Author: Archie Campbell

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Preprints

The genetic structure of the world's first farmers

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Clinical classifiers of COVID-19 infection from novel ultra-high-throughput proteomics

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112,117).

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Mental health during the COVID-19 pandemic in two longitudinal UK population cohorts

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Genetic stratification of depression in UK Biobank suggests a subgroup linked to age of natural menopause

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Epigenetic prediction of complex traits and death

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Genome-wide Meta-analysis of 158,000 Individuals of European Ancestry Identifies Three Loci Associated with Chronic Back Pain

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Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility

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  • In genetic and genomic medicine: 51 out of 488
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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Quantifying the extent to which index event biases influence large genetic association studies

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Electronic Health Record and Genome-wide Genetic Data in Generation Scotland Participants

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Epigenetic clocks predict prevalence and incidence of leading causes of death and disease burden

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A meta-analysis of genome-wide association studies of epigenetic age acceleration

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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DNA methylation age acceleration and risk factors for Alzheimer's disease

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

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VEP-G2P: A Tool for Efficient, Flexible and Scalable Diagnostic Filtering of Genomic Variants

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Insight into the genetic aetiology of retinal detachment by combining small clinical and large population-based datasets

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An epigenetic score for BMI based on DNA methylation correlates with poor physical health and major disease in the Lothian Birth Cohort 1936.

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Meta-analysis of exome array data identifies six novel genetic loci for lung function

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A time-resolved proteomic and diagnostic map characterizes COVID-19 disease progression and predicts outcome

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Birth weight associations with psychiatric and physical health, cognitive function, and DNA methylation differences in an adult population

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Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

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Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

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Genetic and shared couple environmental contributions to smoking and alcohol use in the UK population

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An epigenome-wide association study of sex-specific chronological ageing

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Identification of epigenome-wide DNA methylation differences between carriers of APOE ε4 and APOE ε2

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Epigenome-wide analyses identify DNA methylation signatures of dementia risk

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Epigenetic signatures of starting and stopping smoking

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Shared genetics and couple-associated environment are major contributors to the risk of both clinical and self-declared depression

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Assessment of Dried Blood Spots for DNA Methylation Profiling

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Identification of novel differentially methylated sites with potential as clinical predictors of impaired respiratory function and COPD

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DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan

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DNA methylation in the APOE gene: its link with Alzheimer's and cardiovascular health

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Subthreshold psychosis symptoms associated with molecular genetic risk in a population-based cohort: Findings from Generation Scotland

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Creating and validating a DNA methylation-based proxy for Interleukin-6

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DNA methylation signatures of C-reactive protein associations with structural neuroimaging measures and major depressive disorder

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Using human genetics to understand the causes and consequences of circulating cardiac troponin I in the general population

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Omics versus Questionnaires: Using methylation data to assess the environmental impact of smoking on obesity-related traits

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