| Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders Z Iqbal, G Vandeweyer, M van der Voet, AM Waryah, MY Zahoor, ... Human molecular genetics 22 (10), 1960-1970, 2013 | 172 | 2013 |
| Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39 JM Schultz, SN Khan, ZM Ahmed, S Riazuddin, AM Waryah, D Chhatre, ... The American Journal of Human Genetics 85 (1), 25-39, 2009 | 121 | 2009 |
| Mutations of human TMHS cause recessively inherited non-syndromic hearing loss MI Shabbir, ZM Ahmed, SY Khan, S Riazuddin, AM Waryah, SN Khan, ... Journal of medical genetics 43 (8), 634-640, 2006 | 106 | 2006 |
| Mutational spectrum of MYO15A: the large N‐terminal extension of myosin XVA is required for hearing N Nal, ZM Ahmed, E Erkal, ÖM Alper, G Lüleci, O Dinç, AM Waryah, Q Ain, ... Human mutation 28 (10), 1014-1019, 2007 | 99 | 2007 |
| Consanguinity: A blessing or menace at population level? MA Bhinder, H Sadia, N Mahmood, M Qasim, Z Hussain, MM Rashid, ... Annals of human genetics 83 (4), 214-219, 2019 | 56 | 2019 |
| CDC14A phosphatase is essential for hearing and male fertility in mouse and human A Imtiaz, IA Belyantseva, AJ Beirl, C Fenollar-Ferrer, R Bashir, I Bukhari, ... Human molecular genetics 27 (5), 780-798, 2018 | 56 | 2018 |
| Mutational spectrum of the CYP1B1 gene in Pakistani patients with primary congenital glaucoma: novel variants and genotype-phenotype correlations SA Sheikh, AM Waryah, AK Narsani, H Shaikh, IA Gilal, K Shah, M Qasim, ... Molecular vision 20, 991, 2014 | 38 | 2014 |
| Clinical and hematological profile of acute myeloid leukemia (AML) patients of Sindh F Chang, TS Shamsi, AM Waryah J Hematol Thrombo Dis 4 (239), 2, 2016 | 37 | 2016 |
| MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients: a case control study FF Khidri, YM Waryah, FK Ali, H Shaikh, ID Ujjan, AM Waryah BMC medical genetics 20, 1-12, 2019 | 30 | 2019 |
| Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population M Shahzad, S Yousaf, YM Waryah, H Gul, T Kausar, N Tariq, U Mahmood, ... Scientific reports 7 (1), 44185, 2017 | 29 | 2017 |
| Visual impairment and progressive phthisis bulbi caused by recessive pathogenic variant in MARK3 M Ansar, H Chung, YM Waryah, P Makrythanasis, E Falconnet, AR Rao, ... Human molecular genetics 27 (15), 2703-2711, 2018 | 27 | 2018 |
| A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred AM Waryah, M Shahzad, H Shaikh, SA Sheikh, NA Channa, RB Hufnagel, ... Clinical genetics 90 (1), 90-95, 2016 | 27 | 2016 |
| The novel heterozygous Thr377Arg MYOC mutation causes severe Juvenile Open Angle Glaucoma in a large Pakistani family AM Waryah, AK Narsani, SA Sheikh, H Shaikh, MY Shahani Gene 528 (2), 356-359, 2013 | 27 | 2013 |
| Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani population S Yousaf, M Shahzad, K Tasleem, SA Sheikh, N Tariq, AS Shabbir, M Ali, ... Pigment cell & melanoma research 29 (2), 231, 2016 | 23 | 2016 |
| Identities and frequencies of variants in CYP1B1 causing primary congenital glaucoma in Pakistan M Rashid, S Yousaf, SA Sheikh, Z Sajid, AS Shabbir, T Kausar, N Tariq, ... Molecular vision 25, 144, 2019 | 20 | 2019 |
| Discriminating power of rapidly mutating Y-STRs in deep rooted endogamous pedigrees from Sindhi population of Pakistan A Rakha, YN Oh, HY Lee, S Hussain, AM Waryah, A Adnan, KJ Shin Legal Medicine 34, 17-20, 2018 | 19 | 2018 |
| DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2‐q15 AM Waryah, A Rehman, ZM Ahmed, ZH Bashir, SY Khan, AU Zafar, ... Clinical genetics 76 (3), 270-275, 2009 | 18 | 2009 |
| INPP5K variant causes autosomal recessive congenital cataract in a Pakistani family S Yousaf, SA Sheikh, S Riazuddin, AM Waryah, ZM Ahmed Clinical Genetics 93 (3), 682-686, 2018 | 15 | 2018 |
| SE33 locus as a reliable genetic marker for forensic DNA analysis systems DMA Bhinder, MY Zahoor, H Sadia, M Qasim, R Perveen, GM Anjum, ... Turkish Journal of Medical Sciences 48 (3), 611-614, 2018 | 15 | 2018 |
| IL28B rs12980275 polymorphism shows association with response to treatment in Pakistani patients with Chronic Hepatitis C N Shaikh, AM Waryah, BR Devrajani, MI Rajput, AS Hayat, S Shaikh Journal of Medical Virology 87 (5), 814-820, 2015 | 13 | 2015 |
