Saturation of the 5q31-q33 candidate region for coeliac disease

Annals of Human Genetics

Volumn 67, Issue 3, 2003, Pages 265-268

  Percopo, Selvaggia ^a   Babron, M C ^b   Whalen, M ^c   De Virgiliis, S ^c   Coto, I ^a   Clerget Darpoux, F ^b   Landolfo, F ^a   Greco, L ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^b INSERM   (France)

^c UNIVERSITY OF CAGLIARI   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

HLA ANTIGEN;

ARTICLE; CELIAC DISEASE; CENTROMERE; CHROMOSOME 5Q; CHROMOSOME MARKER; CONTROLLED STUDY; FAMILY STUDY; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN CELL; ITALY; PRIORITY JOURNAL; RISK FACTOR; SIBLING; CHROMOSOME 5; GENETIC MARKER; GENETIC PREDISPOSITION; GENETICS;

CELIAC DISEASE; CHROMOSOMES, HUMAN, PAIR 5; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HUMANS;

EID: 1542360089     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1469-1809.2003.00026.x     Document Type: Article

References (16)

1. Cookson, W. O. & Moffatt, M. F. (2000) Genetics of asthma and allergic disease. Hum Mol Genet 9, 2359-2364.
2. Cox, N. J., Frigge M., Nicolae, D. L. et al. (1999) Loci on chromosome 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans. Nat Gen 21, 213-215
3. Greco, L., Corazza, G., Babron, M. C. et al. (1998) Genome search in Coeliac Disease. Am J Hum Genet 62, 669-675.
4. Greco, L., Babron, M-C., Corazza, G. et al. (2001) Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families. Ann Hum Genet 65, 35-41.
5. Holopainen, P., Mustalahti, K., Uimari, R et al. (2001) Candidate gene regions and genetic heterogeneity in gluten sensitivity. Gut 48, 696-701.
6. Hugot, J. P., Chamaillard, M., Zouali, H. et al. (2001) Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 411, 599-603.
7. Kruglyak, L., Daly, M. J., Reeve-Daly, M. P. & Lander, E. S. (1996) Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 58, 1347-1363.
8. Liu, J., Juo, S. H., Holopainen, P. et al. (2002) Genomewide Linkage Analysis of Celiac Disease in Finnish Families. Am J Hum Genet 70, 51-59.
9. Louka, A. S., Naluai, A. T., Asher, H. et al. (2002) The IL12B does not confer susceptibility to Coeliac Disease. Tissue Antigens 59, 70-72.
10. Marquet, S., Abel, L., Hillaire, D. & Dessein, A. (1999) Full results of the genome-wide scan which localises a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33. Eur J Hum Genet 7, 88-97.
11. Morahan, G., Huang, D., Ymer, S. I. et al. (2001) Linkage disequilibrium of a type 1 diabetes susceptibility locus with a regulatory IL12B allele. Nat Genet 27, 218-221.
12. Naluai, A. T., Nilsson, S., Gudjonsdottir, A. H. et al. (2001) Genome-wide Linkage Analysis of Scandinavian Affected Sib-pairs supports presence of susceptibility loci for Celiac Disease on chromosomes 5 and 11. Eur J Hum Genet 9, 938-944.
13. Ogura, Y., Bonen, D. K., Inohara, N. et al. (2001) A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 411, 603-6.
14. PE Applied Biosystems Amplf/STr Profiler plus™ PCR amplification kit user's manual. (1997) Forster City, CA: Perkin-Elmer Corporation.
15. Rioux, J. D., Daly, M. J., Silverberg, M. S. et al. (2001) Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nature Genetics 29, 223-229.
16. Sollid, L. M. (2000) Molecular basis of cehac disease. Annu Rev Immunol 18, 53-81.