Amber Burt


Ontology type: schema:Person     


Person Info

NAME

Amber

SURNAME

Burt

Publications in SciGraph latest 50 shown

  • 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
  • 2018-01 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-12 Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals in BIODATA MINING
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2017-02 Is “incidental finding” the best term?: a study of patients’ preferences in GENETICS IN MEDICINE
  • 2017-02 Identifying gene–gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts in HUMAN GENETICS
  • 2016-06 Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome in JOURNAL OF GENETIC COUNSELING
  • 2015-12 Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network in GENOME MEDICINE
  • 2015-01 Genetic variation in the HLA region is associated with susceptibility to herpes zoster in GENES & IMMUNITY
  • 2014-12 Effects of dietary components on high-density lipoprotein measures in a cohort of 1,566 participants in NUTRITION & METABOLISM
  • 2014-11 A genome-wide map of adeno-associated virus–mediated human gene targeting in NATURE STRUCTURAL & MOLECULAR BIOLOGY
  • 2013-12 Dietary fatty acid intake is associated with paraoxonase 1 activity in a cohort-based analysis of 1,548 subjects in LIPIDS IN HEALTH AND DISEASE
  • 2009-02 Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate in EUROPEAN JOURNAL OF HUMAN GENETICS
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