about
Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (cmtx5)Analysis of protein-coding genetic variation in 60,706 humansA comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery diseaseGenetic prediction of antidepressant drug response and nonresponse in Korean patientsA genome-wide association study of antidepressant response in KoreansAssociation between air pollution and suicide in South Korea: a nationwide studyExome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians.Predicting national suicide numbers with social media dataCataloging coding sequence variations in human genome databasesComparative analysis of the JAK/STAT signaling through erythropoietin receptor and thrombopoietin receptor using a systems approach.Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe HypercholesterolemiaThe 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations.SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15).Inactivating mutations in NPC1L1 and protection from coronary heart diseaseMultiple associated variants increase the heritability explained for plasma lipids and coronary artery disease.Celebrity suicides and their differential influence on suicides in the general population: a national population-based study in KoreaSystematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction.Paraquat prohibition and change in the suicide rate and methods in South Korea.Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis.Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.Burden of Intracranial Atherosclerosis Is Associated With Long-Term Vascular Outcome in Patients With Ischemic Stroke.NUDT15 genotype distributions in the Korean population.Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels.A Bayesian ensemble approach with a disease gene network predicts damaging effects of missense variants of human cancers.Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity.Whole exome sequencing combined with integrated variant annotation prediction identifies a causative myosin essential light chain variant in hypertrophic cardiomyopathy.Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patients.Breakpoint mapping by whole genome sequencing identifies PTH2R gene disruption in a patient with midline craniosynostosis and a de novo balanced chromosomal rearrangement.A genome-wide association study of antidepressant response in KoreansSequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea.Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families.A genome-wide scan for the Sasang constitution in a Korean family suggests significant linkage at chromosomes 8q11.22-23 and 11q22.1-3.Genetic association study of individual symptoms in depression.The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma.
P50
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P50
description
hulumtues
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wetenschapper
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հետազոտող
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name
Hong-Hee Won
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Hong-Hee Won
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Hong-Hee Won
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Hong-Hee Won
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Hong-Hee Won
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type
label
Hong-Hee Won
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Hong-Hee Won
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Hong-Hee Won
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Hong-Hee Won
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Hong-Hee Won
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prefLabel
Hong-Hee Won
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Hong-Hee Won
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Hong-Hee Won
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Hong-Hee Won
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Hong-Hee Won
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P106
P1153
34573851600
P21
P31
P496
0000-0001-5719-0552
P569
2000-01-01T00:00:00Z