Intrafamilial and Case-Control Association Analysis of D2S152 in Insulin-Dependent Diabetes

References

• Todd J. A., Aitman T. J., Cornall R. J., Ghosh S., Hall J. R. S., Hearne C. M., Knight A. M., Love J. M., McAleer M. A., Prins J. -B., Rodrigues N., Lathrop M., Pressey A., DcLarato N. H., Peterson L. B., Wicker L. S. Genetic analysis of autoimmune type I diabetes mellitus in mice. Nature 1991; 351: 542–546
   PubMed Web of Science ®Google Scholar
• Ghosh S., Palmer S. M., Rodrigues N. R., Cordell H. J., Hearne C. M., Cornall R. J., Prins J. B., McShanc P., Lathrop G. M., Peterson L. B., Wicker L. S., Todd J. A. Polygenic control of autoimmune diabetes in nonobese mice. Nature Genetics 1993; 4: 404–409
   PubMed Web of Science ®Google Scholar
• Davies J. L., Yoshihiko K., Bennett S., Copeman J. B., Cordell H. J., Pritchard L. E., Reed P. W., Gough S. C. L., Jenkins C., Palmer S. M., Balfour K. M., Rowe B. R., Farrall M., Barnett A. H., Bain S. C., Todd J. A. A genome-wide search for human type 1 diabetes susceptibility genes. Nature 1994; 371: 130–136
   PubMed Web of Science ®Google Scholar
• Hashimoto L., Habita C., Beressi J. P., Delepine M., Besse C., Cambon-Thompsen A., Deschamps I., Rotter J. I., Djoulah S., James M. R., Froguel P., Wcissenbach J., Lathrop G. M., Julier C. Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q. Nature 1994; 371: 161–164
   PubMed Web of Science ®Google Scholar
• Field L. L., Tobias R., Magnus T. A locus on chromosome 15q26 (1DDM3) produces susceptibility to insulin-dependent diabetes mellitus. Nature Genetics 1994; 8: 189–194
   PubMedGoogle Scholar
• Owerbach D., Gabbay K. H. The HOXD8 locus (2q31) is linked to type I diabetes: Interaction with chromosome 6 and 11 disease susceptibility genes. Diabetes 1995; 44: 132–136
   PubMedGoogle Scholar
• Copeman J. B., Cucca F., Hearne C. M., Cornall R. J., Reed P. W., Ronningen K. S., Undlien D. E., Nistico L., Buzzetti R., Tosi R., Pociot F., Ncrup J., Cornelis F., Barnett A. H., Bain S. C., Todd J. A. Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33. Nature Genetics 1995; 9: 80–85
   PubMedGoogle Scholar
• Luo D. F., Bui M. M., Muir A., Maclaren N. K., Thomson G., She J. X. Affected sibpair mapping of a novel susceptibility gene to insulin-dependent diabetes mellitus (IDDM8) on chromosome 6q25-q27. Am. J. Hum. Genet. 1995, (In Press)
   Google Scholar
• Risch N. Linkage strategies for genetically complex Traits. II. The power of affceted relative pairs. Am. J. Hum. Ganet. 1990; 46: 229–241
   PubMed Web of Science ®Google Scholar
• Julier C., Hyer R. N., Davies J., Merlin F., Soularue P., Briant L., Cathelineau G., Deschamps I., Rotter J. I., Froguel P., Boitard C., Bell J. I., Lathrop G. M. Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-depcndcnt diabetes susceptibility. Nature 1991; 354: 155–158
   PubMedGoogle Scholar
• Bain S. C., Prins J. B., Hearne C. M., Rodrigues N. R., Rowe B. R., Pritchard L. E., Ritchie R. J., Hall J. R. S., Undlien D. E., Ronningen K. S., Dunger D. B., Barnett A. H., Todd J. A. Insulin gene region-encoded susceptibility to type 1 diabetes is not restricted to HLA-DR4-positive individuals. Nature Genetics 1992; 2: 212–215
   PubMedGoogle Scholar
• Spielman R. S., McGinnis R. E., Ewens W. J. transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am. J. Hum. Genet. 1993; 52: 506–512
   PubMed Web of Science ®Google Scholar
• Nei M., Li W. -H. Linkage disequilibrium in subdivided populations. Genetics 1973; 75: 213–219
   PubMed Web of Science ®Google Scholar
• Franklin I. R., Feldman M. W. Two loci with alleles: linkage equilibrium and linkage disequilibrium can be simultaneously stable. Them. Popul. Biol. 1977; 12: 95–113
   Google Scholar
• Karlin S., Carmelli D. Numerical studies on two-loci selection models with general viabilities. Theor. Popul. Biol. 1975; 7: 399–421
   Google Scholar
• Thomson G. The effect of a selected locus on linked neutral loci. Genetics 1977; 85: 753–788
   PubMed Web of Science ®Google Scholar
• Rubinstein P., Walker M., Carpenter C., Carrier C., Krassner J., Falk C., Ginsberg F. Genetics of HLA association. The use of the haplotype relative risk (HRR) and the “Haplo-Delta” (Dh) estimates in juvenile diabetes from three racial groups. Hum. Immunol. 1981; 3: 384
   Google Scholar
• Field L. L., Fothergill-Payne C., Bertrams J., Baur M. P. HLA-DR effects in a large German IDDM data set. Genet. Epidemiol. 1986, Suppl 1
   Google Scholar
• Falk C. T., Rubinstein P. Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations. Ann. Hum. Genet. 1987; 51: 227–233
   PubMed Web of Science ®Google Scholar
• Bowcock A. M., Tomfohrde J., Weisenbach J., Bonne-Tamir B., Geoge-Hyslop P., Giagheddu M., Cavalli-Sforza L. L., Farrer L. A. Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites. Am. J. Hum. Genet. 1994; 54: 79–87
   Google Scholar
• Lerner T. J., Boustany R. M.N., MacCormack K., Gleitsman J., Schlumpf K., Breakefield X. O., Gusella J. F., Haines J. L. Linkage disequilibrium between the juvenile neuronal ceroid lopofuscinosis gene and marker loci on chromosome 16p12.1. Am. J. Hum. Genet. 1994; 54: 88–94
   Google Scholar
• She J. X., Bui M. M., Tian X. H., Muir A., Wakeland E. K., Zorovich B., Zhang L. P., Liu M. C., Thomson G., Maclaren N. K. Additive susceptibility to insulin-dependent diabetes conferred by HLA-DQB1 and insulin genes. Autoimmunity. 1994; 18: 195–203
   PubMed Web of Science ®Google Scholar