Päivi J Miettinen

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 9

Top Topics

Recombinant Human

Top Venues

Journal of inherited metabolic disease

Nature communications

Journal of the Endocrine Society

This page only lists publications with an associated author ORCID identifier.

Publications

Hazem Ibrahim, Diego Balboa, Jonna Saarimäki-Vire, Hossam Montaser, Oleg Dyachok, Per-Eric Lund, Muhmmad Omar-Hmeadi, Jouni A Kvist, Om Prakash Dwivedi, Väinö Lithovius, Tom Barsby, Vikash Chandra, Solja Eurola, Jarkko Ustinov, Tiinamaija Tuomi, Päivi J Miettinen, Sebastian Barg, Anders Tengholm, Timo Otonkoski
RFX6 haploinsufficiency predisposes to diabetes through impaired beta cell function. Diabetologia 67 (8) (2024)
Hazem Ibrahim, Diego Balboa, Jonna Saarimäki-Vire, Hossam Montaser, Oleg Dyachok, Per-Eric Lund, Muhmmad Omar-Hmeadi, Jouni A Kvist, Om Prakash Dwivedi, Väinö Lithovius, Tom Barsby, Vikash Chandra, Solja Eurola, Jarkko Ustinov, Tiinamaija Tuomi, Päivi J Miettinen, Sebastian Barg, Anders Tengholm, Timo Otonkoski
RFX6 haploinsufficiency predisposes to diabetes through impaired beta cell function. Diabetologia 67 (8) (2024)
Hazem Ibrahim, Diego Balboa, Jonna Saarimäki-Vire, Hossam Montaser, Oleg Dyachok, Per-Eric Lund, Muhmmad Omar-Hmeadi, Jouni A Kvist, Om Prakash Dwivedi, Väinö Lithovius, Tom Barsby, Vikash Chandra, Solja Eurola, Jarkko Ustinov, Tiinamaija Tuomi, Päivi J Miettinen, Sebastian Barg, Anders Tengholm, Timo Otonkoski
RFX6 haploinsufficiency predisposes to diabetes through impaired beta cell function. Diabetologia (2024)
Hazem Ibrahim, Diego Balboa, Jonna Saarimäki-Vire, Hossam Montaser, Oleg Dyachok, Per-Eric Lund, Muhmmad Omar-Hmeadi, Jouni A Kvist, Om Prakash Dwivedi, Väinö Lithovius, Tom Barsby, Vikash Chandra, Solja Eurola, Jarkko Ustinov, Tiinamaija Tuomi, Päivi J Miettinen, Sebastian Barg, Anders Tengholm, Timo Otonkoski
RFX6 haploinsufficiency predisposes to diabetes through impaired beta cell function. Diabetologia 67 (8) (2024)
Minna Harsunen, Jarno L T Kettunen, Taina Härkönen, Om Prakash Dwivedi, Mikko Lehtovirta, Paula Vähäsalo, Riitta Veijola, Jorma Ilonen, Päivi J Miettinen, Olli H Laitinen, Tiinamaija Tuomi
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. Diabetologia (2022)
Jarno L T Kettunen, Elina Rantala, Om Prakash Dwivedi, Bo Isomaa, Leena Sarelin, Paula Kokko, Liisa Hakaste, Päivi J Miettinen, Leif C Groop, Tiinamaija Tuomi
A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY. Diabetologia 65 (4) (2021)
Päivi M Vieira, Irina I Nagy, Elisa Rahikkala, Marja-Leena Väisänen, Katariina Latva, Kari Kaunisto, Pekka Valmari, Riikka Keski-Filppula, Maria K Haanpää, Virpi Sidoroff, Päivi J Miettinen, Tuula Arkkola, Marja Ojaniemi, Matti Nuutinen, Johanna M Uusimaa, Päivi Myllynen
Cytosolic phosphoenolpyruvate carboxykinase deficiency: Expanding the clinical phenotype and novel laboratory findings. Journal of inherited metabolic disease (2021)
Ella Kohva, Hanna Huopio, Matti Hero, Päivi J Miettinen, Kirsi Vaaralahti, Virpi Sidoroff, Jorma Toppari, Taneli Raivio
Recombinant Human FSH Treatment Outcomes in Five Boys With Severe Congenital Hypogonadotropic Hypogonadism. Journal of the Endocrine Society 2 (12) (2018)
Kashyap A Patel, Jarno L T Kettunen, Markku Laakso, Alena Stančáková Yaluri, Thomas W Laver, Kevin Colclough, Matthew B Johnson, Marc Abramowicz, Leif Groop, Päivi J Miettinen, Maggie H Shepherd, Sarah E Flanagan, Sian Ellard, Nobuya Inagaki, Andrew T Hattersley, Tiinamaija Tuomi, Miriam Cnop, Michael N Weedon
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance. Nature communications 8 (1) (2017)