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本文引用的文献
1
Genome-wide association studies for complex traits: consensus, uncertainty and challenges.
Nat Rev Genet. 2008 May;9(5):356-69. doi: 10.1038/nrg2344.
2
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Nat Genet. 2008 May;40(5):638-45. doi: 10.1038/ng.120. Epub 2008 Mar 30.
3
A second generation human haplotype map of over 3.1 million SNPs.
Nature. 2007 Oct 18;449(7164):851-61. doi: 10.1038/nature06258.
4
A new multipoint method for genome-wide association studies by imputation of genotypes.
Nat Genet. 2007 Jul;39(7):906-13. doi: 10.1038/ng2088. Epub 2007 Jun 17.
5
A common allele on chromosome 9 associated with coronary heart disease.
Science. 2007 Jun 8;316(5830):1488-91. doi: 10.1126/science.1142447. Epub 2007 May 3.
6
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
Science. 2007 Jun 8;316(5830):1491-3. doi: 10.1126/science.1142842. Epub 2007 May 3.
7
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
Science. 2007 Jun 1;316(5829):1331-6. doi: 10.1126/science.1142358. Epub 2007 Apr 26.
8
GeneCruiser: a web service for the annotation of microarray data.
Bioinformatics. 2005 Sep 15;21(18):3681-2. doi: 10.1093/bioinformatics/bti587. Epub 2005 Jul 19.
9
Haploview: analysis and visualization of LD and haplotype maps.
Bioinformatics. 2005 Jan 15;21(2):263-5. doi: 10.1093/bioinformatics/bth457. Epub 2004 Aug 5.
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