-
1
-
-
33646806090
-
Concordance, disease progression, and heritability of coeliac disease in Italian twins
-
Nistico L, Fagnani C, Coto I, Percopo S, Cotichini R, Limongelli MG et al. Concordance, disease progression, and heritability of coeliac disease in Italian twins. Gut 2006; 55: 803-808.
-
(2006)
Gut
, vol.55
, pp. 803-808
-
-
Nistico, L.1
Fagnani, C.2
Coto, I.3
Percopo, S.4
Cotichini, R.5
Limongelli, M.G.6
-
2
-
-
0036715684
-
Coeliac disease: Dissecting a complex inflammatory disorder
-
Sollid LM. Coeliac disease: dissecting a complex inflammatory disorder. Nat Rev Immunol 2002; 2: 647-655.
-
(2002)
Nat Rev Immunol
, vol.2
, pp. 647-655
-
-
Sollid, L.M.1
-
3
-
-
0036109726
-
The first large population based twin study of coeliac disease
-
Greco L, Romino R, Coto I, Di CN, Percopo S, Maglio M et al. The first large population based twin study of coeliac disease. Gut 2002; 50: 624-628.
-
(2002)
Gut
, vol.50
, pp. 624-628
-
-
Greco, L.1
Romino, R.2
Coto, I.3
Di Cn Percopo, S.4
Maglio, M.5
-
4
-
-
58149333555
-
Autoimmune diseases: Insights from genome-wide association studies
-
Lettre G, Rioux JD. Autoimmune diseases: insights from genome-wide association studies. Hum Mol Genet 2008; 17: R116-R121.
-
(2008)
Hum Mol Genet
, vol.17
-
-
Lettre, G.1
Rioux, J.D.2
-
5
-
-
34347324029
-
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21
-
van Heel DA, Franke L, Hunt KA, Gwilliam R, Zhernakova A, Inouye M et al. A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21. Nat Genet 2007; 39: 827-829.
-
(2007)
Nat Genet
, vol.39
, pp. 827-829
-
-
Van Heel, D.A.1
Franke, L.2
Hunt, K.A.3
Gwilliam, R.4
Zhernakova, A.5
Inouye, M.6
-
6
-
-
36749054721
-
Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases
-
Zhernakova A, Alizadeh BZ, Bevova M, van Leeuwen MA, Coenen MJ, Franke B et al. Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases. Am J Hum Genet 2007; 81: 1284-1288.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 1284-1288
-
-
Zhernakova, A.1
Alizadeh, B.Z.2
Bevova, M.3
Van Leeuwen, M.A.4
Coenen, M.J.5
Franke, B.6
-
7
-
-
44849084957
-
Association study of IL2/IL21 and FcgRIIa: Significant association with the IL2/IL21 region in Scandinavian coeliac disease families
-
DOI 10.1038/gene.2008.27, PII GENE200827
-
Adamovic S, Amundsen SS, Lie BA, Gudjonsdottir AH, Ascher H, Ek J et al. Association study of IL2/IL21 and FcgRIIa: significant association with the IL2/IL21 region in Scandinavian coeliac disease families. Genes Immun 2008; 9: 364-367. (Pubitemid 351795051)
-
(2008)
Genes and Immunity
, vol.9
, Issue.4
, pp. 364-367
-
-
Adamovic, S.1
Amundsen, S.S.2
Lie, B.A.3
Gudjonsdottir, A.H.4
Ascher, H.5
Ek, J.6
Van Heel, D.A.7
Nilsson, S.8
Sollid, L.M.9
Torinsson Naluai, A.10
-
8
-
-
58549091109
-
Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease
-
Romanos J, Barisani D, Trynka G, Zhernakova A, Bardella MT, Wijmenga C. Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease. J Med Genet 2009; 46: 60-63.
-
(2009)
J Med Genet
, vol.46
, pp. 60-63
-
-
Romanos, J.1
Barisani, D.2
Trynka, G.3
Zhernakova, A.4
Bardella, M.T.5
Wijmenga, C.6
-
9
-
-
41349103493
-
Newly identified genetic risk variants for celiac disease related to the immune response
-
Hunt KA, Zhernakova A, Turner G, Heap GA, Franke L, Bruinenberg M et al. Newly identified genetic risk variants for celiac disease related to the immune response. Nat Genet 2008; 40: 395-402.
-
(2008)
Nat Genet
, vol.40
, pp. 395-402
-
-
Hunt, K.A.1
Zhernakova, A.2
Turner, G.3
Heap, G.A.4
Franke, L.5
Bruinenberg, M.6
-
10
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993; 52: 506-516.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
11
-
-
10844233469
-
The risk of celiac disease in 107 families with at least two affected siblings
-
Gudjonsdottir AH, Nilsson S, Ek J, Kristiansson B, Ascher H. The risk of celiac disease in 107 families with at least two affected siblings. J Pediatr Gastroenterol Nutr 2004; 38: 338-342.
-
(2004)
J Pediatr Gastroenterol Nutr
, vol.38
, pp. 338-342
-
-
Gudjonsdottir, A.H.1
Nilsson, S.2
Ek, J.3
Kristiansson, B.4
Ascher, H.5
-
12
-
-
0036702792
-
HLA in coeliac disease families: A novel test of risk modification by the 'other' haplotype when at least one DQA1*05-DQB1*02 haplotype is carried
-
Louka AS, Nilsson S, Olsson M, Talseth B, Lie BA, Ek J et al. HLA in coeliac disease families: a novel test of risk modification by the 'other' haplotype when at least one DQA1*05-DQB1*02 haplotype is carried. Tissue Antigens 2002; 60: 147-154.
-
(2002)
Tissue Antigens
, vol.60
, pp. 147-154
-
-
Louka, A.S.1
Nilsson, S.2
Olsson, M.3
Talseth, B.4
Lie, B.A.5
Ek, J.6
-
13
-
-
0025341150
-
Report of working group of European Society of Paediatric Gastroenterology and Nutrition: Revised criteria for diagnosis of coeliac disease
-
Walker-Smith J, Guandalini S, Schmitz J, Schmerling D, Visakorpi J. Report of working group of European Society of Paediatric Gastroenterology and Nutrition: revised criteria for diagnosis of coeliac disease. Arch Dis Child 1990; 65: 909-911.
-
(1990)
Arch Dis Child
, vol.65
, pp. 909-911
-
-
Walker-Smith, J.1
Guandalini, S.2
Schmitz, J.3
Schmerling, D.4
Visakorpi, J.5
-
14
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005; 21: 263-265.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
15
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B et al. The structure of haplotype blocks in the human genome. Science 2002; 296: 2225-2229.
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
-
16
-
-
16644373197
-
Haplotype structure and linkage disequilibrium in chemokine and chemokine receptor genes
-
Clark VJ, Dean M. Haplotype structure and linkage disequilibrium in chemokine and chemokine receptor genes. Hum Genomics 2004; 1: 255-273.
-
(2004)
Hum Genomics
, vol.1
, pp. 255-273
-
-
Clark, V.J.1
Dean, M.2
-
17
-
-
16644372641
-
Characterisation of SNP haplotype structure in chemokine and chemokine receptor genes using CEPH pedigrees and statistical estimation
-
Clark VJ, Dean M. Characterisation of SNP haplotype structure in chemokine and chemokine receptor genes using CEPH pedigrees and statistical estimation. Hum Genomics 2004; 1: 195-207.
-
(2004)
Hum Genomics
, vol.1
, pp. 195-207
-
-
Clark, V.J.1
Dean, M.2
-
18
-
-
33745162565
-
The 32-base pair deletion of the chemokine receptor 5 gene (CCR5-Delta32) is not associated with primary sclerosing cholangitis in 363 Scandinavian patients
-
Melum E, Karlsen TH, Broome U, Broome U, Thorsby E, Schrumpf E et al. The 32-base pair deletion of the chemokine receptor 5 gene (CCR5-Delta32) is not associated with primary sclerosing cholangitis in 363 Scandinavian patients. Tissue Antigens 2006; 68: 78-81.
-
(2006)
Tissue Antigens
, vol.68
, pp. 78-81
-
-
Melum, E.1
Karlsen, T.H.2
Broome, U.3
Broome, U.4
Thorsby, E.5
Schrumpf, E.6
-
19
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 1998; 63: 259-266.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
20
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
Dudbridge F. Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 2003; 25: 115-121.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 115-121
-
-
Dudbridge, F.1
-
21
-
-
0033358374
-
The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene
-
Lie BA, Todd JA, Pociot F, Nerup J, Akselsen HE, Joner G et al. The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene. Am J Hum Genet 1999; 64: 793-800.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 793-800
-
-
Lie, B.A.1
Todd, J.A.2
Pociot, F.3
Nerup, J.4
Akselsen, H.E.5
Joner, G.6
-
22
-
-
61849085397
-
Association study of the IL18RAP locus in three European populations with coeliac disease
-
Koskinen LL, Einarsdottir E, Dukes E, Heap GA, Dubois P, Korponay-Szabo IR et al. Association study of the IL18RAP locus in three European populations with coeliac disease. Hum Mol Genet 2009; 18: 1148-1155.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1148-1155
-
-
Koskinen, L.L.1
Einarsdottir, E.2
Dukes, E.3
Heap, G.A.4
Dubois, P.5
Korponay-Szabo, I.R.6
-
23
-
-
0030712312
-
Mechanism of transdominant inhibition of CCR5-mediated HIV-1 infection by ccr5delta32
-
Benkirane M, Jin DY, Chun RF, Koup RA, Jeang KT. Mechanism of transdominant inhibition of CCR5-mediated HIV-1 infection by ccr5delta32. J Biol Chem 1997; 272: 30603-30606.
-
(1997)
J Biol Chem
, vol.272
, pp. 30603-30606
-
-
Benkirane, M.1
Jin, D.Y.2
Chun, R.F.3
Koup, R.A.4
Jeang, K.T.5
-
24
-
-
33646152126
-
Negative association between the chemokine receptor CCR5-Delta32 polymorphism and rheumatoid arthritis: A meta-analysis
-
Prahalad S. Negative association between the chemokine receptor CCR5-Delta32 polymorphism and rheumatoid arthritis: a meta-analysis. Genes Immun 2006; 7: 264-268.
-
(2006)
Genes Immun
, vol.7
, pp. 264-268
-
-
Prahalad, S.1
-
25
-
-
34347373514
-
Lack of association between the chemokine receptor 5 polymorphism CCR5delta32 in rheumatoid arthritis and juvenile idiopathic arthritis
-
Lindner E, Nordang GB, Melum E, Flato B, Selvaag AM, Thorsby E et al. Lack of association between the chemokine receptor 5 polymorphism CCR5delta32 in rheumatoid arthritis and juvenile idiopathic arthritis. BMC Med Genet 2007; 8: 33-38.
-
(2007)
BMC Med Genet
, vol.8
, pp. 33-38
-
-
Lindner, E.1
Nordang, G.B.2
Melum, E.3
Flato, B.4
Selvaag, A.M.5
Thorsby, E.6
-
26
-
-
20044377204
-
The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility
-
Gonzalez E, Kulkarni H, Bolivar H, Mangano A, Sanchez R, Catano G et al. The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility. Science, 2005; 307:1434-1440.
-
(2005)
Science
, vol.307
, pp. 1434-1440
-
-
Gonzalez, E.1
Kulkarni, H.2
Bolivar, H.3
Mangano, A.4
Sanchez, R.5
Catano, G.6
-
27
-
-
47949087731
-
CCL3L1 gene-containing segmental duplications and polymorphisms in CCR5 affect risk of systemic lupus erythaematosus
-
Mamtani M, Rovin B, Brey R, Camargo JF, Kulkarni H, Herrera M et al. CCL3L1 gene-containing segmental duplications and polymorphisms in CCR5 affect risk of systemic lupus erythaematosus. Ann Rheum Dis 2008; 67: 1076-1083.
-
(2008)
Ann Rheum Dis
, vol.67
, pp. 1076-1083
-
-
Mamtani, M.1
Rovin, B.2
Brey, R.3
Camargo, J.F.4
Kulkarni, H.5
Herrera, M.6
-
28
-
-
58149091678
-
Shared and distinct genetic variants in type 1 diabetes and celiac disease
-
Smyth DJ, Plagnol V, Walker NM, Cooper JD, Downes K, Yang JH et al. Shared and distinct genetic variants in type 1 diabetes and celiac disease. N Engl J Med 2008; 359: 2767-2777.
-
(2008)
N Engl J Med
, vol.359
, pp. 2767-2777
-
-
Smyth, D.J.1
Plagnol, V.2
Walker, N.M.3
Cooper, J.D.4
Downes, K.5
Yang, J.H.6
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