Tenesha N. Smith - Concepedia

Concepedia

Author

Tenesha N. Smith

National Institute on Deafness and Other Communication Disorders

Also Known As

Tenesha N Smith, Tenesha N. Smith, Tenesha Smith

8

Publications

1.2K

Citations

7

H-Index

14

Concepts

All Affiliations

National Institute on Deafness and Other Communication Disorders Centre of Excellence in Molecular Biology National Institutes of Health All India Institute of Medical Sciences University of the Punjab

TN

About

Tenesha N. Smith is an author at National Institute on Deafness and Other Communication Disorders specializing in hearing loss, medicine, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	979
2	Arts	3	3	815
3	Molecular Genetics	2	2	255
4	Molecular Medicine	1	1	148
5	Pathology	1	1	148

Tenesha N. Smith

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6

Publications

1.2K

Citations

6

H-Index

	Year	Citations
Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29 Edward R. Wilcox, Quianna Burton, Sadaf Naz, Cell Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiology	2001	437
OTOF Encodes Multiple Long and Short Isoforms: Genetic Evidence That the Long Ones Underlie Recessive Deafness DFNB9 Shin’ichiro Yasunaga, M’hamed Grati, Sébastien Chardenoux, The American Journal of Human Genetics Developmental BiologyShort IsoformsGenetic DisorderGeneticsAudiology	2000	203
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC Zubair M. Ahmed, Tenesha N. Smith, Saima Riazuddin, Human Genetics Mendelian DisorderAllelic MutationsGenetic DisorderGeneticsAudiology	2002	175
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome Nikki Liburd, Manju Ghosh, Saima Riazuddin, Human Genetics Mendelian DisorderGenetic DisorderNovel MutationsPathologyMedicine	2001	148
Dominant modifier DFNM1 suppresses recessive deafness DFNB26 Saima Riazuddin, Caley M. Castelein, Zubair M. Ahmed, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsMedical GeneticsDominant Modifier Dfnm1	2000	139
A Gene for Recessive Nonsyndromic Sensorineural Deafness (DFNB18) Maps to the Chromosomal Region 11p14–p15.1 Containing the Usher Syndrome Type 1C Gene Pawan Kumar Jain, Anil K. Lalwani, Xiaoyan C. Li, Genomics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsMolecular Genetics	1998	52

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