Works by Campbell, Archie
Results: 94
The circulating proteome and brain health: Mendelian randomisation and cross-sectional analyses.
- Published in:
- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-02915-x
- By:
- Publication type:
- Article
Epigenetic prediction of complex traits and death.
- Published in:
- Genome Biology, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s13059-018-1514-1
- By:
- Publication type:
- Article
Pharmaco-epidemiology of antidepressant exposure in a UK cohort record-linkage study.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 9, p. 1, doi. 10.1371/journal.pgen.1007601
- By:
- Publication type:
- Article
Genome-wide characterization of 54 urinary metabolites reveals molecular impact of kidney function.
- Published in:
- Nature Communications, 2025, v. 16, p. 1, doi. 10.1038/s41467-024-55182-1
- By:
- Publication type:
- Article
Mental illness and COVID-19 vaccination: a multinational investigation of observational & register-based data.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-52342-1
- By:
- Publication type:
- Article
Blood-based epigenome-wide analyses of 19 common disease states: A longitudinal, population-based linked cohort study of 18,413 Scottish individuals.
- Published in:
- PLoS Medicine, 2023, v. 20, n. 7, p. 1, doi. 10.1371/journal.pmed.1004247
- By:
- Publication type:
- Article
Using tree-based methods for detection of gene–gene interactions in the presence of a polygenic signal: simulation study with application to educational attainment in the Generation Scotland Cohort Study.
- Published in:
- Bioinformatics, 2019, v. 35, n. 2, p. 181, doi. 10.1093/bioinformatics/bty462
- By:
- Publication type:
- Article
Structural brain correlates of childhood trauma with replication across two large, independent community-based samples.
- Published in:
- European Psychiatry, 2023, v. 66, n. 1, p. 1, doi. 10.1192/j.eurpsy.2022.2347
- By:
- Publication type:
- Article
Association of low-frequency and rare coding variants with information processing speed.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01736-6
- By:
- Publication type:
- Article
Hair glucocorticoids are associated with childhood adversity, depressive symptoms and reduced global and lobar grey matter in Generation Scotland.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01644-9
- By:
- Publication type:
- Article
Integrated methylome and phenome study of the circulating proteome reveals markers pertinent to brain health.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32319-8
- By:
- Publication type:
- Article
Prescreening for European Prevention of Alzheimer Dementia (EPAD) trial-ready cohort: impact of AD risk factors and recruitment settings.
- Published in:
- Alzheimer's Research & Therapy, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13195-019-0576-y
- By:
- Publication type:
- Article
Epigenetic measures of ageing predict the prevalence and incidence of leading causes of death and disease burden.
- Published in:
- Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-020-00905-6
- By:
- Publication type:
- Article
Characterisation of an inflammation-related epigenetic score and its association with cognitive ability.
- Published in:
- Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-020-00903-8
- By:
- Publication type:
- Article
DNA methylation outlier burden, health, and ageing in Generation Scotland and the Lothian Birth Cohorts of 1921 and 1936.
- Published in:
- Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-020-00838-0
- By:
- Publication type:
- Article
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
- Published in:
- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0414-4
- By:
- Publication type:
- Article
Epigenome-wide association study of global cortical volumes in generation Scotland: Scottish family health study.
- Published in:
- Epigenetics, 2022, v. 17, n. 10, p. 1143, doi. 10.1080/15592294.2021.1997404
- By:
- Publication type:
- Article
Birth weight associations with DNA methylation differences in an adult population.
- Published in:
- Epigenetics, 2021, v. 16, n. 7, p. 783, doi. 10.1080/15592294.2020.1827713
- By:
- Publication type:
- Article
Recent genomic heritage in Scotland.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1605-2
- By:
- Publication type:
- Article
Genome-wide methylation data improves dissection of the effect of smoking on body mass index.
- Published in:
- PLoS Genetics, 2021, v. 17, n. 9, p. 1, doi. 10.1371/journal.pgen.1009750
- By:
- Publication type:
- Article
General Framework for Meta-Analysis of Haplotype Association Tests.
- Published in:
- Genetic Epidemiology, 2016, v. 40, n. 3, p. 244, doi. 10.1002/gepi.21959
- By:
- Publication type:
- Article
Regional variation in health is predominantly driven by lifestyle rather than genetics.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00497-5
- By:
- Publication type:
- Article
Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS).
- Published in:
- PLoS ONE, 2015, v. 10, n. 11, p. 1, doi. 10.1371/journal.pone.0142197
- By:
- Publication type:
- Article
Sex-Differences in the Metabolic Health of Offspring of Parents with Diabetes: A Record-Linkage Study.
- Published in:
- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0134883
- By:
- Publication type:
- Article
Association of Genetic Variant at Chromosome 12q23.1 With Neuropathic Pain Susceptibility.
- Published in:
- JAMA Network Open, 2021, v. 4, n. 12, p. e2136560, doi. 10.1001/jamanetworkopen.2021.36560
- By:
- Publication type:
- Article
Epigenetic scores of blood-based proteins as biomarkers of general cognitive function and brain health.
- Published in:
- Clinical Epigenetics, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13148-024-01661-7
- By:
- Publication type:
- Article
Identification of influential probe types in epigenetic predictions of human traits: implications for microarray design.
- Published in:
- Clinical Epigenetics, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13148-022-01320-9
- By:
- Publication type:
- Article
Spectral clustering based on structural magnetic resonance imaging and its relationship with major depressive disorder and cognitive ability.
- Published in:
- European Journal of Neuroscience, 2021, v. 54, n. 6, p. 6281, doi. 10.1111/ejn.15423
- By:
- Publication type:
- Article
Early life predictors of late life cerebral small vessel disease in four prospective cohort studies.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Blunted medial prefrontal cortico-limbic reward-related effective connectivity and depression.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Stratification by Smoking Status Reveals an Association of CHRNA5-A3-B4 Genotype with Body Mass Index in Never Smokers.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 12, p. 1, doi. 10.1371/journal.pgen.1004799
- By:
- Publication type:
- Article
Multiple Cardiac Biomarkers to Improve Prediction of Cardiovascular Events: Findings from the Generation Scotland Scottish Family Health Study.
- Published in:
- Clinical Chemistry, 2024, v. 70, n. 2, p. 403, doi. 10.1093/clinchem/hvad205
- By:
- Publication type:
- Article
Sex Differences in Cardiac Troponin I and T and the Prediction of Cardiovascular Events in the General Population.
- Published in:
- Clinical Chemistry, 2021, v. 67, n. 10, p. 1351, doi. 10.1093/clinchem/hvab109
- By:
- Publication type:
- Article
Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Novel Urinary Peptidomic Classifier Predicts Incident Heart Failure.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Correction: Association of low-frequency and rare coding variants with information processing speed.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Exome Sequencing to Detect Rare Variants Associated With General Cognitive Ability: A Pilot Study.
- Published in:
- Twin Research & Human Genetics, 2015, v. 18, n. 2, p. 117, doi. 10.1017/thg.2015.10
- By:
- Publication type:
- Article
Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations.
- Published in:
- International Journal of Epidemiology, 2022, v. 51, n. 3, p. e108, doi. 10.1093/ije/dyab234
- By:
- Publication type:
- Article
Factors associated with sharing e-mail information and mental health survey participation in large population cohorts.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Evidence for large-scale gene-by-smoking interaction effects on pulmonary function.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness.
- Published in:
- International Journal of Epidemiology, 2013, v. 42, n. 3, p. 689, doi. 10.1093/ije/dys084
- By:
- Publication type:
- Article
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39248-0
- By:
- Publication type:
- Article
Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39248-0
- By:
- Publication type:
- Article
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39248-0
- By:
- Publication type:
- Article
Blood-based epigenome-wide analyses of cognitive abilities.
- Published in:
- Genome Biology, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s13059-021-02596-5
- By:
- Publication type:
- Article
Identification of epigenome-wide DNA methylation differences between carriers of APOE ε4 and APOE ε2 alleles.
- Published in:
- Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-020-00808-4
- By:
- Publication type:
- Article
An epigenome-wide association study of sex-specific chronological ageing.
- Published in:
- Genome Medicine, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s13073-019-0693-z
- By:
- Publication type:
- Article
Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin study.
- Published in:
- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0170653
- By:
- Publication type:
- Article