Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis

A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature

Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect

Comparative genetic architectures of schizophrenia in East Asian and European populations

Polygenic burden in focal and generalized epilepsies

Citrullination of RGG Motifs in FET Proteins by PAD4 Regulates Protein Aggregation and ALS Susceptibility

Re-evaluating classical body type theories: genetic correlation between psychiatric disorders and body mass index

Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer’s disease

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders

A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN

A genome-wide association study of late-onset Alzheimer’s disease in a Japanese population

Large-scale screening of TARDBP mutation in amyotrophic lateral sclerosis in Japanese

Optineurin mutations in Japanese amyotrophic lateral sclerosis

Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese

Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East Asians

A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’s disease

Contribution of germline and somatic mutations to risk of neuromyelitis optica spectrum disorder