Lista de obras - Hong-Hee Won - Dominio Público Uruguay

A Bayesian ensemble approach with a disease gene network predicts damaging effects of missense variants of human cancers.

artículo científico publicado en 2012

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

artículo científico publicado en 2015

A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia ⬇️

artículo científico publicado el 3 de mayo de 2011

A genome-wide association study of antidepressant response in Koreans

artículo científico publicado en 2015

A genome-wide association study of antidepressant response in Koreans

artículo científico publicado en 2015

A genome-wide scan for the Sasang constitution in a Korean family suggests significant linkage at chromosomes 8q11.22-23 and 11q22.1-3.

artículo científico publicado en 2009

A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank

artículo científico publicado en 2022

Analysis of dementia-related gene variants in APOE ε4 noncarrying Korean patients with early-onset Alzheimer's disease

scientific article published on 22 May 2019

Analysis of protein-coding genetic variation in 60,706 humans

artículo científico publicado en 2016

Association between a polymorphism in the lymphotoxin-a promoter region and migraine

artículo científico publicado en 2007

Association between air pollution and suicide in South Korea: a nationwide study

artículo científico publicado en 2015

Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease

artículo científico publicado en 2017

Association of the choline acetyltransferase gene with responsiveness to acetylcholinesterase inhibitors in Alzheimer's disease

artículo científico publicado en 2015

Breakpoint mapping by whole genome sequencing identifies PTH2R gene disruption in a patient with midline craniosynostosis and a de novo balanced chromosomal rearrangement.

artículo científico publicado en 2015

Burden of Intracranial Atherosclerosis Is Associated With Long-Term Vascular Outcome in Patients With Ischemic Stroke.

artículo científico

Cataloging coding sequence variations in human genome databases

artículo científico publicado en 2008

Celebrity suicides and their differential influence on suicides in the general population: a national population-based study in Korea

artículo científico publicado en 2015

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

artículo científico publicado en 2016

Comparative analysis of the JAK/STAT signaling through erythropoietin receptor and thrombopoietin receptor using a systems approach

artículo científico publicado en 2009

Comparison of identical single nucleotide polymorphisms genotyped by the GeneChip Targeted Genotyping 25K, Affymetrix 500K and Illumina 550K platforms.

artículo científico publicado en 2009

DATA MINING FOR GENE EXPRESSION PROFILES FROM DNA MICROARRAY

article

Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

artículo científico publicado en 2016

Differentially expressed genes in human peripheral blood as potential markers for statin response

article

Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.

artículo científico publicado en 2015

Effectiveness of in silico tagSNP selection methods: virtual analysis of the genotypes of pharmacogenetic genes.

artículo científico publicado en 2007

EnsemPro: an ensemble approach to predicting transcription start sites in human genomic DNA sequences

artículo científico publicado en 2008

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

artículo científico publicado en 2014

Founder effects in two predominant intronic mutations of UNC13D, c.118-308C>T and c.754-1G>C underlie the unusual predominance of type 3 familial hemophagocytic lymphohistiocytosis (FHL3) in Korea

artículo científico publicado en 2012

Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patients.

artículo científico publicado en 2016

Genetic analysis for a shared biological basis between migraine and coronary artery disease

artículo científico publicado en 2015

Genetic association study of individual symptoms in depression

artículo científico publicado en 2012

Genetic prediction of antidepressant drug response and nonresponse in Korean patients

artículo científico publicado en 2014

Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families.

artículo científico publicado en 2013

Genome-widely significant evidence of linkage of schizophrenia to chromosomes 2p24.3 and 6q27 in an SNP-Based analysis of Korean families.

artículo científico publicado en 2009

HMGCLL1 is a predictive biomarker for deep molecular response to imatinib therapy in chronic myeloid leukemia

artículo científico publicado en 2018

Heritability estimates of individual psychological distress symptoms from genetic variation

artículo científico publicado en 2019

Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity

artículo científico publicado en 2017

Human knockouts in a cohort with a high rate of consanguinity

Inactivating mutations in NPC1L1 and protection from coronary heart disease

artículo científico publicado en 2014

Interleukin 10 polymorphisms differentially influence the risk of gastric cancer in East Asians and Caucasians.

artículo científico publicado en 2010

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

artículo científico publicado en 2015

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease

artículo científico publicado en 2014

Multiple single-nucleotide polymorphism-based risk model for clinical outcomes after allogeneic stem-cell transplantation, especially for acute graft-versus-host disease.

artículo científico publicado en 2012

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)

artículo científico publicado en 2007

Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries

artículo científico publicado en 2015

NUDT15 genotype distributions in the Korean population

artículo científico publicado en 2017

No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis ⬇️

scientific article published on 12 October 2016

No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study

scientific article published on 15 January 2019

Paraquat prohibition and change in the suicide rate and methods in South Korea ⬇️

artículo científico publicado en 2015

Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels

artículo científico publicado en 2016

Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals

artículo científico publicado en 2020

Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients.

artículo científico publicado en 2011

Predicting national suicide numbers with social media data

artículo científico publicado en 2013

Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease

artículo científico publicado en 2017

Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease

artículo científico publicado en 2019

Risk stratification of organ-specific GVHD can be improved by single-nucleotide polymorphism-based risk models

scientific article published on 03 March 2014

SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15).

artículo científico publicado en 2013

SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians

artículo científico publicado en 2013

Sequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea.

artículo científico publicado en 2010

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

artículo científico publicado en 2017

Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction

artículo científico publicado en 2015

The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations

artículo científico publicado en 2011

The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma

artículo científico publicado en 2017

The association of single nucleotide polymorphisms in the connective tissue growth factor gene with pseudoexfoliation syndrome/glaucoma.

artículo científico publicado en 2015

Tissue-specific genetic features inform prediction of drug side effects in clinical trials

artículo científico publicado en 2020

Whole exome sequencing combined with integrated variant annotation prediction identifies a causative myosin essential light chain variant in hypertrophic cardiomyopathy.

artículo científico publicado en 2015

Lista de obras de Hong-Hee Won

A Bayesian ensemble approach with a disease gene network predicts damaging effects of missense variants of human cancers.

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia ⬇️

A genome-wide association study of antidepressant response in Koreans

A genome-wide association study of antidepressant response in Koreans

A genome-wide scan for the Sasang constitution in a Korean family suggests significant linkage at chromosomes 8q11.22-23 and 11q22.1-3.

A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank

Analysis of dementia-related gene variants in APOE ε4 noncarrying Korean patients with early-onset Alzheimer's disease

Analysis of protein-coding genetic variation in 60,706 humans

Association between a polymorphism in the lymphotoxin-a promoter region and migraine

Association between air pollution and suicide in South Korea: a nationwide study

Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease

Association of the choline acetyltransferase gene with responsiveness to acetylcholinesterase inhibitors in Alzheimer's disease

Breakpoint mapping by whole genome sequencing identifies PTH2R gene disruption in a patient with midline craniosynostosis and a de novo balanced chromosomal rearrangement.

Burden of Intracranial Atherosclerosis Is Associated With Long-Term Vascular Outcome in Patients With Ischemic Stroke.

Cataloging coding sequence variations in human genome databases

Celebrity suicides and their differential influence on suicides in the general population: a national population-based study in Korea

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

Comparative analysis of the JAK/STAT signaling through erythropoietin receptor and thrombopoietin receptor using a systems approach

Comparison of identical single nucleotide polymorphisms genotyped by the GeneChip Targeted Genotyping 25K, Affymetrix 500K and Illumina 550K platforms.

DATA MINING FOR GENE EXPRESSION PROFILES FROM DNA MICROARRAY

Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

Differentially expressed genes in human peripheral blood as potential markers for statin response

Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.

Effectiveness of in silico tagSNP selection methods: virtual analysis of the genotypes of pharmacogenetic genes.

EnsemPro: an ensemble approach to predicting transcription start sites in human genomic DNA sequences

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

Founder effects in two predominant intronic mutations of UNC13D, c.118-308C>T and c.754-1G>C underlie the unusual predominance of type 3 familial hemophagocytic lymphohistiocytosis (FHL3) in Korea

Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patients.

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Genetic association study of individual symptoms in depression

Genetic prediction of antidepressant drug response and nonresponse in Korean patients

Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families.

Genome-widely significant evidence of linkage of schizophrenia to chromosomes 2p24.3 and 6q27 in an SNP-Based analysis of Korean families.

HMGCLL1 is a predictive biomarker for deep molecular response to imatinib therapy in chronic myeloid leukemia

Heritability estimates of individual psychological distress symptoms from genetic variation

Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity

Human knockouts in a cohort with a high rate of consanguinity

Inactivating mutations in NPC1L1 and protection from coronary heart disease

Interleukin 10 polymorphisms differentially influence the risk of gastric cancer in East Asians and Caucasians.

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease

Multiple single-nucleotide polymorphism-based risk model for clinical outcomes after allogeneic stem-cell transplantation, especially for acute graft-versus-host disease.

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)

Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries

NUDT15 genotype distributions in the Korean population

No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis ⬇️

No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study

Paraquat prohibition and change in the suicide rate and methods in South Korea ⬇️

Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels

Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals

Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients.

Predicting national suicide numbers with social media data

Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease

Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease

Risk stratification of organ-specific GVHD can be improved by single-nucleotide polymorphism-based risk models

SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15).

SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians

Sequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea.

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction

The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations

The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma

The association of single nucleotide polymorphisms in the connective tissue growth factor gene with pseudoexfoliation syndrome/glaucoma.

Tissue-specific genetic features inform prediction of drug side effects in clinical trials

Whole exome sequencing combined with integrated variant annotation prediction identifies a causative myosin essential light chain variant in hypertrophic cardiomyopathy.