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- 2022
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Mark
Perinatal famine is associated with excess risk of proliferative retinopathy in patients with type 2 diabetes
(
- Contribution to journal › Article
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Mark
Neuronal Dysfunction Is Linked to the Famine-Associated Risk of Proliferative Retinopathy in Patients With Type 2 Diabetes
(
- Contribution to journal › Article
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
(
- Contribution to journal › Article
- 2021
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Mark
Reduced expression of OXPHOS and DNA damage genes is linked to protection from microvascular complications in long-term type 1 diabetes : the PROLONG study
(
- Contribution to journal › Article
- 2020
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Mark
A diabetes-associated genetic variant is associated with diastolic dysfunction and cardiovascular disease
(
- Contribution to journal › Article
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Mark
Increased Plasma Soluble Interleukin-2 Receptor Alpha Levels in Patients With Long-Term Type 1 Diabetes With Vascular Complications Associated With IL2RA and PTPN2 Gene Polymorphisms
(
- Contribution to journal › Article
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Mark
Liver nucleotide biosynthesis is linked to protection from vascular complications in individuals with long-term type 1 diabetes
(
- Contribution to journal › Article
- 2019
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Mark
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
(
- Contribution to journal › Article
- 2018
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Mark
Perinatal starvation increases risk for diabetic retinopathy in adulthood
2018)(
- Contribution to conference › Abstract
- 2017
-
Mark
Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
(
- Contribution to journal › Article
- 2016
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Mark
Glucose-Dependent Insulinotropic Polypeptide (GIP) Stimulates Osteopontin Expression in the Vasculature via Endothelin-1 and CREB.
(
- Contribution to journal › Article
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Mark
Atrial Natriuretic Peptide in the high normal range is associated with lower prevalence of insulin resistance.
(
- Contribution to journal › Article
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Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article
- 2015
-
Mark
Modelling of OGTT curve identifies 1 h plasma glucose level as a strong predictor of incident type 2 diabetes: results from two prospective cohorts
(
- Contribution to journal › Article
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Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
(
- Contribution to journal › Article
- 2014
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Mark
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
(
- Contribution to journal › Article
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Mark
A Central Role for GRB10 in Regulation of Islet Function in Man.
(
- Contribution to journal › Article
- 2012
-
Mark
Kartläggning av skyddsfaktorer vid typ 1-diabetes har börjat. Vissa patienter tycks skyddade mot sena komplikationer--flera studier pågår.
(
- Contribution to journal › Article
-
Mark
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
(
- Contribution to journal › Article
- 2011
-
Mark
Pleiotropic Effects of GIP on Islet Function Involve Osteopontin
(
- Contribution to journal › Article
-
Mark
FTO, Type 2 Diabetes, and Weight Gain Throughout Adult Life A Meta-Analysis of 41,504 Subjects From the Scandinavian HUNT, MDC, and MPP Studies
(
- Contribution to journal › Article
-
Mark
Power in the Phenotypic Extremes: A Simulation Study of Power in Discovery and Replication of Rare Variants
(
- Contribution to journal › Article
- 2010
-
Mark
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
(
- Contribution to journal › Article
-
Mark
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
(
- Contribution to journal › Article
- 2009
-
Mark
A variant in the KCNQ1 gene predicts future type 2 diabetes and mediates impaired insulin secretion.
(
- Contribution to journal › Article
-
Mark
Assessing the effect of interaction between an FTO variant (rs9939609) and physical activity on obesity in 15,925 Swedish and 2,511 Finnish adults.
(
- Contribution to journal › Article
- 2008
-
Mark
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus
(
- Contribution to journal › Article
-
Mark
Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations
(
- Contribution to journal › Article
-
Mark
Is there a unifying genetic factor predisposing to the metabolic syndrome?
2008) 44th EASD Annual Meeting of the European Association for the Study of Diabetes In Diabetologia 51(S1). p.32-33(
- Contribution to journal › Published meeting abstract
-
Mark
The search for putative unifying genetic factors for components of the metabolic syndrome.
(
- Contribution to journal › Article
-
Mark
Clinical risk factors, DNA variants, and the development of type 2 diabetes.
(
- Contribution to journal › Article
- 2007
-
Mark
Polymorphisms in the gene encoding the voltage-dependent Ca(2+) channel Ca (V)2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretion
(
- Contribution to journal › Article
-
Mark
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- Contribution to journal › Article
-
Mark
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
(
- Contribution to journal › Article
- 2006
-
Mark
Common variants in HNF-1 alpha and risk of type 2 diabetes.
(
- Contribution to journal › Article