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

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Vanita Vanita

Department of Human Genetics

Guru Nanak Dev University

Amritsar

143005

India

[email]@yahoo.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Human Genetics, Guru Nanak Dev University, Amritsar, 143005, India. 2006 - 2012

References

  1. A missense mutation in CRYGD linked with autosomal dominant congenital cataract of aculeiform type. Vanita, V., Singh, D. Mol. Cell. Biochem. (2012) [Pubmed]
  2. Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin. Vanita, V., Sperling, K., Sandhu, H.S., Sandhu, P.S., Singh, J.R. Genet. Test. Mol. Biomarkers (2009) [Pubmed]
  3. Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract. Vanita, V., Singh, J.R., Singh, D., Varon, R., Sperling, K. Mol. Vis. (2009) [Pubmed]
  4. A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin. Vanita, V., Singh, J.R., Singh, D., Varon, R., Sperling, K. Mol. Vis. (2008) [Pubmed]
  5. A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin. Vanita, V., Singh, J.R., Singh, D., Varon, R., Sperling, K. Mol. Vis. (2008) [Pubmed]
  6. A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin. Vanita, V., Singh, J.R., Singh, D., Varon, R., Robinson, P.N., Sperling, K. Mol. Vis. (2007) [Pubmed]
  7. Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin. Vanita, V., Hejtmancik, J.F., Hennies, H.C., Guleria, K., Nürnberg, P., Singh, D., Sperling, K., Singh, J.R. Mol. Vis. (2006) [Pubmed]
  8. A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family. Vanita, V., Singh, J.R., Hejtmancik, J.F., Nuernberg, P., Hennies, H.C., Singh, D., Sperling, K. Mol. Vis. (2006) [Pubmed]
  9. A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin. Vanita, V., Hennies, H.C., Singh, D., Nürnberg, P., Sperling, K., Singh, J.R. Mol. Vis. (2006) [Pubmed]
 
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