Literature DB >> 19416875

The future of the human SNP identification: which individuals to sequence?

Juergen K V Reichardt, Ruty Mehrian-Shai.   

Abstract

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Year:  2009        PMID： 19416875      PMCID： PMC2683127          DOI： 10.1073/pnas.0903681106

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  2 in total

1.  Estimating the number of unseen variants in the human genome.

Authors:  Iuliana Ionita-Laza; Christoph Lange; Nan M Laird
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-10       Impact factor: 11.205

Review 2.  Extreme discordant phenotype methodology: an intuitive approach to clinical pharmacogenetics.

Authors:  D W Nebert
Journal:  Eur J Pharmacol       Date:  2000-12-27       Impact factor: 4.432
  2 in total
  2 in total

Review 1.  Selection of extreme phenotypes: the role of clinical observation in translational research.

Authors:  José Luis Pérez-Gracia; Alfonso Gúrpide; María Gloria Ruiz-Ilundain; Carlos Alfaro Alegría; Ramon Colomer; Jesús García-Foncillas; Ignacio Melero Bermejo
Journal:  Clin Transl Oncol       Date:  2010-03       Impact factor: 3.405

2.  A non-synonymous single nucleotide polymorphism in an OPRM1 splice variant is associated with fentanyl-induced emesis in women undergoing minor gynaecological surgery.

Authors:  Grace Su Yin Pang; Farida Ithnin; Yin Yee Wong; Jing Bo Wang; Yvonne Lim; Alex Tiong Heng Sia; Caroline Guat Lay Lee
Journal:  PLoS One       Date:  2012-11-07       Impact factor: 3.240
  2 in total

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