Free Access
Issue
Med Sci (Paris)
Volume 28, Number 4, Avril 2012
Page(s) 435 - 437
Section Forum
DOI https://doi.org/10.1051/medsci/2012284023
Published online 25 April 2012
  1. Katsnelson A. Breaking the silence. Nat Med 2011 ; 17 : 1536–1538. [CrossRef] [PubMed] [Google Scholar]
  2. Kimchi-Sarfaty C, Oh JM, Kim IW, et al. A « silent » polymorphism in the MDR1 gene changes substrate specificity. Science 2007 ; 315 : 525–528. [CrossRef] [PubMed] [Google Scholar]
  3. Nackley AG, Shabalina SA, Tchivileva IE, et al. Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science 2006 ; 314 : 1930–1933. [CrossRef] [PubMed] [Google Scholar]
  4. Chen R, Davydov EV, Sirota M, Butte AJ. Non-synonymous and synonymous coding SNPs show similar likelihood and effect size of human disease association. PLoS One 2010 ; 5 : e13574. [CrossRef] [PubMed] [Google Scholar]
  5. International HapMap Consortium, Frazer KA, Ballinger DG, Cox DR, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature 2007 ; 449 : 851–861. [CrossRef] [PubMed] [Google Scholar]
  6. Sauna ZE, Kimchi-Sarfaty C. Understanding the contribution of synonymous mutations to human disease. Nat Rev Genet 2011 ; 12 : 683–691. [CrossRef] [PubMed] [Google Scholar]
  7. Sempé JJ. Rien n’est simple. Paris : Denoël 1962. [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.