Literature DB >> 10762555

Evidence for a new Graves disease susceptibility locus at chromosome 18q21.

B Vaidya1, H Imrie, P Perros, E T Young, W F Kelly, D Carr, D M Large, A D Toft, P Kendall-Taylor, S H Pearce.   

Abstract

Graves disease (GD) is a common autoimmune thyroid disorder that is inherited as a complex multigenic trait. By using a single microsatellite marker at each locus, we screened the type 1 diabetes loci IDDM4, IDDM5, IDDM6, IDDM8, and IDDM10 and the fucosyltransferase-2 locus for linkage in sib pairs with GD. This showed a two-point nonparametric linkage (NPL) score of 1.57 (P=.06) at the IDDM6 marker D18S41, but NPL scores were <1.0 at the other five loci. Thus, the investigation of the IDDM6 locus was extended by genotyping 11 microsatellite markers spanning 48 cM across chromosome 18q12-q22 in 81 sib pairs affected with autoimmune thyroid disease (AITD). Multipoint analysis, designating all AITD sib pairs as affected, showed a peak NPL score of 3.46 (P=.0003), at the marker D18S487. Designation of only GD cases as affected (74 sib pairs) showed a peak NPL score of 3.09 (P=.001). Linkage to this region has been demonstrated in type 1 diabetes (IDDM6), rheumatoid arthritis, and systemic lupus erythematosus, which suggests that this locus may have a role in several forms of autoimmunity.

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Year:  2000        PMID: 10762555      PMCID: PMC1378028          DOI: 10.1086/302908

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  33 in total

1.  Parametric and nonparametric linkage analysis: a unified multipoint approach.

Authors:  L Kruglyak; M J Daly; M P Reeve-Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Assessing the role of HLA-linked and unlinked determinants of disease.

Authors:  N Risch
Journal:  Am J Hum Genet       Date:  1987-01       Impact factor: 11.025

3.  Increased prevalence of non-secretors in patients with Graves' disease: evidence for an infective aetiology?

Authors:  A Collier; A W Patrick; A D Toft; C C Blackwell; V James; D M Weir
Journal:  Br Med J (Clin Res Ed)       Date:  1988-04-23

4.  Secretor state of patients with insulin dependent or non-insulin-dependent diabetes mellitus.

Authors:  C C Blackwell; V S James; D M Weir; J D Gemmill; A W Patrick; A Collier; B F Clarke
Journal:  Br Med J (Clin Res Ed)       Date:  1987-10-24

5.  Complete multipoint sib-pair analysis of qualitative and quantitative traits.

Authors:  L Kruglyak; E S Lander
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

6.  Sequence and expression of a candidate for the human Secretor blood group alpha(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype.

Authors:  R J Kelly; S Rouquier; D Giorgi; G G Lennon; J B Lowe
Journal:  J Biol Chem       Date:  1995-03-03       Impact factor: 5.157

7.  Autoimmune thyroid disease in type I diabetic families.

Authors:  H Payami; S Joe; G Thomson
Journal:  Genet Epidemiol       Date:  1989       Impact factor: 2.135

8.  Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q.

Authors:  L Hashimoto; C Habita; J P Beressi; M Delepine; C Besse; A Cambon-Thomsen; I Deschamps; J I Rotter; S Djoulah; M R James
Journal:  Nature       Date:  1994-09-08       Impact factor: 49.962

9.  A genome-wide search for human type 1 diabetes susceptibility genes.

Authors:  J L Davies; Y Kawaguchi; S T Bennett; J B Copeman; H J Cordell; L E Pritchard; P W Reed; S C Gough; S C Jenkins; S M Palmer
Journal:  Nature       Date:  1994-09-08       Impact factor: 49.962

10.  Confirmation of three susceptibility genes to insulin-dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8.

Authors:  D F Luo; R Buzzetti; J I Rotter; N K Maclaren; L J Raffel; L Nisticò; C Giovannini; P Pozzilli; G Thomson; J X She
Journal:  Hum Mol Genet       Date:  1996-05       Impact factor: 6.150

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  7 in total

1.  Association study of autoimmune thyroid disease at 5q23-q33 in Japanese patients.

Authors:  Takashi Akamizu; Hitomi Hiratani; Satoshi Ikegami; Stephen S Rich; Donald W Bowden
Journal:  J Hum Genet       Date:  2003-04-09       Impact factor: 3.172

2.  Genome-wide meta-analysis for rheumatoid arthritis.

Authors:  Carol J Etzel; Wei V Chen; Neil Shepard; Damini Jawaheer; Francois Cornelis; Michael F Seldin; Peter K Gregersen; Christopher I Amos
Journal:  Hum Genet       Date:  2006-04-13       Impact factor: 4.132

Review 3.  GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.

Authors:  Matthew J Simmonds
Journal:  Nat Rev Endocrinol       Date:  2013-03-26       Impact factor: 43.330

4.  Molecular diagnosis in head and neck: what a surgical pathologist must know.

Authors:  Jennifer L Hunt
Journal:  Head Neck Pathol       Date:  2008-02-26

5.  An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family.

Authors:  T P Atkinson; A A Schäffer; B Grimbacher; H W Schroeder; C Woellner; C S Zerbe; J M Puck
Journal:  Am J Hum Genet       Date:  2001-08-21       Impact factor: 11.025

6.  Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families.

Authors:  Yaron Tomer; Yoshiyuki Ban; Erlinda Concepcion; Giuseppe Barbesino; Ronald Villanueva; David A Greenberg; Terry F Davies
Journal:  Am J Hum Genet       Date:  2003-09-12       Impact factor: 11.025

7.  A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.

Authors:  Shih-Jen Hwang; Qiong Yang; James B Meigs; Elizabeth N Pearce; Caroline S Fox
Journal:  BMC Med Genet       Date:  2007-09-19       Impact factor: 2.103

  7 in total

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