Works by Shastry, Barkur S.

Results: 21

Assessment of the contribution of the LOC387715 gene polymorphism in a family with exudative age-related macular degeneration and heterozygous CFH variant (Y402H).

Published in:

Journal of Human Genetics, 2007, v. 52, n. 4, p. 384, doi. 10.1007/s10038-007-0120-y

By:

Shastry, Barkur S.

Publication type:

Article

Developmental dyslexia: an update.

Published in:

Journal of Human Genetics, 2007, v. 52, n. 2, p. 104, doi. 10.1007/s10038-006-0088-z

By:

Shastry, Barkur S.

Publication type:

Article

Recent progress in the genetics of incontinentia pigmenti (Bloch-Sulzberger syndrome).

Published in:

Journal of Human Genetics, 2000, v. 45, n. 6, p. 323, doi. 10.1007/s100380070001

By:

Shastry, Barkur S.

Publication type:

Article

Reply to Bottomley et al.

Published in:

2006

By:

Shastry, Barkur S.;
Trese, Michael T.

Publication type:

Letter

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy.

Published in:

Nature Genetics, 2002, v. 32, n. 2, p. 326, doi. 10.1038/ng957

By:

Robitaille, Johane;
MacDonald, Marcia L.E.;
Kaykas, Ajamete;
Sheldahl, Laird C.;
Zeisler, Jutta;
Dubé, Marie-Pierre;
Zhang, Lin-Hua;
Singaraja, Roshni R.;
Guernsey, Duane L.;
Zheng, Binyou;
Siebert, Lee F.;
Hoskin-Mott, Ann;
Trese, Michael T.;
Pimstone, Simon N.;
Shastry, Barkur S.;
Moon, Randall T.;
Hayden, Michael R.;
Goldberg, Y. Paul;
Samuels, Mark E.

Publication type:

Article

Further Support for the Common Variants in Complement Factor H (Y402H) and LOC387715 (A69S) Genes as Major Risk Factors for the Exudative Age-Related Macular Degeneration.

Published in:

Ophthalmologica, 2006, v. 220, n. 5, p. 291, doi. 10.1159/000094617

By:

Barkur S. Shastry

Publication type:

Article

Coats' Disease and Congenital Retinoschisis in a Single Eye: A Case Report and DNA Analysis.

Published in:

Ophthalmologica, 2001, v. 215, n. 2, p. 132, doi. 10.1159/000050844

By:

Berinstein, Daniel M.;
Hiraoka, Miki;
Trese, Michael T.;
Shastry, Barkur S.

Publication type:

Article

Evaluation of the Peripherin/RDS Gene as a Candidate Gene in Families with Age-Related Macular Degeneration.

Published in:

Ophthalmologica, 1999, v. 213, n. 3, p. 165, doi. 10.1159/000027413

By:

Shastry, Barkur S.;
Trese, Michael T.

Publication type:

Article

Retinal ganglion cell (RGC) death in glaucomatous beagles is not associated with mutations in p53 and NTF4 genes.

Published in:

Veterinary Ophthalmology, 2012, v. 15, p. 8, doi. 10.1111/j.1463-5224.2012.01024.x

By:

Kato, Kumiko;
Sasaki, Noboru;
Shastry, Barkur S.

Publication type:

Article

Genetic risk in the development of Advanced retinopathy of Prematurity.

Published in:

Current Medical Literature: Ophthalmology, 2011, v. 21, n. 3, p. 89

By:

Shastry, Barkur S.

Publication type:

Article

On the functions of lithium: The mood stabilizer.

Published in:

BioEssays, 1997, v. 19, n. 3, p. 199, doi. 10.1002/bies.950190304

By:

Shastry, Barkur S.

Publication type:

Article

Genetic susceptibility to advanced retinopathy of prematurity (ROP).

Published in:

Journal of Biomedical Science, 2010, v. 17, p. 69, doi. 10.1186/1423-0127-17-69

By:

Shastry, Barkur S.

Publication type:

Article

Identification of novel missense mutations in the Norrie disease gene associated with one X-linked and four sporadic cases of Familial Exudative Vitreoretinopathy.

Published in:

Human Mutation, 1997, v. 9, n. 5, p. 396, doi. 10.1002/(SICI)1098-1004(1997)9:5<396::AID-HUMU3>3.0.CO;2-2

By:

Shastry, Barkur S.;
Hejtmancik, James F.;
Trese, Michael T.

Publication type:

Article

Role of Epigenomics in Drug Discovery and Therapies.

Published in:

Drug Development Research, 2012, v. 73, n. 8, p. 513, doi. 10.1002/ddr.21044

By:

Shastry, Barkur S.

Publication type:

Article

Genetics of familial exudative vitreoretinopathy and its implications for management.

Published in:

Expert Review of Ophthalmology, 2012, v. 7, n. 4, p. 377, doi. 10.1586/EOP.12.40

By:

Shastry, Barkur S.

Publication type:

Article

Role of SNP/haplotype map in gene discovery and drug development: An overview.

Published in:

Drug Development Research, 2004, v. 62, n. 2, p. 143, doi. 10.1002/ddr.10377

By:

Barkur S. Shastry

Publication type:

Article

Persistent hyperplastic primary vitreous: congenital malformation of the eye.

Published in:

Clinical & Experimental Ophthalmology, 2009, v. 37, n. 9, p. 884, doi. 10.1111/j.1442-9071.2009.02150.x

By:

Shastry, Barkur S.

Publication type:

Article

Ophthalmic genetics: complexity in paediatric vitreoretinopathies.

Published in:

2006

By:

Shastry, Barkur S.

Publication type:

Editorial

Hereditary Degenerative Retinopathies: Optimism for Somatic Gene Therapy.

Published in:

IUBMB Life, 2000, v. 49, n. 6, p. 479, doi. 10.1080/15216540050167007

By:

Shastry, Barkur S.

Publication type:

Article

Genetic diversity and medicinal drug response in eye care.

Published in:

Graefe's Archive of Clinical & Experimental Ophthalmology, 2010, v. 248, n. 8, p. 1057, doi. 10.1007/s00417-010-1333-x

By:

Shastry, Barkur S.

Publication type:

Article

Evaluation of the Norrie Disease Gene in a Family with Incontinentia pigmenti.

Published in:

Ophthalmic Research, 2000, v. 32, n. 4, p. 181, doi. 10.1159/000055610

By:

Shastry, Barkur S.;
Trese, Michael T.

Publication type:

Article