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- 2024
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A genomic mutational constraint map using variation in 76,156 human genomes
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- Contribution to journal › Article
- 2023
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Mark
Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
(
- Contribution to journal › Article
- 2022
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Mark
Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis : How to Correctly Identify MODY8 Cases
(
- 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
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Mark
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
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- Contribution to journal › Article
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Mark
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease
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- Contribution to journal › Article
- 2021
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Mark
Relationship between insulin sensitivity and gene expression in human skeletal muscle
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- Contribution to journal › Article
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Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health
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- Contribution to journal › Article
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Mark
Cohort profile : Epigenetics in Pregnancy (EPIPREG) - population-based sample of European and South Asian pregnant women with epigenome-wide DNA methylation (850k) in peripheral blood leukocytes
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- Contribution to journal › Article
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Mark
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
(
- Contribution to journal › Article
- 2020
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Mark
Blood-based epigenetic estimators of chronological age in human adults using DNA methylation data from the Illumina MethylationEPIC array
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- Contribution to journal › Article
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Mark
Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC
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- Contribution to journal › Article
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Mark
Hydroxysteroid 17-β dehydrogenase 13 variant increases phospholipids and protects against fibrosis in nonalcoholic fatty liver disease
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- Contribution to journal › Article
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Mark
The effect of LRRK2 loss-of-function variants in humans
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- Contribution to journal › Article
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Mark
MuscleAtlasExplorer : a web service for studying gene expression in human skeletal muscle
(
- Contribution to journal › Article
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Mark
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus
(
- Contribution to journal › Article
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Mark
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
(
- Contribution to journal › Article
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Mark
Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals
(
- Contribution to journal › Article
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Mark
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes
(
- Contribution to journal › Article
- 2019
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Mark
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
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- Contribution to journal › Article
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Mark
Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control
(
- Contribution to journal › Article
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Mark
Associations of autozygosity with a broad range of human phenotypes
(
- Contribution to journal › Article
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Mark
Loss of ZnT8 function protects against diabetes by enhanced insulin secretion
(
- Contribution to journal › Article
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Mark
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
(
- Contribution to journal › Article
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Mark
Roadmap for a precision-medicine initiative in the Nordic region
2019) In Nature Genetics(
- Contribution to journal › Debate/Note/Editorial
- 2018
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Mark
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland
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- Contribution to journal › Article
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Mark
Silencing of the FTO gene inhibits insulin secretion : An in vitro study using GRINCH cells
(
- Contribution to journal › Article
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Mark
Discovering human diabetes-risk gene function with genetics and physiological assays
(
- Contribution to journal › Article
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Mark
Genetic determinants of glucose levels in pregnancy : Genetic risk scores analysis and GWAS in the Norwegian STORK cohort
(
- Contribution to journal › Article
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Mark
A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes
(
- Contribution to journal › Article
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Mark
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
(
- Contribution to journal › Article
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Mark
Melatonin receptor 1B gene rs10830963 polymorphism, depressive symptoms and glycaemic traits
(
- Contribution to journal › Article
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Mark
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
(
- Contribution to journal › Article
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Mark
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
(
- Contribution to journal › Article
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Mark
Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin
(
- Contribution to journal › Article
- 2017
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Mark
LoFtool : a gene intolerance score based on loss-of-function variants in 60 706 individuals
(
- Contribution to journal › Article
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Mark
Exome-wide association study of plasma lipids in >300,000 individuals
(
- Contribution to journal › Article
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Mark
Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
(
- Contribution to journal › Article
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Mark
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
(
- Contribution to journal › Article
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Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
(
- Contribution to journal › Article
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Mark
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
(
- Contribution to journal › Article
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Mark
Human Pancreatic β Cell lncRNAs Control Cell-Specific Regulatory Networks
(
- Contribution to journal › Article
- 2016
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Mark
A Variant of GJD2, Encoding for Connexin 36, Alters the Function of Insulin Producing β-Cells.
(
- Contribution to journal › Article
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Mark
The (in)famous GWAS P-value threshold revisited and updated for low-frequency variants.
(
- Contribution to journal › Article
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Mark
A reference panel of 64,976 haplotypes for genotype imputation
(
- Contribution to journal › Article
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Mark
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
(
- Contribution to journal › Article
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Mark
Transcription factor 7-like 2 (TCF7L2)
2016) p.297-316(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape
(
- Contribution to journal › Article
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Mark
Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes
(
- Contribution to journal › Article
- 2015
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Mark
A novel atlas of gene expression in human skeletal muscle reveals molecular changes associated with aging.
(
- Contribution to journal › Article
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Mark
Identification of novel genes for glucose metabolism based upon expression pattern in human islets and effect on insulin secretion and glycemia.
(
- 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
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Mark
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
(
- Contribution to journal › Article
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Mark
Impact of age, BMI and HbA1c levels on the genome-wide DNA methylation and mRNA expression patterns in human adipose tissue and identification of epigenetic biomarkers in blood.
(
- 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
TCF7L2 is a master regulator of insulin production and processing.
(
- Contribution to journal › Article
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Mark
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
(
- Contribution to journal › Article
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Mark
A Novel Test for Recessive Contributions to Complex Diseases Implicates Bardet-Biedl Syndrome Gene BBS10 in Idiopathic Type 2 Diabetes and Obesity
(
- Contribution to journal › Article
- 2012
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Mark
Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time
(
- Contribution to journal › Article
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Mark
Survival of pancreatic beta cells is partly controlled by a TCF7L2-p53-p53INP1-dependent pathway.
(
- Contribution to journal › Article
- 2011
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Mark
Genetics of type 2 diabetes
(
- Contribution to journal › Scientific review
- 2010
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Mark
NordicDB: a Nordic pool and portal for genome-wide control data
(
- Contribution to journal › Article
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Mark
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes
(
- Contribution to journal › Article
- 2009
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Mark
Prioritizing genes for follow-up from genome wide association studies using information on gene expression in tissues relevant for type 2 diabetes mellitus
(
- Contribution to journal › Article
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Mark
Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs
(
- Contribution to journal › Article
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Mark
The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects
(
- Contribution to journal › Article
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Mark
Tissue-specific alternative splicing of TCF7L2
(
- Contribution to journal › Article
- 2008
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Mark
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture
(
- Contribution to journal › Article
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Mark
Strategies for Conditional Two-Locus Nonparametric Linkage Analysis.
(
- Contribution to journal › Article
- 2007
-
Mark
Associating mitochondrial DNA variation with complex traits - Reply to Elson et al.
(
- Contribution to journal › Letter
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Mark
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans
(
- Contribution to journal › Article
- 2006
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Mark
Comprehensive association testing of common mitochondrial DNA variation in metabolic disease
(
- Contribution to journal › Article
- 2005
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Mark
Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes.
(
- Contribution to journal › Article
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Mark
A male-specific quantitative trait locus on 1p21 controlling human stature
(
- Contribution to journal › Article
- 2004
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Mark
Association between a polymorphism in the carboxyl ester lipase gene and serum cholesterol profile
(
- Contribution to journal › Article
- 2003
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Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
(
- Contribution to journal › Article
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Mark
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.
(
- Contribution to journal › Article
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Mark
Polymorphisms of the HDL receptor gene associated with HDL cholesterol levels in diabetic kindred from three populations
(
- Contribution to journal › Article
- 2002
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Mark
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
(
- Contribution to journal › Article
- 2001
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Mark
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height
(
- Contribution to journal › Article
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Mark
SR-B1 variants associated with HDL cholesterol levels in three populations
(
- Contribution to journal › Article
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Mark
Linkage disequilibrium at PPARG and other genes assessed with dense sets of SNPs.
(
- Contribution to journal › Article