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Author Details
Full Name
Adam S Butterworth
Affiliation
British Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge
ORCID
Career Start Year
2006
Papers
179
H Index
65
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37667866
Genetically predicted plasma cortisol and common chronic diseases: A Mendelian randomization study.
Clin Endocrinol (Oxf)
2024
37667866
Genetically predicted plasma cortisol and common chronic diseases: A Mendelian randomization study.
Clin Endocrinol (Oxf)
2024
37804448
Dietary amino acids and risk of stroke subtypes: a prospective analysis of 356,000 participants in seven European countries.
Eur J Nutr
2024
37804448
Dietary amino acids and risk of stroke subtypes: a prospective analysis of 356,000 participants in seven European countries.
Eur J Nutr
2024
36175368
The common IL1A single nucleotide polymorphism rs17561 is a hypomorphic mutation that significantly reduces interleukin-1α release from human blood cells.
Immunology
2023
36175368
The common IL1A single nucleotide polymorphism rs17561 is a hypomorphic mutation that significantly reduces interleukin-1α release from human blood cells.
Immunology
2023
37679551
Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.
Nat Immunol
2023
37935836
Mendelian randomization for cardiovascular diseases: principles and applications.
Eur Heart J
2023
37596262
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.
Nat Commun
2023
37814896
Cardiovascular Disease Knowledge Portal: A Community Resource for Cardiovascular Disease Research.
Circ Genom Precis Med
2023
37563310
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.
Nat Immunol
2023
37622920
Identification of blood protein biomarkers associated with prostate cancer risk using genetic prediction models: analysis of over 140,000 subjects.
Hum Mol Genet
2023
37414900
A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.
Nat Med
2023
37034649
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
2023
36719157
Fibroblast Growth Factor-23 and Risk of Cardiovascular Diseases: A Mendelian Randomization Study.
Clin J Am Soc Nephrol
2023
37034613
Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders.
Res Sq
2023
36712066
Trans-ethnic Polygenic Risk Scores for Body Mass Index: An International Hundred K+ Cohorts Consortium Study.
medRxiv
2023
36824751
Genetic mechanisms of 184 neuro-related proteins in human plasma.
medRxiv
2023
36576811
Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention.
JAMA Cardiol
2023
36573802
An empirical investigation into the impact of winner's curse on estimates from Mendelian randomization.
Int J Epidemiol
2023
37450379
Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study.
Alzheimers Dement
2023
37367415
Risk Factors of Secondary Cardiovascular Events in a Multi-Ethnic Asian Population with Acute Myocardial Infarction: A Retrospective Cohort Study from Malaysia.
J Cardiovasc Dev Dis
2023
36993312
Genetic regulation of fetal hemoglobin across global populations.
medRxiv
2023
37104291
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 Med
2023
36991119
An atlas of genetic scores to predict multi-omic traits.
Nature
2023
36528346
Mendelian randomisation and vitamin D: the importance of model assumptions - Authors' reply.
Lancet Diabetes Endocrinol
2023
37291107
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.
Nat Commun
2023
36720882
Quality control and removal of technical variation of NMR metabolic biomarker data in ~120,000 UK Biobank participants.
Sci Data
2023
37596262
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.
Nat Commun
2023
37622920
Identification of blood protein biomarkers associated with prostate cancer risk using genetic prediction models: analysis of over 140,000 subjects.
Hum Mol Genet
2023
37935836
Mendelian randomization for cardiovascular diseases: principles and applications.
Eur Heart J
2023
37679551
Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.
Nat Immunol
2023
37814896
Cardiovascular Disease Knowledge Portal: A Community Resource for Cardiovascular Disease Research.
Circ Genom Precis Med
2023
37563310
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.
Nat Immunol
2023
37291107
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.
Nat Commun
2023
36993312
Genetic regulation of fetal hemoglobin across global populations.
medRxiv
2023
36991119
An atlas of genetic scores to predict multi-omic traits.
Nature
2023
37450379
Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study.
Alzheimers Dement
2023
37414900
A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.
Nat Med
2023
37104291
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 Med
2023
37367415
Risk Factors of Secondary Cardiovascular Events in a Multi-Ethnic Asian Population with Acute Myocardial Infarction: A Retrospective Cohort Study from Malaysia.
J Cardiovasc Dev Dis
2023
37034649
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
2023
37034613
Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders.
Res Sq
2023
36720882
Quality control and removal of technical variation of NMR metabolic biomarker data in ~120,000 UK Biobank participants.
Sci Data
2023
36719157
Fibroblast Growth Factor-23 and Risk of Cardiovascular Diseases: A Mendelian Randomization Study.
Clin J Am Soc Nephrol
2023
36712066
Trans-ethnic Polygenic Risk Scores for Body Mass Index: An International Hundred K+ Cohorts Consortium Study.
medRxiv
2023
36576811
Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention.
JAMA Cardiol
2023
36573802
An empirical investigation into the impact of winner's curse on estimates from Mendelian randomization.
Int J Epidemiol
2023
36824751
Genetic mechanisms of 184 neuro-related proteins in human plasma.
medRxiv
2023
36528346
Mendelian randomisation and vitamin D: the importance of model assumptions - Authors' reply.
Lancet Diabetes Endocrinol
2023
1 - 50 of 358
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