NDLI: Guilt beyond a reasonable doubt

Content Provider	Semantic Scholar
Author	Altshuler, David Daly, Mark J.
Copyright Year	2007
Abstract	Genome-wide association studies, exemplified by the Wellcome Trust Case Control Consortium and follow-up studies, have identified dozens of common variants robustly associated with common diseases, providing new clues about genetic architecture in humans. Finding all such loci, and fully defining genotype-phenotype correlation, will be a key to translating initial clues into pathophysiological understanding and clinical prediction.
Starting Page	813
Ending Page	815
Page Count	3
File Format	PDF HTM / HTML
DOI	10.1038/ng0707-813
Alternate Webpage(s)	http://biosun01.biostat.jhsph.edu/~iruczins/teaching/misc/gwas/papers/altshuler2007.pdf
Alternate Webpage(s)	http://www.biostat.jhsph.edu/~iruczins/teaching/misc/gwas/papers/altshuler2007.pdf
Alternate Webpage(s)	https://www.vitagenes.com/media/uploads/papers/ConjuringSNPs.pdf
PubMed reference number	17597768
Alternate Webpage(s)	https://doi.org/10.1038/ng0707-813
Journal	Medline
Volume Number	39
Journal	Nature Genetics
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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Guilt beyond a reasonable doubt