Lista de obras - Matt Simmonds - Dominio Público Uruguay

A nonsense mutation in exon 2 of the DNase I gene is not present in UK subjects with systemic lupus erythematosus and Graves' disease: Comment on the article by Rood et al

artículo científico publicado en 2002

A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect

scientific article published on 27 June 2007

A single nucleotide polymorphism in the CD40 gene on chromosome 20q (GD-2) provides no evidence for susceptibility to Graves' disease in UK Caucasians.

artículo científico publicado en 2004

A systematic approach to the assessment of known TNF-alpha polymorphisms in Graves' disease.

artículo científico publicado en 2004

Analysis of HLA class II genes in Hashimoto's thyroiditis reveals differences compared to Graves' disease

scientific article published on 01 May 2008

Association of Caveolin-1 Gene Polymorphism With Kidney Transplant Fibrosis and Allograft Failure

artículo científico publicado en 2010

Association of FcGRIIa with Graves' disease: a potential role for dysregulated autoantibody clearance in disease onset/progression

artículo científico publicado en 2010

Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta74

scientific article published on 01 October 2006

Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease.

artículo científico publicado en 2009

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

artículo científico publicado en 2007

Caveolin-1 single-nucleotide polymorphism and arterial stiffness in non-dialysis chronic kidney disease.

artículo científico publicado en 2015

Confirmation of association of chromosome 5q31-33 with United Kingdom Caucasian Graves' disease.

artículo científico publicado en 2010

Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease.

artículo científico publicado en 2005

Endothelial nitric oxide synthase single nucleotide polymorphism and left ventricular function in early chronic kidney disease

artículo científico publicado en 2015

Evaluation of five interleukin genes for association with end-stage renal disease in white Europeans

artículo científico publicado en 2010

Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study

artículo científico publicado en 2010

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

artículo científico

Genetic predictors of long-term graft function in kidney and pancreas transplant patients.

artículo científico publicado en 2017

Genetic variation in caveolin-1 correlates with long-term pancreas transplant function

artículo científico publicado en 2015

Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.

artículo científico publicado en 2011

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

artículo científico publicado en 2010

IL-13 and chromosome 5q31-q33: problems of identifying association within regions of linkage to Graves' disease

artículo científico publicado en 2005

Impact of month of birth on the development of autoimmune thyroid disease in the United Kingdom and Europe

artículo científico publicado en 2014

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

artículo científico publicado en 2013

Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves' ophthalmopathy.

artículo científico publicado en 2007

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

artículo científico publicado en 2011

Regression mapping of association between the human leukocyte antigen region and Graves disease

artículo científico publicado en 2004

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

artículo científico publicado en 2007

Seven newly identified loci for autoimmune thyroid disease

artículo científico publicado en 2012

Skewed X chromosome inactivation and female preponderance in autoimmune thyroid disease: an association study and meta-analysis.

artículo científico publicado en 2013

The CD40 Kozak SNP: a new susceptibility loci for Graves' disease?

scientific article published on 01 August 2005

The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency

artículo científico publicado en 2008

The search for the genetic contribution to autoimmune thyroid disease: the never ending story?

artículo científico publicado en 2011

Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.

artículo científico publicado en 2010

Unravelling the genetic complexity of autoimmune thyroid disease: HLA, CTLA-4 and beyond.

artículo científico publicado en 2004

Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: no association with Graves' disease.

artículo científico publicado en 2006

Using Genetic Variation to Predict and Extend Long-term Kidney Transplant Function.

artículo científico

Using PU.1 and Jun dimerization protein 2 transcription factor expression in myelodysplastic syndromes to predict treatment response and leukaemia transformation

scientific article published on 05 February 2019

Lista de obras de Matt Simmonds

A nonsense mutation in exon 2 of the DNase I gene is not present in UK subjects with systemic lupus erythematosus and Graves' disease: Comment on the article by Rood et al

A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect

A single nucleotide polymorphism in the CD40 gene on chromosome 20q (GD-2) provides no evidence for susceptibility to Graves' disease in UK Caucasians.

A systematic approach to the assessment of known TNF-alpha polymorphisms in Graves' disease.

Analysis of HLA class II genes in Hashimoto's thyroiditis reveals differences compared to Graves' disease

Association of Caveolin-1 Gene Polymorphism With Kidney Transplant Fibrosis and Allograft Failure

Association of FcGRIIa with Graves' disease: a potential role for dysregulated autoantibody clearance in disease onset/progression

Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta74

Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Caveolin-1 single-nucleotide polymorphism and arterial stiffness in non-dialysis chronic kidney disease.

Confirmation of association of chromosome 5q31-33 with United Kingdom Caucasian Graves' disease.

Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease.

Endothelial nitric oxide synthase single nucleotide polymorphism and left ventricular function in early chronic kidney disease

Evaluation of five interleukin genes for association with end-stage renal disease in white Europeans

Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study

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

Genetic predictors of long-term graft function in kidney and pancreas transplant patients.

Genetic variation in caveolin-1 correlates with long-term pancreas transplant function

Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

IL-13 and chromosome 5q31-q33: problems of identifying association within regions of linkage to Graves' disease

Impact of month of birth on the development of autoimmune thyroid disease in the United Kingdom and Europe

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves' ophthalmopathy.

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

Regression mapping of association between the human leukocyte antigen region and Graves disease

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

Seven newly identified loci for autoimmune thyroid disease

Skewed X chromosome inactivation and female preponderance in autoimmune thyroid disease: an association study and meta-analysis.

The CD40 Kozak SNP: a new susceptibility loci for Graves' disease?

The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency

The search for the genetic contribution to autoimmune thyroid disease: the never ending story?

Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.

Unravelling the genetic complexity of autoimmune thyroid disease: HLA, CTLA-4 and beyond.

Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: no association with Graves' disease.

Using Genetic Variation to Predict and Extend Long-term Kidney Transplant Function.

Using PU.1 and Jun dimerization protein 2 transcription factor expression in myelodysplastic syndromes to predict treatment response and leukaemia transformation