1. Aninye, Irene O, Matsumoto, Shunichi, Sidhaye, Aniket R, Wondisford, Fredric E. 2014. Circadian regulation of Tshb gene expression by Rev-Erbα (NR1D1) and nuclear corepressor 1 (NCOR1). In The Journal of biological chemistry, 289, 17070-7. doi:10.1074/jbc.M114.569723. https://pubmed.ncbi.nlm.nih.gov/24794873/
2. Huang, D W, Wang, J X, Liu, Q Y, Feng, T, Li, N. 2012. Analysis on DNA sequence of TSHB gene and its association with reproductive seasonality in goats. In Molecular biology reports, 40, 1893-904. doi:10.1007/s11033-012-2245-0. https://pubmed.ncbi.nlm.nih.gov/23076536/
3. Kaplan, Adam I, Luxford, Catherine, Clifton-Bligh, Roderick J. 2022. Novel TSHB variant (c.217A>C) causing severe central hypothyroidism and pituitary hyperplasia. In Endocrinology, diabetes & metabolism case reports, 2022, . doi:10.1530/EDM-22-0230. https://pubmed.ncbi.nlm.nih.gov/36001021/
4. Asirvatham, Adlyne Reena, Deva Reddy, Vaishnavi Reddy, Jagadeesh, Sujatha, Mahadevan, Shriraam. 2025. Central congenital hypothyroidism due to TSHB gene mutation: 25-year follow-up. In BMJ case reports, 18, . doi:10.1136/bcr-2024-263094. https://pubmed.ncbi.nlm.nih.gov/39875149/
5. Borges, Maria de Fátima, Domené, Horacio Mario, Scaglia, Paula Alejandra, Oliveira, Marília Matos, Marqui, Alessandra Bernadete Trovó de. 2019. A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING. In Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo, 37, 520-524. doi:10.1590/1984-0462/;2019;37;4;00017. https://pubmed.ncbi.nlm.nih.gov/31166470/
6. Shaki, David, Eskin-Schwartz, Marina, Hadar, Noam, Birk, Ohad S, Haim, Alon. 2022. TSHB R75G is a founder variant and prevalent cause of low or undetectable TSH in Indian Jews. In European thyroid journal, 11, . doi:10.1530/ETJ-21-0072. https://pubmed.ncbi.nlm.nih.gov/34981755/