Bermseok Oh

Association of lipoprotein lipase (LPL) single nucleotide polymorphisms with type 2 diabetes mellitus.

RAPGEF1 gene variants associated with type 2 diabetes in the Korean population.

Replication of the Wellcome Trust genome-wide association study on essential hypertension in a Korean population.

Genetic variations in the sodium balance-regulating genes ENaC, NEDD4L, NDFIP2 and USP2 influence blood pressure and hypertension.

Recapitulation of two genomewide association studies on blood pressure and essential hypertension in the Korean population.

Gene flow between the Korean peninsula and its neighboring countries.

Overview of personalized medicine in the disease genomic era.

Alternative splicing of human height-related zinc finger and BTB domain-containing 38 gene through Alu exonization.

Type 2 diabetes genetic association database manually curated for the study design and odds ratio.

A regulatory SNP in AKAP13 is associated with blood pressure in Koreans.

Association between renin-angiotensin-aldosterone system-related genes and blood pressure in a Korean population.

Common variants in RYR1 are associated with left ventricular hypertrophy assessed by electrocardiogram.

Recapitulation of the association of the Val66Met polymorphism of BDNF gene with BMI in Koreans.

A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.

Decreases in Casz1 mRNA by an siRNA Complex Do not Alter Blood Pressure in Mice.

Association analysis of reactive oxygen species-hypertension genes discovered by literature mining.

Silencing of Atp2b1 increases blood pressure through vasoconstriction.

Allelic frequencies of 20 visible phenotype variants in the korean population.

Development of a predictive model for type 2 diabetes mellitus using genetic and clinical data.

ANTXR2 is a potential causative gene in the genome-wide association study of the blood pressure locus 4q21.

Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians.

Gene Silencing and Haploinsufficiency of Csk Increase Blood Pressure.

No Interaction with Alcohol Consumption, but Independent Effect of C12orf51 (HECTD4) on Type 2 Diabetes Mellitus in Korean Adults Aged 40-69 Years: The KoGES_Ansan and Ansung Study.

Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes.

Csk Regulates Blood Pressure by Controlling the Synthetic Pathways of Aldosterone.

GAREM1 regulates the PR interval on electrocardiograms.

Allopregnanolone Effects on Transmission in the Brain Stem Solitary Tract Nucleus (NTS).

Identification of five novel genetic loci related to facial morphology by genome-wide association studies.

Importance of family history of diabetes in computing a diabetes risk score in Korean prediabetic population.

Longitudinal analysis to better characterize Asthma-COPD overlap syndrome: Findings from an adult asthma cohort in Korea (COREA).

Gene-environment interactions related to blood pressure traits in two community-based Korean cohorts.

Effect of Interaction between Early Menarche and Genetic Polymorphisms on Triglyceride.

Pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis.

Meta-Qtest: meta-analysis of quadratic test for rare variants.

Incidence of Diabetes Mellitus in Male Moderate Alcohol Drinkers: A Community-Based Prospective Cohort Study.

Direct-to-consumer genetic testing: advantages and pitfalls.

Genome-wide interaction study of single-nucleotide polymorphisms and alcohol consumption on blood pressure: The Ansan and Ansung study of the Korean Genome and Epidemiology Study (KoGES).

Cardiac-specific inactivation of effects cardiac conduction abnormalities and cardiomyopathy-associated phenotypes.