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Lista de obras de Archie I Campbell

35th Annual Meeting of the European Association for the Study of Diabetes

artículo científico

35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999

article

A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila

artículo científico publicado en 2011

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

artículo científico publicado en 2018

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants

artículo científico publicado en 2010

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

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

artículo científico publicado en 2019

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019

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

article

Assessing the genetic overlap between BMI and cognitive function

artículo científico publicado en 2016

Assessment of dried blood spots for DNA methylation profiling

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

artículo científico publicado en 2019

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

artículo científico publicado en 2010

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits

scientific article published on 09 October 2020

Bayesian reassessment of the epigenetic architecture of complex traits

artículo científico publicado en 2020

Birth weight associations with DNA methylation differences in an adult population

artículo científico publicado en 2020

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer.

artículo científico publicado en 2009

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

artículo científico publicado en 2020

Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin study.

artículo científico publicado en 2017

Cohort Profile: Stratifying Resilience and Depression Longitudinally (STRADL): a questionnaire follow-up of Generation Scotland: Scottish Family Health Study (GS:SFHS).

artículo científico publicado en 2017

Cohort profile for the STratifying Resilience and Depression Longitudinally (STRADL) study: A depression-focused investigation of Generation Scotland, using detailed clinical, cognitive, and neuroimaging assessments

artículo científico publicado en 2019

Common genetic variants explain the majority of the correlation between height and intelligence: the generation Scotland study.

artículo científico publicado en 2014

Complex trait methylation scores in the prediction of major depressive disorder

artículo científico publicado en 2022

Correction: Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

artículo científico publicado en 2017

CovidLife: a resource to understand mental health, well-being and behaviour during the COVID-19 pandemic in the UK

artículo científico publicado en 2021

Current versus lifetime depression, APOE variation, and their interaction on cognitive performance in younger and older adults

artículo científico publicado en 2015

Differential effects of the APOE e4 allele on different domains of cognitive ability across the life-course

artículo científico publicado en 2015

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Dissection of major depressive disorder using polygenic risk scores for schizophrenia in two independent cohorts.

artículo científico publicado en 2016

Early life predictors of late life cerebral small vessel disease in four prospective cohort studies

artículo científico publicado en 2021

Early life predictors of late life cerebral small vessel disease in four prospective cohort studies

artículo científico publicado en 2021

Effect of Smoking on Blood Pressure and Resting Heart Rate: A Mendelian Randomization Meta-Analysis in the CARTA Consortium

artículo científico publicado en 2015

Electronic health record and genome-wide genetic data in Generation Scotland participants.

artículo científico publicado en 2017

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)

artículo científico publicado en 2015

Epigenetic prediction of complex traits and death

article by Daniel L McCartney et al published 27 September 2018 in Genome Biology

Epigenetic signatures of starting and stopping smoking

artículo científico publicado en 2018

Epigenome-wide association study of alcohol consumption in N = 8161 individuals and relevance to alcohol use disorder pathophysiology: identification of the cystine/glutamate transporter SLC7A11 as a top target

artículo científico publicado en 2021

Erratum: COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer

article

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

artículo científico publicado en 2017

Estimating human inbreeding coefficients: comparison of genealogical and marker heterozygosity approaches

artículo científico publicado en 2006

Evidence for large-scale gene-by-smoking interaction effects on pulmonary function.

artículo científico publicado en 2017

Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.

artículo científico

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

artículo científico publicado en 2017

Face covering adherence is positively associated with better mental health and wellbeing: a longitudinal analysis of the CovidLife surveys

artículo científico publicado en 2021

Factors associated with sharing e-mail information and mental health survey participation in large population cohorts

artículo científico publicado en 2019

Feasibility and ethics of using data from the Scottish newborn blood spot archive for research

artículo científico publicado en 2022

Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP

artículo científico publicado en 2019

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

scientific article published on 05 May 2020

Generation Scotland - Using Electronic Health Records for Research

article

Generation Scotland participant survey on data collection

artículo científico publicado en 2019

Generation Scotland: using data linkage for longitudinal studies

article

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

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

Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis

artículo científico publicado en 2016

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

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

artículo científico publicado en 2018

Genetic and environmental risk for chronic pain and the contribution of risk variants for psychiatric disorders. Results from Generation Scotland: Scottish Family Health Study and UK Biobank

article

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

artículo científico publicado en 2019

Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression

artículo científico publicado en 2020

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

artículo científico publicado en 2015

Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study

artículo científico publicado en 2006

Genetic parameters for periodontal disease: an analysis of electronic dental treatment records linked to pedigree, genomic, sociodemographic and clinical data

Genetic stratification of depression in UK Biobank

scientific article published on 24 May 2020

Genetic variants linked to education predict longevity

artículo científico publicado en 2016

Genome-Wide and Abdominal MRI-Imaging Data Provides Evidence that a Genetically Determined Favourable Adiposity Phenotype is Characterized by Lower Ectopic Liver Fat and Lower Risk of Type 2 Diabetes, Heart Disease and Hypertension

scientific article published on 23 October 2018

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets

artículo científico publicado en 2017

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

article

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

artículo científico publicado en 2017

Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP

article

Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain

artículo científico publicado en 2018

Genome-wide methylation data improves dissection of the effect of smoking on body mass index

artículo científico publicado en 2021

Genome-wide methylation data improves dissection of the effect of smoking on body mass index

artículo científico publicado en 2020

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

artículo científico publicado en 2016

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

artículo científico publicado en 2017

Genomic insights into the origin of farming in the ancient Near East

artículo científico publicado en 2016

Heavier smoking may lead to a relative increase in waist circumference: evidence for a causal relationship from a Mendelian randomisation meta-analysis. The CARTA consortium

artículo científico publicado en 2015

Homozygous loss-of-function variants in European cosmopolitan and isolate populations

artículo científico publicado en 2015

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

artículo científico publicado en 2019

Investigating the possible causal association of smoking with depression and anxiety using Mendelian randomisation meta-analysis: the CARTA consortium

artículo científico publicado en 2014

Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease

artículo científico publicado en 2018

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

artículo científico publicado en 2016

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

scientific article published on 12 January 2018

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

Methylome-wide association study of antidepressant use in Generation Scotland and the Netherlands Twin Register implicates the innate immune system

artículo científico publicado en 2021

Methylome-wide association study of early life stressors and adult mental health

artículo científico publicado en 2022

Molecular genetic contributions to socioeconomic status and intelligence.

artículo científico publicado en 2014

Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

article

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

artículo científico publicado en 2019

Multi-ethnic genome-wide association study for atrial fibrillation

article

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

artículo científico publicado en 2017

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

artículo científico publicado en 2018

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

artículo científico publicado en 2016

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

artículo científico publicado en 2019

Participation and item missingness in a depression questionnaire in Generation Scotland: The Scottish Family Health Study

artículo científico publicado en 2023

Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

artículo científico publicado en 2022

Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

artículo científico publicado en 2016

Pharmaco-epidemiology of antidepressant exposure in a UK cohort record-linkage study

scientific article published on 27 February 2019

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

scientific article published on 29 October 2019

Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study

artículo científico publicado en 2018

Polygenic risk of ischemic stroke is associated with cognitive ability

artículo científico publicado en 2015

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

artículo científico publicado en 2019

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer ⬇️

artículo científico publicado en 2015

Regional variation in health is predominantly driven by lifestyle rather than genetics

artículo científico publicado en 2017

Runs of Homozygosity in European Populations

artículo científico publicado en 2008

RuralCovidLife: A new resource for the impact of the pandemic on rural Scotland

artículo científico publicado en 2022

SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function

artículo científico publicado en 2016

Self-reported medication use validated through record linkage to national prescribing data

artículo científico publicado en 2017

Sex-Differences in the Metabolic Health of Offspring of Parents with Diabetes: A Record-Linkage Study

artículo científico publicado en 2015

Socioeconomic Deprivation: An Important, Largely Unrecognized Risk Factor in Primary Prevention of Cardiovascular Disease

Stability of adiposity phenotypes from childhood and adolescence into young adulthood with contribution of parental measures.

artículo científico publicado en 2001

Stratification by smoking status reveals an association of CHRNA5-A3-B4 genotype with body mass index in never smokers

artículo científico publicado en 2014

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

artículo científico publicado en 2019

TeenCovidLife: a resource to understand the impact of the COVID-19 pandemic on adolescents in Scotland

artículo científico publicado en 2022

The genetic landscape of Scotland and the Isles

artículo científico publicado en 2019

The genetic structure of the world's first farmers

The power of genetic diversity in genome-wide association studies of lipids

The role of neuroticism in self-harm and suicidal ideation: results from two UK population-based cohorts

artículo científico publicado en 2019

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

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