A SRF 2014

Articles

• personalized medicine
  22 April 2007

  The utility and limitations of personal genomic data can be discussed in three domains:
  pharmacogenomics,
  assessment of genetic predispositions for common diseases,
  identification of rare disease-causing genetic variants.
  Open references
  Personalized medicine: hope or hype? Salari K, Watkins H, Ashley EA. Eur Heart J. 2012 Jul;33(13):1564-70. doi:10.1093/eurheartj/ehs112. PMID: #22659199# [Free]
  References
  G-DOC: A Systems Medicine Platform for Personalized Oncology. Madhavan (...)

• genotype-phenotype correlation
  29 October 2003

  genotype-phenotype relation; gen2phen
  See also
  pleiotropy
  Open references
  Genotype to phenotype via network analysis. Carter H, Hofree M, Ideker T. Curr Opin Genet Dev. 2013 Dec;23(6):611-21. doi:10.1016/j.gde.2013.10.003 . PMID: #24238873# [Free]
  Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease. Cooper DN, Krawczak M, Polychronakos C, Tyler-Smith C, Kehrer-Sawatzki H. Hum Genet. 2013 (...)

• disease-causing mutation
  24 September 2014

  disease-causing mutations
  See also
  disease-causing mutation database
  References
  Genotype to phenotype via network analysis. Carter H, Hofree M, Ideker T. Curr Opin Genet Dev. 2013 Dec;23(6):611-21. doi:10.1016/j.gde.2013.10.003 . PMID: #24238873# [Free]