2022
CATEGORY
2022.1.31
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus
2022.1.31
Genetic diversity fuels gene discovery for tobacco and alcohol use
2022.1.31
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
2022.1.30
Genetic Architectures Underlie Onset Age of Atopic Dermatitis
2022.1.28
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
2022.1.27
Association between germline pathogenic variants in cancer-predisposing genes and lymphoma risk
2022.1.26
Population-based Screening for Hereditary Colorectal Cancer Variants in Japan
2022.1.25
Stroke genetics informs drug discovery and risk prediction across ancestries
2022.1.23
DOCK2 is involved in the host genetics and biology of severe COVID-19
2022.1.22
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
2022.1.21
Genetic analysis of right heart structure and function in 40,000 people
2022.1.20
Developing and validating polygenic risk scores for colorectal cancer risk prediction in East Asians
2022.1.19
Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component
2022.1.18
Association of germline TYK2 variation with lung cancer and non-Hodgkin lymphoma risk
2022.1.17
Different risk genes contribute to clear cell and non-clear cell renal cell carcinoma in 1532 Japanese patients and 5996 controls
2022.1.16
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
2022.1.15
Large-scale Integrated Analysis of Genetics and Metabolomic Data Reveals Potential Links Between Lipids and Colorectal Cancer Risk
2022.1.14
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
2022.1.13
Biological insights into systemic lupus erythematosus through an immune cell-specific transcriptome-wide association study
2022.1.12
A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study
2022.1.11
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores
2022.1.10
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
2022.1.9
Editorial: Current Status and Future Challenges of Biobank Data Analysis
2022.1.8
Expansion of Cancer Risk Profile for BRCA1 and BRCA2 Pathogenic Variants
2022.1.7
Genome-wide risk prediction of common diseases across ancestries in one million people
2022.1.6
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
2022.1.5
Genome-wide association study of colorectal polyps identified highly overlapping polygenic architecture with colorectal cancer
2022.1.4
Federated analysis of BRCA1 and BRCA2 variation in a Japanese cohort
2022.1.3
Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes
2022.1.2
[Cohorts and Biobanks as Essential Resources for Cancer Research]
2022.1.1
A single-nucleotide-polymorphism in the 5′-flanking region of MSX1 gene as a predictive marker candidate for platinum-based therapy of esophageal carcinoma
2022.1.1
Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease