Adam S Butterworth


Ontology type: schema:Person     


Person Info

NAME

Adam S

SURNAME

Butterworth

Publications in SciGraph latest 50 shown

  • 2018-12 Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits in NATURE COMMUNICATIONS
  • 2018-12 Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels in NATURE COMMUNICATIONS
  • 2018-12 Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits in NATURE COMMUNICATIONS
  • 2018-12 Author Correction: Genome‐wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease in NATURE COMMUNICATIONS
  • 2018-12 Genome‐wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease in NATURE COMMUNICATIONS
  • 2018-11-02 Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps in NATURE GENETICS
  • 2018-06 Genomic atlas of the human plasma proteome in NATURE
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-04 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-01-23 Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2018-01 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-12-19 Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-12 Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity in SCIENTIFIC REPORTS
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-10 Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease in NATURE GENETICS
  • 2017-09 Association analyses based on false discovery rate implicate new loci for coronary artery disease in NATURE GENETICS
  • 2017-07-13 Platelet function is modified by common sequence variation in megakaryocyte super enhancers in NATURE COMMUNICATIONS
  • 2017-07 Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms in NATURE GENETICS
  • 2017-06 A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2016-11 Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps in NATURE GENETICS
  • 2016-10 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension in NATURE GENETICS
  • 2016-08 The genetic architecture of type 2 diabetes in NATURE
  • 2015-12 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 in BMC PUBLIC HEALTH
  • 2015-07 The Bangladesh Risk of Acute Vascular Events (BRAVE) Study: objectives and design in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 2009-03 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 in GENETICS IN MEDICINE
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