DOI: 10.1038/ng1801. Evaluating coverage of genome-wide association studies

Evaluating coverage of genome-wide association studies

10.1038/ng1801

Crossref journal-article

Springer Science and Business Media LLC

Nature Genetics (297)

Bibliography

Barrett, J. C., & Cardon, L. R. (2006). Evaluating coverage of genome-wide association studies. Nature Genetics, 38(6), 659â662.

Authors 2

Jeffrey C Barrett (first)
Lon R Cardon (additional)

References 19 Referenced 323

Altshuler, D. et al. A haplotype map of the human genome. Nature 437, 1299–1320 (2005). (10.1038/nature04226) / Nature by D Altshuler (2005)
Hinds, D.A. et al. Whole-genome patterns of common DNA variation in three human populations. Science 307, 1072–1079 (2005). (10.1126/science.1105436) / Science by DA Hinds (2005)
Wang, W.Y., Barratt, B.J., Clayton, D.G. & Todd, J.A. Genome-wide association studies: theoretical and practical concerns. Nat. Rev. Genet. 6, 109–118 (2005). (10.1038/nrg1522) / Nat. Rev. Genet. by WY Wang (2005)
Hirschhorn, J.N. & Daly, M.J. Genome-wide association studies for common diseases and complex traits. Nat. Rev. Genet. 6, 95–108 (2005). (10.1038/nrg1521) / Nat. Rev. Genet. by JN Hirschhorn (2005)
Palmer, L.J. & Cardon, L.R. Shaking the tree: mapping complex disease genes with linkage disequilibrium. Lancet 366, 1223–1234 (2005). (10.1016/S0140-6736(05)67485-5) / Lancet by LJ Palmer (2005)
Botstein, D. & Risch, N. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nat. Genet. 33 (Suppl.), 228–237 (2003). (10.1038/ng1090) / Nat. Genet. by D Botstein (2003)
Neale, B.M. & Sham, P.C. The future of association studies: gene-based analysis and replication. Am. J. Hum. Genet. 75, 353–362 (2004). (10.1086/423901) / Am. J. Hum. Genet. by BM Neale (2004)
Clayton, D.G. et al. Population structure, differential bias and genomic control in a large-scale, case-control association study. Nat. Genet. 37, 1243–1246 (2005). (10.1038/ng1653) / Nat. Genet. by DG Clayton (2005)
de Bakker, P.I. et al. Efficiency and power in genetic association studies. Nat. Genet. 37, 1217–1223 (2005). (10.1038/ng1669) / Nat. Genet. by PI de Bakker (2005)
Dong, S. et al. Flexible use of high-density oligonucleotide arrays for single-nucleotide polymorphism discovery and validation. Genome Res. 11, 1418–1424 (2001). (10.1101/gr.171101) / Genome Res. by S Dong (2001)
Carlson, C.S. et al. Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. Am. J. Hum. Genet. 74, 106–120 (2004). (10.1086/381000) / Am. J. Hum. Genet. by CS Carlson (2004)
Ke, X. et al. A comparison of tagging methods and their tagging space. Hum. Mol. Genet. 14, 2757–2767 (2005). (10.1093/hmg/ddi309) / Hum. Mol. Genet. by X Ke (2005)
Pritchard, J.K. & Przeworski, M. Linkage disequilibrium in humans: models and data. Am. J. Hum. Genet. 69, 1–14 (2001). (10.1086/321275) / Am. J. Hum. Genet. by JK Pritchard (2001)
Jorgenson, E. & Witte, J.S. Coverage and power in genomewide association studies. Am. J. Hum. Genet. 78, 884–888 (2006). (10.1086/503751) / Am. J. Hum. Genet. by E Jorgenson (2006)
Daly, M. et al. Evaluating and improving power in whole-genome association studies using fixed marker sets. Nat. Genet. advance online publication 21 May 2006 (doi:10.1038/ng1816). (10.1038/ng1816)
Klein, R.J. et al. Complement factor H polymorphism in age-related macular degeneration. Science 308, 385–389 (2005). (10.1126/science.1109557) / Science by RJ Klein (2005)
Rieder, M.J. et al. Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose. N. Engl. J. Med. 352, 2285–2293 (2005). (10.1056/NEJMoa044503) / N. Engl. J. Med. by MJ Rieder (2005)
Hardenbol, P. et al. Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay. Genome Res. 15, 269–275 (2005). (10.1101/gr.3185605) / Genome Res. by P Hardenbol (2005)
Barrett, J.C., Fry, B., Maller, J. & Daly, M.J. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21, 263–265 (2005). (10.1093/bioinformatics/bth457) / Bioinformatics by JC Barrett (2005)

Dates

Type	When
Created	19 years, 3 months ago (May 21, 2006, 1:58 p.m.)
Deposited	2 years, 3 months ago (May 18, 2023, 6:11 p.m.)
Indexed	4 months, 2 weeks ago (April 11, 2025, 8:27 a.m.)
Issued	19 years, 3 months ago (May 21, 2006)
Published	19 years, 3 months ago (May 21, 2006)
Published Online	19 years, 3 months ago (May 21, 2006)
Published Print	19 years, 2 months ago (June 1, 2006)

Funders 0

None

BibTeX

@article{Barrett_2006, title={Evaluating coverage of genome-wide association studies}, volume={38}, ISSN={1546-1718}, url={http://dx.doi.org/10.1038/ng1801}, DOI={10.1038/ng1801}, number={6}, journal={Nature Genetics}, publisher={Springer Science and Business Media LLC}, author={Barrett, Jeffrey C and Cardon, Lon R}, year={2006}, month=may, pages={659–662} }

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