内分泌代謝疾患
CATEGORY
2023.1.9
Identification of serum metabolome signatures associated with retinal and renal complications of type 2 diabetes
2023.1.15
Genetic Risk of Primary Aldosteronism and Its Contribution to Hypertension: A Cross-Ancestry Meta-Analysis of Genome-Wide Association Studies
2022.1.19
Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component
2022.1.16
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
2022.1.14
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
2022.1.7
Genome-wide risk prediction of common diseases across ancestries in one million people
2022.1.6
Response to Comment on Dawed et al. Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to Sulfonylureas. Diabetes Care 2021;44:2673-2682
2021.1.23
The power of genetic diversity in genome-wide association studies of lipids
2021.1.5
A deep learning method for HLA imputation and trans-ethnic MHC fine-mapping of type 1 diabetes
2020.1.23
Cause-specific mortality rates in patients with diabetes according to comorbid macro- and microvascular complications: BioBank Japan Cohort
2020.1.19
Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients
2020.1.7
Identification of type 2 diabetes loci in 433,540 East Asian individuals
2020.1.2
Diabetes and cancer risk: A Mendelian randomization study
2019.1.5
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
2018.1.30
Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetes
2018.1.8
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
2017.1.25
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes
2016.1.20
Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes
2016.1.3
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
2010.3.22
A single nucleotide polymorphism in KCNQ1 is associated with susceptibility to diabetic nephropathy in japanese subjects with type 2 diabetes
2010.3.22
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B
2009.3.22
Replication study for the association of new meta-analysis-derived risk loci with susceptibility to type 2 diabetes in 6,244 Japanese individuals
2008.3.22
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
2024.1.3
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
2024.1.5
Body mass index stratification optimizes polygenic prediction of type 2 diabetes in cross-biobank analyses
2017.1.1
Characteristics of patients with liver cancer in the BioBank Japan project
2017.1.1
Cholesterol levels of Japanese dyslipidaemic patients with various comorbidities: BioBank Japan
2017.1.1
Serum glucose, cholesterol and blood pressure levels in Japanese type 1 and 2 diabetic patients: BioBank Japan
2017.1.1
Statin use and all-cause and cancer mortality: BioBank Japan cohort
2015.1.9
Construction of a population-specific HLA imputation reference panel and its application to Graves’ disease risk in Japanese
2017.1.1
Survival of macrovascular disease, chronic kidney disease, chronic respiratory disease, cancer and smoking in patients with type 2 diabetes: BioBank Japan cohort
2014.1.14
Genome-wide association study identifies three novel loci for type 2 diabetes
2024.1.5
Genetic Risk, Healthy Lifestyle Adherence, and Risk of Developing Diabetes in the Japanese Population
2014.1.5
The construction of risk prediction models using GWAS data and its application to a type 2 diabetes prospective cohort
2012.1.13
A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations
2011.3.22
Association between single nucleotide polymorphisms within genes encoding sirtuin families and diabetic nephropathy in Japanese subjects with type 2 diabetes
2011.3.22
Identification of independent risk loci for Graves’ disease within the MHC in the Japanese population