2023
CATEGORY
2023.1.31
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
2023.1.31
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity
2023.1.31
Helicobacter pylori, Homologous-Recombination Genes, and Gastric Cancer
2023.1.31
Hereditary Cancer Variants and Homologous Recombination Deficiency in Biliary Tract Cancer
2023.1.31
Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction
2023.1.31
Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals
2023.1.31
Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention
2023.1.31
Association Between Glycemic Traits and Primary Open-Angle Glaucoma: A Mendelian Randomization Study in the Japanese Population
2023.1.31
Genetic footprints of assortative mating in the Japanese population
2023.1.31
Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts
2023.1.31
Identification of serum metabolome signatures associated with retinal and renal complications of type 2 diabetes
2023.1.31
Comparison of the loci associated with HbA1c and blood glucose levels identified by a genome-wide association study in the Japanese population
2023.1.31
Genome-Wide Association Study of Intracranial Artery Stenosis Followed by Phenome-Wide Association Study
2023.1.30
Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study
2023.1.30
Prediction Model with HLA-A*33:03 Reveals Number of Days to Develop Liver Cancer from Blood Test
2023.1.29
Genetic Risk of Primary Aldosteronism and Its Contribution to Hypertension: A Cross-Ancestry Meta-Analysis of Genome-Wide Association Studies
2023.1.28
Population-Based Impact of Smoking, Drinking, and Genetic Factors on HDL-Cholesterol Levels in J-MICC Study Participants
2023.1.26
Genome-Wide Association Study of Lung Adenocarcinoma in East Asia and Comparison with a European Population
2023.1.27
Investigating the Association between Glycaemic Traits and Colorectal Cancer in the Japanese Population using Mendelian Randomisation
2023.1.25
Mobile Element Variation Contributes to Population-Specific Genome Diversification, Gene Regulation and Disease Risk
2023.1.24
Prediction of the Cell-Type-Specific Transcription of Non-Coding RNAs from Genome Sequences Via Machine Learning
2023.1.23
Improved Genetic Prediction of the Risk of Knee Osteoarthritis using the Risk Factor-Based Polygenic Score
2023.1.22
Detection of trait-associated structural variations using short-read sequencing
2023.1.21
Pan-Cancer and Cross-Population Genome-Wide Association Studies Dissect Shared Genetic Backgrounds Underlying Carcinogenesis
2023.1.20
Genome-Wide Association Study Identifies Risk Loci within the Major Histocompatibility Complex Region for Hunner-Type Interstitial Cystitis
2023.1.19
GWAS of Folate Metabolism with Gene-Environment Interaction Analysis Revealed the Possible Role of Lifestyles in the Control of Blood Folate Metabolites in Japanese – the J-MICC Study
2023.1.18
Genome-wide Association Studies Categorized by Class of Antihypertensive Drugs Reveal Complex Pathogenesis of Hypertension with Drug Resistance
2023.1.17
Hyperfructosemia in Sleep Disordered Breathing: Metabolome Analysis of Nagahama Study
2023.1.16
A whole-genome reference panel of 14,393 individuals for East Asian populations accelerates discovery of rare functional variants
2023.1.15
Contribution of an Asian-prevalent HLA haplotype to the risk of HBV-related hepatocellular carcinoma
2023.1.14
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk
2023.1.13
Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects
2023.1.12
GWAS Meta-Analysis of Over 29,000 People with Epilepsy Identifies 26 Risk Loci and Subtype-Specific Genetic Architecture
2023.1.11
Multi-Ancestry Genome-Wide Analysis Identifies Shared Genetic Effects and Common Genetic Variants for Self-Reported Sleep Duration
2023.1.10
Boosting the power of genome-wide association studies within and across ancestries by using polygenic scores
2023.1.9
Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations
2023.1.9
Natural Selection Signatures in the Hondo and Ryukyu Japanese Subpopulations
2023.1.8
Polygenic Prediction Across Populations is Influenced by Ancestry, Genetic Architecture, and Methodology
2023.1.7
Identification of Telomere Maintenance Gene Variations Related to Lung Adenocarcinoma Risk by Genome-Wide Association and Whole Genome Sequencing Analyses
2023.1.6
A large-scale microRNA transcriptome-wide association study identifies two susceptibility microRNAs, miR-1307-5p and miR-192-3p, for colorectal cancer risk
2023.1.5
Extracting immunological and clinical heterogeneity across autoimmune rheumatic diseases by cohort-wide immunophenotyping
2023.1.4
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
2023.1.3
East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease
2023.1.2
Genetic Risk Score of Cerebral Infarction in Atrial Fibrillation Genome-Wide Association Study
2023.1.1
Genetic insights into ossification of the posterior longitudinal ligament of the spine