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

Association of Fc receptor-like 5 (FCRL5) with Graves’ disease is secondary to the effect of FCRL3

(2010) Matthew J. Simmonds et al.   CLINICAL ENDOCRINOLOGY

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

(2010) Paul R Newby et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetics of thyroid autoimmunity and the role of the TSHR

(2010) O.J. Brand et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

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

(2010)   NATURE

Uncovering the roles of rare variants in common disease through whole-genome sequencing

(2010) Elizabeth T. Cirulli et al.   NATURE REVIEWS GENETICS

Missing heritability and strategies for finding the underlying causes of complex disease

(2010) Evan E. Eichler et al.   NATURE REVIEWS GENETICS

Confirmation of Association of Chromosome 5q31–33 with United Kingdom Caucasian Graves' Disease

(2010) Matthew J. Simmonds et al.   THYROID

The Association of HLA with Autoimmune Thyroid Disease in Newfoundland. The Influence of HLA Homozygosity in Graves’ Disease

(2010) Nadir R. Farid et al.   TISSUE ANTIGENS

The HapMap and Genome-Wide Association Studies in Diagnosis and Therapy

(2009) Teri A. Manolio et al.   Annual Review of Medicine

Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence

(2009) Xun Chu et al.   BMC Medical Genetics

Polymorphisms in the interleukin 3 gene show strong association with susceptibility to Graves’ disease in Chinese population

(2009) X Chu et al.   GENES AND IMMUNITY

Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease

(2009) Huai-Dong Song et al.   HUMAN MOLECULAR GENETICS

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

(2009) O. J. Brand et al.   HUMAN MOLECULAR GENETICS

Transgenerational genetic effects on phenotypic variation and disease risk

(2009) J. H. Nadeau   HUMAN MOLECULAR GENETICS

DNA variations in human and medical genetics: 25 years of my experience

(2009) Yusuke Nakamura   JOURNAL OF HUMAN GENETICS

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

Parental origin of sequence variants associated with complex diseases

(2009) Augustine Kong et al.   NATURE

Origins and functional impact of copy number variation in the human genome

(2009) Donald F. Conrad et al.   NATURE

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

(2009) Jeffrey C Barrett et al.   NATURE GENETICS

Sequencing technologies — the next generation

(2009) Michael L. Metzker   NATURE REVIEWS GENETICS

Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes

(2009) S. Nejentsev et al.   SCIENCE

Autoimmune Disease Classification by Inverse Association with SNP Alleles

(2009) Marina Sirota et al.   PLoS Genetics

Genetic developments in autoimmune thyroid disease: an evolutionary process

(2008) Abigail A. Zeitlin et al.   CLINICAL ENDOCRINOLOGY

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

(2008) A A Zeitlin et al.   GENES AND IMMUNITY

Human QTL linkage mapping

(2008) Laura Almasy et al.   GENETICA

How to Interpret a Genome-wide Association Study

(2008) Thomas A. Pearson   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Type 2 diabetes: new genes, new understanding

(2008) Inga Prokopenko et al.   TRENDS IN GENETICS

Interleukin (IL)-23 Receptor Is a Major Susceptibility Gene for Graves’ Ophthalmopathy: The IL-23/T-helper 17 Axis Extends to Thyroid Autoimmunity

(2007) Amanda K. Huber et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM