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References (29)
-
A. Collins, J. Frézal, J. Teague, N. Morton (1996)
A metric map of humans: 23,500 loci in 850 bands.Proceedings of the National Academy of Sciences of the United States of America, 93 25
-
L. Sollid, G. Markussen, J. Ek, H. Gjerde, F. Vartdal, E. Thorsby (1989)
Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimerThe Journal of Experimental Medicine, 169
-
S. Eichenbaum‐Voline, M. Babron, B. Prum, F. Clerget-Darpoux (1998)
Variation of the Maximum Likelihood Score.Annals of Human Genetics, 62
-
L. Sollid, E. Thorsby (1993)
HLA susceptibility genes in celiac disease: genetic mapping and role in pathogenesis.Gastroenterology, 105 3
-
L. Nisticò, R. Buzzetti, L. Pritchard, B. Auwera, C. Giovannini, E. Bosi, M. Larrad, M. Ríos, C. Chow, C. Cockram, K. Jacobs, C. Mijovic, S. Bain, A. Barnett, C. Vandewalle, F. Schuit, F. Gorus, Belgian Registry, R. Tosi, P. Pozzilli, J. Todd (1996)
The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry.Human molecular genetics, 5 7
-
J. Walker-Smith, S. Guandalini, J. Schmitz, D. Shmerling, J. Visakorpi (1990)
Revised criteria for diagnosis of coeliac disease -
A. Polvi, E. Arranz, M. Fernández‐Arquero, P. Collin, M. Mäki, Alberto Sanz, C. Calvo, C. Maluenda, P. Westman, E. Concha, J. Partanen (1998)
HLA-DQ2-negative celiac disease in Finland and Spain.Human immunology, 59 3
-
R. Houlston, Ian Tomlinson, D. Ford, S. Seal, A. Marossy, A. Ferguson, G. Holmes, K. Hosie, P. Howdle, D. Jewell, A. Godkin, G. Kerr, P. Kumar, R. Logan, A. Love, S. Johnston, M. Marsh, S. Mitton, D. O'Donoghue, A. Roberts, J. Walker-Smith, M. Stratton (1997)
Linkage analysis of candidate regions for coeliac disease genes.Human molecular genetics, 6 8
-
M. Marron, L. Raffel, H. Garchon, C. Jacob, M. Serrano-Ríos, M. Larrad, W. Teng, Yongsoo Park, Zhi Zhang, D. Goldstein, Yi Tao, G. Beaurain, J. Bach, Hong‐So Huang, D. Luo, A. Zeidler, J. Rotter, M. Yang, T. Modilevsky, N. Maclaren, J. She (1997)
Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups.Human molecular genetics, 6 8
-
F. Zhong, C. McCombs, J. Olson, R. Elston, F. Stevens, C. McCarthy, J. Michalski (1996)
An autosomal screen for genes that predispose to celiac disease in the western counties of IrelandNature Genetics, 14
-
A. Todorov, D. Rao (1997)
Trade‐off between false positives and false negatives in the linkage analysis of complex traitsGenetic Epidemiology, 14
-
(1997)
Behavior of the maximum likelihood score when many affected sibpairs are issued from a few untyped parents -
L. Kruglyak (1997)
The use of a genetic map of biallelic markers in linkage studiesNature Genetics, 17
-
L. Kruglyak, E. Lander (1995)
Complete multipoint sib-pair analysis of qualitative and quantitative traits.American journal of human genetics, 57 2
-
P. Holopainen, Mikko Arvas, P. Sistonen, K. Mustalahti, P. Collin, M. Mäki, J. Partanen (1999)
CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study.Tissue antigens, 53 5
-
Elizabeth Hauser, M. Boehnke, Sun-Wei Guo, N. Risch (1996)
Affected‐sib‐pair interval mapping and exclusion for complex genetic traits: Sampling considerationsGenetic Epidemiology, 13
-
Knut Lundin, Hege Gjertsen, Helge Scott, Ludvig Sollid, E. Thorsby (1994)
Function of DQ2 and DQ8 as HLA susceptibility molecules in celiac disease.Human immunology, 41 1
-
C. Dib, S. Fauré, C. Fizames, D. Samson, N. Drouot, A. Vignal, P. Millasseau, S. Marc, J. Kazan, E. Seboun, M. Lathrop, G. Gyapay, J. Morissette, J. Weissenbach (1996)
A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 380
-
I. Djilali-Saiah, J. Schmitz, E. Harfouch-Hammoud, J. Mougenot, J. Bach, S. Caillat-Zucman (1998)
CTLA-4 gene polymorphism is associated with predisposition to coeliac diseaseGut, 43
-
F. Ginot, I. Bordelais, S. Nguyen, G. Gyapay (1996)
Correction of some genotyping errors in automated fluorescent microsatellite analysis by enzymatic removal of one base overhangs.Nucleic acids research, 24 3
-
P. Concannon, Kathryn Gogolin-Ewens, David Hinds, B. Wapelhorst, V. Morrison, B. Stirling, M. Mitra, J. Farmer, Sloan Williams, N. Cox, G. Bell, N. Risch, R. Spielman (1998)
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitusNature Genetics, 19
-
D. Rao (1998)
CAT scans, PET scans, and genomic scansGenetic Epidemiology, 15
-
V. Mantovani, G. Corazza, M. Bragliani, M. Frisoni, M. Zaniboni, G. Gasbarrini (1993)
Asp57‐negative HLA DQβ chain and DQA1*0501 allele are essential for the onset of DQw2‐positive and DQw2‐negative coeliac diseaseClinical & Experimental Immunology, 91
-
F. Clot, C. Gianfrani, M. Babron, F. Bouguerrà, S. Southwood, M. Kagnoff, R. Troncone, S. Percopo, J. Eliaou, F. Clerget-Darpoux, A. Sette, L. Greco (1999)
HLA-DR53 molecules are associated with susceptibility to celiac disease and selectively bind gliadin-derived peptidesImmunogenetics, 49
-
Neil Risch (1990)
Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs.American journal of human genetics, 46 2
-
L. Wise, J. Lanchbury, Cathryn Lewis (1999)
Meta‐analysis of genome searchesAnnals of Human Genetics, 63
-
(1997)
CTLA 4 alanine - 17 confers genetic susceptibility to Graves ’ disease and to type 1 diabetes mellitus -
Luigi Greco, G. Corazza, M. Babron, F. Clot, M. Fulchignoni-Lataud, S. Percopo, Patrizia Zavattari, F. Bouguerrà, Colette Dib, Roberto Tosi, Riccardo Troncone, Alessandro Ventura, Wilma Mantavoni, Giuseppe Magazzù, Rosanna Gatti, Rosanna Lazzari, Annamaria Giunta, Francesco Perri, Giuseppe Iacono, Ettore Cardi, S. Virgiliis, Francesco Cataldo, G. Angelis, S. Musumeci, Roberto Ferrari, Fiorella Balli, M. Bardella, U. Volta, C. Catassi, Giuliano Torre, J. Eliaou, J. Serre, Françoise Clerget-Darpoux (1998)
Genome search in celiac disease.American journal of human genetics, 62 3
-
(1999)
The CTLA - 4 gene ( 2 q 33 ) is associated with coeliac disease in Scandinavia
- Publisher
- Wiley
- Copyright
- Copyright © 2001 Wiley Subscription Services
- ISSN
- 0003-4800
- eISSN
- 1469-1809
- DOI
- 10.1046/j.1469-1809.2001.6510035.x
- Publisher site
- See Article on Publisher Site
Abstract
Coeliac disease (CD) is a malabsorptive disorder of the small intestine resulting from ingestion of gluten. The HLA risk factors involved in CD are well known but do not explain the whole genetic susceptibility. Several regions of potential linkage on chromosomes 3q, 5q, 10q, 11q, 15q and 19q have already been reported in the literature. These six regions were analyzed with the Maximum Lod Score method on a dense set of markers. A new sample of 89 Italian sibpairs was available for study. There was no evidence for linkage for any of the regions tested, except for chromosome 5q. For this region, our data, as well as a sample of 93 sibpairs from our first genome screen (Greco et al. 1998), are compatible with the presence of a risk factor for CD with a moderate effect.
Journal
Annals of Human Genetics – Wiley
Published: Jan 1, 2001