Shahid Yar Khan
Shahid Yar Khan
Verified email at
Cited by
Cited by
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
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
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), 1-12, 2012
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
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
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
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
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, 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
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), 1-15, 2016
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
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 (5), 407-412, 2005
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 (6), 789-793, 2007
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
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
Distinctive microRNA expression signatures in proton-irradiated mice
SY Khan, MA Tariq, JP Perrott, CD Brumbaugh, HJ Kim, MI Shabbir, ...
Molecular and cellular biochemistry 382 (1-2), 225-235, 2013
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
Non-coding RNA profiling of the developing murine lens
SY Khan, SF Hackett, SA Riazuddin
Experimental eye research 145, 347-351, 2016
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
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34. 3
SY Khan, S Riazuddin, M Shahzad, N Ahmed, AU Zafar, AU Rehman, ...
European journal of human genetics 18 (1), 125-129, 2010
The system can't perform the operation now. Try again later.
Articles 1–20