| human | Q5 |
| P856 | official website | https://research-information.bristol.ac.uk/en/persons/hannah-r-elliott(985fc0ff-21d1-43af-aa61-cfe914b9d1a8).html |
| P496 | ORCID iD | 0000-0002-1500-3533 |
| P1153 | Scopus author ID | 24479518800 |
| P69 | educated at | Durham University | Q458393 |
| Newcastle University | Q837164 | ||
| P108 | employer | University of Bristol | Q459506 |
| Newcastle University | Q837164 | ||
| Bristol Medical School | Q4968954 | ||
| P734 | family name | Elliott | Q21449521 |
| Elliott | Q21449521 | ||
| Elliott | Q21449521 | ||
| P735 | given name | Hannah | Q39138052 |
| Hannah | Q39138052 | ||
| P106 | occupation | researcher | Q1650915 |
| Q28262949 | An investigation of mitochondrial haplogroups in autism |
| Q112644728 | Association of medically assisted reproduction with offspring cord blood DNA methylation across cohorts |
| Q122951782 | Characterisation of ethnic differences in DNA methylation between UK-resident South Asians and Europeans |
| Q56511231 | Commentary: Migrant study designs for epigenetic studies of disease risk |
| Q40333942 | Commentary: Migrant study designs for epigenetic studies of disease risk. |
| Q50955526 | Commentary: Migrant study designs for epigenetic studies of disease risk. |
| Q44389222 | Competitors who choose to be red have higher testosterone levels. |
| Q37559432 | Differences in smoking associated DNA methylation patterns in South Asians and Europeans |
| Q63352567 | Differential methylation of the type 2 diabetes susceptibility locus KCNQ1 is associated with insulin sensitivity and is predicted by CpG site specific genetic variation |
| Q37775410 | Epigenetics and child health: basic principles. |
| Q35832776 | Epigenetics, epidemiology and mitochondrial DNA diseases. |
| Q36496178 | 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 |
| Q109309630 | Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging |
| Q122951773 | Investigating causality in the association between DNA methylation and type 2 diabetes using bidirectional two-sample Mendelian randomisation |
| Q36370325 | Leveraging genomic data in smoking cessation trials in the era of Precision Medicine: Why and how. |
| Q97539776 | Leveraging the urban-rural divide for epigenetic research |
| Q36807943 | Migration and DNA methylation: a comparison of methylation patterns in type 2 diabetes susceptibility genes between indians and europeans |
| Q57531289 | PGP-UK: a research and citizen science hybrid project in support of personalized medicine |
| Q36808847 | Pathogenic mitochondrial DNA mutations are common in the general population |
| Q38752250 | Role of DNA Methylation in Type 2 Diabetes Etiology: Using Genotype as a Causal Anchor |
| Q57943302 | Role of the mitochondrial DNA 16184–16193 poly-C tract in type 2 diabetes |
| Q122951791 | The EWAS Catalog: a database of epigenome-wide association studies |
| Q58208506 | The Mitochondrial DNA A3243A>G Mutation Must Be An Infrequent Cause Of Asperger Syndrome |
| Q39284073 | The Value of Biosamples in Smoking Cessation Trials: A Review of Genetic, Metabolomic, and Epigenetic Findings |
| Q47667579 | The effects of being in a "new relationship" on levels of testosterone in men. |
| Q34238501 | The expression and function of microRNAs in chondrogenesis and osteoarthritis. |
| Q38088972 | Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure |
| Q35986692 | Titin mutation segregates with hereditary myopathy with early respiratory failure |
| Q33581698 | Valproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblasts |
| Q64095964 | miR-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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