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An investigation of mitochondrial haplogroups in autismValproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblasts.The expression and function of microRNAs in chondrogenesis and osteoarthritis.Epigenetics, epidemiology and mitochondrial DNA diseases.Leveraging genomic data in smoking cessation trials in the era of Precision Medicine: Why and how.Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study.Migration and DNA methylation: a comparison of methylation patterns in type 2 diabetes susceptibility genes between indians and europeansPathogenic mitochondrial DNA mutations are common in the general populationDifferences in smoking associated DNA methylation patterns in South Asians and EuropeansEpigenetics and child health: basic principles.Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure.Role of DNA Methylation in Type 2 Diabetes Etiology: Using Genotype as a Causal Anchor.The Value of Biosamples in Smoking Cessation Trials: A Review of Genetic, Metabolomic, and Epigenetic Findings.Commentary: Migrant study designs for epigenetic studies of disease risk.Competitors who choose to be red have higher testosterone levels.The effects of being in a "new relationship" on levels of testosterone in men.Commentary: Migrant study designs for epigenetic studies of disease risk.Commentary: Migrant study designs for epigenetic studies of disease riskPGP-UK: a research and citizen science hybrid project in support of personalized medicineRole of the mitochondrial DNA 16184–16193 poly-C tract in type 2 diabetesThe Mitochondrial DNA A3243A>G Mutation Must Be An Infrequent Cause Of Asperger SyndromeDifferential methylation of the type 2 diabetes susceptibility locus KCNQ1 is associated with insulin sensitivity and is predicted by CpG site specific genetic variationmiR-324-5p is up regulated in end-stage osteoarthritis and regulates Indian Hedgehog signalling by differing mechanisms in human and mouse
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P50
description
researcher ORCID ID = 0000-0002-1500-3533
@en
wetenschapper
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name
Hannah R Elliott
@ast
Hannah R Elliott
@en
Hannah R Elliott
@es
Hannah R Elliott
@nl
type
label
Hannah R Elliott
@ast
Hannah R Elliott
@en
Hannah R Elliott
@es
Hannah R Elliott
@nl
prefLabel
Hannah R Elliott
@ast
Hannah R Elliott
@en
Hannah R Elliott
@es
Hannah R Elliott
@nl
P1153
24479518800
P31
P496
0000-0002-1500-3533