A genome-wide family-based linkage study of coeliac disease

Annals of Human Genetics

Volumn 64, Issue 6, 2000, Pages 479-490

  King, A L ^a   Yiannakou, J Y ^b   Brett, P M ^c   Curtis, D ^d   Morris, M A ^e   Dearlove, A M ^f   Rhodes, M ^e   Rosen Bronson, S ^d   Mathew, C ^c   Ellis, H J ^b   Ciclitira, P J ^a,b  

^a KING'S COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c ST BARTHOLOMEW S HOSPITAL   (United Kingdom)

^d MRC UK HGMP Resource Centre   (United Kingdom)

^e GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

^f GUY S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOTOXIC T LYMPHOCYTE ANTIGEN 4; HLA ANTIGEN; MICROSATELLITE DNA; T LYMPHOCYTE RECEPTOR GAMMA CHAIN;

ARTICLE; CELIAC DISEASE; CHROMOSOME 10Q; CHROMOSOME 11P; CHROMOSOME 16Q; CHROMOSOME 19Q; CHROMOSOME 6Q; CHROMOSOME MAP; CLINICAL RESEARCH; CONTROLLED STUDY; DISEASE PREDISPOSITION; FEMALE; GENE LOCUS; GENETIC LINKAGE; GENOME; HLA SYSTEM; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MAJOR HISTOCOMPATIBILITY COMPLEX; MALE; MODEL; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SIBLING; T LYMPHOCYTE RECEPTOR GENE;

ANTIGENS, CD; ANTIGENS, DIFFERENTIATION; CELIAC DISEASE; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 16; DNA, INTERGENIC; FEMALE; GENES, T-CELL RECEPTOR GAMMA; GENOME, HUMAN; HUMANS; IMMUNOCONJUGATES; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; PEDIGREE;

EID: 0034472398     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480000008381     Document Type: Article

References (43)

1. A pedigree-based linkage study of coeliac disease: Failure to replicate previous positive findings
2. Common HLA alleles, rather than rare mutants, confer susceptibility to coeliac disease
3. Modulation of non-templated nucleotide addition by Taq DNA polymerase: Primer modifications that facilitate genotyping
4. Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations
5. Serological screening of coeliac disease: Choosing the optimal procedure according to prevalence values
6. Faster sequential genetic linkage computations
7. Model-free linkage analysis using likelihoods
8. Population stratifications can cause false positive linkage results if founders are untyped
9. Comparison of GENEHUNTER and MFLINK for analysis of COGA linkage data
10. A comprehensive genetic map of the human genome based on 5,264 microsatellites
11. Autoantibodies to tissue transglutaminase as predictors of celiac disease
12. CTLA-4 gene polymorphism is associated with predisposition to coeliac disease
13. Further evidence for the increased power of LOD scores compared with nonparametric methods
14. Coeliac disease: Previous family studies
15. From the Neolithic revolution to gluten intolerance: Benefits and problems associated with cultivation of wheat
16. Genome search in coeliac disease
17. A maximum likelihood test of the two locus model for coeliac disease
18. The power to detect linkage in complex disease by means of simple LOD-score analysis
19. The 1993-94 Genethon human genetic linkage map
20. CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study
21. Genetics of coeliac disease
22. Linkage analysis of candidate regions for coeliac disease genes
23. Gluten, major histocompatibility complex and the small intestine. A molecular and immunobiologic approach to the spectrum of gluten sensitivity ('coeliac sprue')
24. Coeliac Disease risk in the USA: High prevalence of anti-endomysium antibodies in healthy blood donors
25. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recording and fuzzy inheritance
26. PedCheck: A program for identification of genotype incompatibilities in linkage analysis
27. HLA-DQB1 and -DQA1 typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours
28. Genetic basis of gluten-sensitive enteropathy
29. Gluten sensitive enteropathy in Spain: Genetic and environmental factors
30. Linkage detection tests under heterogeneity
31. Model misspecification and multipoint linkage analysis
32. Late onset coeliac disease in the monozygotic twin of a coeliac child
33. Faster linkage analysis computations for pedigrees with loops or unused alleles
34. Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer
35. HLA susceptibility genes in coeliac disease: Genetic mapping and role in pathogenesis
36. Tissue transglutaminase autoantibody enzyme-linked immunosorbent assay in detecting celiac disease
37. HLA-class II alleles associated with coeliac disease in a Southern European population
38. Coeliac disease among Ashkenazi Jews from Israel: A study of the HLA-class II alleles and their association with disease susceptibility
39. Revised criteria for the diagnosis of coeliac disease
40. A second-generation linkage map of the human genome
41. Detection and characterisation of anti-endomysial antibody in coeliac disease using human umbilical cord
42. Family linkage study of the T-cell receptor genes in coeliac disease
43. An autosomal screen for genes that predispose to coeliac disease in the western counties of Ireland