A variable number of tandem repeats polymorphism in an E2F-1 binding element in the 5′ flanking region of SMYD3 is a risk factor for human cancers

Genetic architecture of alcohol consumption identified by a genotype-stratified GWAS and impact on esophageal cancer risk in Japanese people

Helicobacter pylori, Homologous-Recombination Genes, and Gastric Cancer

Hereditary Cancer Variants and Homologous Recombination Deficiency in Biliary Tract Cancer

Prediction Model with HLA-A*33:03 Reveals Number of Days to Develop Liver Cancer from Blood Test

Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population

Investigating the Association between Glycaemic Traits and Colorectal Cancer in the Japanese Population using Mendelian Randomisation

Pan-Cancer and Cross-Population Genome-Wide Association Studies Dissect Shared Genetic Backgrounds Underlying Carcinogenesis

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

Contribution of an Asian-prevalent HLA haplotype to the risk of HBV-related hepatocellular carcinoma

ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects

Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations

Identification of Telomere Maintenance Gene Variations Related to Lung Adenocarcinoma Risk by Genome-Wide Association and Whole Genome Sequencing Analyses

A large-scale microRNA transcriptome-wide association study identifies two susceptibility microRNAs, miR-1307-5p and miR-192-3p, for colorectal cancer risk

Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

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

Population-based Screening for Hereditary Colorectal Cancer Variants in Japan

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

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

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

Expansion of Cancer Risk Profile for BRCA1 and BRCA2 Pathogenic Variants

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

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

[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

Genetic susceptibility to hepatocellular carcinoma in chromosome 22q13.31, findings of a genome-wide association study

Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis

Cancer-associated miRNAs and their therapeutic potential

Germline pathogenic variants in 7,636 Japanese patients with prostate cancer and 12,366 controls

Fine Mapping of the Major Histocompatibility Complex Region and Association of the HLA-B*52:01 Allele With Cervical Cancer in Japanese Women

Genome-wide association meta-analysis identifies GP2 gene risk variants for pancreatic cancer

Genetic characterization of pancreatic cancer patients and prediction of carrier status of germline pathogenic variants in cancer-predisposing genes

Prevalence and spectrum of pathogenic germline variants in Japanese patients with early-onset colorectal, breast, and prostate cancer

12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population

Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population

Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion

Novel Common Genetic Susceptibility Loci for Colorectal Cancer

Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection

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

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

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

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

Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations

Clinical and Genome-Wide Analysis of Cisplatin-Induced Peripheral Neuropathy in Survivors of Adult-Onset Cancer

Breast cancer chemoprevention pharmacogenomics: Deep sequencing and functional genomics of the ZNF423 and CTSO genes

Calmodulin-like protein 3 is an estrogen receptor alpha coregulator for gene expression and drug response in a SNP, estrogen, and SERM-dependent fashion

TCL1A Single-Nucleotide Polymorphisms and Estrogen-Mediated Toll-Like Receptor-MYD88-Dependent Nuclear Factor-κB Activation: Single-Nucleotide Polymorphism- and Selective Estrogen Receptor Modulator-Dependent Modification of Inflammation and Immune Response