| scholarly article | Q13442814 |
| P50 | author | Ian Deary | Q1631578 |
| Anna Dominiczak | Q4766963 | ||
| Andrew D Morris | Q92527781 | ||
| Shona M Kerr | Q37634767 | ||
| Lynne J Hocking | Q37635316 | ||
| Blair H. Smith | Q37635980 | ||
| Donald J. MacIntyre | Q37650227 | ||
| Robert S Lindsay | Q40664138 | ||
| Colin Palmer | Q42603882 | ||
| P2093 | author name string | David J Porteous | |
| Mark McGilchrist | |||
| Harry Campbell | |||
| Ian Ford | |||
| Archie Campbell | |||
| Bridie Fitzpatrick | |||
| Cathy Jackson | |||
| Pamela Linksted | |||
| Lucy Wisely | |||
| Robin Morton | |||
| P2860 | cites work | Heritability of chronic pain in 2195 extended families | Q42636486 |
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| P433 | issue | 3 | |
| P304 | page(s) | 689-700 | |
| P577 | publication date | 2012-07-10 | |
| P1433 | published in | International Journal of Epidemiology | Q6051393 |
| P1476 | title | Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness | |
| P478 | volume | 42 |
| Q37603810 | A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder |
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| Q50027870 | Age at Menarche and Cardiometabolic Health: A Sibling Analysis in the Scottish Family Health Study. |
| Q64444694 | An epigenetic score for BMI based on DNA methylation correlates with poor physical health and major disease in the Lothian Birth Cohort |
| Q92354916 | An epigenome-wide association study of sex-specific chronological ageing |
| Q36892416 | Assessing the genetic overlap between BMI and cognitive function |
| Q33635647 | Assessing the presence of shared genetic architecture between Alzheimer's disease and major depressive disorder using genome-wide association data. |
| Q63363688 | Assessment of dried blood spots for DNA methylation profiling |
| Q64056497 | Association analyses identify 31 new risk loci for colorectal cancer susceptibility |
| Q47562858 | Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism. |
| Q37219260 | Association between cognition and gene polymorphisms involved in thrombosis and haemostasis |
| Q50080897 | Association between exposure to second-hand smoke and telomere length: cross-sectional study of 1303 non-smokers. |
| Q47152158 | Balancing the local and the universal in maintaining ethical access to a genomics biobank |
| Q96230335 | Bayesian reassessment of the epigenetic architecture of complex traits |
| Q90242232 | Cardiac Troponin T and Troponin I in the General Population |
| Q42692376 | Chronic pain in families: a cross-sectional study of shared social, behavioural, and environmental influences. |
| Q36287396 | Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin study. |
| Q55429019 | Coding variants in NOD-like receptors: An association study on risk and survival of colorectal cancer. |
| Q91810031 | Cohort Profile: Extended Cohort for E-health, Environment and DNA (EXCEED) |
| Q50100048 | Cohort Profile: Genetics of Diabetes Audit and Research in Tayside Scotland (GoDARTS). |
| Q47736676 | Cohort Profile: Stratifying Resilience and Depression Longitudinally (STRADL): a questionnaire follow-up of Generation Scotland: Scottish Family Health Study (GS:SFHS). |
| Q37610508 | Common genetic variants explain the majority of the correlation between height and intelligence: the generation Scotland study. |
| Q56992616 | DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies |
| Q94453566 | DNA methylation in APOE: The relationship with Alzheimer's and with cardiovascular health |
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| Q56992625 | DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders |
| Q57830320 | DOLORisk: study protocol for a multi-centre observational study to understand the risk factors and determinants of neuropathic pain |
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| Q45758035 | Does a history of depression actually mediate smoking-related pain? Findings from a cross-sectional general population-based study. |
| Q42698641 | Electronic health record and genome-wide genetic data in Generation Scotland participants. |
| Q35841930 | 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) |
| Q58691970 | Epigenetic prediction of complex traits and death |
| Q96303336 | Epigenetic prediction of major depressive disorder |
| Q58591011 | Epigenetic signatures of starting and stopping smoking |
| Q98395490 | Epigenome-wide analyses identify DNA methylation signatures of dementia risk |
| Q94599916 | Epigenome-wide association study and multi-tissue replication of individuals with alcohol use disorder: evidence for abnormal glucocorticoid signaling pathway gene regulation |
| Q38466084 | Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study. |
| Q30840891 | Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants |
| Q56992638 | Exploring causality in the association between circulating 25-hydroxyvitamin D and colorectal cancer risk: a large Mendelian randomisation study |
| Q64444047 | Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP |
| Q92955570 | Generation Scotland participant survey on data collection |
| Q37744445 | Genetic Evidence for a Link Between Favorable Adiposity and Lower Risk of Type 2 Diabetes, Hypertension, and Heart Disease |
| Q37693382 | Genetic Stratification to Identify Risk Groups for Alzheimer's Disease |
| Q36104781 | Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis |
| Q57316759 | Genetic and environmental contributions to psychological resilience and coping |
| Q60677966 | Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism |
| Q91452346 | Genetic and shared couple environmental contributions to smoking and alcohol use in the UK population |
| Q63352453 | Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life |
| Q104287299 | Genetic mechanisms of critical illness in Covid-19 |
| Q104439908 | Genetic mechanisms of critical illness in Covid-19 |
| Q47594715 | Genetic risk of major depressive disorder: the moderating and mediating effects of neuroticism and psychological resilience on clinical and self-reported depression. |
| Q28314981 | Genetic variants linked to education predict longevity |
| Q37603806 | Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium |
| Q40353484 | Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder |
| Q92024341 | Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income |
| Q104795221 | Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability |
| Q52560096 | Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. |
| Q42367819 | Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117). |
| Q64444709 | Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP |
| Q61801103 | Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland |
| Q47394982 | Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank. |
| Q60641775 | Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder |
| Q47556039 | Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank. |
| Q63433067 | Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions |
| Q48266836 | Genomic analysis of family data reveals additional genetic effects on intelligence and personality. |
| Q64444689 | Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits |
| Q90016822 | Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases |
| Q42361174 | Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank |
| Q36065471 | Homozygous loss-of-function variants in European cosmopolitan and isolate populations |
| Q64444712 | Identification of novel differentially methylated sites with potential as clinical predictors of impaired respiratory function and COPD |
| Q34048230 | Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis |
| Q92827686 | Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing |
| Q64454287 | Insulin resistance: Genetic associations with depression and cognition in population based cohorts |
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| Q90715551 | Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease |
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| Q56992661 | Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease |
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| Q37458960 | Molecular Genetic Contributions to Social Deprivation and Household Income in UK Biobank. |
| Q90715062 | Molecular Genetic Risk for Psychosis Is Associated With Psychosis Risk Symptoms in a Population-Based UK Cohort: Findings From Generation Scotland |
| Q33735573 | Molecular genetic contributions to socioeconomic status and intelligence. |
| Q28392317 | Mosaic structural variation in children with developmental disorders |
| Q40091740 | Novel Urinary Peptidomic Classifier Predicts Incident Heart Failure |
| Q35607087 | Opportunities for longitudinal data linkage in Scotland |
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| Q40229593 | Rapid Fractionation and Isolation of Whole Blood Components in Samples Obtained from a Community-based Setting. |
| Q28645673 | Recent genomic heritage in Scotland |
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