Adam S. Butterworth
Reproducibility track record
1
assessed papers
93/100
mean reproducibility
1
reproduced (C1–C2)
0
flagged
724
total citations
flag rate:
0%
(0/1)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 0
last author: 0
Topics
Funders
—
Frequent co-authors
Anette Kalnapenkis 1Tõnu Esko 1Elise J. Needham 1Mari Nelis 1Barbara Thorand 1Leonid Padyukov 1Michael Roden 1Dirk S. Paul 1Mikael Landén 1Ulf Gyllensten 1
Institutions
University of Cambridge 1University of South Australia 1South Australian Health and Medical Research Institute 1Uppsala University 1University of Edinburgh 1Karolinska Institutet 1
Geography (author institutions)
GB 1AU 1SE 1EE 1DE 1HR 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (1)
Complete publication record (428)
Request a reproduction →1 assessed by us (1 reproduced) · 427 not yet assessed — every PubMed paper on record, linked below.
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The proteomic profile of leisure time physical activity across two decades: implications for future cardiovascular risk and mortality ↗European Journal of Preventive Cardiology · 2026 · PMID 41505439not yet assessed
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Genetic Association of Circulating Proteins and Gene Transcripts With Spontaneous Coronary Artery Dissection ↗Circulation Genomic and Precision Medicine · 2026 · PMID 41608794not yet assessed
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Glaucoma in the UK Biobank ↗Ophthalmology · 2026 · PMID 42309491not yet assessed
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Multicohort assessment of plasma metabolomic measurements across the atherosclerosis continuum ↗medRxiv · 2026not yet assessed
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not yet assessed
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Predicted Effector Gene Aggregation, Standards and Unified Schema (PEGASUS): A Community Framework for Effector Gene Reporting ↗bioRxiv (Cold Spring Harbor Laboratory) · 2026 · PMID 42367912not yet assessed
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not yet assessed
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A proteome-wide association study of cardiovascular diseases in 640,000 participants of multiple ancestries ↗medRxiv · 2026 · PMID 42620066not yet assessed
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Liver fat accumulation contributes to discordant genetic risk between coronary artery disease and type 2 diabetes ↗medRxiv · 2026not yet assessed
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The contribution of genetic determinants of blood gene expression and splicing to molecular phenotypes and health outcomes ↗Nature Genetics · 2025 · PMID 40038547not yet assessed
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Performance of deep-learning-based approaches to improve polygenic scores ↗Nature Communications · 2025 · PMID 40456720not yet assessed
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Proteins Involved in Endothelial Function and Inflammation Are Implicated in Cerebral Small Vessel Disease ↗Stroke · 2025 · PMID 39818967not yet assessed
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Large-scale characterisation of the nasal microbiome redefines Staphylococcus aureus colonisation status ↗Nature Communications · 2025 · PMID 41330943not yet assessed
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Combined clinical, metabolomic, and polygenic scores for cardiovascular risk prediction ↗European Heart Journal · 2025 · PMID 41392353not yet assessed
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Robust Metabolomic Age Prediction Based on a Wide Selection of Metabolites ↗The Journals of Gerontology Series A · 2025 · PMID 39821408not yet assessed
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Cohort profile: the BangladEsh Longitudinal Investigation of Emerging Vascular and nonvascular Events (BELIEVE) cohort study ↗BMJ Open · 2025 · PMID 39843382not yet assessed
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Cross-species studies implicate the melanocortin 3 receptor more strongly in the control of pubertal development than energy balance ↗Molecular Metabolism · 2025 · PMID 41386534not yet assessed
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Improved genetic discovery and fine-mapping resolution through multivariate latent factor analysis of high-dimensional traits ↗Cell Genomics · 2025 · PMID 40220762not yet assessed
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UK Longitudinal Linkage Collaboration (UK LLC): The National Trusted Research Environment for Longitudinal Research ↗International Journal for Population Data Science · 2025 · PMID 40129687not yet assessed
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The International Health Cohorts Consortium (IHCC) advances population health research and genomic discovery ↗Communications Medicine · 2025 · PMID 40841586not yet assessed
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Reassessing the association between age at menarche and cardiovascular disease: observational and Mendelian randomization analyses ↗European Journal of Preventive Cardiology · 2025 · PMID 40099743not yet assessed
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Higher Circulating Testosterone Linked to Higher CAD Risk in Men: Mendelian Randomization and Survival Analyses ↗The Journal of Clinical Endocrinology & Metabolism · 2025 · PMID 41131989not yet assessed
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Leveraging large-scale biobanks for therapeutic target discovery ↗Human Genetics and Genomics Advances · 2025 · PMID 41376171not yet assessed
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Polygenic Risk Scores for Preeclampsia Prediction Beyond Gold‐Standard Clinical Models in Multiethnic Populations ↗Journal of the American Heart Association · 2025 · PMID 41378510not yet assessed
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CARRIAGE study - a prospective cohort study of determinants of Staphylococcus aureus nasal colonisation in healthy adults in England. ↗Wellcome Open Research · 2025not yet assessed
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not yet assessed
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The nasal microbiome redefines Staphylococcus aureus colonisation ↗Research Square · 2025not yet assessed
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The genetic determinants of plasma protein variance across ancestries and effects on cardiometabolic disease risk ↗medRxiv · 2025not yet assessed
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Metabolic reaction fluxes as amplifiers and buffers of risk alleles for coronary artery disease ↗Molecular Systems Biology · 2025 · PMID 40175777not yet assessed
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Genetic susceptibility to adverse arsenic-related cardiometabolic outcomes: a systematic review ↗Reviews on Environmental Health · 2025 · PMID 40566704not yet assessed
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Immune Cell-Based Transcriptomic Mendelian Randomization and Colocalization Study on Type 1 Diabetes ↗medRxiv · 2025not yet assessed
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Genetic Landscape of the ACE2 Coronavirus Receptor ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2025not yet assessed
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Protocol for genetic discovery and fine-mapping of multivariate latent factors from high-dimensional traits ↗STAR Protocols · 2025 · PMID 41241937not yet assessed
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Towards defining endotype-specific mechanisms of sub-clinical atherosclerosis to advance precision medicine for cardiovascular disease ↗Cardiovascular Research · 2025 · PMID 41264490not yet assessed
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Immune cell-based transcriptomic Mendelian randomization and colocalization study on type 1 diabetes ↗BMC Medicine · 2025 · PMID 41299435not yet assessed
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Immune cell-based transcriptomic Mendelian randomization and colocalization study on type 1 diabetes. ↗Apollo (University of Cambridge) · 2025not yet assessed
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Immune cell-based transcriptomic Mendelian randomization and colocalization study on type 1 diabetes ↗Figshare · 2025not yet assessed
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Additional file 1 of Immune cell-based transcriptomic Mendelian randomization and colocalization study on type 1 diabetes ↗Figshare · 2025not yet assessed
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Immune cell-based transcriptomic Mendelian randomization and colocalization study on type 1 diabetes ↗Figshare · 2025not yet assessed
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Additional file 1 of Immune cell-based transcriptomic Mendelian randomization and colocalization study on type 1 diabetes ↗Figshare · 2025not yet assessed
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Large-scale characterisation of the nasal microbiome redefines Staphylococcus aureus colonisation status.Apollo (University of Cambridge) · 2025not yet assessed
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Higher Circulating Testosterone Linked to Higher CAD Risk in Men: Mendelian Randomization and Survival Analyses.Apollo (University of Cambridge) · 2025not yet assessed
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Genetic drivers of heterogeneity in type 2 diabetes pathophysiology ↗Nature · 2024 · PMID 38374256not yet assessed
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Genome-wide characterization of circulating metabolic biomarkers ↗Nature · 2024 · PMID 38448586not yet assessed
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Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction ↗Nature Genetics · 2024 · PMID 38839884not yet assessed
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Genetic Associations of Circulating Cardiovascular Proteins With Gestational Hypertension and Preeclampsia ↗JAMA Cardiology · 2024 · PMID 38170504not yet assessed
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Association of circulating fatty acids with cardiovascular disease risk: analysis of individual-level data in three large prospective cohorts and updated meta-analysis ↗European Journal of Preventive Cardiology · 2024 · PMID 39365172not yet assessed
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Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers ↗Nature Communications · 2024 · PMID 38684708not yet assessed
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Dietary intake of plant- and animal-derived protein and incident cardiovascular diseases: the pan-European EPIC-CVD case–cohort study ↗American Journal of Clinical Nutrition · 2024 · PMID 38479550not yet assessed
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Associations between genetically predicted plasma protein levels and Alzheimer’s disease risk: a study using genetic prediction models ↗Alzheimer s Research & Therapy · 2024 · PMID 38212844not yet assessed
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Markers of imminent myocardial infarction ↗Nature Cardiovascular Research · 2024 · PMID 39196201not yet assessed
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The genetic landscape of neuro-related proteins in human plasma ↗Nature Human Behaviour · 2024 · PMID 39210026not yet assessed
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Proteome- and Transcriptome-Wide Genetic Analysis Identifies Biological Pathways and Candidate Drug Targets for Preeclampsia ↗Circulation Genomic and Precision Medicine · 2024 · PMID 39119725not yet assessed
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Novel loci and biomedical consequences of iron homoeostasis variation ↗Communications Biology · 2024 · PMID 39643614not yet assessed
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Proteome-wide association study and functional validation identify novel protein markers for pancreatic ductal adenocarcinoma ↗GigaScience · 2024 · PMID 38608280not yet assessed
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Misexpression of inactive genes in whole blood is associated with nearby rare structural variants ↗The American Journal of Human Genetics · 2024 · PMID 39053458not yet assessed
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Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure ↗Kidney International Reports · 2024 · PMID 38899223not yet assessed
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Polygenic Prediction of Recurrent Events After Early-Onset Myocardial Infarction ↗Circulation Genomic and Precision Medicine · 2024 · PMID 39611259not yet assessed
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Conventional and regionally distinctive risk factors for first-onset myocardial infarction: the Bangladesh Risk of Acute Vascular Events (BRAVE) case–control study ↗The Lancet Regional Health - Southeast Asia · 2024 · PMID 39811539not yet assessed
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Cardiovascular risk prediction using metabolomic biomarkers and polygenic risk scores: a cohort study and modelling analyses ↗European Heart Journal · 2024not yet assessed
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The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleeding ↗Blood Advances · 2024 · PMID 39365993not yet assessed
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Integrated clinical risk prediction of type 2 diabetes with a multifactorial polygenic risk score ↗medRxiv · 2024 · PMID 39228710not yet assessed
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Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries ↗Nature Genetics · 2024 · PMID 38641645not yet assessed
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Associations of 2,922 genetically predicted plasma protein levels with mental illness and response to treatment ↗Research Square · 2024not yet assessed
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Transcriptome- and proteome-wide Mendelian randomization to prioritize therapeutic targets for coronary heart disease ↗medRxiv · 2024not yet assessed
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Improved genetic discovery and fine-mapping resolution through multivariate latent factor analysis of high-dimensional traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2024not yet assessed
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A lipidomic dataset for epidemiological studies of acute myocardial infarction ↗Data in Brief · 2024 · PMID 39411341not yet assessed
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not yet assessed
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Abstract 6153: Proteome-wide association study and functional validation identify novel protein markers for pancreatic ductal adenocarcinoma ↗Cancer Research · 2024not yet assessed
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GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2024not yet assessed
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Metabolic reaction fluxes as amplifiers and buffers of risk alleles for coronary artery disease ↗medRxiv · 2024not yet assessed
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T12. ASSOCIATIONS OF 2,922 GENETICALLY PREDICTED PLASMA PROTEIN LEVELS WITH NINE PSYCHIATRIC DISORDER AND SUBSTANCE MISUSE TRAITS ↗European Neuropsychopharmacology · 2024not yet assessed
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Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits ↗Nature Genetics · 2024 · PMID 38689001not yet assessed
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Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targetsNature Immunology · 2023 · PMID 37563310L1 93/100
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Mendelian randomization for cardiovascular diseases: principles and applications ↗European Heart Journal · 2023 · PMID 37935836not yet assessed
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A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease ↗Nature Medicine · 2023 · PMID 37414900not yet assessed
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An atlas of genetic scores to predict multi-omic traits ↗Nature · 2023 · PMID 36991119not yet assessed
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Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation ↗Nature Genetics · 2023 · PMID 37248441not yet assessed
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Estimating dose-response relationships for vitamin D with coronary heart disease, stroke, and all-cause mortality: observational and Mendelian randomisation analyses ↗The Lancet Diabetes & Endocrinology · 2023 · PMID 38048800not yet assessed
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South Asian medical cohorts reveal strong founder effects and high rates of homozygosity ↗Nature Communications · 2023 · PMID 37291107not yet assessed
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A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology ↗Nature Communications · 2023 · PMID 37596262not yet assessed
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Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity ↗Stroke · 2023 · PMID 36655558not yet assessed
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A nutritional biomarker score of the Mediterranean diet and incident type 2 diabetes: Integrated analysis of data from the MedLey randomised controlled trial and the EPIC-InterAct case-cohort study ↗PLoS Medicine · 2023 · PMID 37104291not yet assessed
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Cardiovascular Disease Knowledge Portal: A Community Resource for Cardiovascular Disease Research ↗Circulation Genomic and Precision Medicine · 2023 · PMID 37814896not yet assessed
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Age at Menopause and the Risk of Stroke: Observational and Mendelian Randomization Analysis in 204 244 Postmenopausal Women ↗Journal of the American Heart Association · 2023 · PMID 37681566not yet assessed
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Genetically predicted plasma cortisol and common chronic diseases: A Mendelian randomization study ↗Clinical Endocrinology · 2023 · PMID 37667866not yet assessed
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Identification of blood protein biomarkers associated with prostate cancer risk using genetic prediction models: analysis of over 140,000 subjects ↗Human Molecular Genetics · 2023 · PMID 37622920not yet assessed
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Trans‐ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study ↗Alzheimer s & Dementia · 2023 · PMID 37450379not yet assessed
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Dietary amino acids and risk of stroke subtypes: a prospective analysis of 356,000 participants in seven European countries ↗European Journal of Nutrition · 2023 · PMID 37804448not yet assessed
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Trans‐ethnic polygenic risk scores for body mass index: An international hundred K+ cohorts consortium study ↗Clinical and Translational Medicine · 2023 · PMID 37337639not yet assessed
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Risk Factors of Secondary Cardiovascular Events in a Multi-Ethnic Asian Population with Acute Myocardial Infarction: A Retrospective Cohort Study from Malaysia ↗Journal of Cardiovascular Development and Disease · 2023 · PMID 37367415not yet assessed
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Quality control and removal of technical variation of NMR metabolic biomarker data in ~120,000 UK Biobank participants ↗Scientific Data · 2023 · PMID 36720882not yet assessed
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Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets ↗Nature Immunology · 2023 · PMID 37679551not yet assessed
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Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications ↗medRxiv · 2023 · PMID 37034649not yet assessed
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Human genetics implicates a BACH2-NRF2 axis in fetal heamoglobin activation ↗medRxiv · 2023 · PMID 36993312not yet assessed
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Genetic determinants of blood gene expression and splicing and their contribution to molecular phenotypes and health outcomes ↗medRxiv · 2023not yet assessed
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Misexpression of inactive genes in whole blood is associated with nearby rare structural variants ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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not yet assessed
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not yet assessed
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Identifying therapeutic targets for cancer: 2,094 circulating proteins and risk of nine cancers ↗medRxiv · 2023not yet assessed
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Cardiovascular risk prediction using metabolomic biomarkers and polygenic risk scores: A cohort study and modelling analyses ↗medRxiv · 2023not yet assessed
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Genetic mechanisms of 184 neuro-related proteins in human plasma ↗medRxiv · 2023 · PMID 36824751not yet assessed
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Trans-ethnic Polygenic Risk Scores for Body Mass Index: An International Hundred K+ Cohorts Consortium Study ↗medRxiv · 2023 · PMID 36712066not yet assessed
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Age at menopause and the risk of stroke: Observational and Mendelian Randomization analysis in 204,244 postmenopausal women ↗medRxiv · 2023not yet assessed
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not yet assessed
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flashfmZoom: a tool for joint fine-mapping and exploration of GWAS results in the UK Biobank ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Mapping pQTLs of circulating inflammatory proteins identifies drivers of immune-related disease risk and novel therapeutic targets ↗medRxiv · 2023not yet assessed
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Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders ↗Research Square · 2023 · PMID 37034613not yet assessed
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Dietary amino acids and risk of stroke subtypes: a prospective analysis of 356,000 participants in seven European countries ↗medRxiv · 2023not yet assessed
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not yet assessed
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Risk factors of secondary cardiovascular events in a multi-ethnic Asian population with acute myocardial infarction ↗International Journal of Cardiology · 2023not yet assessed
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Environmental arsenic exposure, hypertension, and diabetes mellitus: a systematic review and dose-response meta-analysis ↗ISEE Conference Abstracts · 2023not yet assessed
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Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants ↗Nature Genetics · 2022 · PMID 36474045not yet assessed
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Stroke genetics informs drug discovery and risk prediction across ancestries ↗Nature · 2022 · PMID 36180795not yet assessed
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Whole-genome sequencing reveals host factors underlying critical COVID-19 ↗Nature · 2022 · PMID 35255492not yet assessed
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Measurement and initial characterization of leukocyte telomere length in 474,074 participants in UK Biobank ↗Nature Aging · 2022 · PMID 37117760not yet assessed
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Identifying and visualising multimorbidity and comorbidity patterns in patients in the English National Health Service: a population-based study ↗The Lancet Digital Health · 2022 · PMID 36460578not yet assessed
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A first update on mapping the human genetic architecture of COVID-19 ↗Nature · 2022 · PMID 35922517not yet assessed
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Rare and common genetic determinants of metabolic individuality and their effects on human health ↗Nature Medicine · 2022 · PMID 36357675not yet assessed
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Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention ↗JAMA Cardiology · 2022 · PMID 36576811not yet assessed
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Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke ↗Nature Communications · 2022 · PMID 36253349not yet assessed
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Modifiable traits, healthy behaviours, and leukocyte telomere length: a population-based study in UK Biobank ↗The Lancet Healthy Longevity · 2022 · PMID 35685390not yet assessed
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An empirical investigation into the impact of winner’s curse on estimates from Mendelian randomization ↗International Journal of Epidemiology · 2022 · PMID 36573802not yet assessed
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Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative ↗PLoS Genetics · 2022 · PMID 36327219not yet assessed
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Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses ↗Circulation · 2022 · PMID 36314129not yet assessed
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Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites ↗The American Journal of Human Genetics · 2022 · PMID 35568032not yet assessed
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Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke ↗Neurology · 2022 · PMID 36240095not yet assessed
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Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans ↗eLife · 2022 · PMID 35916366not yet assessed
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Genetic landscape of the ACE2 coronavirus receptor ↗Apollo (University of Cambridge) · 2022not yet assessed
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Association of shorter leucocyte telomere length with risk of frailty ↗Journal of Cachexia Sarcopenia and Muscle · 2022 · PMID 35297226not yet assessed
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Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease ↗Cell Genomics · 2022 · PMID 35072137not yet assessed
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Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization ↗The Journal of Clinical Endocrinology & Metabolism · 2022 · PMID 35306566not yet assessed
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Genetically personalised organ-specific metabolic models in health and disease ↗Nature Communications · 2022 · PMID 36446790not yet assessed
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Higher body mass index raises immature platelet count: potential contribution to obesity-related thrombosis ↗Platelets · 2022 · PMID 35068290not yet assessed
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Fibroblast Growth Factor-23 and Risk of Cardiovascular Diseases ↗Clinical Journal of the American Society of Nephrology · 2022 · PMID 36719157not yet assessed
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Physical activity attenuates but does not eliminate coronary heart disease risk amongst adults with risk factors: EPIC-CVD case-cohort study ↗European Journal of Preventive Cardiology · 2022 · PMID 35403197not yet assessed
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Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease ↗Circulation Genomic and Precision Medicine · 2022 · PMID 36215124not yet assessed
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Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer’s disease ↗PLoS Genetics · 2022 · PMID 36048760not yet assessed
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Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations ↗Scientific Reports · 2022 · PMID 35064169not yet assessed
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Flashfm-ivis : interactive visualization for fine-mapping of multiple quantitative traits ↗Bioinformatics · 2022 · PMID 35792838not yet assessed
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The common IL1A single nucleotide polymorphism rs17561 is a hypomorphic mutation that significantly reduces interleukin‐1α release from human blood cells ↗Immunology · 2022 · PMID 36175368not yet assessed
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An empirical investigation into the impact of winner’s curse on estimates from Mendelian randomization ↗medRxiv · 2022not yet assessed
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Mendelian randomisation and vitamin D: the importance of model assumptions – Authors' reply ↗The Lancet Diabetes & Endocrinology · 2022 · PMID 36528346not yet assessed
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Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressure ↗Research Square · 2022not yet assessed
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Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries ↗Nature · 2022 · PMID 36376532not yet assessed
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An atlas of genetic scores to predict multi-omic traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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not yet assessed
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not yet assessed
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Dose–response relationships for vitamin D and all-cause mortality – Authors' reply ↗The Lancet Diabetes & Endocrinology · 2022 · PMID 35202588not yet assessed
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Genome-wide characterization of circulating metabolic biomarkers reveals substantial pleiotropy and novel disease pathways ↗medRxiv · 2022not yet assessed
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Fibroblast Growth Factor-23 and Risk of Cardiovascular Diseases: a Mendelian Randomisation study ↗medRxiv · 2022not yet assessed
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Trans-ethnic Genomic Informed Risk Assessment for Alzheimer’s disease: An International Hundred K+ Cohorts Consortium Study ↗medRxiv · 2022not yet assessed
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flashfm-ivis : interactive visualisation for fine-mapping of multiple quantitative traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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not yet assessed
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Inhibition of MRP1 Induces Fetal Hemoglobin through NRF2 Activation to Protect Human Erythroid Cells from Sickling ↗Blood · 2022not yet assessed
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Higher body mass index raises immature platelet count: potential contribution to obesity-related thrombosis ↗Figshare · 2022not yet assessed
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Genetic Landscape of the ACE2 Coronavirus Receptor ↗Circulation · 2022 · PMID 35387486not yet assessed
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SCORE2 risk prediction algorithms: new models to estimate 10-year risk of cardiovascular disease in Europe ↗European Heart Journal · 2021 · PMID 34120177not yet assessed
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Mapping the human genetic architecture of COVID-19 ↗Nature · 2021 · PMID 34237774not yet assessed
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Polygenic basis and biomedical consequences of telomere length variation ↗Nature Genetics · 2021 · PMID 34611362not yet assessed
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Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19 ↗Nature Medicine · 2021 · PMID 33837377not yet assessed
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A cross-platform approach identifies genetic regulators of human metabolism and health ↗Nature Genetics · 2021 · PMID 33414548not yet assessed
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RETRACTED: Estimating dose-response relationships for vitamin D with coronary heart disease, stroke, and all-cause mortality: observational and Mendelian randomisation analyses ↗The Lancet Diabetes & Endocrinology · 2021 · PMID 34717822not yet assessed
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Polygenic risk scores in cardiovascular risk prediction: A cohort study and modelling analyses ↗PLoS Medicine · 2021 · PMID 33444330not yet assessed
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A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis ↗Communications Biology · 2021 · PMID 33536631not yet assessed
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Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases ↗Nature Metabolism · 2021 · PMID 34750571not yet assessed
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Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates ↗International Journal of Obesity · 2021 · PMID 34226637not yet assessed
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Shorter leukocyte telomere length is associated with adverse COVID-19 outcomes: A cohort study in UK Biobank ↗EBioMedicine · 2021 · PMID 34304048not yet assessed
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Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases ↗Nature Medicine · 2021 · PMID 34426706not yet assessed
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Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci ↗BMC Medicine · 2021 · PMID 34503513not yet assessed
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Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program ↗The American Journal of Human Genetics · 2021 · PMID 33887194not yet assessed
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SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues ↗Cell Reports · 2021 · PMID 34762851not yet assessed
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Plasma Proteomics of Renal Function: A Transethnic Meta-Analysis and Mendelian Randomization Study ↗Journal of the American Society of Nephrology · 2021 · PMID 34135082not yet assessed
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The blood metabolome of incident kidney cancer: A case–control study nested within the MetKid consortium ↗PLoS Medicine · 2021 · PMID 34543281not yet assessed
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Risk Factors and Prediction Models for Incident Heart Failure with Reduced and Preserved Ejection Fraction ↗ESC Heart Failure · 2021 · PMID 34528757not yet assessed
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Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program ↗The American Journal of Human Genetics · 2021 · PMID 34582791not yet assessed
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Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative ↗Human Molecular Genetics · 2021 · PMID 34553764not yet assessed
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An Expanded Genome-Wide Association Study of Fructosamine Levels Identifies RCN3 as a Replicating Locus and Implicates FCGRT as the Effector Transcript ↗Diabetes · 2021 · PMID 34753797not yet assessed
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Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program ↗The American Journal of Human Genetics · 2021not yet assessed
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Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study ↗Nutrients · 2021 · PMID 34836419not yet assessed
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Milk intake and incident stroke and CHD in populations of European descent: a Mendelian randomisation study ↗British Journal Of Nutrition · 2021 · PMID 34670632not yet assessed
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Investigating Genetic and Other Determinants of First-Onset Myocardial Infarction in Malaysia: Protocol for the Malaysian Acute Vascular Events Risk Study ↗JMIR Research Protocols · 2021 · PMID 35142634not yet assessed
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Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants ↗medRxiv · 2021not yet assessed
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not yet assessed
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not yet assessed
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Quality control and removal of technical variation of NMR metabolic biomarker data in ∼120,000 UK Biobank participants ↗medRxiv · 2021not yet assessed
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Mapping genetic determinants of 184 circulating proteins in 26,494 individuals to connect proteins and diseases ↗medRxiv · 2021not yet assessed
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Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19 ↗medRxiv · 2021 · PMID 33851187not yet assessed
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Older biological age is associated with adverse COVID-19 outcomes: A cohort study in UK Biobank ↗medRxiv · 2021not yet assessed
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Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals ↗Nature Genetics · 2021 · PMID 33727701not yet assessed
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Higher body mass index raises immature platelet count: evidence from Mendelian randomization analyses ↗medRxiv · 2021not yet assessed
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Abstract 882: Associations of genetically predicted blood protein biomarkers with pancreatic ductal adenocarcinoma risk: A study using comprehensive protein genetic prediction models ↗Cancer Research · 2021not yet assessed
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Salicylic acid and risk of colorectal cancer: a two sample Mendelian randomization study ↗medRxiv · 2021not yet assessed
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Integrated Analyses of Growth Differentiation Factor-15 Concentration and Cardiometabolic Diseases in Humans ↗medRxiv · 2021not yet assessed
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Genetically predicted levels of the human plasma proteome and risk of stroke: a Mendelian Randomization study ↗medRxiv · 2021not yet assessed
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Association of leucocyte telomere length with frailty: a large–scale cross–sectional analysis in UK Biobank ↗medRxiv · 2021not yet assessed
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SCORE2 risk prediction algorithms: new models to estimate 10-year risk of cardiovascular disease in EuropeSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
204Effects of adiposity on the human proteome: Mendelian randomization study using individual-level data ↗International Journal of Epidemiology · 2021not yet assessed
-
Genetically predicted levels of the human plasma proteome and risk of stroke: a Mendelian Randomization study ↗Research Square · 2021not yet assessed
-
not yet assessed
-
Abstract 12224: Predictive Power and Value of a CAD Polygenic Risk Score in Primary Prevention Based on Age and Clinical Risk ↗Circulation · 2021not yet assessed
-
not yet assessed
-
not yet assessed
-
not yet assessed
-
not yet assessed
-
Association of Cardiometabolic Multimorbidity With Mortality ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2021not yet assessed
-
UKB_telomere_gwas_summarystats.tsv.gz ↗Figshare · 2021not yet assessed
-
Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases ↗Nature Genetics · 2020 · PMID 32895551not yet assessed
-
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals ↗Nature Metabolism · 2020 · PMID 33067605not yet assessed
-
The Polygenic and Monogenic Basis of Blood Traits and Diseases ↗Cell · 2020 · PMID 32888494not yet assessed
-
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations ↗Cell · 2020 · PMID 32888493not yet assessed
-
Lifestyle factors and risk of multimorbidity of cancer and cardiometabolic diseases: a multinational cohort study ↗BMC Medicine · 2020 · PMID 31918762not yet assessed
-
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals ↗Nature Genetics · 2020 · PMID 33230300not yet assessed
-
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length ↗The American Journal of Human Genetics · 2020 · PMID 32109421not yet assessed
-
Association of plasma biomarkers of fruit and vegetable intake with incident type 2 diabetes: EPIC-InterAct case-cohort study in eight European countries ↗BMJ · 2020 · PMID 32641421not yet assessed
-
Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations ↗Diabetes Care · 2020 · PMID 33203707not yet assessed
-
Validation of a Genome-Wide Polygenic Score for Coronary Artery Disease in South Asians ↗Journal of the American College of Cardiology · 2020 · PMID 32762905not yet assessed
-
Metabolic profiling of angiopoietin-like protein 3 and 4 inhibition: a drug-target Mendelian randomization analysis ↗European Heart Journal · 2020 · PMID 33351885not yet assessed
-
Lipoprotein(a) in Alzheimer, Atherosclerotic, Cerebrovascular, Thrombotic, and Valvular Disease ↗Circulation · 2020 · PMID 32479194not yet assessed
-
The associations of major foods and fibre with risks of ischaemic and haemorrhagic stroke: a prospective study of 418 329 participants in the EPIC cohort across nine European countries ↗European Heart Journal · 2020 · PMID 32090257not yet assessed
-
High-throughput multivariable Mendelian randomization analysis prioritizes apolipoprotein B as key lipid risk factor for coronary artery disease ↗International Journal of Epidemiology · 2020 · PMID 33130851not yet assessed
-
Neurology-related protein biomarkers are associated with cognitive ability and brain volume in older age ↗Nature Communications · 2020 · PMID 32041957not yet assessed
-
The association between circulating 25-hydroxyvitamin D metabolites and type 2 diabetes in European populations: A meta-analysis and Mendelian randomisation analysis ↗PLoS Medicine · 2020 · PMID 33064751not yet assessed
-
Large genome-wide association study identifies three novel risk variants for restless legs syndrome ↗Communications Biology · 2020 · PMID 33239738not yet assessed
-
Development and validation of a universal blood donor genotyping platform: a multinational prospective study ↗Blood Advances · 2020 · PMID 32750130not yet assessed
-
Glycemic index, glycemic load, and risk of coronary heart disease: a pan-European cohort study ↗American Journal of Clinical Nutrition · 2020 · PMID 32619242not yet assessed
-
Plant foods, dietary fibre and risk of ischaemic heart disease in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort ↗International Journal of Epidemiology · 2020 · PMID 33245137not yet assessed
-
ACE inhibition and cardiometabolic risk factors, lung ACE2 and TMPRSS2 gene expression, and plasma ACE2 levels: a Mendelian randomization study ↗Royal Society Open Science · 2020 · PMID 33391794not yet assessed
-
The influence of rare variants in circulating metabolic biomarkers ↗PLoS Genetics · 2020 · PMID 32150548not yet assessed
-
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2020not yet assessed
-
The genetic architecture of type 2 diabetes ↗UNC Libraries · 2020not yet assessed
-
not yet assessed
-
Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19 ↗medRxiv · 2020not yet assessed
-
Cross-platform genetic discovery of small molecule products of metabolism and application to clinical outcomes ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
not yet assessed
-
Genomic evaluation of circulating proteins for drug target characterisation and precision medicine ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
not yet assessed
-
Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program ↗medRxiv · 2020not yet assessed
-
Genetic Analyses of Blood Cell Structure for Biological and Pharmacological Inference ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
Learning polygenic scores for human blood cell traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
not yet assessed
-
South Asian Patient Population Genetics Reveal Strong Founder Effects and High Rates of Homozygosity – New Resources for Precision Medicine ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
not yet assessed
-
Effects of adiposity on the human plasma proteome: Observational and Mendelian randomization estimates ↗medRxiv · 2020not yet assessed
-
South Asian Patient Population Genetics Reveal Strong Founder Effects and High Rates of Homozygosity – New Resources for Precision Medicine ↗SSRN Electronic Journal · 2020not yet assessed
-
Author Correction: Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke ↗Nature Communications · 2020 · PMID 32080192not yet assessed
-
Correction: Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition ↗PLoS Biology · 2020 · PMID 32142508not yet assessed
-
not yet assessed
-
The influence of rare variants in circulating metabolic biomarkers. ↗Apollo (University of Cambridge) · 2020not yet assessed
-
Metabolic profiling of angiopoietin-like protein 3 and 4 inhibition: a drug-target Mendelian randomization analysis. ↗STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length. ↗Research Repository (Kingston University London) · 2020not yet assessed
-
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2020not yet assessed
-
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ↗UNC Libraries · 2020not yet assessed
-
Genome-Wide Association Studies, Field Synopses, and the Development of the Knowledge Base on Genetic Variation and Human Diseases ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2020not yet assessed
-
PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations ↗Bioinformatics · 2019 · PMID 31233103not yet assessed
-
A catalog of genetic loci associated with kidney function from analyses of a million individuals ↗Nature Genetics · 2019 · PMID 31152163not yet assessed
-
Association of Triglyceride-Lowering LPL Variants and LDL-C–Lowering LDLR Variants With Risk of Coronary Heart Disease ↗JAMA · 2019 · PMID 30694319not yet assessed
-
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries ↗Nature Genetics · 2019 · PMID 30804560not yet assessed
-
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels ↗Nature Genetics · 2019 · PMID 31578528not yet assessed
-
Cardiovascular Risk Factors Associated With Venous Thromboembolism ↗JAMA Cardiology · 2019 · PMID 30649175not yet assessed
-
Mendelian Randomization Study of ACLY and Cardiovascular Disease ↗New England Journal of Medicine · 2019 · PMID 30865797not yet assessed
-
Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status ↗Nature Communications · 2019 · PMID 31719529not yet assessed
-
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria ↗Nature Communications · 2019 · PMID 31511532not yet assessed
-
Body mass index and all cause mortality in HUNT and UK Biobank studies: linear and non-linear mendelian randomisation analyses ↗BMJ · 2019 · PMID 30957776not yet assessed
-
Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke ↗Nature Communications · 2019 · PMID 31862893not yet assessed
-
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income ↗Nature Communications · 2019 · PMID 31844048not yet assessed
-
Consumption of Meat, Fish, Dairy Products, and Eggs and Risk of Ischemic Heart Disease ↗Circulation · 2019 · PMID 31006335not yet assessed
-
Genetic Determinants of Lipids and Cardiovascular Disease Outcomes ↗Circulation Genomic and Precision Medicine · 2019 · PMID 31756303not yet assessed
-
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci ↗Molecular Psychiatry · 2019 · PMID 30617275not yet assessed
-
Assessing the causal association of glycine with risk of cardio-metabolic diseases ↗Nature Communications · 2019 · PMID 30837465not yet assessed
-
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution ↗Nature Genetics · 2019 · PMID 30778226not yet assessed
-
Serum magnesium and calcium levels in relation to ischemic stroke ↗Neurology · 2019 · PMID 30804065not yet assessed
-
Association of menopausal characteristics and risk of coronary heart disease: a pan-European case–cohort analysis ↗International Journal of Epidemiology · 2019 · PMID 30796459not yet assessed
-
An Unbiased Lipid Phenotyping Approach To Study the Genetic Determinants of Lipids and Their Association with Coronary Heart Disease Risk Factors ↗Journal of Proteome Research · 2019 · PMID 30887811not yet assessed
-
Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition ↗PLoS Biology · 2019 · PMID 31860674not yet assessed
-
Interleukin-6 Receptor Signaling and Abdominal Aortic Aneurysm Growth Rates ↗Circulation Genomic and Precision Medicine · 2019 · PMID 30657332not yet assessed
-
Effect of communicating phenotypic and genetic risk of coronary heart disease alongside web-based lifestyle advice: the INFORM Randomised Controlled Trial ↗Heart · 2019 · PMID 30928969not yet assessed
-
Genome-Wide Association Study of Over One Million Participants Identifies 49 Novel Loci Associated With Coronary Artery DiseaseCirculation · 2019not yet assessed
-
Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes ↗Nature Genetics · 2019 · PMID 31160810not yet assessed
-
Genetic determinants of lipids and cardiovascular disease outcomes: a wide-angled Mendelian randomization investigation ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries ↗Nature Genetics · 2019 · PMID 31110354not yet assessed
-
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2019not yet assessed
-
Genetic analysis identifies molecular systems and biological pathways associated with household income ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Use of polygenic risk scores and other molecular markers to enhance cardiovascular risk prediction: prospective cohort study and modelling analysis ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Cardiovascular Risk Factors Associated With Venous Thromboembolism ↗Apollo (University of Cambridge) · 2019not yet assessed
-
Effect of communicating phenotypic and genetic risk of coronary heart disease alongside web-based lifestyle advice ↗Apollo (University of Cambridge) · 2019not yet assessed
-
Neurology-related protein biomarkers are associated with general fluid cognitive ability and brain volume in older age ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Identification of Novel Variants Associated with Fetal Hemoglobin Levels in Healthy Donors (the INTERVAL study) ↗Blood · 2019not yet assessed
-
Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke. ↗Apollo (University of Cambridge) · 2019not yet assessed
-
Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition. ↗Apollo (University of Cambridge) · 2019not yet assessed
-
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. ↗Figshare · 2019not yet assessed
-
Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition ↗UCL Discovery (University College London) · 2019not yet assessed
-
Abstract 15391: Genome-Wide Association Study of Over One Million Participants Identifies 49 Novel Loci Associated With Coronary Artery DiseaseCirculation · 2019not yet assessed
-
Abstract 11431: Risk Factors and Risk Prediction Models for Incident HFrEF and HFpEF in U.S. VeteransCirculation · 2019not yet assessed
-
Publisher correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes(Nature Genetics, (2018) 50, 4, (524-537), 10.1038/s41588-018-0058-3) ↗Institutional Repositories DataBase (IRDB) · 2019not yet assessed
-
Genomic atlas of the human plasma proteome ↗Nature · 2018 · PMID 29875488not yet assessed
-
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes ↗Nature Genetics · 2018 · PMID 29531354not yet assessed
-
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits ↗Nature Genetics · 2018 · PMID 30224653not yet assessed
-
Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults ↗Journal of the American College of Cardiology · 2018 · PMID 30309464not yet assessed
-
Association ofLPAVariants With Risk of Coronary Disease and the Implications for Lipoprotein(a)-Lowering Therapies ↗JAMA Cardiology · 2018 · PMID 29926099not yet assessed
-
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ↗Nature Genetics · 2018 · PMID 29632382not yet assessed
-
Genome‐wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease ↗Nature Communications · 2018 · PMID 30111768not yet assessed
-
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels ↗Nature Communications · 2018 · PMID 29343764not yet assessed
-
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes ↗ARAN (University of Galway Research Repository) (Ollscoil na Gaillimhe – University of Galway) · 2018not yet assessed
-
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes ↗Nature Communications · 2018 · PMID 30510157not yet assessed
-
ProGeM: a framework for the prioritization of candidate causal genes at molecular quantitative trait loci ↗Nucleic Acids Research · 2018 · PMID 30239796not yet assessed
-
Metabolomic Consequences of Genetic Inhibition of PCSK9 Compared With Statin Treatment ↗Circulation · 2018 · PMID 30524137not yet assessed
-
Alcohol intake in relation to non-fatal and fatal coronary heart disease and stroke: EPIC-CVD case-cohort study ↗BMJ · 2018 · PMID 29844013not yet assessed
-
Risk thresholds for alcohol consumption: combined analysis of individual-participant data for 599 912 current drinkers in 83 prospective studies ↗UEF eRepo (University of Eastern Finland) · 2018not yet assessed
-
Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study ↗The Lancet Haematology · 2018 · PMID 29780001not yet assessed
-
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ↗Biological Psychiatry · 2018 · PMID 30679032not yet assessed
-
Development and evaluation of a transfusion medicine genome wide genotyping array ↗Transfusion · 2018 · PMID 30456907not yet assessed
-
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits ↗Nature Communications · 2018 · PMID 30405126not yet assessed
-
Association of Plasma Vitamin D Metabolites With Incident Type 2 Diabetes: EPIC-InterAct Case-Cohort Study ↗The Journal of Clinical Endocrinology & Metabolism · 2018 · PMID 30418614not yet assessed
-
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits ↗Nature Genetics · 2018 · PMID 30429575not yet assessed
-
Genomic risk prediction of coronary artery disease in nearly 500,000 adults: implications for early screening and primary prevention ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Author Correction: Genome‐wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease ↗Nature Communications · 2018 · PMID 30228274not yet assessed
-
Protein-Coding Variants Implicate Novel Genes Related to Lipid Homeostasis Contributing to Body Fat Distribution ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2018 · PMID 29549329not yet assessed
-
Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits : (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x)Nature Genetics · 2018not yet assessed
-
New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2018 · PMID 29549330not yet assessed
-
Lipoprotein Signatures of Cholesteryl Ester Transfer Protein and HMG-CoA Reductase Inhibition ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls ↗Scientific Data · 2018not yet assessed
-
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
The influence of rare variants in circulating metabolic biomarkers ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Erratum to: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps : (Nature Genetics, (2016), 48, 11, (1303-1312), 10.1038/ng.3668)Nature Genetics · 2018not yet assessed
-
Interleukin-6 Receptor Signalling and Abdominal Aortic Aneurysm Growth Rates ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps ↗Nature Genetics · 2018 · PMID 30390057not yet assessed
-
Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits ↗Nature Communications · 2018 · PMID 30568165not yet assessed
-
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. ↗Kölner Universitäts PublikationsServer (Universität zu Köln) · 2018not yet assessed
-
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. ↗Tampere University Institutional Repository (Tampere University) · 2018not yet assessed
-
Metabolomic consequences of genetic inhibition of PCSK9 compared with statin treatment ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci ↗UCL Discovery (University College London) · 2018not yet assessed
-
Association analyses based on false discovery rate implicate new loci for coronary artery disease ↗Nature Genetics · 2017 · PMID 28714975not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Nature · 2017 · PMID 28146470not yet assessed
-
Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention Setting ↗Circulation · 2017 · PMID 28223407not yet assessed
-
Exome-wide association study of plasma lipids in >300,000 individuals ↗Nature Genetics · 2017 · PMID 29083408not yet assessed
-
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2017 · PMID 29273807not yet assessed
-
Association of Genetic Variants Related to CETP Inhibitors and Statins With Lipoprotein Levels and Cardiovascular Risk ↗JAMA · 2017 · PMID 28846118not yet assessed
-
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms ↗Nature Genetics · 2017 · PMID 28530674not yet assessed
-
Separate and combined associations of obesity and metabolic health with coronary heart disease: a pan-European case-cohort analysis ↗European Heart Journal · 2017 · PMID 29020414not yet assessed
-
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease ↗Nature Genetics · 2017 · PMID 28869590not yet assessed
-
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ↗Journal of the American College of Cardiology · 2017 · PMID 28209224not yet assessed
-
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis ↗The Lancet Neurology · 2017 · PMID 29029846not yet assessed
-
Coffee Drinking and Mortality in 10 European Countries ↗Annals of Internal Medicine · 2017 · PMID 28693038not yet assessed
-
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits ↗The American Journal of Human Genetics · 2017 · PMID 28552196not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2017not yet assessed
-
Exome-wide association study of plasma lipids in > 300,000 individualsFigshare · 2017not yet assessed
-
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity ↗Scientific Reports · 2017 · PMID 28663568not yet assessed
-
A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design ↗European Journal of Human Genetics · 2017 · PMID 28594416not yet assessed
-
Platelet function is modified by common sequence variation in megakaryocyte super enhancers ↗Nature Communications · 2017 · PMID 28703137not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Apollo (University of Cambridge) · 2017not yet assessed
-
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls ↗Scientific Data · 2017 · PMID 29257133not yet assessed
-
Consequences of natural perturbations in the human plasma proteome ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Genetic analysis of over one million people identifies 535 novel loci for blood pressure ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
ProGeM: A framework for the prioritisation of candidate causal genes at molecular quantitative trait loci ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Separate and combined associations of obesity and metabolic health with coronary heart diseaseEuropean Heart Journal · 2017not yet assessed
-
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. ↗eScholarship@McGill (McGill) · 2017not yet assessed
-
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsDSpace@MIT (Massachusetts Institute of Technology) · 2017not yet assessed
-
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease (vol 374, pg 1134, 2016)Data Archiving and Networked Services (DANS) · 2017not yet assessed
-
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. ↗Apollo (University of Cambridge) · 2017not yet assessed
-
PhenoScanner: a database of human genotype–phenotype associations ↗Bioinformatics · 2016 · PMID 27318201not yet assessed
-
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease ↗Cell · 2016 · PMID 27863252not yet assessed
-
The genetic architecture of type 2 diabetes ↗Nature · 2016 · PMID 27398621not yet assessed
-
The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery ↗Cell · 2016 · PMID 27863232not yet assessed
-
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease ↗Science · 2016 · PMID 26965621not yet assessed
-
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ↗Nature Genetics · 2016 · PMID 27618447not yet assessed
-
Natriuretic peptides and integrated risk assessment for cardiovascular disease: an individual-participant-data meta-analysis ↗The Lancet Diabetes & Endocrinology · 2016 · PMID 27599814not yet assessed
-
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease ↗Science Translational Medicine · 2016 · PMID 27252175not yet assessed
-
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps ↗Nature Genetics · 2016 · PMID 27668658not yet assessed
-
Association of Multiple Biomarkers of Iron Metabolism and Type 2 Diabetes: The EPIC-InterAct Study ↗Diabetes Care · 2016 · PMID 26861925not yet assessed
-
Parity, breastfeeding and risk of coronary heart disease: A pan-European case–cohort study ↗European Journal of Preventive Cardiology · 2016 · PMID 27378766not yet assessed
-
Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles ↗European Journal of Preventive Cardiology · 2016 · PMID 27940953not yet assessed
-
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease ↗New England Journal of Medicine · 2016 · PMID 27123876not yet assessed
-
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease ↗Apollo (University of Cambridge) · 2016not yet assessed
-
Genomics of lipid metabolism: Identifying novel causal pathways and new therapeutic targets for reducing risk of coronary heart disease ↗Apollo (University of Cambridge) · 2016not yet assessed
-
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. ↗Apollo (University of Cambridge) · 2016not yet assessed
-
The genetic architecture of type 2 diabetes. ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2016not yet assessed
-
Abstract 16735: Effect of Communicating Phenotypic and Genetic Risk of Coronary Heart Disease Alongside Web-based Lifestyle Advice - The Inform Randomized Clinical TrialCirculation · 2016not yet assessed
-
Natriuretic peptides and integrated risk assessment for cardiovascular disease: an individual-participant-data meta-analysisUCL Discovery (University College London) · 2016not yet assessed
-
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease (vol 374, pg 1134, 2016, Correction)STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2016not yet assessed
-
Association of Cardiometabolic Multimorbidity With Mortality ↗JAMA · 2015 · PMID 26151266not yet assessed
-
Beyond Mendelian randomization: how to interpret evidence of shared genetic predictors ↗Journal of Clinical Epidemiology · 2015 · PMID 26291580not yet assessed
-
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals ↗Human Molecular Genetics · 2015 · PMID 25784503not yet assessed
-
The Bangladesh Risk of Acute Vascular Events (BRAVE) Study: objectives and design ↗European Journal of Epidemiology · 2015 · PMID 25930055not yet assessed
-
Comparative validity of vitamin C and carotenoids as indicators of fruit and vegetable intake: a systematic review and meta-analysis of randomised controlled trials ↗British Journal Of Nutrition · 2015 · PMID 26349405not yet assessed
-
Information and Risk Modification Trial (INFORM): design of a randomised controlled trial of communicating different types of information about coronary heart disease risk, alongside lifestyle advice, to achieve change in health-related behaviour ↗BMC Public Health · 2015 · PMID 26345710not yet assessed
-
Association of Cardiometabolic Multimorbidity With Mortality The Emerging Risk Factors Collaboration ↗Research Publications (Maastricht University) · 2015not yet assessed
-
Investigating the Association of Rare Genetic Variants with Blood Pressure traitsData Archiving and Networked Services (DANS) · 2015not yet assessed
-
Beyond Mendelian randomization: in which the authors discussed how to interpret evidence of shared genetic predictors2015not yet assessed
-
not yet assessed
-
Association of Dietary, Circulating, and Supplement Fatty Acids With Coronary Risk ↗Annals of Internal Medicine · 2014 · PMID 24723079not yet assessed
-
Leucocyte telomere length and risk of cardiovascular disease: systematic review and meta-analysis ↗BMJ · 2014 · PMID 25006006not yet assessed
-
Network Mendelian randomization: using genetic variants as instrumental variables to investigate mediation in causal pathways ↗International Journal of Epidemiology · 2014 · PMID 25150977not yet assessed
-
Glycated Hemoglobin Measurement and Prediction of Cardiovascular Disease ↗JAMA · 2014 · PMID 24668104not yet assessed
-
Leucocyte Telomere Length and Risk of Type 2 Diabetes Mellitus: New Prospective Cohort Study and Literature-Based Meta-Analysis ↗PLoS ONE · 2014 · PMID 25390655not yet assessed
-
Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data ↗Genetic Epidemiology · 2013 · PMID 24114802not yet assessed
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Inflammatory cytokines and risk of coronary heart disease: new prospective study and updated meta-analysis ↗European Heart Journal · 2013 · PMID 24026779not yet assessed
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Functional IL6R 358Ala Allele Impairs Classical IL-6 Receptor Signaling and Influences Risk of Diverse Inflammatory Diseases ↗PLoS Genetics · 2013 · PMID 23593036not yet assessed
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GUESS-ing Polygenic Associations with Multiple Phenotypes Using a GPU-Based Evolutionary Stochastic Search Algorithm ↗PLoS Genetics · 2013 · PMID 23950726not yet assessed
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Assessing Risk Prediction Models Using Individual Participant Data From Multiple Studies ↗American Journal of Epidemiology · 2013 · PMID 24366051not yet assessed
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Lipid-Related Markers and Cardiovascular Disease Prediction ↗EUR Research Repository (Erasmus University Rotterdam) · 2012not yet assessed
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Use of Mendelian randomisation to assess potential benefit of clinical intervention ↗BMJ · 2012 · PMID 23131671not yet assessed
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Adult height and the risk of cause-specific death and vascular morbidity in 1 million people: individual participant meta-analysis ↗International Journal of Epidemiology · 2012 · PMID 22825588not yet assessed
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Clinical Utility of Genetic Variants for Cardiovascular Risk Prediction ↗Circulation Cardiovascular Genetics · 2012 · PMID 22896012not yet assessed
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Abstract B76: Evidence of a causal association between fasting insulin concentrations and endometrial cancer: A Mendelian randomization analysis ↗Cancer Prevention Research · 2012not yet assessed
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Association of the 9p21.3 Locus With Risk of First-Ever Myocardial Infarction in Pakistanis ↗Arteriosclerosis Thrombosis and Vascular Biology · 2010 · PMID 20395598not yet assessed
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Genetic Determinants of Major Blood Lipids in Pakistanis Compared With Europeans ↗Circulation Cardiovascular Genetics · 2010 · PMID 20570915not yet assessed
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Integrated Multi-Trophic Aquaculture systems incorporating abalone and seaweeds2010not yet assessed
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Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects ↗Genetics in Medicine · 2009 · PMID 19367186not yet assessed
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Genome-Wide Association Studies, Field Synopses, and the Development of the Knowledge Base on Genetic Variation and Human Diseases ↗American Journal of Epidemiology · 2009 · PMID 19498075not yet assessed
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Coronary heart disease ↗Oxford University Press eBooks · 2009 · PMID 22997872not yet assessed
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Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases ↗Oxford University Press eBooks · 2009not yet assessed
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Seven Lipoprotein Lipase Gene Polymorphisms, Lipid Fractions, and Coronary Disease: A HuGE Association Review and Meta-Analysis ↗American Journal of Epidemiology · 2008 · PMID 18922999not yet assessed
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Turning the Pump Handle: Evolving Methods for Integrating the Evidence on Gene-Disease Association ↗American Journal of Epidemiology · 2007 · PMID 17804859not yet assessed
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Linkage analysis of rheumatoid arthritis in US and UK families reveals interactions between HLA–DRB1 and loci on chromosomes 6q and 16p ↗Arthritis & Rheumatism · 2006 · PMID 16646029not yet assessed
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Relative and absolute risk of colorectal cancer for individuals with a family history: A meta-analysis ↗European Journal of Cancer · 2005 · PMID 16338133not yet assessed
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Nursing in Slovenia ↗Journal of research in nursing · 2005not yet assessed
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HIV infection and the duration and control of prevalent tuberculosis disease in Harare, ZimbabweLSHTM Research Online (London School of Hygiene and Tropical Medicine) · 2005not yet assessed
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STUDENTS' PAPER. LOUGHBOROUGH SEWAGE AND REFUSE DISPOSAL WORKS. (INCLUDING PLATE AT BACK OF VOLUME). ↗Minutes of the Proceedings of the Institution of Civil Engineers · 1896not yet assessed
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. ↗Archive ouverte UNIGE (University of Geneva) ·not yet assessed
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Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles ↗Institutional Repositories DataBase (IRDB) ·not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
Merged across profiles sharing this ORCID where present. See every “Butterworth A” paper on PubMed ↗