Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases

GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.

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

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks

Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetes

Decrease in PSCA expression caused by Helicobacter pylori infection may promote progression to severe gastritis

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries

Amino acid position 37 of HLA-DRβ1 affects susceptibility to Crohn’s disease in Asians

Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study

Elucidating the genetic architecture of reproductive ageing in the Japanese population

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

Development of a Highly Sensitive Device for Counting the Number of Disease-Specific Exosomes in Human Sera

Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci

Identification of LEF1 as a Susceptibility Locus for Kawasaki Disease in Patients Younger than 6 Months of Age

Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis

A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis

Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls

Association of HLA-A*31:01 Screening With the Incidence of Carbamazepine-Induced Cutaneous Adverse Reactions in a Japanese Population

Deep whole-genome sequencing reveals recent selection signatures linked to evolution and disease risk of Japanese

Multi-ethnic genome-wide association study for atrial fibrillation

Integration of genetics and miRNA-target gene network identified disease biology implicated in tissue specificity

A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes

Blood lipid-related low-frequency variants in LDLR and PCSK9 are associated with onset age and risk of myocardial infarction in Japanese

Interethnic analyses of blood pressure loci in populations of East Asian and European descent

Genome-wide association study identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.

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

Genome-wide association study (GWAS) of ovarian cancer in Japanese predicted regulatory variants in 22q13.1

Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma

本人通知制度の実態と住民票を用いた予後調査への影響の検討