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Contribution of Single Nucleotide Polymorphisms within FCRL3 and MAP3K7IP2 to the Pathogenesis of Graves’ Disease

The journal of clinical endocrinology and metabolism, 2006-03, Vol.91 (3), p.1056-1061

2006

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

Genes and immunity, 2008-06, Vol.9 (4), p.358-363

2008

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Linkage disequilibrium between the human leukocyte antigen class II region of the major histocompatibility complex and Graves' disease : Replication using a population case control and family-based study

The journal of clinical endocrinology and metabolism, 1998-10, Vol.83 (10), p.3394-3397

1998

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The development of Graves' disease and the CTLA-4 gene on chromosome 2q33

The journal of clinical endocrinology and metabolism, 1999-07, Vol.84 (7), p.2398-2401

1999

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Association of a Rare Thyroglobulin Gene Microsatellite Variant with Autoimmune Thyroid Disease

The journal of clinical endocrinology and metabolism, 2003-10, Vol.88 (10), p.5039-5042

2003

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Tag SNP screening of the PDCD1 gene for association with Graves' disease

Clinical endocrinology (Oxford), 2007-07, Vol.67 (1), p.125-128

2007

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Common Allelic Variants of Exons 10, 12, and 33 of the Thyroglobulin Gene Are Not Associated with Autoimmune Thyroid Disease in the United Kingdom

The journal of clinical endocrinology and metabolism, 2004-12, Vol.89 (12), p.6336-6339

2004

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Lack of association of the vitamin D receptor gene with Graves' disease in UK Caucasians

Clinical endocrinology (Oxford), 2004-05, Vol.60 (5), p.618-624

2004

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Mannose-binding lectin gene polymorphisms in a cohort study of ANCA-associated small vessel vasculitis

Rheumatology (Oxford, England), 2007-07, Vol.46 (7), p.1076-1078

2007

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

Clinical endocrinology (Oxford), 2007-11, Vol.67 (5), p.663-667

2007

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No association of an interleukin 4 gene promoter polymorphism with Graves' disease in the United Kingdom

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3861-3863

2001

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

Clinical endocrinology (Oxford), 2005-08, Vol.63 (2), p.232-233

2005

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A heterozygous deletion of the autoimmune regulator (AIRE1) gene, autoimmune thyroid disease, and type 1 diabetes : No evidence for association

The journal of clinical endocrinology and metabolism, 2000-03, Vol.85 (3), p.1320-1322

2000

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MHC class II region, CTLA4 gene, and ophthalmopathy in patients with Graves' disease

The Lancet (British edition), 2001-09, Vol.358 (9286), p.984-985

2001

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Molecular Cloning of Complex Chromosomal Translocation t(8;14;12)(q24.1;q32.3;q24.1) in a Burkitt Lymphoma Cell Line Defines a New Gene (BCL7A) With Homology to Caldesmon

Blood, 1996-04, Vol.87 (8), p.3124-3134

1996

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Evidence for a Type 1 diabetes-specific mechanism for the insulin gene-associated IDDM2 locus rather than a general influence on autoimmunity

Diabetic medicine, 2004-03, Vol.21 (3), p.267-270

2004

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No evidence for allelic association of a human CTLA-4 promoter polymorphism with autoimmune thyroid disease in either population-based case-control or family-based studies

Clinical endocrinology (Oxford), 1998-09, Vol.49 (3), p.331-334

1998

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

Clinical endocrinology (Oxford), 2006-09, Vol.65 (3), p.380-384

2006

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BCL2 Translocations in Leukemias of Mature B Cells

Blood, 1994-06, Vol.83 (12), p.3682-3688

1994

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

Clinical endocrinology (Oxford), 2005-12, Vol.63 (6), p.695-697

2005

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Association of the large multifunctional proteasome (LMP2) gene with Graves' disease is a result of linkage disequilibrium with the HLA haplotype DRB10304-DQB102-DQA10501

Clinical endocrinology (Oxford), 1999-07, Vol.51 (1), p.115-118

1999

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Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position β74

Clinical endocrinology (Oxford), 2006-10, Vol.65 (4), p.429-432

2006

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Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta 74

Clinical endocrinology (Oxford), 2006-10, Vol.65 (4), p.429-432

2006

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Lack of Association Between Polymorphism of the Thyrotropin Receptor Gene and Graves' Disease in United Kingdom and Hong Kong Chinese Patients: Case Control and Family-Based Studies

Thyroid (New York, N.Y.), 1998-09, Vol.8 (9), p.777-780

1998

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Concurrent activation of MYC and BCL2 in B cell non-Hodgkin lymphoma cell lines by translocation of both oncogenes to the same immunoglobulin heavy chain locus

Leukemia, 1996-07, Vol.10 (7), p.1198-1208

1996

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Contribution of Single Nucleotide Polymorphisms within FCRL3 and MAP3K7IP2 to the Pathogenesis of Graves’ Disease

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

Linkage disequilibrium between the human leukocyte antigen class II region of the major histocompatibility complex and Graves' disease : Replication using a population case control and family-based study

The development of Graves' disease and the CTLA-4 gene on chromosome 2q33

Association of a Rare Thyroglobulin Gene Microsatellite Variant with Autoimmune Thyroid Disease

Tag SNP screening of the PDCD1 gene for association with Graves' disease

Common Allelic Variants of Exons 10, 12, and 33 of the Thyroglobulin Gene Are Not Associated with Autoimmune Thyroid Disease in the United Kingdom

Lack of association of the vitamin D receptor gene with Graves' disease in UK Caucasians

Mannose-binding lectin gene polymorphisms in a cohort study of ANCA-associated small vessel vasculitis

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

No association of an interleukin 4 gene promoter polymorphism with Graves' disease in the United Kingdom

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

A heterozygous deletion of the autoimmune regulator (AIRE1) gene, autoimmune thyroid disease, and type 1 diabetes : No evidence for association

MHC class II region, CTLA4 gene, and ophthalmopathy in patients with Graves' disease

Molecular Cloning of Complex Chromosomal Translocation t(8;14;12)(q24.1;q32.3;q24.1) in a Burkitt Lymphoma Cell Line Defines a New Gene (BCL7A) With Homology to Caldesmon

Evidence for a Type 1 diabetes-specific mechanism for the insulin gene-associated IDDM2 locus rather than a general influence on autoimmunity

No evidence for allelic association of a human CTLA-4 promoter polymorphism with autoimmune thyroid disease in either population-based case-control or family-based studies

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

BCL2 Translocations in Leukemias of Mature B Cells

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

Association of the large multifunctional proteasome (LMP2) gene with Graves' disease is a result of linkage disequilibrium with the HLA haplotype DRB10304-DQB102-DQA10501

Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position β74

Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta 74

Lack of Association Between Polymorphism of the Thyrotropin Receptor Gene and Graves' Disease in United Kingdom and Hong Kong Chinese Patients: Case Control and Family-Based Studies

Concurrent activation of MYC and BCL2 in B cell non-Hodgkin lymphoma cell lines by translocation of both oncogenes to the same immunoglobulin heavy chain locus

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