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Shahid Yar Khan
Shahid Yar Khan
Adresse e-mail validée de jhmi.edu
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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
13142*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
2262010
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
2092014
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
1622012
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
1062006
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
962007
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
902009
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
892009
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
882008
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
512015
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
492019
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
422015
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
412016
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
322007
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
292005
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
282015
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
272018
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
272016
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
252018
Non-coding RNA profiling of the developing murine lens
SY Khan, SF Hackett, SA Riazuddin
Experimental eye research 145, 347-351, 2016
252016
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