Johanna Ojala
johanna.o.ojala@utu.fi |
Publications
- Finnish-Enriched SLC26A7 Variant in Congenital Hypothyroidism: Clinical Spectrum, Thyroid Histopathology, and Expression Analysis (2026)
- Thyroid
(A1 Refereed original research article in a scientific journal) - Altered skull and bone morphology in hyperthyroid knock-in mice with TSHR M453T and D633H mutations (2024)
- Endocrine Abstracts
(Other publication) - Decoding SLC26A7'S role in congenital hypothyroidism: delayed onset, very large goiters, and thyrotropin dependent basolateral expression (2024)
- Endocrine Abstracts
(Poster) - Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model (2024)
- JCI Insight
(A1 Refereed original research article in a scientific journal)
UTU Research Portal