Päivi J Miettinen
7PUBLICATIONS
35CO-AUTHORS
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Publications (7)
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|May 14, 2024
RFX6 haploinsufficiency predisposes to diabetes through impaired beta cell function.Hazem Ibrahim, Diego Balboa, Jonna Saarimäki-Vire
|Nov 23, 2022
Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register.Minna Harsunen, Jarno L T Kettunen, Taina Härkönen
|Dec 24, 2021
A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY.Jarno L T Kettunen, Elina Rantala, Om P Dwivedi
|Oct 08, 2021
Cytosolic phosphoenolpyruvate carboxykinase deficiency: Expanding the clinical phenotype and novel laboratory findings.Päivi Vieira, Irina I Nagy, Elisa Rahikkala
|Dec 07, 2018
Recombinant Human FSH Treatment Outcomes in Five Boys With Severe Congenital Hypogonadotropic Hypogonadism.Ella Kohva, Hanna Huopio, Matti Hero
|Oct 14, 2017
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance.Kashyap A Patel, Jarno Kettunen, Markku Laakso
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Frequent Collaborators
5 joint publications
Tiinamaija Tuomi
4 joint publications
Jarno L T Kettunen
4 joint publications
Om P Dwivedi
2 joint publications
Leif C Groop
2 joint publications
Liisa Hakaste
1 joint publications
Alena Stančáková
1 joint publications
Timo Otonkoski
1 joint publications
Ella Kohva
1 joint publications
Matti Hero
1 joint publications
Jorma Toppari
