Manganese transport in mammals by zinc transporter family proteins, ZNT and ZIP
A genome‐wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder
Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies
The Arachidonic Acid Metabolome Serves as a Conserved Regulator of Cholesterol Metabolism
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases
First case of sitosterolemia caused by double heterozygous mutations in ABCG5 and ABCG8 genes
Interethnic analyses of blood pressure loci in populations of East Asian and European descent
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Genes associated with diabetes: potential for novel therapeutic targets?
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data
Genomewide Association Study Confirming the Association of
<i>NAT2</i>
with Susceptibility to Antituberculosis Drug-Induced Liver Injury in Thai Patients
Genomics of hypertriglyceridemia
Impact of Cortisol on Reduction in Muscle Strength and Mass: A Mendelian Randomization Study
Trans-ethnic polygenic analysis supports genetic overlaps of lumbar disc degeneration with height, body mass index, and bone mineral density
The interaction between ABCA1 polymorphism and physical activity on the HDL-cholesterol levels in a Japanese population
Clinical whole exome sequencing in severe hypertriglyceridemia
Directional dominance on stature and cognition in diverse human populations
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
Biomarkers of Dietary Omega-6 Fatty Acids and Incident Cardiovascular Disease and Mortality
The power of genetic diversity in genome-wide association studies of lipids
Stroke genetics informs drug discovery and risk prediction across ancestries
Genome‐wide association studies of bipolar disorder: A systematic review of recent findings and their clinical implications
Whole exome sequencing combined with integrated variant annotation prediction identifies asymptomatic Tangier disease with compound heterozygous mutations in ABCA1 gene
Molecular and functional characterization of familial chylomicronemia syndrome
Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease
TTC39B deficiency stabilizes LXR reducing both atherosclerosis and steatohepatitis
Identification of genetic elements in metabolism by high-throughput mouse phenotyping
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genetic invalidation of Lp-PLA<sub>2</sub> as a therapeutic target: Large-scale study of five functional Lp-PLA<sub>2</sub>-lowering alleles
Different inverse association of large high-density lipoprotein subclasses with exacerbation of insulin resistance and incidence of type 2 diabetes: The Nagahama study
A Transethnic Mendelian Randomization Study Identifies Causality of Obesity on Risk of Psoriasis
Comprehensive genotyping in dyslipidemia: mendelian dyslipidemias caused by rare variants and Mendelian randomization studies using common variants
Significant impact of miRNA–target gene networks on genetics of human complex traits
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease
Association of genetic variants with dyslipidemia and chronic kidney disease in a longitudinal population-based genetic epidemiological study
Association of genetic variants with dyslipidemia
Investigating the causal effect of fibroblast growth factor 23 on osteoporosis and cardiometabolic disorders: A Mendelian randomization study
Identification of type 2 diabetes loci in 433,540 East Asian individuals
GPR146 Deficiency Protects against Hypercholesterolemia and Atherosclerosis
Beneficial effect of ezetimibe-atorvastatin combination therapy in patients with a mutation in ABCG5 or ABCG8 gene
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
Gene-exercise interactions in the development of cardiometabolic diseases
V．ゲノムから展望する脂質管理のあり方
New Insights into the Roles of ZIP8, a Cadmium and Manganese Transporter, and Its Relation to Human Diseases