| Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ... autophagy 17 (1), 1-382, 2021 | 13112* | 2021 |
| Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79 AU Rehman, RJ Morell, IA Belyantseva, SY Khan, ET Boger, M Shahzad, ... The American Journal of Human Genetics 86 (3), 378-388, 2010 | 226 | 2010 |
| Single-cell analyses of transcriptional heterogeneity during drug tolerance transition in cancer cells by RNA sequencing MCW Lee, FJ Lopez-Diaz, SY Khan, MA Tariq, Y Dayn, CJ Vaske, ... Proceedings of the National Academy of Sciences 111 (44), E4726-E4735, 2014 | 208 | 2014 |
| Sequencing three crocodilian genomes to illuminate the evolution of archosaurs and amniotes JA St John, EL Braun, SR Isberg, LG Miles, AY Chong, J Gongora, ... Genome biology 13, 1-12, 2012 | 161 | 2012 |
| 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 |
| Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus SY Khan, ZM Ahmed, MI Shabbir, S Kitajiri, S Kalsoom, S Tasneem, ... Human mutation 28 (5), 417-423, 2007 | 96 | 2007 |
| Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome S Riazuddin, S Anwar, M Fischer, ZM Ahmed, SY Khan, AGH Janssen, ... The American Journal of Human Genetics 85 (2), 273-280, 2009 | 90 | 2009 |
| SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis S Anwar, S Riazuddin, ZM Ahmed, S Tasneem, SY Khan, AJ Griffith, ... Journal of human genetics 54 (5), 266-270, 2009 | 89 | 2009 |
| Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans ZM Ahmed, S Masmoudi, E Kalay, IA Belyantseva, MA Mosrati, ... Nature genetics 40 (11), 1335-1340, 2008 | 87 | 2008 |
| Transcriptome Profiling of Developing Murine Lens Through RNA Sequencing. SY Khan, SF Hackett, MCW Lee, N Pourmand, CCJ Talbot, SA Riazuddin Invest Ophthalmol Vis Sci. 56 (8), 4919-26, 2015 | 51 | 2015 |
| SnS2 quantum dots growth on MoS2: Atomic-level heterostructure for electrocatalytic hydrogen evolution T Ali, X Wang, K Tang, Q Li, S Sajjad, S Khan, SA Farooqi, C Yan Electrochimica Acta 300, 45-52, 2019 | 47 | 2019 |
| Missense mutations in CRYAB are liable for recessive congenital cataracts X Jiaox, SY Khan, B Irum, AO Khan, Q Wang, F Kabir, AA Khan, ... PloS one 10 (9), e0137973, 2015 | 42 | 2015 |
| FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1 SY Khan, S Vasanth, F Kabir, JD Gottsch, AO Khan, R Chaerkady, ... Nature communications 7 (1), 10953, 2016 | 40 | 2016 |
| Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3 SY Khan, S Riazuddin, M Tariq, S Anwar, MI Shabbir, SA Riazuddin, ... Human genetics 120, 789-793, 2007 | 32 | 2007 |
| DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1 J Ahmad, SN Khan, SY Khan, K Ramzan, S Riazuddin, ZM Ahmed, ... Human genetics 116, 407-412, 2005 | 29 | 2005 |
| Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families SY Khan, S Ali, MA Naeem, SN Khan, T Husnain, NH Butt, ZA Qazi, ... Molecular vision 21, 871, 2015 | 28 | 2015 |
| Generation and proteome profiling of PBMC-originated, iPSC-derived corneal endothelial cells M Ali, SY Khan, S Vasanth, MR Ahmed, R Chen, CH Na, JJ Thomson, ... Investigative Ophthalmology & Visual Science 59 (6), 2437-2444, 2018 | 27 | 2018 |
| Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts B Irum, SY Khan, M Ali, H Kaul, F Kabir, B Rauf, F Fatima, R Nadeem, ... PloS one 11 (11), e0162620, 2016 | 27 | 2016 |
| Proteome profiling of developing murine lens through mass spectrometry SY Khan, M Ali, F Kabir, S Renuse, CH Na, CC Talbot, SF Hackett, ... Investigative Ophthalmology & Visual Science 59 (1), 100-107, 2018 | 25 | 2018 |
| Non-coding RNA profiling of the developing murine lens SY Khan, SF Hackett, SA Riazuddin Experimental eye research 145, 347-351, 2016 | 25 | 2016 |
Firoz KabirThe Singapore Eye Research Institute (SERI)Verified email at seri.com.sg
