A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY

por Kettunen, Jarno L. T., Rantala, Elina, Dwivedi, Om P., Isomaa, Bo, Sarelin, Leena, Kokko, Paula, Hakaste, Liisa, Miettinen, Päivi J., Groop, Leif C., Tuomi, Tiinamaija
Publicado 2021

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

por Harsunen, Minna, Kettunen, Jarno L. T., Härkönen, Taina, Dwivedi, Om, Lehtovirta, Mikko, Vähäsalo, Paula, Veijola, Riitta, Ilonen, Jorma, Miettinen, Päivi J., Knip, Mikael, Tuomi, Tiinamaija
Publicado 2022

Systematic Review of Treatment of Beta-Cell Monogenic Diabetes

por Naylor, Rochelle N., Patel, Kashyap A., Kettunen, Jarno L.T., Männistö, Jonna M.E., Støy, Julie, Beltrand, Jacques, Polak, Michel, Vilsbøll, Tina, Greeley, Siri A.W., Hattersley, Andrew T., Tuomi, Tiinamaija
Publicado 2023

Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance

por Patel, Kashyap A., Kettunen, Jarno, Laakso, Markku, Stančáková, Alena, Laver, Thomas W., Colclough, Kevin, Johnson, Matthew B., Abramowicz, Marc, Groop, Leif, Miettinen, Päivi J., Shepherd, Maggie H., Flanagan, Sarah E., Ellard, Sian, Inagaki, Nobuya, Hattersley, Andrew T., Tuomi, Tiinamaija, Cnop, Miriam, Weedon, Michael N.
Publicado 2017