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TKG
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Author Details
Full Name
Kijoung Song
Affiliation
ORCID
Career Start Year
2003
Papers
57
H Index
33
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37108061
Clinicopathological Significance of Cell Adhesion Molecule 4 Expression in Gallbladder Cancer and Its Prognostic Role.
2023
37021827
Effect of case and control definitions on genome-wide association study (GWAS) findings.
2023
36865145
Identifying COPD subtypes using multi-trait genetics.
medRxiv
2023
36686437
Association between circulating resistin levels and thyroid dysfunction: A systematic review and meta-analysis.
2022
33981765
Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank.
ERJ Open Res
2021
30804560
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Nat Genet
2019
27523435
No evidence of large genetic effects on steroid response in asthma patients.
Journal of Allergy and Clinical Immunology
2017
28472345
STOPGAP: a database for systematic target opportunity assessment by genetic association predictions.
Bioinformatics
2017
26833246
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.
Nat Commun
2016
27023328
Pyrexia in dabrafenib-treated melanoma patients is not associated with common genetic variation or HLA polymorphisms.
Pharmacogenomics
2016
25922065
Different effects of the BIM deletion polymorphism on treatment of solid tumors by the tyrosine kinase inhibitors (TKI) pazopanib, sunitinib, and lapatinib.
Annals of Oncology
2015
23541341
The benefits of using genetic information to design prevention trials.
Am J Hum Genet
2013
24391740
Urotensin-II system in genetic control of blood pressure and renal function.
PLoS One
2013
23934621
The effects of alcohol on the pharmacokinetics and pharmacodynamics of the selective mu-opioid receptor antagonist GSK1521498 in healthy subjects.
Journal of Clinical Pharmacology
2013
23746178
Practical limitations to estimating heritability in pharmacogenetic studies.
Pharmacogenomics
2013
23358095
Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology.
J Invest Dermatol
2013
23147384
Effects of the mu-opioid receptor antagonist GSK1521498 on hedonic and consummatory eating behaviour: a proof of mechanism study in binge-eating obese subjects.
Molecular Psychiatry
2013
21606947
Sequencing of Lp-PLA2-encoding PLA2G7 gene in 2000 Europeans reveals several rare loss-of-function mutations.
Pharmacogenomics J
2012
22479202
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
PLoS Genet
2012
22885924
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.
Nat Genet
2012
22693459
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
PLoS Genet
2012
22008728
An 18-kDa translocator protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28.
J Cereb Blood Flow Metab
2012
22238593
A genome-wide association search for type 2 diabetes genes in African Americans.
PLoS One
2012
21706003
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.
Nat Genet
2011
21490708
Carriage of the V279F null allele within the gene encoding Lp-PLAâ¿¿ is protective from coronary artery disease in South Korean males.
PLoS One
2011
21915365
Prospective study of insulin-like growth factor-I, insulin-like growth factor-binding protein 3, genetic variants in the IGF1 and IGFBP3 genes and risk of coronary artery disease.
Int J Mol Epidemiol Genet
2011
20018283
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals.
Atherosclerosis
2010
20686565
Biological, clinical and population relevance of 95 loci for blood lipids.
Nature
2010
21060006
Genetic architecture of ambulatory blood pressure in the general population: insights from cardiovascular gene-centric array.
Hypertension
2010
20864672
Genetic variants influencing circulating lipid levels and risk of coronary artery disease.
Arterioscler Thromb Vasc Biol
2010
20858683
Common variants at 10 genomic loci influence hemoglobin Aâ¿(C) levels via glycemic and nonglycemic pathways.
Diabetes
2010
20717167
FGF21 signalling pathway and metabolic traits - genetic association analysis.
Eur J Hum Genet
2010
20081858
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
Nat Genet
2010
20081857
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.
Nat Genet
2010
20011104
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.
PLoS Genet
2009
19448623
Genetic variation in LIN28B is associated with the timing of puberty.
Nat Genet
2009
19139842
Risk prediction of prevalent diabetes in a Swiss population using a weighted genetic score--the CoLaus Study.
Diabetologia
2009
19079261
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
Nat Genet
2009
19430483
Genome-wide association study identifies eight loci associated with blood pressure.
Nat Genet
2009
19060907
Variants in MTNR1B influence fasting glucose levels.
Nat Genet
2009
19557161
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.
PLoS Genet
2009
18262040
LDL-cholesterol concentrations: a genome-wide association study.
Lancet
2008
17888929
Genetic and phenotypic architecture of metabolic syndrome-associated components in dyslipidemic and normolipidemic subjects: the GEMS Study.
Atherosclerosis
2008
18849991
Male-pattern baldness susceptibility locus at 20p11.
Nat Genet
2008
18940312
Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.
Am J Hum Genet
2008
18787507
Pharmacological effects of lipid-lowering drugs recapitulate with a larger amplitude the phenotypic effects of common variants within their target genes.
Pharmacogenet Genomics
2008
18454148
Common variants near MC4R are associated with fat mass, weight and risk of obesity.
Nat Genet
2008
18227835
Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking.
Mol Psychiatry
2008
18366642
The CoLaus study: a population-based study to investigate the epidemiology and genetic determinants of cardiovascular risk factors and metabolic syndrome.
BMC Cardiovasc Disord
2008
18466491
Genome-wide association studies using an adaptive two-stage analysis for a case-control design.
BMC Proceedings
2007
1 - 50 of 57
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