| Identification of mutations in TRAPPC9, which encodes the NIK-and IKK-β-binding protein, in nonsyndromic autosomal-recessive mental retardation A Mir, L Kaufman, A Noor, MM Motazacker, T Jamil, M Azam, K Kahrizi, ... The American Journal of Human Genetics 85 (6), 909-915, 2009 | 179 | 2009 |
| Identification of mutations in TRAPPC9, which encodes the NIK-and IKK-β-binding protein, in nonsyndromic autosomal-recessive mental retardation A Mir, L Kaufman, A Noor, MM Motazacker, T Jamil, M Azam, K Kahrizi, ... The American Journal of Human Genetics 85 (6), 909-915, 2009 | 179 | 2009 |
| Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families R Harripaul, N Vasli, A Mikhailov, MA Rafiq, K Mittal, C Windpassinger, ... Molecular psychiatry, 2017 | 177 | 2017 |
| Epigenetics in Alzheimer’s disease: perspective of DNA methylation TJ Qazi, Z Quan, A Mir, H Qing Molecular neurobiology 55 (2), 1026-1044, 2018 | 147 | 2018 |
| Concept of halal food and biotechnology JZK Khattak, A Mir, Z Anwar, G Abbas, HZK Khattak, H Ismatullah Advance Journal of Food Science and Technology 3 (5), 385-389, 2011 | 138 | 2011 |
| Hutchinson–gilford progeria syndrome: a premature aging disease MS Ahmed, S Ikram, N Bibi, A Mir Molecular neurobiology 55 (5), 4417-4427, 2018 | 119 | 2018 |
| The genetics of intellectual disability: advancing technology and gene editing M Ilyas, A Mir, S Efthymiou, H Houlden F1000Research 9 (22), 22, 2020 | 87 | 2020 |
| Susceptibility pattern of Pseudomonas aeruginosa against various antibiotics F Anjum, A Mir African Journal of Microbiology Research 4 (10), 1005-1012, 2010 | 83 | 2010 |
| Application of proteomics to investigate stress-induced proteins for improvement in crop protection A Afroz, GM Ali, A Mir, S Komatsu Plant cell reports 30 (5), 745-763, 2011 | 70 | 2011 |
| Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairment RLP Santos, M Wajid, MN Khan, N McArthur, TL Pham, A Bhatti, K Lee, ... Human mutation 26 (4), 396-396, 2005 | 70 | 2005 |
| Effect of organic manures with recommended dose of NPK on the performance of wheat (Triticum aestivum L.) G Abbas, JZK Khattak, A Mir, M Ishaque, M Hussain, HM Wahedi, ... J. Anim. Plant. Sci 22 (3), 683-687, 2012 | 66 | 2012 |
| A novel familial BBS12 mutation associated with a mild phenotype: implications for clinical and molecular diagnostic strategies B Pawlik, A Mir, H Iqbal, Y Li, G Nürnberg, C Becker, R Qamar, ... Molecular syndromology 1 (1), 27-34, 2010 | 54 | 2010 |
| Structural, phylogenetic and docking studies of D-amino acid oxidase activator (DAOA), a candidate schizophrenia gene SA Sehgal, NA Khattak, A Mir Theoretical Biology and Medical Modelling 10 (1), 3, 2013 | 53 | 2013 |
| Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly R Kousar, MJ Hassan, B Khan, S Basit, S Mahmood, A Mir, W Ahmad, ... BMC neurology 11 (1), 119, 2011 | 46 | 2011 |
| Identification of bioflavonoid as fusion inhibitor of dengue virus using molecular docking approach A Mir, H Ismatullah, S Rauf, UHK Niazi Informatics in Medicine Unlocked 3, 1-6, 2016 | 42 | 2016 |
| Carbon Tetrachloride (CCl4)-induced hepatotoxicity in rats: Curative role of Solanum nigrum A Mir, F Anjum, N Riaz, H Iqbal, HM Wahedi, JZK Khattak, MA Khan, ... J Med Plant Res 4 (23), 2525-2532, 2010 | 40 | 2010 |
| Tumor necrosis factor receptor superfamily 10B (TNFRSF10B): an insight from structure modeling to virtual screening for designing drug against head and neck cancer RA Tahir, SA Sehgal, NA Khattak, JZK Khattak, A Mir Theoretical Biology and Medical Modelling 10 (1), 38, 2013 | 35 | 2013 |
| Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family A Mir, K Sritharan, K Mittal, N Vasli, C Araujo, T Jamil, MA Rafiq, Z Anwar, ... Human genetics 133 (8), 975-984, 2014 | 32 | 2014 |
| Adaptive evolution and elucidating the potential inhibitor against schizophrenia to target DAOA (G72) isoforms SA Sehgal, S Mannan, S Kanwal, I Naveed, A Mir Drug design, development and therapy 9, 3471, 2015 | 30 | 2015 |
| An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan S Rasool, JM Baig, A Moawia, I Ahmad, M Iqbal, SS Waseem, M Asif, ... Molecular genetics & genomic medicine, e1408, 0 | 27 | |
