Autoimmune Addison disease: pathophysiology and genetic complexity

Partial recovery of adrenal function in a patient with autoimmune Addison’s disease

(2014) L. C. C. J. Smans et al.   JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

The Soluble CTLA-4 Splice Variant Protects From Type 1 Diabetes and Potentiates Regulatory T-Cell Function

(2011) K. D. Gerold et al.   DIABETES

Multiple Loci in the HLA Complex Are Associated with Addison's Disease

(2011) Beate Skinningsrud et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

The autoimmune disease–associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness

(2011) Jinyi Zhang et al.   NATURE GENETICS

Genetic Variant of the Scavenger Receptor BI in Humans

(2011) Menno Vergeer et al.   NEW ENGLAND JOURNAL OF MEDICINE

A coding variant in NLRP1 is associated with autoimmune Addison's disease

(2010) Magdalena Żurawek et al.   HUMAN IMMUNOLOGY

Multiple common variants for celiac disease influencing immune gene expression

(2010) Patrick C A Dubois et al.   NATURE GENETICS

The role of AIRE in human autoimmune disease

(2010) Eitan M. Akirav et al.   Nature Reviews Endocrinology

Association of a dog leukocyte antigen class II haplotype with hypoadrenocorticism in Nova Scotia Duck Tolling Retrievers

(2010) A. M. Hughes et al.   TISSUE ANTIGENS

A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis

(2009) B. Skinningsrud et al.   ANNALS OF THE RHEUMATIC DISEASES

Familial association between type 1 diabetes and other autoimmune and related diseases

(2009) K. Hemminki et al.   DIABETOLOGIA

Soluble CTLA-4 receptor an immunological marker of Graves' disease and severity of ophthalmopathy is associated with CTLA-4 Jo31 and CT60 gene polymorphisms

(2009) Jacek Daroszewski et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15− Crohn's disease patients

(2009) Ana Márquez et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison’s Disease and Graves’ Disease Susceptibility

(2009) Anna L. Mitchell et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Homozygosity of the Polymorphism MICA5.1 Identifies Extreme Risk of Progression to Overt Adrenal Insufficiency among 21-Hydroxylase Antibody-Positive Patients with Type 1 Diabetes

(2009) Taylor M. Triolo et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Cutting Edge: The PTPN22 Allelic Variant Associated with Autoimmunity Impairs B Cell Signaling

(2009) A. F. Arechiga et al.   JOURNAL OF IMMUNOLOGY

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease

(2008) Matthew Roycroft et al.   CLINICAL ENDOCRINOLOGY

Association of an A/C single nucleotide polymorphism in programmed cell death-ligand 1 gene with Graves' disease in Japanese patients.

(2008) Mina Hayashi et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease

(2008) Beate Skinningsrud et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia

(2008) M Zoledziewska et al.   GENES AND IMMUNITY

A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes

(2008) N F Magitta et al.   GENES AND IMMUNITY

Polymorphisms inCLEC16AandCIITAat 16p13 Are Associated with Primary Adrenal Insufficiency

(2008) Beate Skinningsrud et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM