Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genome-wide association study of hyperthyroidism based on electronic medical record from Taiwan

27 Jul 2022

Abstract excerpt

Excess thyroid hormones have complex metabolic effects, particularly hyperthyroidism, and are associated with various cardiovascular risk factors. Previous candidate gene studies have indicated that genetic variants may contribute to this variable response. Electronic medical record (EMR) biobanks containing clinical and genomic data on large numbers of individuals have great potential to inform the disease...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic Associations and Epidemiology
Share to Genomics and Rare Diseases
Share to Thyroid Disorders and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35991636
DOI: 10.3389/fmed.2022.830621

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide association study of hyperthyroidism based on electronic medical record from TaiwanPMID 35991636Read ↗

Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid diseaseSemantic proximity Read ↗

Analysis of HLA Variants and Graves' Disease and Its Comorbidities Using a High Resolution Imputation System to Examine Electronic Medical Health Records.Semantic proximity Read ↗

Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease susceptibility and age-of-onsetSemantic proximity Read ↗

Association analysis of clinical phenotype and exon gene mutation locus in children with hyperthyroidismSemantic proximity Read ↗

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.Semantic proximity Read ↗

Association of Thyroid Function Genetic Predictors With Atrial FibrillationSemantic proximity Read ↗

Genome-wide association study and polygenic risk prediction of hypothyroidismSemantic proximity Read ↗

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.Semantic proximity Read ↗

Excess mortality in hyperthyroidism: the influence of preexisting comorbidity and genetic confounding: a danish nationwide register-based cohort study of twins and singletons.Semantic proximity Read ↗

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulationSemantic proximity Read ↗

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implicationsSemantic proximity Read ↗

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

⌁Select a neighboring publication to make it the new centre.