Related references
Note: Only part of the references are listed.Genetics of 35 blood and urine biomarkers in the UK Biobank
Nasa Sinnott-Armstrong et al.
NATURE GENETICS (2021)
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Daniel Taliun et al.
NATURE (2021)
Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts
Elizabeth T. Cirulli et al.
NATURE COMMUNICATIONS (2020)
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic et al.
CELL (2020)
Monogenic and polygenic inheritance become instruments for clonal selection
Po-Ru Loh et al.
NATURE (2020)
Exome sequencing and characterization of 49,960 individuals in the UK Biobank
Cristopher V. Van Hout et al.
NATURE (2020)
Identity-by-descent detection across 487,409 British samples reveals fine scale population structure and ultra-rare variant associations
Juba Nait Saada et al.
NATURE COMMUNICATIONS (2020)
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Jason Flannick et al.
NATURE (2019)
Exome sequencing of Finnish isolates enhances rare-variant association power
Adam E. Locke et al.
NATURE (2019)
Rare-variant collapsing analyses for complex traits: guidelines and applications
Gundula Povysil et al.
NATURE REVIEWS GENETICS (2019)
Predicting Splicing from Primary Sequence with Deep Learning
Kishore Jaganathan et al.
CELL (2019)
PANTHER version 14: more genomes, a new PANTHER GO-slim and improvements in enrichment analysis tools
Huaiyu Mi et al.
NUCLEIC ACIDS RESEARCH (2019)
CADD: predicting the deleteriousness of variants throughout the human genome
Philipp Rentzsch et al.
NUCLEIC ACIDS RESEARCH (2019)
The Gene Ontology Resource: 20 years and still GOing strong
S. Carbon et al.
NUCLEIC ACIDS RESEARCH (2019)
The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019
Annalisa Buniello et al.
NUCLEIC ACIDS RESEARCH (2019)
Apparent latent structure within the UK Biobank sample has implications for epidemiological analysis
Simon Haworth et al.
NATURE COMMUNICATIONS (2019)
ClinVar: improving access to variant interpretations and supporting evidence
Melissa J. Landrum et al.
NUCLEIC ACIDS RESEARCH (2018)
Mixed-model association for biobank-scale datasets
Po-Ru Loh et al.
NATURE GENETICS (2018)
From genome-wide associations to candidate causal variants by statistical fine-mapping
Daniel J. Schaid et al.
NATURE REVIEWS GENETICS (2018)
Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study
Christopher DeBoever et al.
NATURE COMMUNICATIONS (2018)
Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease
Connor A. Emdin et al.
NATURE COMMUNICATIONS (2018)
Structures of Angptl3 and Angptl4, modulators of triglyceride levels and coronary artery disease
Ekaterina Biterova et al.
SCIENTIFIC REPORTS (2018)
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies
Wei Zhou et al.
NATURE GENETICS (2018)
The UK Biobank resource with deep phenotyping and genomic data
Clare Bycroft et al.
NATURE (2018)
The SWISS-MODEL Repository-new features and functionality
Stefan Bienert et al.
NUCLEIC ACIDS RESEARCH (2017)
Exome-wide association study of plasma lipids in >300,000 individuals
Dajiang J. Liu et al.
NATURE GENETICS (2017)
An Expanded View of Complex Traits: From Polygenic to Omnigenic
Evan A. Boyle et al.
CELL (2017)
Genotype Imputation with Millions of Reference Samples
Brian L. Browning et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
FINEMAP: efficient variable selection using summary data from genome-wide association studies
Christian Benner et al.
BIOINFORMATICS (2016)
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
Chunyu Liu et al.
NATURE GENETICS (2016)
Reference-based phasing using the Haplotype Reference Consortium panel
Po-Ru Loh et al.
NATURE GENETICS (2016)
Fast and accurate long-range phasing in a UK Biobank cohort
Po-Ru Loh et al.
NATURE GENETICS (2016)
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy et al.
NATURE GENETICS (2016)
Next-generation genotype imputation service and methods
Sayantan Das et al.
NATURE GENETICS (2016)
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR Study
Frederick E. Dewey et al.
SCIENCE (2016)
The Structural Basis for Cdc42-Induced Dimerization of IQGAPs
Louis LeCour et al.
STRUCTURE (2016)
The Ensembl Variant Effect Predictor
William McLaren et al.
GENOME BIOLOGY (2016)
Efficient Bayesian mixed-model analysis increases association power in large cohorts
Po-Ru Loh et al.
NATURE GENETICS (2015)
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Jie Huang et al.
NATURE COMMUNICATIONS (2015)
Second-generation PLINK: rising to the challenge of larger and richer datasets
Christopher C. Chang et al.
GIGASCIENCE (2015)
Rho GTPases in platelet function
J. E. Aslan et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2013)
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
Wenqing Fu et al.
NATURE (2013)
Differential confounding of rare and common variants in spatially structured populations
Iain Mathieson et al.
NATURE GENETICS (2012)
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits
Jian Yang et al.
NATURE GENETICS (2012)
Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
Jacob A. Tennessen et al.
SCIENCE (2012)
Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
Michael C. Wu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Perilipin Deficiency and Autosomal Dominant Partial Lipodystrophy
Sheetal Gandotra et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Structural and biophysical studies of PCSK9 and its mutants linked to familial hypercholesterolemia
David Cunningham et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2007)
Medical sequencing at the extremes of human body mass
Nadav Ahituv et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
A phosphatidylinositol 3kinase-phosphodiesterase 3B-cyclic AMP pathway in hypothalamic action of leptin on feeding
AZ Zhao et al.
NATURE NEUROSCIENCE (2002)
The Protein Data Bank
HM Berman et al.
NUCLEIC ACIDS RESEARCH (2000)