S.S. Bhattacharya - Concepedia

Author

S.S. Bhattacharya

Also Known As

S Bhattacharya, S S BHATTACHARYA, S S Bhattacharya, S. Bhattacharya, S. S Bhattacharya, S. S. Bhattacharya, S.S Bhattacharya, S.S. Bhattacharya, Samadrita Bhattacharya, Shomi S. Bhattacharya

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

University College London Western General Hospital Moorfields Eye Hospital Moorfields Eye Hospital NHS Foundation Trust University of London

About

S.S. Bhattacharya is an author at University College London specializing in molecular genetics, genetics, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	226
2	Public Health	2	2	47
3	Biology	1	1	10
4	Cell Biology	1	1	40
5	Genetic Medicine	1	1	28

S.S. Bhattacharya

Publications

983

Citations

H-Index

Page 1

	Year	Citations
TGF-beta1, -beta2, and -beta3 in vitro: biphasic effects on Tenon's fibroblast contraction, proliferation, and migration. M. Francesca Cordeiro, S.S. Bhattacharya, Gregory S. Schultz, PubMed	2000	160
Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy L. V. B. Nicholson, Mark A. Johnson, D. Gardner‐Medwin, Acta Neuropathologica UrologyKinesiologyDystrophin ExpressionBecker Muscular DystrophyDegenerative Disease	1990	149
Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. Peter Wieacker, Kay E. Davies, Howard J. Cooke, PubMed	1984	145
Single exposures to antiproliferatives: long-term effects on ocular fibroblast wound-healing behavior. Nick L. Occleston, Julie T. Daniels, Roy Tarnuzzer, PubMed	1997	120
A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa family Mai Al-Maghtheh, Richard Kim, Alison J. Hardcastle, Human Molecular Genetics Molecular Diagnostic TechniquesRetinaBp InsertionOphthalmologyGenetic Disorder	1994	49
Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14. Alan F. Wright, S.S. Bhattacharya, John Clayton, PubMed	1987	42
Novel Mutations in CHST6 Gene Causing Macular Corneal Dystrophy MF El-Ashry, MM Abd El-Aziz, ND Ebenezer, Investigative Ophthalmology & Visual Science Ocular DiseaseOphthalmologyCorneal DystrophyGeneticsNovel Mutations	2002	42
Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous. Shagufta Khaliq, Asif Hameed, M. Ismail, PubMed	2001	41
OPA1, encoding a dynamin-related GTPase is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 C B Alexander, Marcela Votruba, U. E.A. Pesch, American Journal of Ophthalmology	2001	41
New model of conjunctival scarring in the mouse eye Martin Reichel, M. Francesca Cordeiro, R. A Alexander, British Journal of Ophthalmology	1998	40

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