Genetics. Harvesting medical information from the hu... [Science. 2005] - PubMed

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Whole-genome patterns of common DNA variation in three human populations. [Science. 2005]
Whole-genome patterns of common DNA variation in three human populations.
Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR. Science. 2005 Feb 18; 307(5712):1072-9.
Linkage disequilibrium maps constructed with common SNPs are useful for first-pass disease association screens. [Genomics. 2004]
Linkage disequilibrium maps constructed with common SNPs are useful for first-pass disease association screens.
Taillon-Miller P, Saccone SF, Saccone NL, Duan S, Kloss EF, Lovins EG, Donaldson R, Phong A, Ha C, Flagstad L, et al. Genomics. 2004 Dec; 84(6):899-912.
The structure of haplotype blocks in the human genome. [Science. 2002]
The structure of haplotype blocks in the human genome.
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, et al. Science. 2002 Jun 21; 296(5576):2225-9. Epub 2002 May 23.
Review Finding genes underlying risk of complex disease by linkage disequilibrium mapping. [Curr Opin Genet Dev. 2003]
Review Finding genes underlying risk of complex disease by linkage disequilibrium mapping.
Clark AG. Curr Opin Genet Dev. 2003 Jun; 13(3):296-302.
Review Toward positional cloning with SNPs. [Curr Opin Mol Ther. 2002]
Review Toward positional cloning with SNPs.
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Genetic association tests: a method for the joint analysis of family and case-control data. [Hum Genomics. 2009]
Genetic association tests: a method for the joint analysis of family and case-control data.
Gray-McGuire C, Bochud M, Goodloe R, Elston RC. Hum Genomics. 2009 Oct; 4(1):2-20.
Strategy for mapping quantitative trait loci (QTL) by using human metapopulations. [Croat Med J. 2006]
Strategy for mapping quantitative trait loci (QTL) by using human metapopulations.
Rudan I, Biloglav Z, Carothers AD, Wright AF, Campbell H. Croat Med J. 2006 Aug; 47(4):532-42.
High-throughput discovery of rare human nucleotide polymorphisms by Ecotilling. [Nucleic Acids Res. 2006]
High-throughput discovery of rare human nucleotide polymorphisms by Ecotilling.
Till BJ, Zerr T, Bowers E, Greene EA, Comai L, Henikoff S. Nucleic Acids Res. 2006 Aug 7; 34(13):e99. Epub 2006 Aug 7.

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Genetics. Harvesting medical information from the human family tree.
Genetics. Harvesting medical information from the human family tree.
Science. 2005 Feb 18 ;307(5712):1052-3.

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