Author:
Alsmadi Osama,John Sumi E.,Thareja Gaurav,Hebbar Prashantha,Antony Dinu,Behbehani Kazem,Thanaraj Thangavel Alphonse
Publisher
Public Library of Science (PLoS)
Reference118 articles.
1. The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes;D Altshuler;Nat Genet,2000
2. Exome sequencing identifies the cause of a mendelian disorder;SB Ng;Nat Genet,2010
3. Progress and promise of genome-wide association studies for human complex trait genetics;BE Stranger;Genetics,2011
4. Zhu J, Cui L, Wang W, Hang XY, Xu AX, et al.. (2013) Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia. Fam Cancer.
5. De La Vega F, Hyland F, McLaughlin S, Ni J, Fu Y, et al.. (2009) Functional analysis of the genetic variation within the genomes of three HapMap individuals obtained by whole-genome, second-generation sequencing. (Data downloaded from http://www.sequenceontology.org/resources/10Gen.html).
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