David Melzer

University of Exeter — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

87h-index36.4kcitations410works5.62yr avg
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Research Topics

Genetic Associations and Epidemiology(51), Health disparities and outcomes(40), Health Systems, Economic Evaluations, Quality of Life(27), Frailty in Older Adults(26), Nutrition and Health in Aging(23)

Publications406 total

Chondrocalcinosis and the haemochromatosis-linked HFE C282Y homozygous variant in the UK Biobank
EULAR Rheumatology Open·2025Open Access
Data from Hereditary Hemochromatosis Variant Associations with Incident Nonliver Malignancies: 11-Year Follow-up in UK Biobank
2025Open Access
Supplementary Table from Hereditary Hemochromatosis Variant Associations with Incident Nonliver Malignancies: 11-Year Follow-up in UK Biobank
2025Open Access
Predictors of MRI-estimated brain iron deposition in dementia and Parkinson's disease-associated subcortical regions: Genetic and observational analysis in UK Biobank
Journal of Alzheimer s Disease·2025Open Access
Predictors of brain iron deposition in dementia and Parkinson’s disease-associated subcortical regions: genetic and observational analysis in UK Biobank
2025Open Access
A systematic analysis of the contribution of genetics to multimorbidity and comparisons with primary care data
EBioMedicine·2025· 9 citedOpen Access
Mitochondrial DNA copy number from human blood is associated with specific cognitive function
Alzheimer s & Dementia·2024Open Access
Mitochondrial DNA copy number associated dementia risk by somatic mutations and frailty
GeroScience·2024· 5 citedOpen Access
Incidence of liver complications with hemochromatosis-associated HFE p.C282Y homozygosity: The role of central adiposity
Hepatology·2024· 7 citedOpen Access
MRI-derived brain iron, grey matter volume, and risk of dementia and Parkinson's disease: Observational and genetic analysis in the UK Biobank cohort
Neurobiology of Disease·2024· 17 citedOpen Access
A systematic analysis of the contribution of genetics to multimorbidity and comparisons with primary care data
2024· 3 citedOpen Access
SLCO1B1 Exome Sequencing and Statin Treatment Response in 64,000 UK Biobank Patients
International Journal of Molecular Sciences·2024· 2 citedOpen Access
Polygenic scores for cardiovascular risk factors improve estimation of clinical outcomes in CCB treatment compared to pharmacogenetic variants alone
The Pharmacogenomics Journal·2024· 4 citedOpen Access
<i>HFE</i> genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank
BMJ Open·2024· 33 citedOpen Access
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women
UNC Libraries·2024Open Access
Is Mitochondrial DNA Copy Number from Human Blood Associated with Iron Deposits in the Brain?
Antioxidants and Redox Signaling·2024· 1 citedOpen Access
Iron and risk of dementia: Mendelian randomisation analysis in UK Biobank
Journal of Medical Genetics·2024· 15 citedOpen Access
Mitochondrial DNA copy number predicts dementia risk with early mobility impairment
Alzheimer s & Dementia·2023· 3 citedOpen Access
<i>HFE</i> genotypes, haemochromatosis diagnosis and clinical outcomes to age 80: a prospective cohort study in UK Biobank
2023Open Access
Does physical activity moderate the association between shorter leukocyte telomere length and incident coronary heart disease? Data from 54,180 UK Biobank participants
GeroScience·2023· 2 citedOpen Access
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Frequent Co-authors

Luigi Ferrucci(24), Luke C. Pilling(15), Timothy M. Frayling(11), Stefania Bandinelli(11), André G. Uitterlinden(9), Albert Hofman(9), John R. B. Perry(8), Dena Hernández(8), Andrew Singleton(8), Anna Murray(8), Joanne M. Murabito(7), William Henley(7), Iain Lang(7), Nicholas J. Wareham(6), Toshiko Tanaka(6), Tamara S. Galloway(6), Jack M. Guralnik(6), George A. Kuchel(6), Michael N. Weedon(5), Lorna W. Harries(5)