2021
CATEGORY
2021.1.23
The power of genetic diversity in genome-wide association studies of lipids
2021.1.22
Genetic susceptibility to hepatocellular carcinoma in chromosome 22q13.31, findings of a genome-wide association study
2021.1.21
A cross-population atlas of genetic associations for 220 human phenotypes
2021.1.20
Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus
2021.1.19
A genome-wide association study identifies a novel candidate locus at the DLGAP1 gene with susceptibility to resistant hypertension in the Japanese population
2021.1.18
Genetic insights into biological mechanisms governing human ovarian ageing
2021.1.17
Intracellular Accumulation of IFN-λ4 Induces ER Stress and Results in Anti-Cirrhotic but Pro-HCV Effects
2021.1.16
All-cause and cardiovascular disease mortality in underweight patients with diabetic nephropathy: BioBank Japan cohort
2021.1.15
Susceptibility loci and polygenic architecture highlight population specific and common genetic features in inguinal hernias: genetics in inguinal hernias
2021.1.14
Genetics of autosomal mosaic chromosomal alteration (mCA)
2021.1.13
Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis
2021.1.12
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection
2021.1.11
Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs
2021.1.10
Cancer-associated miRNAs and their therapeutic potential
2021.1.9
Eight novel susceptibility loci and putative causal variants in atopic dermatitis
2021.1.8
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
2021.1.7
Genetic analyses identify widespread sex-differential participation bias
2021.1.6
An X chromosome-wide meta-analysis based on Japanese cohorts revealed that non-autosomal variations are associated with serum urate
2021.1.5
A deep learning method for HLA imputation and trans-ethnic MHC fine-mapping of type 1 diabetes
2021.1.4
Obelisc: an identical-by-descent mapping tool based on SNP streak
2021.1.3
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
2021.1.2
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
2021.1.1
Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power
2021.1.1
Genome-wide SNP data of Izumo and Makurazaki populations support inner-dual structure model for origin of Yamato people