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- 2022
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Mark
Telomere length is not a main factor for the development of islet autoimmunity and type 1 diabetes in the TEDDY study
(
- Contribution to journal › Article
- 2019
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Mark
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
(
- Contribution to journal › Article
- 2018
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Mark
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
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- Contribution to journal › Article
- 2017
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Mark
The complex genetics of gait speed : Genome-wide meta-analysis approach
(
- Contribution to journal › Article
- 2016
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Mark
Association of Lipid-Related Genetic Variants with the Incidence of Atrial Fibrillation : The AFGen Consortium
(
- Contribution to journal › Article
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Mark
Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2
(
- Contribution to journal › Article
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Mark
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
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- Contribution to journal › Article
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Mark
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
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- Contribution to journal › Article
- 2015
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Mark
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease
(
- Contribution to journal › Article
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Mark
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis
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- Contribution to journal › Article
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Mark
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
(
- Contribution to journal › Letter
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Mark
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
(
- Contribution to journal › Article
- 2014
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Mark
Association of Low-Density Lipoprotein Cholesterol-Related Genetic Variants With Aortic Valve Calcium and Incident Aortic Stenosis.
(
- 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
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
(
- Contribution to journal › Article
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Mark
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.
(
- Contribution to journal › Article
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Mark
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
(
- Contribution to journal › Article
- 2013
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Mark
Genetic Associations with Valvular Calcification and Aortic Stenosis
(
- Contribution to journal › Article
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Mark
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
(
- Contribution to journal › Article
- 2012
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Mark
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
(
- Contribution to journal › Article
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Mark
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
(
- Contribution to journal › Article
-
Mark
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
(
- Contribution to journal › Article
- 2011
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Mark
A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease
(
- Contribution to journal › Article
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Mark
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
(
- Contribution to journal › Article
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Mark
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
(
- Contribution to journal › Article
- 2010
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Mark
Biological, clinical and population relevance of 95 loci for blood lipids
(
- Contribution to journal › Article