Empirical evaluation of analytic validity of polygenic scores

Pitfalls in estimating and interpreting the contribution of ultra-rare genetic variants to the heritability of complex traits

Genetics of skeletal proportions across two different populations

Distinct genetic profiles influence body mass index between infancy and adolescence

Family-GWAS reveals effects of environment and mating on genetic associations

Estimation and mapping of the missing heritability of human phenotypes

Polygenic prediction of body mass index and obesity through the life course and across ancestries

The contribution of gametic phase disequilibrium to the heritability of complex traits

One Health Approach to the Computational Design of a Lipoprotein-Based Multi-Epitope Vaccine Against Human and Livestock Tuberculosis

Genetic architecture reconciles linkage and association studies of complex traits

Genome-wide fine-mapping improves identification of causal variants

Genetic influence on within-person longitudinal change in anthropometric traits in the UK Biobank

Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

The impact of assortative mating, participation bias and socioeconomic status on the polygenic risk of behavioural and psychiatric traits

Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity

Cross-ancestry analyses identify new genetic loci associated with 25-hydroxyvitamin D

Identification and analysis of individuals who deviate from their genetically-predicted phenotype

Boosting the power of genome-wide association studies within and across ancestries by using polygenic scores

Direct and INdirect effects analysis of Genetic lOci (DINGO): A software package to increase the power of locus discovery in GWAS meta-analyses of perinatal phenotypes and traits influenced by indirect genetic effects

Genetics of skeletal proportions in two different populations

Genome-wide CRISPR screening of chondrocyte maturation newly implicates genes in skeletal growth and height-associated GWAS loci

Mate choice through a genomic lens

The effect of the scale of grant scoring on ranking accuracy

Estimation and implications of the genetic architecture of fasting and non-fasting blood glucose

15 years of GWAS discovery: Realizing the promise

Genomics and phenomics of body mass index reveals a complex disease network

Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study

A saturated map of common genetic variants associated with human height

Genetic footprints of assortative mating in the Japanese population

Genetic and modifiable risk factors combine multiplicatively in common disease

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Constrained human genes under scrutiny

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Assortative mating biases marker-based heritability estimators

Polygenic burden could explain high rates of affective disorders in a community with restricted founder population

Discovery and implications of polygenicity of common diseases

Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization

Genomic partitioning of inbreeding depression in humans

The trans-ancestral genomic architecture of glycemic traits

Corrigendum to: Alzheimer’s disease genetic risk and sleep phenotypes in healthy young men: association with more slow waves and daytime sleepiness

Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals

Triangulating evidence from longitudinal and Mendelian randomization studies of metabolomic biomarkers for type 2 diabetes

Quantifying genetic heterogeneity between continental populations for human height and body mass index

Widespread signatures of natural selection across human complex traits and functional genomic categories

Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Integrative analyses identify susceptibility genes underlying COVID-19 hospitalization

Pathogenic variants in actionable MODY genes are associated with type 2 diabetes

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

Risk prediction of late-onset Alzheimer’s disease implies an oligogenic architecture

Using prior information from humans to prioritize genes and gene-associated variants for complex traits in livestock

Theoretical and empirical quantification of the accuracy of polygenic scores in ancestry divergent populations

Risk in Relatives, Heritability, SNP-Based Heritability, and Genetic Correlations in Psychiatric Disorders: A Review

A unified framework for association and prediction from vertex-wise grey-matter structure

Alzheimer’s disease genetic risk and sleep phenotypes in healthy young men: association with more slow waves and daytime sleepiness

No Evidence for Social Genetic Effects or Genetic Similarity Among Friends Beyond that Due to Population Stratification: A Reappraisal of Domingue et al (2018)

Improved polygenic prediction by Bayesian multiple regression on summary statistics

Genetic correlates of social stratification in Great Britain

Extreme inbreeding in a European ancestry sample from the contemporary UK population

Assortative Mating in Autism Spectrum Disorder: Toward an Evidence Base From DNA Data, but Not There Yet

Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals

Genome-wide association study of medication-use and associated disease in the UK Biobank

Imprint of assortative mating on the human genome

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

ALDH2 Polymorphism rs671, but Not ADH1B Polymorphism rs1229984, Increases Risk for Hypo-HDL-Cholesterolemia in a/a Carriers Compared to the G/G Carriers

Assortative mating on complex traits revisited: Double first cousins and the X-chromosome

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry

Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry

Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Misestimation of heritability and prediction accuracy of male-pattern baldness

Association Between Population Density and Genetic Risk for Schizophrenia

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

Increased Hepatic PDGF-AA Signaling Mediates Liver Insulin Resistance in Obesity-Associated Type 2 Diabetes

Signatures of negative selection in the genetic architecture of human complex traits

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

Reply to Kardos et al.: Estimation of inbreeding depression from SNP data

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis

Detection and quantification of inbreeding depression for complex traits from SNP data

Low-dose exposure to bisphenols A, F and S of human primary adipocyte impacts coding and non-coding RNA profiles

Early metabolic markers identify potential targets for the prevention of type 2 diabetes

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

Genome-wide physical activity interactions in adiposity – A meta-analysis of 200,452 adults

Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

Relationship between salivary/pancreatic amylase and body mass index: a systems biology approach

KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

Detection of human adaptation during the past 2000 years

Impact of statistical models on the prediction of type 2 diabetes using non-targeted metabolomics profiling

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

Associations Between Type 2 Diabetes-Related Genetic Scores and Metabolic Traits, in Obese and Normal-Weight Youths

Erratum: The kynurenine pathway is activated in human obesity and shifted toward kynurenine monooxygenase activation

Genomic insights into the origin of farming in the ancient Near East

The genetic architecture of type 2 diabetes

Post-Bariatric Surgery Changes in Quinolinic and Xanthurenic Acid Concentrations Are Associated with Glucose Homeostasis