019 | 16 | 2019 |
| MTHFR polymorphisms as Risk for Male Infertility in Pakistan and its Comparison with Socioeconomic Status in the World N Ullah, A Mansoor, S Micheal, B Mirza, R Qamar, K Mazhar, S Siddiqi Personalized Medicine 16 (1), 35-49, 2019 | 16 | 2019 |
| Direct‐acting antiviral agents in the treatment of chronic hepatitis C—Real‐life experience from clinical practices in Pakistan S Mushtaq, A Mansoor, M Umar, A Khan, S Siddiqi, S Manzoor Journal of Medical Virology 92 (12), 3475-3487, 2020 | 15 | 2020 |
| Identification and in silico characterization of a novel p. P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family M Ajmal, A Mir, S Wahid, CC Khor, JN Foo, S Siddiqi, M Kauser, SA Malik, ... BMC Medical Genetics 18 (1), 148, 2017 | 12 | 2017 |
| 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 | 12 | 2014 |
Atika MansoorVerified email at ibge.edu.pk
