Johanna Ojala

Finnish-Enriched SLC26A7 Variant in Congenital Hypothyroidism: Clinical Spectrum, Thyroid Histopathology, and Expression Analysis (2026)

Thyroid

Niuro, Laura; Ojala, Johanna; Ravi, Rowmika; Melnyk, Vladyslav; Linnossuo, Veli; Palmu, Sofia; Jännäri, Meeri; Tyystjärvi, Sofia; Löf, Christoffer; Patyra, Konrad; Makkonen, Kristiina; Jääskeläinen, Jarmo; Danner, Emmi; Huopio, Hanna; Niinikoski, Harri; Viikari, Liisa; Kero, Andreina; Miettinen, Päivi; Schoenmakers, Nadia; FinnGen, FinnGen; Reeve, Mary Pat; Kero, Jukka

(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )

Altered skull and bone morphology in hyperthyroid knock-in mice with TSHR M453T and D633H mutations (2024)

Endocrine Abstracts

Makkonen Kristiina; Määttä Jorma; Ivaska Kaisa; Patyra Konrad; Melnyk Vladyslav; Linnossuo Veli; Ojala Johanna; Ravi Rowmika; Jaschke Holger; Undeutsch Julian; Kero Jukka

(O2 Muu julkaisu )

Decoding SLC26A7'S role in congenital hypothyroidism: delayed onset, very large goiters, and thyrotropin dependent basolateral expression (2024)

Endocrine Abstracts

Ojala Johanna; Niuro Laura; Ravi Rowmika; Melnyk Vladyslav; Linnossuo Veli; Makkonen Kristiina; Jääskelainen Jarmo; Danner Emmi; Huopio Hanna; Niinikoski Harri; Viikari Liisa; Miettinen Paivi; Schoenmakers Nadia; Pat Reeve Mary; Kero Jukka

(Konferenssiposteri)

Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model (2024)

JCI Insight

Makkonen Kristiina, Jännäri Meeri, Crisostomo Luis, Kuusi Matilda, Patyra Konrad, Melnyk Vladyslav, Linnossuo Veli, Ojala Johanna, Ravi Rowmika, Löf Christoffer, Makela Juho-Antti, Miettinen Paivi, Laakso Saila, Ojaniemi Marja, Jaaskelainen Jarmo, Laakso Markku, Bossowski Filip, Sawicka Beata, Stozek Karolina, Bossowski Artur, Kleinau Gunnar, Scheerer Patrick; FinnGen, Reeve Mary Pat, Kero Jukka

(Vertaisarvioitu alkuperäisartikkeli tai data-artikkeli tieteellisessä aikakauslehdessä (A1))

Johanna

Ojala

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Finnish-Enriched SLC26A7 Variant in Congenital Hypothyroidism: Clinical Spectrum, Thyroid Histopathology, and Expression Analysis (2026)

Altered skull and bone morphology in hyperthyroid knock-in mice with TSHR M453T and D633H mutations (2024)

Decoding SLC26A7'S role in congenital hypothyroidism: delayed onset, very large goiters, and thyrotropin dependent basolateral expression (2024)

Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model (2024)