D. Maraganore, M. De-andrade, and T. Lesnick, High-Resolution Whole-Genome Association Study of Parkinson Disease, The American Journal of Human Genetics, vol.77, issue.5, pp.685-693, 2005.
DOI : 10.1086/496902

R. Klein, C. Zeiss, and E. Chew, Complement Factor H Polymorphism in Age-Related Macular Degeneration, Science, vol.308, issue.5720, pp.385-389, 2005.
DOI : 10.1126/science.1109557

A. Herbert, N. Gerry, and M. Mcqueen, A Common Genetic Variant Is Associated with Adult and Childhood Obesity, Science, vol.312, issue.5771, pp.279-283, 2006.
DOI : 10.1126/science.1124779

S. Lesage, H. Zouali, and J. Cezard, CARD15/NOD2 Mutational Analysis and Genotype-Phenotype Correlation in 612 Patients with Inflammatory Bowel Disease, The American Journal of Human Genetics, vol.70, issue.4, pp.845-857, 2002.
DOI : 10.1086/339432

S. Vermeire, G. Wild, and K. Kocher, CARD15 Genetic Variation in a Quebec Population: Prevalence, Genotype-Phenotype Relationship, and Haplotype Structure, The American Journal of Human Genetics, vol.71, issue.1, pp.74-83, 2002.
DOI : 10.1086/341124

J. Pritchard and N. Cox, The allelic architecture of human disease genes: common disease-common variant... or not?, Human Molecular Genetics, vol.11, issue.20, pp.2417-2423, 2002.
DOI : 10.1093/hmg/11.20.2417

J. Pritchard, Are Rare Variants Responsible for Susceptibility to Complex Diseases?, The American Journal of Human Genetics, vol.69, issue.1, pp.124-137, 2001.
DOI : 10.1086/321272

S. Mccarroll, T. Hadnott, and G. Perry, Common deletion polymorphisms in the human genome, Nature Genetics, vol.21, issue.1, pp.86-92, 2006.
DOI : 10.1038/ng1696

D. Hinds, A. Kloek, J. M. Chen, X. Frazer, and K. , Common deletions and SNPs are in linkage disequilibrium in the human genome, Nature Genetics, vol.13, issue.1, pp.82-85, 2006.
DOI : 10.1038/ng1695

K. Lohmueller, C. Pearce, M. Pike, E. Lander, and J. Hirschhorn, Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease, Nature Genetics, vol.33, issue.2, pp.177-182, 2003.
DOI : 10.1038/ng1071

T. Mackay, The genetic architecture of quantitative traits: lessons from Drosophila, Current Opinion in Genetics & Development, vol.14, issue.3, pp.253-257, 2004.
DOI : 10.1016/j.gde.2004.04.003

J. Terwilliger, F. Haghighi, T. Hiekkalinna, and H. Goring, A bias-ed assessment of the use of SNPs in human complex traits, Current Opinion in Genetics & Development, vol.12, issue.6, pp.726-734, 2002.
DOI : 10.1016/S0959-437X(02)00357-X

D. Reich, N. Patterson, D. Jager, and P. , A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility, Nature Genetics, vol.12, issue.10, pp.1113-1118, 2005.
DOI : 10.1086/426405

J. Todd, J. Bell, and H. Mcdevitt, HLA-DQ?? gene contributes to susceptibility and resistance to insulin-dependent diabetes mellitus, Nature, vol.329, issue.6140, pp.599-604, 1987.
DOI : 10.1038/329599a0

F. Clerget-darpoux, M. Babron, I. Deschamps, and J. Hors, Complementation and maternal effect in insulin-dependent diabetes, Am J Hum Genet, vol.49, pp.42-48, 1991.

L. Sollid and E. Thorsby, The primary association of celiac disease to a given HLA-DQ ??/?? heterodimer explains the divergent HLA-DR associations observed in various Caucasian populations, Tissue Antigens, vol.86, issue.3, pp.136-137, 1990.
DOI : 10.1111/j.1399-0039.1990.tb01816.x

L. Sollid and E. Thorsby, HLA susceptibility genes in celiac disease: Genetic mapping and role in pathogenesis, Gastroenterology, vol.105, issue.3, pp.910-922, 1993.
DOI : 10.1016/0016-5085(93)90912-V

P. Margaritte-jeannin, M. Babron, and M. Bourgey, HLA-DQ relative risks for coeliac disease in European populations: a study of the European Genetics Cluster on Coeliac Disease, Tissue Antigens, vol.14, issue.6, pp.562-567, 2004.
DOI : 10.1016/S0198-8859(02)00822-4

M. Lincoln, A. Montpetit, and M. Cader, A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis, Nature Genetics, vol.25, issue.10, pp.1108-1112, 2005.
DOI : 10.1002/gepi.10252