UK Biobank

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UK Biobank

metasource: bio.tools
version: extracted_at: 2022-11-04T11:26:33.260010

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929

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uk-biobank

metasource: bio.tools
version: extracted_at: 2022-11-04T11:26:33.260010

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Other names: uk-biobank

UK Biobank is a large-scale biomedical database and research resource that provides researchers access to detailed longitudinal phenotype, medical and genetic data from 500,000 volunteer participants.

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Publications

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Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts
PMID: 31992710

metasource: bio.tools
version: extracted_at: 2022-11-04T11:26:33.260010

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• Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts PubMed citations: 32.

  32 articles citing: Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts

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  The Impact of ACEs on BMI: An Investigation of the Genotype-Environment Effects of BMI. PMID:35342390

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  Investigating underlying human immunity genes, implicated diseases and their relationship to COVID-19. PMID:35261286

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  Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank. PMID:35177841

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  HLA-A∗03:01 is associated with increased risk of fever, chills, and stronger side effects from Pfizer-BioNTech COVID-19 vaccination. PMID:35005651

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  Biomarker discovery studies for patient stratification using machine learning analysis of omics data: a scoping review. PMID:34873011

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  Sequencing-based genome-wide association studies reporting standards. PMID:34870259

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  A Novel Quality-Control Procedure to Improve the Accuracy of Rare Variant Calling in SNP Arrays. PMID:34764980

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  Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization. PMID:34752750

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  Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes. PMID:34732801

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  Exome-Wide Pan-Cancer Analysis of Germline Variants in 8,719 Individuals Finds Little Evidence of Rare Variant Associations. PMID:34718237

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  Variance-component-based meta-analysis of gene-environment interactions for rare variants. PMID:34544119

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  Positive predictive value highlights four novel candidates for actionable genetic screening from analysis of 220,000 clinicogenomic records. PMID:34385667

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  Rare variant contribution to human disease in 281,104 UK Biobank exomes. PMID:34375979

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  A study of elective genome sequencing and pharmacogenetic testing in an unselected population. PMID:34313030

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  A role for zinc transporter gene SLC39A12 in the nervous system and beyond. PMID:34252531

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  Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. PMID:34226706

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  Genetic pleiotropy of ERCC6 loss-of-function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries. PMID:34005834

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  Comprehensive Allele Genotyping in Critical Pharmacogenes Reduces Residual Clinical Risk in Diverse Populations. PMID:33930192

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  Response by Pan and Tsao to Letter Regarding Article, "Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program". PMID:33900828

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  Brain Magnetic Resonance Imaging Phenome-Wide Association Study With Metal Transporter Gene SLC39A8. PMID:33790950

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  Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population. PMID:33763119

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  Prioritizing non-coding regions based on human genomic constraint and sequence context with deep learning. PMID:33686085

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  Loss of Znt8 function in diabetes mellitus: risk or benefit? PMID:33666829

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  Exome Chip Analyses and Genetic Risk for IgA Nephropathy among Han Chinese. PMID:33462083

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  Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations. PMID:33432171

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  Assessing the Role of Rare Genetic Variation in Patients With Heart Failure. PMID:33326012

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  Whole-genome sequencing analysis of the cardiometabolic proteome. PMID:33303764

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  Identity-by-descent detection across 487,409 British samples reveals fine scale population structure and ultra-rare variant associations. PMID:33257650

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  Pathogenic variants in actionable MODY genes are associated with type 2 diabetes. PMID:33046911

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  Scalability and cost-effectiveness analysis of whole genome-wide association studies on Google Cloud Platform and Amazon Web Services. PMID:32719837

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  Tumour predisposition and cancer syndromes as models to study gene-environment interactions. PMID:32472073

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  Taking One Step Back in Familial Hypercholesterolemia: STAP1 Does Not Alter Plasma LDL (Low-Density Lipoprotein) Cholesterol in Mice and Humans. PMID:31996024

Tags:

Tags

More detailed information about this field from each metasource. ×

UK BIOBANK

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Genomics

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Exome sequencing

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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WGS

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Omics

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Pain

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Research

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Cognitive Measures

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Physical Measures

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Magnetic resonance imaging

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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DXA

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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ECG

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Accelerometer

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Mental Health

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Environment

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Primary Care

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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COVID-19

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Hospital episode statistics

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Cancer Registry

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Deaths

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Sociodemographics

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Digestive Health

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Occupational Health

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Biomarkers

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Lifestyle

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Health Data

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Cardiac MRI

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Brain MRI

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Abdominal MRI

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Carotid Ultrasound

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Diet

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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Pain Hub

metasource: HDR UK
version: extracted_at: 2022-09-05T08:28:24.125862

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biobank

metasource: bio.tools
version: extracted_at: 2022-11-04T11:26:33.260010

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exome sequencing

metasource: bio.tools
version: extracted_at: 2022-11-04T11:26:33.260010

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genotype and phenotype

metasource: bio.tools
version: extracted_at: 2022-11-04T11:26:33.260010

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genomics

metasource: bio.tools
version: extracted_at: 2022-11-04T11:26:33.260010

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chip-on-chip

metasource: bio.tools
version: extracted_at: 2022-11-04T11:26:33.260010

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rare diseases

metasource: bio.tools
version: extracted_at: 2022-11-04T11:26:33.260010

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uk biobank genomics exome sequencing wgs omics pain research cognitive measures physical measures magnetic resonance imaging dxa ecg accelerometer mental health environment primary care covid-19 hospital episode statistics cancer registry deaths sociodemographics digestive health occupational health biomarkers lifestyle health data cardiac mri brain mri abdominal mri carotid ultrasound diet pain hub biobank exome sequencing genotype and phenotype genomics chip-on-chip rare diseases