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

K.S. Reddy

Quest Diagnostics Incorporated

San Juan Capistrano

California 92690

USA

[email]@questdiagnostics.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Quest Diagnostics Incorporated, San Juan Capistrano, California 92690, USA. 1999 - 2001
  • Cytogenetic Laboratory, Quest Diagnostics Inc., Nichols Institute, San Juan Capistrano, USA. 1999 - 2001
  • Quest Diagnostics Inc., Nichols Institute, Cytogenetics Department, 33608 Ortega Highway, USA. 2001

References

  1. Mosaic unbalanced structural abnormalities confirmed using FISH on buccal mucosal cells. Reddy, K.S., Mak, L. Ann. Genet. (2001) [Pubmed]
  2. Segmental amplification of 11q23 region identified by fluorescence in situ hybridization in four patients with myeloid disorders: a review. Reddy, K.S., Parsons, L., Mak, L., Dighe, P., Saphner, T., Crow, M.K., Scott, M. Cancer Genet. Cytogenet. (2001) [Pubmed]
  3. An hsr on chromosome 7 was shown to be an insertion of four copies of the 11q23 MLL gene region in an HIV-related lymphoma. Reddy, K.S., Parsons, L., Mak, L., Chan, J.A. Cancer Genet. Cytogenet. (2001) [Pubmed]
  4. Mosaic tetrasomy 8q: inverted duplication of 8q23.3qter in an analphoid marker. Reddy, K.S., Sulcova, V., Schwartz, S., Noble, J.E., Phillips, J., Brasel, J.A., Huff, K., Lin, H.J. Am. J. Med. Genet. (2000) [Pubmed]
  5. A child with ALL and ETV6/AML1 fusion on a chromosome 12 due to an insertion of AML1 and loss of ETV6 from the homolog involved in a t(12;15)(p13;q15). Reddy, K.S., Yang, X., Mak, L., Wang, S., Johnston, M. Genes. Chromosomes. Cancer (2000) [Pubmed]
  6. Intrachromosomal triplications: molecular cytogenetic and clinical studies. Reddy, K.S., Logan, J.J. Clin. Genet. (2000) [Pubmed]
  7. Fusion of 9 beta-satellite and telomere (TTAGGG)n sequences results in a jumping translocation. Reddy, K.S., Murphy, T. Hum. Genet. (2000) [Pubmed]
  8. De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes. Reddy, K.S., Sulcova, V., Young, H., Blancato, J.K., Haddad, B.R. Am. J. Med. Genet. (1999) [Pubmed]
  9. Microdeletion of chromosome sub-band 2q37.3 in two patients with abnormal situs viscerum. Reddy, K.S., Flannery, D., Farrer, R.J. Am. J. Med. Genet. (1999) [Pubmed]
  10. A paternally inherited terminal deletion, del(8)(p23.1)pat, detected prenatally in an amniotic fluid sample: a review of deletion 8p23.1 cases. Reddy, K.S. Prenat. Diagn. (1999) [Pubmed]
 
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