| Convergent transcriptional programs regulate cAMP levels in C. elegans GABAergic motor neurons B Yu, X Wang, S Wei, T Fu, EE Dzakah, A Waqas, WW Walthall, G Shan Developmental cell 43 (2), 212-226. e7, 2017 | 36 | 2017 |
| Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features MA Rafiq, CS Leblond, MAN Saqib, AK Vincent, A Ambalavanan, ... BMC medical genetics 16, 1-10, 2015 | 34 | 2015 |
| Clinical and molecular delineation of PUS3‐associated neurodevelopmental disorders M Nøstvik, SM Kateta, B Schönewolf‐Greulich, A Afenjar, M Barth, ... Clinical Genetics 100 (5), 628-633, 2021 | 27 | 2021 |
| Intratracheally instillated diesel PM2. 5 significantly altered the structure and composition of indigenous murine gut microbiota Y Liu, T Wang, B Si, H Du, Y Liu, A Waqas, S Huang, G Zhao, S Chen, ... Ecotoxicology and Environmental Safety 210, 111903, 2021 | 26 | 2021 |
| Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability K Mittal, MA Rafiq, R Rafiullah, R Harripaul, H Ali, M Ayaz, M Aslam, ... Journal of human genetics 61 (10), 867-872, 2016 | 24 | 2016 |
| Aging-independent and size-dependent genotoxic response induced by titanium dioxide nanoparticles in mammalian cells J Wang, J Wang, Y Liu, Y Nie, B Si, T Wang, A Waqas, G Zhao, M Wang, ... Journal of Environmental Sciences 85, 94-106, 2019 | 21 | 2019 |
| Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type A M Umair, O Palander, M Bilal, B Almuzzaini, Q Alam, F Ahmad, M Younus, ... Genomics 113 (4), 2495-2502, 2021 | 20 | 2021 |
| Case report: biallelic variant in the tRNA methyltransferase domain of the AlkB homolog 8 causes syndromic intellectual disability A Waqas, A Nayab, S Shaheen, S Abbas, M Latif, MM Rafeeq, ... Frontiers in Genetics 13, 878274, 2022 | 15 | 2022 |
| Targeted exome sequencing identified a novel frameshift variant in the PGAM2 gene causing glycogen storage disease type X A Nayab, Q Alam, OR Alzahrani, R Khan, S Sarfaraz, AA Albaz, ... European Journal of Medical Genetics 64 (9), 104283, 2021 | 13 | 2021 |
| Loss of miR-83 extends lifespan and affects target gene expression in an age-dependent manner in Caenorhabditis elegans EE Dzakah, A Waqas, S Wei, B Yu, X Wang, T Fu, L Liu, G Shan Journal of genetics and genomics 45 (12), 651-662, 2018 | 13 | 2018 |
| Computational analysis of Cyclin D1 gene SNPs and association with breast cancer A Aftab, R Khan, W Shah, M Azhar, A Unar, HM Jafar Hussain, A Waqas Bioscience Reports 41 (1), BSR20202269, 2021 | 12 | 2021 |
| Gain-of-function p. F28S variant in RAC3 disrupts neuronal differentiation, migration and axonogenesis during cortical development, leading to neurodevelopmental disorder M Nishikawa, M Scala, M Umair, H Ito, A Waqas, P Striano, F Zara, ... Journal of Medical Genetics 60 (3), 223-232, 2023 | 10 | 2023 |
| Quantifying the impacts of COVID-19 lockdown and spring festival on air quality over Yangtze river delta region Z Javed, A Tanvir, Y Wang, A Waqas, M Xie, A Abbas, O Sandhu, C Liu Atmosphere 12 (6), 735, 2021 | 8 | 2021 |
| Variants in the PNPLA1 Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance F Ahmad, I Ahmed, Q Alam, T Ahmad, A Khan, I Ahmad, M Bilal, A Hayat, ... Molecular Syndromology 12 (6), 351-361, 2021 | 7 | 2021 |
| Sero-prevalence of hepatitis B, hepatitis C, Human immunodeficiency virus, Syphilis and Malaria in blood donors of Mirpur, Azad Jammu Kashmir M Umair, RT Mahmood, M Inam, A Waqas, I Wazir Pakistan. J Public Health Biol Sci 1 (4), 110-4, 2012 | 6 | 2012 |
| Uptake and Reaction of C. elegans to Environmental RNAs A Waqas, G Shan Non-coding RNAs and Inter-kingdom Communication, 117-124, 2016 | 3 | 2016 |
| CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family MD Ghouchanatigh, R Khan, M Mojarrad, U Hameed, M Zubair, A Waqas, ... Asian Journal of Andrology 24 (4), 416-421, 2022 | 2 | 2022 |
| Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment MU Kakar, M Akram, M Zubair Mehboob, M Younus, M Bilal, A Waqas, ... Plos one 17 (6), e0268078, 2022 | 2 | 2022 |
| Exonuclease 5 is dispensable for meiotic progression and male fertility in mouse Q Zaman, R Khan, U Hameed, W Shah, A Waqas, M Zubair, S Dil, T Zafar, ... Gene 769, 145254, 2021 | 2 | 2021 |
