rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation

The rs9789446 G allele confers a sex-specific protective effect against CH, particularly in males. This supports its potential utility in genetic risk assessment and personalized screening strategies for early intervention.

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Publication Details

Journal
Frontiers in Genetics
Published
2025-12-17
DOI
https://doi.org/10.3389/fgene.2025.1721264
Primary Topic
Thyroid Disorders and Treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation

Frontiers in Genetics
Thyroid Disorders and Treatments
article

rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation

article en

Abstract

The rs9789446 G allele confers a sex-specific protective effect against CH, particularly in males. This supports its potential utility in genetic risk assessment and personalized screening strategies for early intervention.

Frontiers in GeneticsVol. 16
Qingdao University (CN), Weifang People's Hospital (CN), Affiliated Hospital of Qingdao University (CN)
Good health and well-being
Openalex Percentile: Top 32%
Thyroid Disorders and Treatments
DOIOpen Access PDFOpenAlex
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rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation · Frontiers in Genetics (2025) | TGRS Research Map | TGRS