|Pathogenic mitochondrial DNA mutations are common in the general population|
HR Elliott, DC Samuels, JA Eden, CL Relton, PF Chinnery
The American journal of human genetics 83 (2), 254-260, 2008
|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|
JC Chambers, M Loh, B Lehne, A Drong, J Kriebel, V Motta, S Wahl, ...
The lancet Diabetes & endocrinology 3 (7), 526-534, 2015
|Differences in smoking associated DNA methylation patterns in South Asians and Europeans|
HR Elliott, T Tillin, WL McArdle, K Ho, A Duggirala, TM Frayling, ...
Clinical epigenetics 6 (1), 1-10, 2014
|The expression and function of microRNAs in chondrogenesis and osteoarthritis|
TE Swingler, G Wheeler, V Carmont, HR Elliott, MJ Barter, M Abu‐Elmagd, ...
Arthritis & Rheumatism 64 (6), 1909-1919, 2012
|Epigenetics, epidemiology and mitochondrial DNA diseases|
PF Chinnery, HR Elliott, G Hudson, DC Samuels, CL Relton
International journal of epidemiology 41 (1), 177-187, 2012
|Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation|
JL Min, G Hemani, E Hannon, KF Dekkers, J Castillo-Fernandez, R Luijk, ...
Nature genetics 53 (9), 1311-1321, 2021
|Titin mutation segregates with hereditary myopathy with early respiratory failure|
G Pfeffer, HR Elliott, H Griffin, R Barresi, J Miller, J Marsh, A Evilä, ...
Brain 135 (6), 1695-1713, 2012
|The EWAS Catalog: a database of epigenome-wide association studies|
T Battram, P Yousefi, G Crawford, C Prince, MS Babaei, G Sharp, ...
Wellcome open research 7, 2022
|Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study|
PF Chinnery, HR Elliott, A Syed, PM Rothwell
The Lancet Neurology 9 (5), 498-503, 2010
|Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure|
G Pfeffer, R Barresi, IJ Wilson, SA Hardy, H Griffin, J Hudson, HR Elliott, ...
Journal of Neurology, Neurosurgery & Psychiatry 85 (3), 331-338, 2014
|Role of the mitochondrial DNA 16184–16193 poly-C tract in type 2 diabetes|
PF Chinnery, HR Elliott, S Patel, C Lambert, SM Keers, SE Durham, ...
The Lancet 366 (9497), 1650-1651, 2005
|Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging|
DL McCartney, JL Min, RC Richmond, T Palviainen, M Ollikainen, ...
|Epigenetics and child health: basic principles|
A Groom, HR Elliott, ND Embleton, CL Relton
Archives of disease in childhood 96 (9), 863-869, 2011
|Epigenetics and gestational diabetes: a review of epigenetic epidemiology studies and their use to explore epigenetic mediation and improve prediction|
HR Elliott, GC Sharp, CL Relton, DA Lawlor
Diabetologia 62, 2171-2178, 2019
|Valproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblasts|
KS Sitarz, HR Elliott, BS Karaman, C Relton, PF Chinnery, R Horvath
Molecular genetics and metabolism 112 (1), 57-63, 2014
|Associations between high blood pressure and DNA methylation|
N Kazmi, HR Elliott, K Burrows, T Tillin, AD Hughes, N Chaturvedi, ...
PloS one 15 (1), e0227728, 2020
|Role of DNA methylation in type 2 diabetes etiology: using genotype as a causal anchor|
HR Elliott, HA Shihab, GA Lockett, JW Holloway, AF McRae, GD Smith, ...
Diabetes 66 (6), 1713-1722, 2017
|miR-324-5p is up regulated in end-stage osteoarthritis and regulates Indian Hedgehog signalling by differing mechanisms in human and mouse|
S Woods, MJ Barter, HR Elliott, CM McGillivray, MA Birch, IM Clark, ...
Matrix Biology 77, 87-100, 2019
|Episodic ataxia and hemiplegia caused by the 8993T→ C mitochondrial DNA mutation|
K Craig, HR Elliott, SM Keers, C Lambert, A Pyle, TD Graves, ...
Journal of medical genetics 44 (12), 797-799, 2007
|DNA methylation of blood cells is associated with prevalent type 2 diabetes in a meta-analysis of four European cohorts|
DL Juvinao-Quintero, RE Marioni, C Ochoa-Rosales, TC Russ, IJ Deary, ...
Clinical epigenetics 13, 1-14, 2021