CURRICULUM VITAE NAME Shom Shanker Bhattacharya, PhD ...

dystrophies. Papaioannou, M., Ocaka, L., Bessant, D., Lois, N., Bird, A., Payne,
A. and Bhattacharya, S. (2000). Invest. Ophthalmol. Vis.Sci. 41: 16-19.
164. A novel locus for Leber Congenital Amaurosis with Anterior Keratoconus
mapping to chromosome 17p13. Hameed, A., Khaliq, S., Ismail, M., Anwar, K.,
Ebenezer, N. D., Jordan, T., Mehdi, S.Q., Payne, A.M. and Bhattacharya S.S.
(2000). Invest. Ophthalmol. Vis. Sci. 41: 629-633.
165. Mutations in a novel photoreceptor-pineal gene on 17p cause Leber
congenital amaurosis (LCA4). Sohocki, M.M., Bowne, S.J., Sullivan, L.S.,
Blackshaw,S., Cepko, C.L., Payne, A.M., Bhattacharya, S.S., Khaliq, S., Qasim
Mehdi, S., Birch, D.G., Harrison, W.R., Elder, F.F., Heckenlively, J.R. and Daiger,
S.P. (2000). Nat. Genet. 24: 79-83.
166. Novel mutations of the RPGR gene in RP3 families. Zito, I., Gorin, M.B.,
Plant, C., Bird, A.C., Bhattacharya, S.S. and Hardcastle, A.J. (2000). Hum.
Mutat. (Online), 15: 386.
167. TGF-beta1,-beta2, and –beta3 in vitro: biphasic effects on Tenon’s
fibroblast contraction, proliferation, and migration. Cordeiro, M.F., Bhattacharya
S.S., Schultz, G.S. and Khaw, P.T. (2000). Invest. Ophthalmol. Vis. Sci. 41:
756-763.
168. Importance of the autosomal recessive retinitis pigmentosa locus on
1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGSr).
Bessant, D.A.R., Payne, A.M., Snow, B., Antinolo, G., Mehdi, S.Q., Bird, A.C.,
Siderovski, D.P. and Bhattacharya, S.S. (2000). J. Med. Genet. 37: 384-387.
169. Novel frameshift mutations in the RP2 gene and polymorphic variants.
Thiselton, D.L., Zito, I., Plant, C., Jay, M., Hodgson, S.V., Bird, A.C.,
Bhattacharya, S.S. and Hardcastle, A.J. (2000). Hum. Mutat. (Online), 15: 580.
170. Missense mutations in MIP underlie autosomal dominant ‘polymorphic’
and lamellar cataracts linked to 12q. Berry, V., Francis, P., Kaushal, S., Moore,
A. and Bhattacharya, S. (2000). Nat. Genet. 25: 15-17.
171. Restoration of photoreceptor ultrastructure and function in retinal
degeneration slow mice by gene therapy. Ali, R.R., Sarra, G.M., Stephens, C.,
Alwis, M.D., Bainbridge, J.W., Munro, P.M., Fauser, S., Reichel, M.B., Kinnon,
C., Hunt, D.M., Bhattacharya, S.S. and Thrasher, A.J. (2000). Nat. Genet. 25:
306-310.
172. Mutations in a novel photoreceptor-pineal gene on 17p cause Leber
congenital amaurosis (LCA4). Sohocki, M.M., Bowne, S.J., Sullivan, L.S.,
Blackshaw,S., Cepko, C.L., Payne, A.M., Bhattacharya, S.S., Khaliq, S., Qasim
Mehdi, S., Birch, D.G., Harrison, W.R., Elder, F.F., Heckenlively, J.R. and Daiger,
S.P. (2000). Am. J. Ophthalmol.129: 834-5.
173. MRI of the intraorbital optic nerve in patients with autosomal dominant
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