Related references
Note: Only part of the references are listed.Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation
Oleksandr Frei et al.
NATURE COMMUNICATIONS (2019)
SumHer better estimates the SNP heritability of complex traits from summary statistics
Doug Speed et al.
NATURE GENETICS (2019)
Genetic architecture: the shape of the genetic contribution to human traits and disease
Nicholas J. Timpson et al.
NATURE REVIEWS GENETICS (2018)
Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model
Naomi R. Wray et al.
CELL (2018)
Meta-analysis of genome-wide association studies for height and body mass index in ∼700 000 individuals of European ancestry
Loic Yengo et al.
HUMAN MOLECULAR GENETICS (2018)
The UK Biobank resource with deep phenotyping and genomic data
Clare Bycroft et al.
NATURE (2018)
An atlas of genetic associations in UK Biobank
Oriol Canela-Xandri et al.
NATURE GENETICS (2018)
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Anubha Mahajan et al.
NATURE GENETICS (2018)
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
Jie Zheng et al.
BIOINFORMATICS (2017)
Genetic effects on gene expression across human tissues
Francois Aguet et al.
NATURE (2017)
Reevaluation of SNP heritability in complex human traits
Doug Speed et al.
NATURE GENETICS (2017)
Functional mapping and annotation of genetic associations with FUMA
Kyoko Watanabe et al.
NATURE COMMUNICATIONS (2017)
Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies
Christian Benner et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
10 Years of GWAS Discovery: Biology, Function, and Translation
Peter M. Visscher et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
An Expanded View of Complex Traits: From Polygenic to Omnigenic
Evan A. Boyle et al.
CELL (2017)
FINEMAP: efficient variable selection using summary data from genome-wide association studies
Christian Benner et al.
BIOINFORMATICS (2016)
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek et al.
NATURE (2016)
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets
Zhihong Zhu et al.
NATURE GENETICS (2016)
Integrative analysis of 111 reference human epigenomes
Anshul Kundaje et al.
NATURE (2015)
A global reference for human genetic variation
David M. Altshuler et al.
NATURE (2015)
Meta-analysis of the heritability of human traits based on fifty years of twin studies
Tinca J. C. Polderman et al.
NATURE GENETICS (2015)
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
Kyle J. Gaulton et al.
NATURE GENETICS (2015)
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
Brendan K. Bulik-Sullivan et al.
NATURE GENETICS (2015)
Making sense of GWAS: using epigenomics and genome engineering to understand the functional relevance of SNPs in non-coding regions of the human genome
Yu Gyoung Tak et al.
EPIGENETICS & CHROMATIN (2015)
MAGMA: Generalized Gene-Set Analysis of GWAS Data
Christiaan A. de Leeuw et al.
PLOS COMPUTATIONAL BIOLOGY (2015)
Evaluating the Performance of Fine-Mapping Strategies at Common Variant GWAS Loci
Martijn van de Bunt et al.
PLOS GENETICS (2015)
Rare-Variant Association Analysis: Study Designs and Statistical Tests
Seunggeung Lee et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Yukinori Okada et al.
NATURE (2014)
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
Danielle Welter et al.
NUCLEIC ACIDS RESEARCH (2014)
Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples
Peter M. Visscher et al.
PLOS GENETICS (2014)
Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
Claudia Giambartolomei et al.
PLOS GENETICS (2014)
Pleiotropy in complex traits: challenges and strategies
Nadia Solovieff et al.
NATURE REVIEWS GENETICS (2013)
Molecular signatures database (MSigDB) 3.0
Arthur Liberzon et al.
BIOINFORMATICS (2011)
Initial impact of the sequencing of the human genome
Eric S. Lander
NATURE (2011)
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
Kai Wang et al.
NUCLEIC ACIDS RESEARCH (2010)
Finding the missing heritability of complex diseases
Teri A. Manolio et al.
NATURE (2009)
PLINK: A tool set for whole-genome association and population-based linkage analyses
Shaun Purcell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
The human disease network
Kwang-Il Goh et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Complement factor H polymorphism and age-related macular degeneration
AO Edwards et al.
SCIENCE (2005)