A. Brookes, HGBASE ??? a unified human SNP database, Trends in Genetics, vol.17, issue.4, p.229, 2001.
DOI : 10.1016/S0168-9525(01)02227-2

G. Johnson, L. Esposito, B. Barratt, A. Smith, J. Heward et al., Haplotype tagging for the identification of common disease genes, Nature Genetics, vol.29, issue.2, pp.233-237, 2001.
DOI : 10.1038/ng1001-233

D. Stram, C. Haiman, J. Hirschhorn, D. Altshuler, L. Kolonel et al., Choosing Haplotype-Tagging SNPS Based on Unphased Genotype Data Using a Preliminary Sample of Unrelated Subjects with an Example from the Multiethnic Cohort Study, Human Heredity, vol.55, issue.1, pp.27-36, 2003.
DOI : 10.1159/000071807

E. Cousin, E. Génin, S. Macé, R. S. Chansac, C. Del-zompo et al., Association Studies in Candidate Genes: Strategies to Select SNPs to Be Tested, Human Heredity, vol.56, issue.4, pp.151-159, 2003.
DOI : 10.1159/000073200

C. Carlson, M. Eberle, M. Rieder, Q. Yi, L. Kruglyak et al., Selecting a Maximally Informative Set of Single-Nucleotide Polymorphisms for Association Analyses Using Linkage Disequilibrium, The American Journal of Human Genetics, vol.74, issue.1, pp.106-120, 2004.
DOI : 10.1086/381000

B. Devlin and N. Risch, A Comparison of Linkage Disequilibrium Measures for Fine-Scale Mapping, Genomics, vol.29, issue.2, pp.311-322, 1995.
DOI : 10.1006/geno.1995.9003

G. Abecasis and W. Cookson, GOLD--Graphical Overview of Linkage Disequilibrium, Bioinformatics, vol.16, issue.2, pp.182-183, 2000.
DOI : 10.1093/bioinformatics/16.2.182

W. Zhang, A. Collins, and E. Morton, Does haplotype diversity predict power for association mapping of disease susceptibility?, Human Genetics, vol.115, issue.2, pp.157-164, 2004.
DOI : 10.1007/s00439-004-1122-x

P. Sebastiani, L. R. Weiss, S. Kunkel, L. Kohane, I. Ramoni et al., Minimal haplotype tagging, Proceedings of the National Academy of Sciences, vol.408, issue.6813, pp.9900-9905, 2003.
DOI : 10.1038/35047064
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC187880

Z. Meng, D. Zaykin, C. Xu, M. Wagner, and M. Ehm, Selection of Genetic Markers for Association Analyses, Using Linkage Disequilibrium and Haplotypes, The American Journal of Human Genetics, vol.73, issue.1, pp.115-130, 2003.
DOI : 10.1086/376561

B. Horne and N. Camp, Principal component analysis for selection of optimal SNP-sets that capture intragenic genetic variation, Genetic Epidemiology, vol.63, issue.1, pp.11-21, 2004.
DOI : 10.1002/gepi.10292

T. Rebbeck, M. Spitz, and X. Wu, Assessing the function of genetic variants in candidate gene association studies, Nature Reviews Genetics, vol.13, issue.8, pp.589-597, 2004.
DOI : 10.1159/000066695

D. Nyholt, A Simple Correction for Multiple Testing for Single-Nucleotide Polymorphisms in Linkage Disequilibrium with Each Other, The American Journal of Human Genetics, vol.74, issue.4, pp.765-769, 2004.
DOI : 10.1086/383251