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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Barkur S. Shastry

Department of Biological Sciences

Oakland University


MI 48309



Name/email consistency: high



  • Department of Biological Sciences, Oakland University, Rochester, MI 48309, USA. 2003 - 2010


  1. Common polymorphisms of the CFH, LOC 387715/ARMS2 and HTRA1 genes may not influence the intra-familial variability of X-linked juvenile retinoschisis. Shastry, B.S. Mol. Med. Report (2010) [Pubmed]
  2. Persistent hyperplastic primary vitreous: congenital malformation of the eye. Shastry, B.S. Clin. Experiment. Ophthalmol. (2009) [Pubmed]
  3. Evaluation of the common variants of the ABCA4 gene in families with Stargardt disease and autosomal recessive retinitis pigmentosa. Shastry, B.S. Int. J. Mol. Med. (2008) [Pubmed]
  4. Lack of association of the VEGF gene promoter (-634 G-->C and -460 C-->T) polymorphism and the risk of advanced retinopathy of prematurity. Shastry, B.S., Qu, X. Graefes Arch. Clin. Exp. Ophthalmol. (2007) [Pubmed]
  5. Assessment of the contribution of insulin-like growth factor I receptor 3174 G-->A polymorphism to the progression of advanced retinopathy of prematurity. Shastry, B.S. Eur. J. Ophthalmol (2007) [Pubmed]
  6. Developmental dyslexia: an update. Shastry, B.S. J. Hum. Genet. (2007) [Pubmed]
  7. Assessment of the contribution of the LOC387715 gene polymorphism in a family with exudative age-related macular degeneration and heterozygous CFH variant (Y402H). Shastry, B.S. J. Hum. Genet. (2007) [Pubmed]
  8. SNPs in disease gene mapping, medicinal drug development and evolution. Shastry, B.S. J. Hum. Genet. (2007) [Pubmed]
  9. Pharmacogenetics and the concept of individualized medicine. Shastry, B.S. Pharmacogenomics J. (2006) [Pubmed]
  10. 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. Shastry, B.S. Ophthalmologica (2006) [Pubmed]
  11. Bipolar disorder: an update. Shastry, B.S. Neurochem. Int. (2005) [Pubmed]
  12. Genetic diversity and new therapeutic concepts. Shastry, B.S. J. Hum. Genet. (2005) [Pubmed]
  13. Cosegregation of two unlinked mutant alleles in some cases of autosomal dominant familial exudative vitreoretinopathy. Shastry, B.S., Trese, M.T. Eur. J. Hum. Genet. (2004) [Pubmed]
  14. Molecular genetics of attention-deficit hyperactivity disorder (ADHD): an update. Shastry, B.S. Neurochem. Int. (2004) [Pubmed]
  15. Evaluation of the ABCR and glutathione peroxidase-3 genes in familial and sporadic cases of exudative age-related macular degeneration. Shastry, B.S. Int. J. Mol. Med. (2004) [Pubmed]
  16. Neurodegenerative disorders of protein aggregation. Shastry, B.S. Neurochem. Int. (2003) [Pubmed]
  17. Molecular genetics of autism spectrum disorders. Shastry, B.S. J. Hum. Genet. (2003) [Pubmed]
  18. Overproduction and partial purification of the Norrie disease gene product, norrin, from a recombinant baculovirus. Shastry, B.S., Trese, M.T. Biochem. Biophys. Res. Commun. (2003) [Pubmed]
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