Search Results - "GROVE, Megan L"
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Evaluation of mitochondrial DNA copy number estimation techniques
Published in PloS one (31-01-2020)“…Mitochondrial DNA copy number (mtDNA-CN), a measure of the number of mitochondrial genomes per cell, is a minimally invasive proxy measure for mitochondrial…”
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2
Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci
Published in Human molecular genetics (01-08-2015)“…Obesity is an important component of the pathophysiology of chronic diseases. Identifying epigenetic modifications associated with elevated adiposity,…”
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3
Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities Study
Published in Journal of the American Society of Nephrology (01-08-2016)“…Mitochondrial dysfunction in kidney cells has been implicated in the pathogenesis of CKD. Mitochondrial DNA (mtDNA) copy number is a surrogate measure of…”
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4
A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos
Published in American journal of human genetics (05-11-2020)“…Variation in levels of the human metabolome reflect changes in homeostasis, providing a window into health and disease. The genetic impact on circulating…”
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5
MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertension
Published in PloS one (03-08-2017)“…In older adults (aged 70-74 years), African-Americans have 4-fold higher risk of developing hypertension-attributed end-stage renal disease (ESRD) than…”
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Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs
Published in Genome medicine (28-09-2020)“…Mitochondrial DNA copy number (mtDNA-CN) has been associated with a variety of aging-related diseases, including all-cause mortality. However, the mechanism by…”
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Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality
Published in Nature communications (30-09-2023)“…Mitochondria carry their own circular genome and disruption of the mitochondrial genome is associated with various aging-related diseases. Unlike the nuclear…”
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Longitudinal change in blood DNA epigenetic signature after smoking cessation
Published in Epigenetics (03-10-2022)“…Cigarette smoking is associated with epigenetic changes that may be reversible following smoking cessation. Whole blood DNA methylation was evaluated in…”
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Factors associated with blood mercury concentrations and their interactions with three glutathione S-transferase genes (GSTT1, GSTM1, and GSTP1): an exposure assessment study of typically developing Jamaican children
Published in BMC pediatrics (04-01-2024)“…Jamaican soil is abundant in heavy metals including mercury (Hg). Due to availability and ease of access, fish is a traditional dietary component in Jamaica…”
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10
Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections
Published in American journal of human genetics (01-09-2016)“…Acute aortic dissections are a preventable cause of sudden death if individuals at risk are identified and surgically repaired in a non-emergency setting…”
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Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers
Published in PloS one (18-09-2019)“…Hypertension (HTN) disproportionately affects African Americans (AAs), who respond better to thiazide diuretics than other antihypertensives. Variants of the…”
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Lipoprotein-associated phospholipase A2 and risk of incident peripheral arterial disease: Findings from The Atherosclerosis Risk in Communities study (ARIC)
Published in Atherosclerosis (01-01-2018)“…Results from prospective studies evaluating the relationship between elevated lipoprotein-associated phospholipase A2 (Lp-PLA2) activity and incident…”
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Cerebral white matter hyperintensities on MRI and acceleration of epigenetic aging: the atherosclerosis risk in communities study
Published in Clinical epigenetics (14-02-2017)“…Cerebral white matter hyperintensities (WMH) on magnetic resonance imaging (MRI) are part of the spectrum of brain vascular injury accompanying aging and are…”
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14
The diagnosis of autism and autism spectrum disorder in low- and middle-income countries: Experience from Jamaica
Published in Autism : the international journal of research and practice (01-07-2017)“…The administration requirements of the Autism Diagnostic Observation Schedule and the Autism Diagnostic Interview–Revised, widely used in high-income…”
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Chromosome 9p21 Single Nucleotide Polymorphisms Are Not Associated With Recurrent Myocardial Infarction in Patients With Established Coronary Artery Disease
Published in Circulation Journal (2012)“…Background: Chromosome 9p21 single nucleotide polymorphisms (SNPs) have been shown to be associated with coronary heart disease in multiple studies. The aim of…”
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16
Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program
Published in European journal of human genetics : EJHG (01-12-2008)“…Essential hypertension is a principal cardiovascular risk factor whose origin remains unknown. Classical genetic studies have shown that blood pressure is at…”
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Corrigendum to ‘Association of sickle cell trait with measures of cognitive function and dementia in African Americans’ eNeurologicalSci, Vol. 16 (2019), 100,201
Published in eNeurologicalSci (01-12-2020)“…[This corrects the article DOI: 10.1016/j.ensci.2019.100201.]…”
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Single Nucleotide Polymorphisms in Cholesteryl Ester Transfer Protein Gene and Recurrent Coronary Heart Disease or Mortality in Patients With Established Atherosclerosis
Published in The American journal of cardiology (01-11-2013)“…It is not known whether genetic variants in the cholesteryl ester transfer protein (CETP) gene are associated with recurrent coronary heart disease events or…”
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Association of sickle cell trait with measures of cognitive function and dementia in African Americans
Published in eNeurologicalSci (01-09-2019)“…The incidence and prevalence of cognitive decline and dementia are significantly higher among African Americans compared with non-Hispanic Whites. The aim of…”
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Host and gut microbial tryptophan metabolism and type 2 diabetes: an integrative analysis of host genetics, diet, gut microbiome and circulating metabolites in cohort studies
Published in Gut (01-06-2022)“…Tryptophan can be catabolised to various metabolites through host kynurenine and microbial indole pathways. We aimed to examine relationships of host and…”
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