Shahid Y. Khan - Concepedia

Author

Shahid Y. Khan

Also Known As

Khan, Shahid, Khan, Shahid Y., Khan, Shahid Yar, S Khan, S Y Khan, S. Khan, Shahid Khan, Shahid Y Khan, Shahid Y. Khan, Shahid Yar Khan

Publications

4.3K

Citations

H-Index

Concepts

All Affiliations

Johns Hopkins Medicine University of the Punjab Centre of Excellence in Molecular Biology Johns Hopkins University National Institutes of Health

About

Shahid Y. Khan is an author at Johns Hopkins Medicine specializing in medicine, genetics, and gene expression.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	1.1K
2	Natural Sciences	3	3	410
3	Arts	2	2	106
4	Education	1	1	30
5	Biology	1	1	134

Shahid Y. Khan

Publications

4.2K

Citations

H-Index

Page 1

	Year	Citations
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)<sup>1</sup> Daniel J. Klionsky, Amal Kamal Abdel‐Aziz, Sara Abdelfatah, Autophagy	2021	2.5K
CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness Lisa M. Astuto, Julie M. Bork, Michael D. Weston, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderPhenotype HeterogeneityGeneticsGenetic Epidemiology	2002	230
Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79 Atteeq U. Rehman, Robert J. Morell, Inna A. Belyantseva, The American Journal of Human Genetics Mutated GeneGenetic DisorderMedicineGeneticsEncoding Taperin	2010	193
Single-cell analyses of transcriptional heterogeneity during drug tolerance transition in cancer cells by RNA sequencing Wendy Lee, Fernando J. López-Díaz, Shahid Y. Khan, Proceedings of the National Academy of Sciences	2014	182
Sequencing three crocodilian genomes to illuminate the evolution of archosaurs and amniotes John A. St John, Edward L. Braun, Sally R. Isberg, Genome biology Comparative GenomicsGeneticsGenomicsCrocodilian GenomesPhylogenetics	2012	134
Mutations of human <i>TMHS</i> cause recessively inherited non-syndromic hearing loss Muhammad Imran Shabbir, Zubair M. Ahmed, Shahid Y. Khan, Journal of Medical Genetics	2006	100
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis Saima Anwar, Saima Riazuddin, Zubair M. Ahmed, Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologySlc26a4 Mutation Spectrum	2009	98
Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome Saima Riazuddin, Saima Anwar, Martin Fischer, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyDegenerative Disease	2009	86
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans Zubair M. Ahmed, Saber Masmoudi, Ersan Kalay, Nature Genetics Nonsyndromic DeafnessMendelian DisorderGenetic DisorderGeneticsAudiology	2008	84
Mutations of the<i>RDX</i>gene cause nonsyndromic hearing loss at the<i>DFNB24</i>locus Shahid Y. Khan, Zubair M. Ahmed, Muhammad Imran Shabbir, Human Mutation Genetic DisorderNatural SciencesGeneticsMolecular BiologyInner Ear	2007	83

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