Works matching AU Porteous, David J.
Results: 102
Epigenetic prediction of complex traits and death.
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- Genome Biology, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s13059-018-1514-1
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- Article
CpG-free plasmids confer reduced inflammation and sustained pulmonary gene expression.
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- Nature Biotechnology, 2008, v. 26, n. 5, p. 549, doi. 10.1038/nbt1399
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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
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
Genome-wide characterization of 54 urinary metabolites reveals molecular impact of kidney function.
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- Nature Communications, 2025, v. 16, p. 1, doi. 10.1038/s41467-024-55182-1
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- Article
Human-Specific Cystic Fibrosis Transmembrane Conductance Regulator Antibodies Detect In Vivo Gene Transfer to Ovine Airways.
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- American Journal of Respiratory Cell & Molecular Biology, 2006, v. 35, n. 1, p. 72, doi. 10.1165/rcmb.2005-0377OC
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- Article
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
Home working and social and mental wellbeing at different stages of the COVID-19 pandemic in the UK: Evidence from 7 longitudinal population surveys.
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- PLoS Medicine, 2023, v. 19, n. 4, p. 1, doi. 10.1371/journal.pmed.1004214
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- Article
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
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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- Article
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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- Article
A Century of Mendelism in Human Genetics. Eds. MILO KEYNES, A. W. F. EDWARDS & ROBERT PEEL. CRC Press. 2004.
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- Genetics Research, 2005, v. 85, n. 3, p. 249, doi. 10.1017/s0016672305007639
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- Article
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
A t(1;11) translocation linked to schizophrenia and affective disorders gives rise to aberrant chimeric DISC1 transcripts that encode structurally altered, deleterious mitochondrial proteins.
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- Human Molecular Genetics, 2012, v. 21, n. 15, p. 3374, doi. 10.1093/hmg/dds169
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- Article
The DISC1 promoter: characterization and regulation by FOXP2.
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- Human Molecular Genetics, 2012, v. 21, n. 13, p. 2862, doi. 10.1093/hmg/dds111
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- Article
DISC1 variants 37W and 607F disrupt its nuclear targeting and regulatory role in ATF4-mediated transcription.
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- Human Molecular Genetics, 2012, v. 21, n. 12, p. 2779, doi. 10.1093/hmg/dds106
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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
SuRFing the genomics wave: an R package for prioritizing SNPs by functionality.
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- Genome Medicine, 2014, v. 6, n. 10, p. 31, doi. 10.1186/s13073-014-0079-1
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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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- Article
Birth weight associations with DNA methylation differences in an adult population.
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- Epigenetics, 2021, v. 16, n. 7, p. 783, doi. 10.1080/15592294.2020.1827713
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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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- Article
Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder.
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- 2018
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- Publication type:
- journal article
The NPAS3 gene—emerging evidence for a role in psychiatric illness.
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- Annals of Medicine, 2006, v. 38, n. 6, p. 439, doi. 10.1080/07853890600946500
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- 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).
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- PLoS ONE, 2015, v. 10, n. 11, p. 1, doi. 10.1371/journal.pone.0142197
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- Article
Sex-Differences in the Metabolic Health of Offspring of Parents with Diabetes: A Record-Linkage Study.
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- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0134883
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- Article
APOE/TOMM40 genetic loci, white matter hyperintensities, and cerebral microbleeds.
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- International Journal of Stroke, 2015, v. 10, n. 8, p. 1297, doi. 10.1111/ijs.12615
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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
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
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
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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- Article
Sex Differences in Cardiac Troponin I and T and the Prediction of Cardiovascular Events in the General Population.
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- Clinical Chemistry, 2021, v. 67, n. 10, p. 1351, doi. 10.1093/clinchem/hvab109
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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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- Publication type:
- journal article
Response to Amar J. Klar: The Chromosome 1;11 Translocation Provides the Best Evidence Supporting Genetic Etiology for Schizophrenia and Bipolar Affective Disorders.
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- Genetics, 2003, v. 163, n. 2, p. 833, doi. 10.1093/genetics/163.2.833
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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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- Article
Evidence for large-scale gene-by-smoking interaction effects on pulmonary function.
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- 2017
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- Publication type:
- 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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- 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.
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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
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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- Article
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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- 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
Identification of epigenome-wide DNA methylation differences between carriers of APOE ε4 and APOE ε2 alleles.
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- Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-020-00808-4
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- Article
An epigenome-wide association study of sex-specific chronological ageing.
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- Genome Medicine, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s13073-019-0693-z
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- Article
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
Genetic prediction of male pattern baldness.
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- PLoS Genetics, 2017, v. 13, n. 2, p. 1, doi. 10.1371/journal.pgen.1006594
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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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- Article
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