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| 37017090 | Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy. | Circ Genom Precis Med | 2023 |
| 34672391 | Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes. | Genetic Epidemiology | 2022 |
| 32732227 | Data-driven modelling of mutational hotspots and in silico predictors in hypertrophic cardiomyopathy. | Journal of Medical Genetics | 2021 |
| 33437986 | Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. | Hum Mol Genet | 2021 |
| 33230300 | Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. | Nat Genet | 2020 |
| 32873833 | Heritability of haemodynamics in the ascending aorta. | Sci Rep | 2020 |
| 31537879 | Marked variation in heritability estimates of left ventricular mass depending on modality of measurement. | Sci Rep | 2019 |
| 31775616 | Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers. | BMC Bioinformatics | 2019 |
| 30531895 | Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield. | Genet Med | 2019 |
| 29273806 | Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. | Nat 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 |
| 30224653 | Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. | Nat Genet | 2018 |
| 29713486 | Plasma cytokines and risk of coronary heart disease in the PROCARDIS study. | Open Heart | 2018 |
| 29740026 | Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer's disease. | Scientific Reports | 2018 |
| 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 |
| 28209224 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. | J Am Coll Cardiol | 2017 |
| 28506971 | Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease. | Circ Res | 2017 |
| 28951623 | Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. | Nat Genet | 2017 |
| 28770004 | Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals. | BioData Min | 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 |
| 28714975 | Association analyses based on false discovery rate implicate new loci for coronary artery disease. | Nat Genet | 2017 |
| 28486474 | Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study. | PLoS Med | 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 |
| 27532257 | Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. | Genet Med | 2017 |
| 28267856 | Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease. | JAMA | 2017 |
| 28135244 | Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. | Nat Genet | 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 |
| 27013693 | Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits. | Circ Cardiovasc Genet | 2016 |
| 27050191 | Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia. | 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 |
| 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 |
| 28007139 | Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels. | J Am Coll Cardiol | 2016 |
| 27876822 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. | Nat Commun | 2016 |
| 24474739 | Mendelian randomization of blood lipids for coronary heart disease. | Eur Heart J | 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 |
| 25487149 | Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. | Nature | 2015 |
| 25853659 | Genetically determined height and coronary artery disease. | N Engl J Med | 2015 |
| 25934857 | Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants. | Neurology | 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 |
| 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 |