|
| 36598836 | Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. | Circ Genom Precis Med | 2023 |
| 36778260 | Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy. | medRxiv | 2023 |
| 37017090 | Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy. | Circ Genom Precis Med | 2023 |
| 36918541 | Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. | Nat Commun | 2023 |
| 34672391 | Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes. | Genetic Epidemiology | 2022 |
| 33402679 | Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 33558525 | Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 31584065 | A key role for the novel coronary artery disease gene JCAD in atherosclerosis via shear stress mechanotransduction. | Cardiovascular Research | 2020 |
| 31127295 | A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. | Hum Mol Genet | 2019 |
| 31775616 | Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers. | BMC Bioinformatics | 2019 |
| 31089183 | Genetic variation in CADM2 as a link between psychological traits and obesity. | Scientific Reports | 2019 |
| 29455858 | A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. | Am J Hum Genet | 2018 |
| 30354237 | Differential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk Variants. | Arteriosclerosis, Thrombosis, and Vascular Biology | 2018 |
| 30429575 | Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. | Nat Genet | 2018 |
| 29912962 | Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. | PLoS One | 2018 |
| 30048712 | Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion. | Journal of Molecular and Cellular Cardiology | 2018 |
| 30287978 | Neonatal Micro-RNA Profile Determines Endothelial Function in Offspring of Hypertensive Pregnancies. | Hypertension | 2018 |
| 30224653 | Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. | Nat Genet | 2018 |
| 29467471 | Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets. | Scientific Reports | 2018 |
| 29740026 | Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer's disease. | Scientific Reports | 2018 |
| 28209224 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. | J Am Coll Cardiol | 2017 |
| 28461624 | Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions. | Circulation | 2017 |
| 28459806 | Identifying systematic heterogeneity patterns in genetic association meta-analysis studies. | PLoS Genetics | 2017 |
| 28898252 | 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. | PLoS Med | 2017 |
| 28714975 | Association analyses based on false discovery rate implicate new loci for coronary artery disease. | Nat Genet | 2017 |
| 28970529 | A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11. | Scientific Reports | 2017 |
| 28739976 | Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. | Hypertension | 2017 |
| 29040868 | Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation. | Atherosclerosis | 2017 |
| 27731410 | No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis. | Sci Rep | 2016 |
| 26934567 | Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. | N Engl J Med | 2016 |
| 26821629 | Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study. | J Am Coll Cardiol | 2016 |
| 27355579 | Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. | PLoS Genet | 2016 |
| 26561523 | A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. | Hum Mol Genet | 2016 |
| 25979724 | Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis. | Int J Epidemiol | 2016 |
| 27618452 | The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. | Nat Genet | 2016 |
| 27876822 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. | Nat Commun | 2016 |
| 26105150 | Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF. | Blood | 2015 |
| 25673413 | Genetic studies of body mass index yield new insights for obesity biology. | Nature | 2015 |
| 25673412 | New genetic loci link adipose and insulin biology to body fat distribution. | Nature | 2015 |
| 25631608 | Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. | Nat Commun | 2015 |
| 25781951 | Analysis of the role of interleukin 6 receptor haplotypes in the regulation of circulating levels of inflammatory biomarkers and risk of coronary heart disease. | PLoS ONE | 2015 |
| 25487149 | Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. | Nature | 2015 |
| 25811787 | Modulation of genetic associations with serum urate levels by body-mass-index in humans. | PLoS One | 2015 |
| 26426971 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. | PLoS Genet | 2015 |
| 26343387 | A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. | Nat Genet | 2015 |
| 24954895 | Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. | Am J Hum Genet | 2014 |
| 25551457 | No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects. | PLoS One | 2014 |
| 25282103 | Defining the role of common variation in the genomic and biological architecture of adult human height. | Nat Genet | 2014 |
| 25390462 | Inactivating mutations in NPC1L1 and protection from coronary heart disease. | N Engl J Med | 2014 |
| 24336170 | Meta-analysis of gene-level tests for rare variant association. | Nat Genet | 2014 |