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CATEGORY
2024.1.1
Genetic architecture of alcohol consumption identified by a genotype-stratified GWAS and impact on esophageal cancer risk in Japanese people
2023.1.13
Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals
2023.1.1
Genetic footprints of assortative mating in the Japanese population
2023.1.11
Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts
2023.1.15
Comparison of the loci associated with HbA1c and blood glucose levels identified by a genome-wide association study in the Japanese population
2023.1.15
Population-Based Impact of Smoking, Drinking, and Genetic Factors on HDL-Cholesterol Levels in J-MICC Study Participants
2023.1.17
Mobile element variation contributes to population-specific genome diversification, gene regulation and disease risk
2023.1.17
Prediction of the cell-type-specific transcription of non-coding RNAs from genome sequences via machine learning
2023.1.18
Detection of trait-associated structural variations using short-read sequencing
2023.1.18
A whole-genome reference panel of 14,393 individuals for East Asian populations accelerates discovery of rare functional variants
2023.1.19
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration
2023.1.19
Boosting the power of genome-wide association studies within and across ancestries by using polygenic scores
2023.1.19
Natural Selection Signatures in the Hondo and Ryukyu Japanese Subpopulations
2023.1.19
Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology
2022.1.31
Genetic diversity fuels gene discovery for tobacco and alcohol use
2022.1.11
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores
2022.1.9
Editorial: Current Status and Future Challenges of Biobank Data Analysis
2021.1.21
A cross-population atlas of genetic associations for 220 human phenotypes
2021.1.14
Genetics of autosomal mosaic chromosomal alteration (mCA)
2021.1.11
Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs
2021.1.7
Genetic analyses identify widespread sex-differential participation bias
2021.1.4
Obelisc: an identical-by-descent mapping tool based on SNP streak
2021.1.1
Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power
2020.1.28
Evidence of Polygenic Adaptation in Sardinia at Height-Associated Loci Ascertained from the Biobank Japan
2020.1.22
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
2020.1.21
The Polygenic and Monogenic Basis of Blood Traits and Diseases
2020.1.13
Chromosomal alterations among age-related haematopoietic clones in Japan
2020.1.11
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
2020.1.10
Dimensionality reduction reveals fine-scale structure in the Japanese population with consequences for polygenic risk prediction
2020.1.9
Trans-biobank analysis with 676,000 individuals elucidates the association of polygenic risk scores of complex traits with human lifespan
2020.1.8
Genetic and phenotypic landscape of the mitochondrial genome in the Japanese population
2020.1.5
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits
2020.1.3
Genome-Wide Natural Selection Signatures Are Linked to Genetic Risk of Modern Phenotypes in the Japanese Population
2019.1.27
Characterizing rare and low-frequency height-associated variants in the Japanese population
2019.1.26
Associations of autozygosity with a broad range of human phenotypes
2019.1.25
Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles
2019.1.22
Genetic and phenotypic landscape of the major histocompatibilty complex region in the Japanese population
2019.1.17
Empirical evaluation of variant calling accuracy using ultra-deep whole-genome sequencing data.
2019.1.3
GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation
2019.1.2
Genetic predisposition to mosaic Y chromosome loss in blood
2019.1.1
GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture
2018.1.31
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases
2018.1.31
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.
2018.1.27
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
2018.1.24
Elucidating the genetic architecture of reproductive ageing in the Japanese population
2018.1.22
Development of a Highly Sensitive Device for Counting the Number of Disease-Specific Exosomes in Human Sera
2018.1.15
Deep whole-genome sequencing reveals recent selection signatures linked to evolution and disease risk of Japanese
2018.1.13
Integration of genetics and miRNA-target gene network identified disease biology implicated in tissue specificity
2018.1.10
Interethnic analyses of blood pressure loci in populations of East Asian and European descent
2018.1.1
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