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

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

doi:10.1007/s00125-021-05631-z

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

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

Research output: Contribution to journal › Article › Scientific › peer-review

Original language	English
Journal	Diabetologia
Volume	65
Issue number	4
Pages (from-to)	632-643
Number of pages	12
ISSN	0012-186X
DOIs	https://doi.org/10.1007/s00125-021-05631-z
Publication status	Published - Apr 2022
MoE publication type	A1 Journal article-refereed

Bibliographical note

Correction: Volume65, Issue5
Page: 912-912
DOI: 10.1007/s00125-022-05663-z
Published: MAY 2022
Early Access: MAR 2022

Fields of Science

Age at onset
Glucagon
HNF1A-MODY
Insulin deficiency
Lipolysis
Maturity-onset diabetes of the young (MODY)
MODY3
Monogenic diabetes
NEFA
Polygenic risk score for type 2 diabetes
HEPATIC NUCLEAR FACTOR-1-ALPHA
HOMEOSTASIS MODEL ASSESSMENT
INSULIN SENSITIVITY
CELL DYSFUNCTION
ALPHA-GENE
YOUNG MODY
C-PEPTIDE
ONSET
GLUCOSE
MUTATION
3111 Biomedicine

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10.1007/s00125-021-05631-z

Kettunen2022_Article_CorrectionToAMultigenerationalFinal published version, 127 KBLicence: CC BY
Kettunen2022_Article_AMultigenerationalStudyOnPhenoFinal published version, 787 KBLicence: CC BY

Cite this

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title = "A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY",

keywords = "Age at onset, Glucagon, HNF1A-MODY, Insulin deficiency, Lipolysis, Maturity-onset diabetes of the young (MODY), MODY3, Monogenic diabetes, NEFA, Polygenic risk score for type 2 diabetes, HEPATIC NUCLEAR FACTOR-1-ALPHA, HOMEOSTASIS MODEL ASSESSMENT, INSULIN SENSITIVITY, CELL DYSFUNCTION, ALPHA-GENE, YOUNG MODY, C-PEPTIDE, ONSET, GLUCOSE, MUTATION, 3111 Biomedicine",

author = "Kettunen, {Jarno L.T.} and Elina Rantala and Dwivedi, {Om P.} and Bo Isomaa and Leena Sarelin and Paula Kokko and Liisa Hakaste and Miettinen, {P{\"a}ivi J.} and Groop, {Leif C.} and Tiinamaija Tuomi",

note = "Correction: Volume65, Issue5 Page: 912-912 DOI: 10.1007/s00125-022-05663-z Published: MAY 2022 Early Access: MAR 2022",

year = "2022",

month = apr,

doi = "10.1007/s00125-021-05631-z",

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AU - Kettunen, Jarno L.T.

AU - Rantala, Elina

AU - Dwivedi, Om P.

AU - Isomaa, Bo

AU - Sarelin, Leena

AU - Kokko, Paula

AU - Hakaste, Liisa

AU - Miettinen, Päivi J.

AU - Groop, Leif C.

AU - Tuomi, Tiinamaija

N1 - Correction: Volume65, Issue5 Page: 912-912 DOI: 10.1007/s00125-022-05663-z Published: MAY 2022 Early Access: MAR 2022

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KW - Glucagon

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KW - Insulin deficiency

KW - Lipolysis

KW - Maturity-onset diabetes of the young (MODY)

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KW - Polygenic risk score for type 2 diabetes

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KW - HOMEOSTASIS MODEL ASSESSMENT

KW - INSULIN SENSITIVITY

KW - CELL DYSFUNCTION

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KW - YOUNG MODY

KW - C-PEPTIDE

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EP - 643

JO - Diabetologia

JF - Diabetologia

IS - 4

ER -

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

Bibliographical note

Fields of Science

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