A Blood Transcriptomic Resource for ALS Highlights Disease-Associated Signatures and Alternative Splicing Events

A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts

A cross-disorder analysis of CNVs finds novel loci and dose-dependent relationships of genes to psychiatric traits

A methylome-wide association study of major depression with out-of-sample case-control classification and trans-ancestry comparison

Antidepressant Exposure and DNA Methylation: Insights from a Methylome-Wide Association Study

Antidepressant switching as a proxy phenotype for drug non-response: investigating clinical, demographic and genetic characteristics

Applying Machine-Learning and Deep-Learning to Predict Depression from Brain MRI and Identify Depression-Related Brain Biology

Atypical depression is associated with a distinct clinical, neurobiological, treatment response and polygenic risk profile

Bayesian analysis of GWAS summary data reveals differential signatures of natural selection across human complex traits and functional genomic categories

Clinical trials in depression: Integrated collection across EU and US registries

Cohort profile: Cell-omics Resource of the Australian Genetics of Depression Study (AGDS:Cell-o)

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Conditional GWAS analysis identifies putative disorder-specific SNPs for psychiatric disorders

Connecting genomic results for psychiatric disorders to human brain cell types and regions reveals convergence with functional connectivity

Cross-disorder GWAS meta-analysis for Attention Deficit/Hyperactivity Disorder, Autism Spectrum Disorder, Obsessive Compulsive Disorder, and Tourette Syndrome

Decoding Treatment Choice: Genetic and Phenotypic Analyses of Long-term Antidepressant Acceptability

Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

Examining sex-differentiated genetic effects across neuropsychiatric and behavioral traits

Extensive antagonistic variants across human genome

Familial co-aggregation and shared heritability between clinically diagnosed neurodevelopmental problems and cardiometabolic conditions: a nationwide register study across three generations

GWAS of epigenetic ageing rates in blood reveals a critical role forTERT

Gene expression and RNA splicing explain large proportions of the heritability for complex traits in cattle

Genetic Association Study of Childhood Aggression across raters, instruments and age

Genetic correlates of vitamin D-binding protein and 25 hydroxyvitamin D in neonatal dried blood spots

Genetic structure of major depression symptoms across clinical and community cohorts

Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration

Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling

Genome-wide fine-mapping improves identification of causal variants

Genome-wide fine-mapping improves identification of causal variants

Genome-wide insights into generalised anxiety using a dimensional symptom severity approach

Genome-wide meta-analyses of non-response to antidepressants identify novel loci and potential drugs

Genome-wide meta-analysis identifies genetic risk factors and implicates multiple body systems in panic attacks and disorder

Genome-wide study of DNA methylation in Amyotrophic Lateral Sclerosis identifies differentially methylated loci and implicates metabolic, inflammatory and cholesterol pathways

Genomic and Functional studies identify RPSA as a risk gene for ALS and other neurological diseases

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

Lithium Response in Bipolar Disorder is Associated with Focal Adhesion and PI3K-Akt Networks: A Multi-omics Replication Study

MELODY trial: Study protocol for a 12-week randomised controlled trial of adjunctive melatonin, digital cognitive behaviour therapy for insomnia, or pill placebo to improve depressive symptoms in young adults with mood disorders

Methylome-wide association study of early life stressors and adult mental health reveals a relationship between birth date and cell type composition in blood

Multi-ancestry GWAS of major depression aids locus discovery, fine-mapping, gene prioritisation, and causal inference

Polygenic Prediction of Molecular Traits using Large-Scale Meta-analysis Summary Statistics

Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects

R2ROC: An efficient method of comparing two or more correlated AUC from out-of-sample prediction using polygenic scores

RNA-seq analysis of skeletal muscle in motor neurone disease cases and controls

Sex-Specific Association Between Genetic Risk of Psychiatric Disorders and Cardiovascular Diseases

Sex-stratified genome-wide association meta-analysis of Major Depressive Disorder

Significance tests for R2 of out-of-sample prediction using polygenic scores

The Australian Genetics of Depression Study: Study Description and Sample Characteristics

The Landscape of Shared and Divergent Genetic Influences across 14 Psychiatric Disorders

The genetic and phenotypic correlates of neonatal Complement Component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders

Unsupervised Variant Clustering Identifies Genetic Subtypes of Disease

Using genotype data to distinguish pleiotropy from heterogeneity: deciphering coheritability in autoimmune and neuropsychiatric diseases

mBAT-combo: a more powerful test to detect gene-trait associations from GWAS data