Search details
1.
A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY.
Diabetologia
; 65(4): 632-643, 2022 04.
Article
in English
| MEDLINE | ID: mdl-34951657
2.
Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin.
Hum Mol Genet
; 27(3): 546-558, 2018 02 01.
Article
in English
| MEDLINE | ID: mdl-29186428
3.
Correction to: A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY.
Diabetologia
; 65(5): 912, 2022 May.
Article
in English
| MEDLINE | ID: mdl-35238956
4.
Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin.
PLoS Genet
; 10(12): e1004854, 2014 Dec.
Article
in English
| MEDLINE | ID: mdl-25521368
5.
A central role for GRB10 in regulation of islet function in man.
PLoS Genet
; 10(4): e1004235, 2014 Apr.
Article
in English
| MEDLINE | ID: mdl-24699409
6.
[Update on Current Care Guideline. Diabetes]. / Diabetes.
Duodecim
; 132(9): 881-2, 2016.
Article
in Fi
| MEDLINE | ID: mdl-27319085
7.
Modelling of OGTT curve identifies 1 h plasma glucose level as a strong predictor of incident type 2 diabetes: results from two prospective cohorts.
Diabetologia
; 58(1): 87-97, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-25292440
8.
The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis.
PLoS Med
; 10(6): e1001474, 2013.
Article
in English
| MEDLINE | ID: mdl-23824655
9.
Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants.
Genet Epidemiol
; 35(4): 236-46, 2011 May.
Article
in English
| MEDLINE | ID: mdl-21308769
10.
Clinical risk factors, DNA variants, and the development of type 2 diabetes.
N Engl J Med
; 359(21): 2220-32, 2008 Nov 20.
Article
in English
| MEDLINE | ID: mdl-19020324
11.
A common variant near the PRL gene is associated with increased adiposity in males.
Mol Genet Metab
; 102(1): 78-81, 2011 Jan.
Article
in English
| MEDLINE | ID: mdl-20846890
12.
The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts.
PLoS Genet
; 3(4): e61, 2007 Apr 27.
Article
in English
| MEDLINE | ID: mdl-17465681
13.
Low-cost exercise interventions improve long-term cardiometabolic health independently of a family history of type 2 diabetes: a randomized parallel group trial.
BMJ Open Diabetes Res Care
; 8(2)2020 11.
Article
in English
| MEDLINE | ID: mdl-33219117
14.
The associations of daylight and melatonin receptor 1B gene rs10830963 variant with glycemic traits: the prospective PPP-Botnia study.
Ann Med
; 51(1): 58-67, 2019 02.
Article
in English
| MEDLINE | ID: mdl-30592226
15.
Melatonin receptor 1B gene rs10830963 polymorphism, depressive symptoms and glycaemic traits.
Ann Med
; 50(8): 704-712, 2018 12.
Article
in English
| MEDLINE | ID: mdl-30089436
16.
HAPT2D: high accuracy of prediction of T2D with a model combining basic and advanced data depending on availability.
Eur J Endocrinol
; 178(4): 331-341, 2018 Apr.
Article
in English
| MEDLINE | ID: mdl-29371336
17.
Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals.
Diabetes
; 55(10): 2890-5, 2006 Oct.
Article
in English
| MEDLINE | ID: mdl-17003358
18.
Improved prandial glucose control with lower risk of hypoglycemia with nateglinide than with glibenclamide in patients with maturity-onset diabetes of the young type 3.
Diabetes Care
; 29(2): 189-94, 2006 Feb.
Article
in English
| MEDLINE | ID: mdl-16443858
19.
Predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes.
Diabetes
; 54(1): 166-74, 2005 Jan.
Article
in English
| MEDLINE | ID: mdl-15616025
20.
Increased Melatonin Signaling Is a Risk Factor for Type 2 Diabetes.
Cell Metab
; 23(6): 1067-1077, 2016 06 14.
Article
in English
| MEDLINE | ID: mdl-27185156