Megan L Grove


Ontology type: schema:Person     


Person Info

NAME

Megan L

SURNAME

Grove

Publications in SciGraph latest 50 shown

  • 2018-12 An epigenome-wide study of obesity in African American youth and young adults: novel findings, replication in neutrophils, and relationship with gene expression in CLINICAL EPIGENETICS
  • 2018-08 Maternal Exposures Associated with Autism Spectrum Disorder in Jamaican Children in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 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 Novel associations between blood DNA methylation and body mass index in middle-aged and older adults in INTERNATIONAL JOURNAL OF OBESITY
  • 2018-04 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes 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
  • 2018-01 Genetic variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population in HUMAN GENETICS
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-12 Cerebral white matter hyperintensities on MRI and acceleration of epigenetic aging: the atherosclerosis risk in communities study in CLINICAL EPIGENETICS
  • 2017-09 Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease in NATURE GENETICS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2016-10 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci in NATURE GENETICS
  • 2016-09 Rare coding TTN variants are associated with electrocardiographic QT interval in the general population in SCIENTIFIC REPORTS
  • 2016-08 Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits in NATURE GENETICS
  • 2016-05 Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans in MOLECULAR PSYCHIATRY
  • 2015-12 Rare coding variants and X-linked loci associated with age at menarche in NATURE COMMUNICATIONS
  • 2015-12 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility in NATURE COMMUNICATIONS
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-04 PLD3 variants in population studies in NATURE
  • 2015-02 Association of mitochondrial DNA levels with frailty and all-cause mortality in JOURNAL OF MOLECULAR MEDICINE
  • 2014-12 Blood manganese concentrations in Jamaican children with and without autism spectrum disorders in ENVIRONMENTAL HEALTH
  • 2014-12 Evaluation of microarray-based DNA methylation measurement using technical replicates: the Atherosclerosis Risk In Communities (ARIC) Study in BMC BIOINFORMATICS
  • 2013-01 Seafood Consumption and Blood Mercury Concentrations in Jamaican Children With and Without Autism Spectrum Disorders in NEUROTOXICITY RESEARCH
  • 2012-09 Maternal and Paternal Age are Jointly Associated with Childhood Autism in Jamaica in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2010-12 Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations in ACTA DIABETOLOGICA
  • 2008-12 Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2008-12 Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD in BMC MEDICAL GENETICS
  • 2008-05 Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease in HUMAN GENETICS
  • 2007-11 Quantitative effects of common genetic variations in the 3′UTR of the human LDL-receptor gene and their associations with plasma lipid levels in the Atherosclerosis Risk in Communities study in HUMAN GENETICS
  • 2007-06 Gene–environment interaction and the GNB3 gene in the Atherosclerosis Risk in Communities Study in INTERNATIONAL JOURNAL OF OBESITY
  • 2007-05 Quantitative effects of common genetic variations in the 3′UTR of the human LDL-receptor gene and their associations with plasma lipid levels in the Atherosclerosis Risk in Communities study in HUMAN GENETICS
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