Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus

Genetic diversity fuels gene discovery for tobacco and alcohol use

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Genetic Architectures Underlie Onset Age of Atopic Dermatitis

Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis

Association between germline pathogenic variants in cancer-predisposing genes and lymphoma risk

Population-based Screening for Hereditary Colorectal Cancer Variants in Japan

Stroke genetics informs drug discovery and risk prediction across ancestries

DOCK2 is involved in the host genetics and biology of severe COVID-19

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

Genetic analysis of right heart structure and function in 40,000 people

Developing and validating polygenic risk scores for colorectal cancer risk prediction in East Asians

Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component

Association of germline TYK2 variation with lung cancer and non-Hodgkin lymphoma risk

Different risk genes contribute to clear cell and non-clear cell renal cell carcinoma in 1532 Japanese patients and 5996 controls

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Large-scale Integrated Analysis of Genetics and Metabolomic Data Reveals Potential Links Between Lipids and Colorectal Cancer Risk

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

Biological insights into systemic lupus erythematosus through an immune cell-specific transcriptome-wide association study

A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study

Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Editorial: Current Status and Future Challenges of Biobank Data Analysis

Expansion of Cancer Risk Profile for BRCA1 and BRCA2 Pathogenic Variants

Genome-wide risk prediction of common diseases across ancestries in one million people

Response to Comment on Dawed et al. Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to Sulfonylureas. Diabetes Care 2021;44:2673-2682

Genome-wide association study of colorectal polyps identified highly overlapping polygenic architecture with colorectal cancer

Federated analysis of BRCA1 and BRCA2 variation in a Japanese cohort

Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes

[Cohorts and Biobanks as Essential Resources for Cancer Research]

A single-nucleotide-polymorphism in the 5′-flanking region of MSX1 gene as a predictive marker candidate for platinum-based therapy of esophageal carcinoma

Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease