Works matching AU Porteous, David J.
Results: 104
Genetic contributions to stability and change in intelligence from childhood to old age.
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- Nature, 2012, v. 482, n. 7384, p. 212, doi. 10.1038/nature10781
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- Article
Genome-wide association study of cardiac troponin I in the general population.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 2027, doi. 10.1093/hmg/ddab124
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- Article
Epigenetic measures of ageing predict the prevalence and incidence of leading causes of death and disease burden.
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- Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-020-00905-6
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- Article
Investigating Shared Aetiology Between Type 2 Diabetes and Major Depressive Disorder in a Population Based Cohort.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 3, p. 227, doi. 10.1002/ajmg.b.32478
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- Article
Speeding disease gene discovery by sequence based candidate prioritization.
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- BMC Bioinformatics, 2005, v. 6, p. 55, doi. 10.1186/1471-2105-6-55
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- Article
Elimination of contaminant Escherichia coli chromosomal DNA from preparations of P1 artifical chromosome recombinants facilitates directed subcloning.
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- Electrophoresis, 1999, v. 20, n. 7, p. 1469, doi. 10.1002/(SICI)1522-2683(19990601)20:7<1469::AID-ELPS1469>3.0.CO;2-W
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- Article
Disrupted in schizophrenia 1 and phosphodiesterase 4B: towards an understanding of psychiatric illness.
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- Journal of Physiology, 2007, v. 584, n. 2, p. 401, doi. 10.1113/jphysiol.2007.140210
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- Article
GWAS on family history of Alzheimer’s disease.
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- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0150-6
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- Article
Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study.
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- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0111-0
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- Article
Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.
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- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-017-0034-1
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- Article
Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.
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- Translational Psychiatry, 2017, p. 1, doi. 10.1038/s41398-017-0010-9
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- Article
SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis.
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- Nucleic Acids Research, 2002, v. 30, n. 15, p. e74, doi. 10.1093/nar/gnf070
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- Article
Identification of influential probe types in epigenetic predictions of human traits: implications for microarray design.
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- Clinical Epigenetics, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13148-022-01320-9
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- Article
A Phase I/IIa Safety and Efficacy Study of Nebulized Liposome-mediated Gene Therapy for Cystic Fibrosis Supports a Multidose Trial.
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- 2015
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- journal article
Assessment of F/HN-Pseudotyped Lentivirus as a Clinically Relevant Vector for Lung Gene Therapy.
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- American Journal of Respiratory & Critical Care Medicine, 2012, v. 186, n. 9, p. 846, doi. 10.1164/rccm.201206-1056OC
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- Article
Sputum proteomics in inflammatory and suppurative respiratory diseases.
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- 2008
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- journal article
The Lothian Birth Cohort 1936: a study to examine influences oncognitive ageing from age 11 to age 70 and beyond.
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- BMC Geriatrics, 2007, v. 7, p. 28, doi. 10.1186/1471-2318-7-28
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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.
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- Bioinformatics, 2019, v. 35, n. 2, p. 181, doi. 10.1093/bioinformatics/bty462
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Cloning the shared components of complex DNA resources.
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- Human Molecular Genetics, 1994, v. 3, n. 11, p. 2011
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High frequency gene targeting using insertional vectors.
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- Human Molecular Genetics, 1993, v. 2, n. 8, p. 1299
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- Article
Gene therapy for cystic fibrosis—Where and When?
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- Human Molecular Genetics, 1993, v. 2, n. 3, p. 211
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- Article
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I.
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- Human Molecular Genetics, 1993, v. 2, n. 2, p. 115
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What the papers say: Cystic fibrosis: Prospects for therapy.
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- BioEssays, 1993, v. 15, n. 7, p. 485, doi. 10.1002/bies.950150708
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- Article
Translational Neuroscience of Schizophrenia: Seeking a Meeting of Minds Between Mouse and Man.
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- Science Translational Medicine, 2011, v. 3, n. 102, p. 1, doi. 10.1126/scitranslmed.3002917
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- Article
Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans.
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- Genome Biology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13059-023-02953-6
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- Article
Blood-based epigenome-wide analyses of cognitive abilities.
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- Genome Biology, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s13059-021-02596-5
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- Article
Apolipoprotein E is not Related to Memory Abilities at 70 Years of Age.
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- Behavior Genetics, 2009, v. 39, n. 1, p. 6, doi. 10.1007/s10519-008-9236-x
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- Article
Pharmaco-epidemiology of antidepressant exposure in a UK cohort record-linkage study.
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- 2019
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- journal article
Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis.
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- 2016
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- journal article
Isolation and characterization of the mouse translin-associated protein X (Trax) gene.
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- Mammalian Genome, 2000, v. 11, n. 5, p. 395, doi. 10.1007/s003350010074
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- Article
DNAmethylation in APOE: The relationshipwith Alzheimer's andwith cardiovascular health.
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- Alzheimer's & Dementia: Translational Research & Clinical Interventions, 2020, v. 6, n. 1, p. 1, doi. 10.1002/trc2.12026
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Genome‐ and epigenome‐wide studies of plasma protein biomarkers for Alzheimer's disease implicate TBCA and TREM2 in disease risk.
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- Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2022, v. 14, n. 1, p. 1, doi. 10.1002/dad2.12280
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- Article
Evolutionary conserved longevity genes and human cognitive abilities in elderly cohorts.
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- European Journal of Human Genetics, 2012, v. 20, n. 3, p. 341, doi. 10.1038/ejhg.2011.201
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Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin study.
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- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0170653
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- Article
Association between cognition and gene polymorphisms involved in thrombosis and haemostasis.
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- Age, 2015, v. 37, n. 4, p. 1, doi. 10.1007/s11357-015-9820-y
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- Article
Molecular Genetic Risk for Psychosis Is Associated With Psychosis Risk Symptoms in a Population-Based UK Cohort: Findings From Generation Scotland.
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- Schizophrenia Bulletin, 2020, v. 46, n. 5, p. 1045, doi. 10.1093/schbul/sbaa042
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- Article
DISC1 in Schizophrenia: Genetic Mouse Models and Human Genomic Imaging.
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- Schizophrenia Bulletin, 2011, v. 37, n. 1, p. 14, doi. 10.1093/schbul/sbq135
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- Article
Structural Brain MRI Trait Polygenic Score Prediction of Cognitive Abilities.
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- 2015
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- journal article
Exome Sequencing to Detect Rare Variants Associated With General Cognitive Ability: A Pilot Study.
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- Twin Research & Human Genetics, 2015, v. 18, n. 2, p. 117, doi. 10.1017/thg.2015.10
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Evidence for large-scale gene-by-smoking interaction effects on pulmonary function.
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- 2017
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- journal article
Polygenic risk for coronary artery disease is associated with cognitive ability in older adults.
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- 2016
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- 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.
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- International Journal of Epidemiology, 2013, v. 42, n. 3, p. 689, doi. 10.1093/ije/dys084
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- Article
Loss of SORCS2 is Associated with Neuronal DNA Double-Strand Breaks.
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- Cellular & Molecular Neurobiology, 2023, v. 43, n. 1, p. 237, doi. 10.1007/s10571-021-01163-7
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Methods applied to neonatal dried blood spot samples for secondary research purposes: a scoping review.
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- Critical Reviews in Clinical Laboratory Sciences, 2024, v. 61, n. 8, p. 685, doi. 10.1080/10408363.2024.2360996
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- Article
Genome-wide methylation data improves dissection of the effect of smoking on body mass index.
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- PLoS Genetics, 2021, v. 17, n. 9, p. 1, doi. 10.1371/journal.pgen.1009750
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Are Some Genetic Risk Factors Common to Schizophrenia, Bipolar Disorder and Depression? Evidence from DISC1, GRIK4 and NRG1.
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- Neurotoxicity Research, 2007, v. 11, n. 1, p. 73, doi. 10.1007/BF03033484
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Hair glucocorticoids are associated with childhood adversity, depressive symptoms and reduced global and lobar grey matter in Generation Scotland.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01644-9
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- Article
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-13585-5
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- Article
Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
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- 2019
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- Correction Notice
Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09301-y
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- Article