UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age - Test2 - elhamkhani - TriplyDB

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age

http://www.wikidata.org/entity/Q28650740

about

Inherited platelet disorders: toward DNA-based diagnosis Longitudinal Intergenerational Birth Cohort Designs: A Systematic Review of Australian and New Zealand Studies Genomics of Cancer and a New Era for Cancer Prevention Accuracy of Electronic Health Record Data for Identifying Stroke Cases in Large-Scale Epidemiological Studies: A Systematic Review from the UK Biobank Stroke Outcomes Group Commonly prescribed drugs associate with cognitive function: a cross-sectional study in UK Biobank The LifeLines Cohort Study: a resource providing new opportunities for environmental epidemiology Beyond Our Borders? Public Resistance to Global Genomic Data Sharing Sex differences in body anthropometry and composition in individuals with and without diabetes in the UK Biobank Association of Cardiometabolic Multimorbidity With Mortality Cognitive Test Scores in UK Biobank: Data Reduction in 480,416 Participants and Longitudinal Stability in 20,346 Participants Shared genetic aetiology between cognitive functions and physical and mental health in UK Biobank (N=112 151) and 24 GWAS consortia Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records Genetics, lifestyle and environment. UK Biobank is an open access resource following the lives of 500,000 participants to improve the health of future generations.Validity of Cardiovascular Disease Event Ascertainment Using Linkage to UK Hospital Records A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data.Can mental health diagnoses in administrative data be used for research? A systematic review of the accuracy of routinely collected diagnoses.Network-Based Biomedical Data Analysis.Improved Genetic Profiling of Anthropometric Traits Using a Big Data Approach Accuracy of routinely-collected healthcare data for identifying motor neurone disease cases: A systematic review Dawning of the age of genomics for platelet granule disorders: improving insight, diagnosis and management.METACOHORTS for the study of vascular disease and its contribution to cognitive decline and neurodegeneration: An initiative of the Joint Programme for Neurodegenerative Disease Research Semiparametric methods for estimation of a nonlinear exposure-outcome relationship using instrumental variables with application to Mendelian randomization.Phenome-wide heritability analysis of the UK Biobank Assessing the presence of shared genetic architecture between Alzheimer's disease and major depressive disorder using genome-wide association data.Multi-omics approaches to disease.The 'cognitive footprint' of psychiatric and neurological conditions: cross-sectional study in the UK Biobank cohort.Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan.Validation of the AX3 triaxial accelerometer in older functionally impaired people.Cognitive ability and physical health: a Mendelian randomization study.Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study.Tissue Sources for Accurate Measurement of Germline DNA Genotypes in Prostate Cancer Patients Treated With Radical Prostatectomy.Phenome-Wide Association Studies as a Tool to Advance Precision Medicine.Intelligence and neuroticism in relation to depression and psychological distress: Evidence from two large population cohorts.Central adiposity and the overweight risk paradox in aging: follow-up of 130,473 UK Biobank participants Genetics of Depression: Progress at Last.Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity.Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits Development of a Cancer Risk Prediction Tool for Use in the UK Primary Care and Community Settings.

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UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age

http://www.wikidata.org/entity/Q28650740

description

2015 nî lūn-bûn

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2015 թուականի Մարտին հրատարակուած գիտական յօդուած

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2015 թվականի մարտին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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UK biobank: an open access res ...... diseases of middle and old age

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JOURNAL.PMED.1001779

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Alan Young

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Bette Liu

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P2860

Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology

The causes of cancer: quantitative estimates of avoidable risks of cancer in the United States today

The UK Biobank sample handling and storage protocol for the collection, processing and archiving of human blood and urine.

What makes UK Biobank special?

Epidemiological methods for studying genes and environmental factors in complex diseases.

Enhancing the feasibility of large cohort studies.

One in 30 people in the UK take part in cohort studies.

Design and implementation of a high-throughput biological sample processing facility using modern manufacturing principles.

UK Biobank: from concept to reality.

Development and evaluation of the Oxford WebQ, a low-cost, web-based method for assessment of previous 24 h dietary intakes in large-scale prospective studies.

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e1001779

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Paul M. Matthews

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2015-03-01T00:00:00Z

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