Manju Ghosh - Concepedia

Author

Manju Ghosh

All India Institute of Medical Sciences

Also Known As

M Ghosh, M. Ghosh, Manju Ghosh, Monideep Ghosh

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

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

About

Manju Ghosh is an author at All India Institute of Medical Sciences specializing in medicine, genetics, and hearing loss.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	15	1.2K
2	Arts	6	6	864
3	Engineering	1	1	28
4	Natural Sciences	1	1	18
5	Public Health	1	1	15

Manju Ghosh

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function Kiyoto Kurima, Linda Peters, Yandan Yang, Nature Genetics Novel GeneGenetic DisorderGeneticsCochlear Hair-cell FunctionAudiology	2002	471
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
Risk factors for severe acute lower respiratory tract infection in under-five children. Shobha Broor, Rudra Pandey, Manju Ghosh, PubMed	2001	155
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
Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39 Julie M. Schultz, Shaheen N. Khan, Zubair M. Ahmed, The American Journal of Human Genetics GeneticsAudiologyPathologyAuditory PhysiologyNonsyndromic Hearing Loss	2009	120
Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness Saima Riazuddin, Shaheen N. Khan, Zubair M. Ahmed, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsPutative Cytoskeletal-organizing Protein	2005	110
Allelic hierarchy of <i>CDH23</i> mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes Julie M. Schultz, Rashid Bhatti, Anne C. Madeo, Journal of Medical Genetics	2011	103
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
Mutational spectrum of<i>MYO15A</i>: the large N-terminal extension of myosin XVA is required for hearing N. Nal, Zubair M. Ahmed, Engin Erkal, Human Mutation	2007	91
Clinical profile and frequency of delta f508 mutation in Indian children with cystic fibrosis. S. K. Kabra, Madhulika Kabra, Rakesh Lodha, PubMed	2003	70

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