Jukka Kero

Genetic Rescue of a Subset of Thyroid Follicular Cells Restores Thyroid Function in Dyshormonogenic Duoxa−/− Mice (2025)

Thyroid

Djerbib, Sami; Grasberger, Helmut; Goossens, Steven; Haigh, Jody; Haenebalcke, Lieven; Pieters, Tim; Kero, Jukka; Miot, Françoise; De Deken, Xavier

(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )

β-Cell Function and Glucose Tolerance in Persons With Multiple Islet Autoantibodies Randomized to a Gluten-free Diet (2025)

Journal of the Endocrine Society

Maziarz, Marlena; Koskenniemi, Jaakko J; Martinez, Maria Månsson; Spiliopoulos, Lampros; Salami, Falastin; Toppari, Jorma; Kero, Jukka; Veijola, Riitta; Tossavainen, Päivi; Palmu, Sauli; Aronsson, Carin Andrén; Lundgren, Markus; Borg, Henrik; Katsarou, Anastasia; Elding, Larsson Helena; Knip, Mikael; Lou, Olivia; Dunne, Jessica L; Törn, Carina; Lernmark, Åke

(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )

Altered Glucagon Response to Oral Glucose in Individuals at Different Stages of Type 1 Diabetes Development (2025)

Journal of Clinical Endocrinology and Metabolism

Kontola, Helena; Crisóstomo, Luís; Löyttyniemi, Eliisa; Koskenniemi, Jaakko J.; Veijola, Riitta; Toppari, Jorma; Kero, Jukka

(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )

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))

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 )

Higher initial levothyroxine doses and very early treatment start may lead to better cognitive outcomes in children with congenital hypothyroidism (2024)

Acta Paediatrica

Danner, Emmi; Niuro, Laura; Lapinoja, Sonja; Huopio, Hanna; Viikari, Liisa A.; Kero, Jukka; Jääskeläinen, Jarmo; Niinikoski, Harri

(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )

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)

Identification of a stat3 mutation, P.THR716MET in two cases of very early-onset autoimmune hypothyroidism (2024)

Endocrine Abstracts

Ravi Rowmika; Nuutinen Anita; Makkonen Kristiina; Toppari Jorma; Kero Jukka

(Konferenssiposteri)

Comorbidity in Congenital Hypothyroidism—A Nationwide, Population-based Cohort Study (2023)

Journal of Clinical Endocrinology and Metabolism

Danner Emmi, Jääskeläinen Jarmo, Niuro Laura, Huopio Hanna, Niinikoski Harri, Viikari Liisa, Kero Jukka, Sund Reijo

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

Incidence of primary congenital hypothyroidism over 24 years in Finland (2023)

Pediatric Research

Danner Emmi, Niuro Laura, Huopio Hanna, Niinikoski Harri, Viikari Liisa, Kero Jukka, Jääskeläinen Jarmo

(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )

Jukka

Kero

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Genetic Rescue of a Subset of Thyroid Follicular Cells Restores Thyroid Function in Dyshormonogenic Duoxa−/− Mice (2025)

β-Cell Function and Glucose Tolerance in Persons With Multiple Islet Autoantibodies Randomized to a Gluten-free Diet (2025)

Altered Glucagon Response to Oral Glucose in Individuals at Different Stages of Type 1 Diabetes Development (2025)

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

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

Higher initial levothyroxine doses and very early treatment start may lead to better cognitive outcomes in children with congenital hypothyroidism (2024)

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

Identification of a stat3 mutation, P.THR716MET in two cases of very early-onset autoimmune hypothyroidism (2024)

Comorbidity in Congenital Hypothyroidism—A Nationwide, Population-based Cohort Study (2023)

Incidence of primary congenital hypothyroidism over 24 years in Finland (2023)