Barkur S. Shastry - Concepedia

Author

Barkur S. Shastry

Also Known As

BARKUR S. SHASTRY, Barkur S Shastry, Barkur S. Shastry, Barkur Shastry, Barkur S. Shastry, Shastry, B.S., Shastry, Barkur S.

Publications

4.4K

Citations

H-Index

Concepts

All Affiliations

Oakland University Beaumont Hospital, Royal Oak Smith-Kettlewell Eye Research Institute National Eye Institute Beaumont Eye Institute

About

Barkur S. Shastry is an author at Oakland University specializing in medicine, genetics, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	19	2.1K
2	Public Health	7	7	147
3	Natural Sciences	2	2	1K
4	Allergy	1	1	35
5	Anatomy	1	1	14

Barkur S. Shastry

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
[36] Eukaryotic gene transcription with purified components John David Dignam, Paul L. Martin, Barkur S. Shastry, Methods in enzymology on CD-ROM/Methods in enzymology Transcriptional RegulationNatural SciencesGene StructureGene RegulationMolecular Biology	1983	989
Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy Johane M. Robitaille, Marcia L.E. MacDonald, Ajamete Kaykas, Nature Genetics Ocular DiseaseVitreous BodyFamilial Exudative VitreoretinopathyOphthalmologyPathology	2002	473
Autosomal Recessive Familial Exudative Vitreoretinopathy Is Associated with Mutations in LRP5 Xiaodong Jiao, V. Ventruto, Michael T. Trese, The American Journal of Human Genetics Ocular DiseaseVitreous BodyOphthalmologyGenetic DisorderGenetics	2004	208
Identification of Missense Mutations in the Norrie Disease Gene Associated With Advanced Retinopathy of Prematurity Barkur S. Shastry Archives of Ophthalmology	1997	176
X-Linked Recessive Familial Exudative Vitreoretinopathy David A. Plager, Ira K. Orgel, Forrest D. Ellis, American Journal of Ophthalmology Ocular DiseaseVitreous BodyOphthalmologyPathogenesisFragile X Spectrum	1992	84
Identification of novel missense mutations in the Norrie disease gene associated with one X-linked and four sporadic cases of Familial Exudative Vitreoretinopathy Barkur S. Shastry, J. Fielding Hejtmancik, Michael T. Trese Human Mutation	1997	79
Linkage and Candidate Gene Analysis of X-Linked Familial Exudative Vitreoretinopathy Barkur S. Shastry, J. Fielding Hejtmancik, David A. Plager, Genomics Ocular DiseaseVitreous BodyOphthalmologyGenetic DisorderGenetics	1995	52
Study of the Norrie Disease Gene in 2 Patients With Bilateral Persistent Hyperplastic Primary Vitreous Scott Pendergast, Michael T. Trese, Xuyang Liu, Archives of Ophthalmology	1998	38
SNPs and haplotypes: Genetic markers for disease and drug response (Review) Barkur S. Shastry International Journal of Molecular Medicine GeneticsGenetic EpidemiologyHuman PolymorphismGenomicsDrug Treatment	2003	35
Lack of association of the VEGF gene promoter (−634 G→C and −460 C→T) polymorphism and the risk of advanced retinopathy of prematurity Barkur S. Shastry, Xianggui Qu Graefe s Archive for Clinical and Experimental Ophthalmology Ocular DiseaseOphthalmologyGeneticsAdvanced RetinopathyGenetic Epidemiology	2006	35

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