Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease

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Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease

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scientific article published on 27 February 2015

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wetenschappelijk artikel

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наукова стаття, опублікована в лютому 2015

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Common genetic variants associ ...... 's disease and Graves' disease

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Common genetic variants associ ...... 's disease and Graves' disease

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Common genetic variants associ ...... 's disease and Graves' disease

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Common genetic variants associ ...... 's disease and Graves' disease

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Common genetic variants associ ...... 's disease and Graves' disease

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Common genetic variants associ ...... 's disease and Graves' disease

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Common genetic variants associ ...... 's disease and Graves' disease

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Laszlo Hegedüs

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Lynley C Ward

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Purdey Campbell

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Thomas H Brix

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P2860

Mechanisms of autoimmune thyroid diseases: from genetics to epigenetics

Discovery of common variants associated with low TSH levels and thyroid cancer risk

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

Whole-genome sequence-based analysis of thyroid function.

A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study.

Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III).

Laboratory medicine practice guidelines. Laboratory support for the diagnosis and monitoring of thyroid disease.

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.

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278-283

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scholarly article

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10.1111/CEN.12746

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P478

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2015-02-27T00:00:00Z

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25683181

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