About: Adam S. Butterworth

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researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy)
rdfs:label	Adam S. Butterworth (en) Adam S. Butterworth (es) Adam S. Butterworth (nl) Adam S. Butterworth (sl) Adam S. Butterworth (ast)
skos:prefLabel	Adam S. Butterworth (en) Adam S. Butterworth (es) Adam S. Butterworth (nl) Adam S. Butterworth (sl) Adam S. Butterworth (ast)
name	Adam S. Butterworth (en) Adam S. Butterworth (es) Adam S. Butterworth (nl) Adam S. Butterworth (sl) Adam S. Butterworth (ast)
Scopus author ID	wds:Q55313240-6AB241C2-276D-4558-81CD-648B1F19E2ED
Scopus author ID	57190167995
given name	wds:Q55313240-EA1018B4-0434-4F2C-B0CB-F9ABCF040768
given name	Adam
instance of	wds:Q55313240-C62D8F39-D942-492B-A68F-D4B28240C8A2
instance of	Homo sapiens
skos:altLabel	AS Butterworth (en) Adam Butterworth (en) Adam S Butterworth (en)
occupation	wds:Q55313240-BBD77289-7D51-4C37-8A85-D9D9A031FC51
employer	wds:Q55313240-6c2d188f-4844-9cd5-04d2-b59253d5536d
sex or gender	wds:Q55313240-0fcb9a6a-4ed5-c5ec-3e73-492315428e79
DBLP author ID	wds:Q55313240-2F4EBCE7-181A-4D24-B937-CC2878EBA525
family name	wds:Q55313240-466DD92E-D1B2-43CE-A312-E672FFDF3D90
DBLP author ID	https://dblp.org/pid/187/5721.rdf
occupation	researcher
employer	John Ffowcs Williams
sex or gender	male
DBLP author ID	187/5721
family name	Butterworth
ORCID iD	wds:Q55313240-5C03FDFB-9133-4A7F-BD7A-0B870CA2A6FD
ORCID iD	https://orcid.org/0000-0002-6915-9015
ORCID iD	0000-0002-6915-9015
Gateway to Research person ID	wds:Q55313240-73D79F6C-8EB6-43E7-AD67-4900718D98E0
Gateway to Research person ID	9E72C8B3-6137-45DC-A650-FF9C45331610
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55313240
is author of	Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: a HuGE association review and meta-analysis Comparative validity of vitamin C and carotenoids as indicators of fruit and vegetable intake: a systematic review and meta-analysis of randomised controlled trials Beyond Mendelian randomization: how to interpret evidence of shared genetic predictors Linkage analysis of rheumatoid arthritis in US and UK families reveals interactions between HLA–DRB1 and loci on chromosomes 6q and 16p Mendelian randomization analysis with multiple genetic variants using summarized data Lipid-related markers and cardiovascular disease prediction C-reactive protein, fibrinogen, and cardiovascular disease prediction Use of Mendelian randomisation to assess potential benefit of clinical intervention 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 Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases Glycated hemoglobin measurement and prediction of cardiovascular disease Relative and absolute risk of colorectal cancer for individuals with a family history: a meta-analysis Functional IL6R 358Ala allele impairs classical IL-6 receptor signaling and influences risk of diverse inflammatory diseases Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease Inflammatory cytokines and risk of coronary heart disease: new prospective study and updated meta-analysis Association of Cardiometabolic Multimorbidity With Mortality Leucocyte telomere length and risk of cardiovascular disease: systematic review and meta-analysis Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies The genetic architecture of type 2 diabetes Rare and low-frequency coding variants alter human adult height Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension Association of the 9p21.3 locus with risk of first-ever myocardial infarction in Pakistanis: case-control study in South Asia and updated meta-analysis of Europeans Leucocyte telomere length and risk of type 2 diabetes mellitus: new prospective cohort study and literature-based meta-analysis Turning the Pump Handle: Evolving Methods for Integrating the Evidence on Gene-Disease Association Genetic determinants of major blood lipids in Pakistanis compared with Europeans. Coffee Drinking and Mortality in 10 European Countries: A Multinational Cohort Study Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles PhenoScanner: a database of human genotype-phenotype associations. Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease Association analyses based on false discovery rate implicate new loci for coronary artery disease Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease 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 Network Mendelian randomization: using genetic variants as instrumental variables to investigate mediation in causal pathways Separate and combined associations of obesity and metabolic health with coronary heart disease: a pan-European case-cohort analysis. Association of Multiple Biomarkers of Iron Metabolism and Type 2 Diabetes: The EPIC-InterAct Study Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals. Natriuretic peptides and integrated risk assessment for cardiovascular disease: an individual-participant-data meta-analysis GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits Exome-wide association study of plasma lipids in >300,000 individuals Risk thresholds for alcohol consumption: combined analysis of individual-participant data for 599 912 current drinkers in 83 prospective studies. Assessing the causal association of glycine with risk of cardio-metabolic diseases Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.

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