Detalhe da pesquisa
1.
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.
Nature
; 498(7453): 232-5, 2013 Jun 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-23698362
2.
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.
PLoS Genet
; 10(2): e1004123, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24586183
3.
Caveolin-1 single-nucleotide polymorphism and arterial stiffness in non-dialysis chronic kidney disease.
Nephrol Dial Transplant
; 31(7): 1140-4, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26433014
4.
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.
Nat Genet
; 39(7): 857-64, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17554260
5.
Seven newly identified loci for autoimmune thyroid disease.
Hum Mol Genet
; 21(23): 5202-8, 2012 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22922229
6.
Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.
PLoS Genet
; 7(8): e1002216, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21829393
7.
Donor ABCB1 variant associates with increased risk for kidney allograft failure.
J Am Soc Nephrol
; 23(11): 1891-9, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23064017
8.
Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease.
Hum Mol Genet
; 18(9): 1704-13, 2009 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19244275
9.
Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3.
Clin Endocrinol (Oxf)
; 73(5): 654-60, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20626413
10.
Association of FcGRIIa with Graves' disease: a potential role for dysregulated autoantibody clearance in disease onset/progression.
Clin Endocrinol (Oxf)
; 73(1): 119-25, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20148910
11.
Association of caveolin-1 gene polymorphism with kidney transplant fibrosis and allograft failure.
JAMA
; 303(13): 1282-7, 2010 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20371787
12.
Genetic developments in autoimmune thyroid disease: an evolutionary process.
Clin Endocrinol (Oxf)
; 68(5): 671-82, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18081880
13.
The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency.
Respir Res
; 9: 52, 2008 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-18620570
14.
Phenotypic differences in alpha 1 antitrypsin-deficient sibling pairs may relate to genetic variation.
COPD
; 5(6): 353-9, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19353349
15.
Genetic predictors of long-term graft function in kidney and pancreas transplant patients.
Brief Funct Genomics
; 16(4): 228-237, 2017 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28110269
16.
Using Genetic Variation to Predict and Extend Long-term Kidney Transplant Function.
Transplantation
; 99(10): 2038-48, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26262502
17.
Endothelial nitric oxide synthase single nucleotide polymorphism and left ventricular function in early chronic kidney disease.
PLoS One
; 10(1): e0116160, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25612295
18.
Skewed X chromosome inactivation and female preponderance in autoimmune thyroid disease: an association study and meta-analysis.
J Clin Endocrinol Metab
; 99(1): E127-31, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24187400
19.
Impact of month of birth on the development of autoimmune thyroid disease in the United Kingdom and Europe.
J Clin Endocrinol Metab
; 99(8): E1459-65, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24840812
20.
GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.
Nat Rev Endocrinol
; 9(5): 277-87, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23529038