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Author Details
Full Name
Ruifang Li-Gao
Affiliation
ORCID
Career Start Year
2005
Papers
76
H Index
25
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36602522
Computational Study of Iron-Catalyzed Intramolecular [2 + 2] Cycloaddition and Cycloisomerization of Enyne Acetates: Mechanism and Selectivity.
2023
37034649
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
2023
36715614
Normal range CAG repeat size variations in the HTT gene are associated with an adverse lipoprotein profile partially mediated by body mass index.
2023
37402774
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.
Commun Biol
2023
37202875
Altered high-density lipoprotein composition is associated with risk for complications in type 2 diabetes mellitus in South Asian descendants: A cross-sectional, case-control study on lipoprotein subclass profiling.
Diabetes Obes Metab
2023
37017544
Hepatic triglyceride content is intricately associated with numerous metabolites and biochemical pathways.
Liver Int
2023
37398003
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
medRxiv
2023
37301258
Sex-specific association between microvascular health and coagulation parameters: the Netherlands Epidemiology of Obesity study.
2023
34739073
Depression and Inflammatory Bowel Disease: A Bidirectional Two-sample Mendelian Randomization Study.
2022
35511521
Genetic and environmental contributions to stability and change in social inhibition across the adolescent and adult life span.
Developmental Psychology
2022
36154123
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.
Circulation
2022
36144194
The Roles of Gut Microbiome and Plasma Metabolites in the Associations between ABO Blood Groups and Insulin Homeostasis: The Microbiome and Insulin Longitudinal Evaluation Study (MILES).
Metabolites
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
34588469
Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function.
Sci Rep
2021
34270325
Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations.
Circ Genom Precis Med
2021
33731105
Investigating the relationships between unfavourable habitual sleep and metabolomic traits: evidence from multi-cohort multivariable regression and Mendelian randomization analyses.
BMC Med
2021
33727701
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
2021
33512453
Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation.
Blood
2021
33064246
The Heritability of Type D Personality by an Extended Twin-Pedigree Analysis in the Netherlands Twin Register.
Behavior Genetics
2021
34727949
Higher thyrotropin leads to unfavorable lipid profile and somewhat higher cardiovascular disease risk: evidence from multi-cohort Mendelian randomization and metabolomic profiling.
BMC Med
2021
34610981
Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism.
2021
32603185
Genome-Wide Association Study of the Postprandial Triglyceride Response Yields Common Genetic Variation in LIPC (Hepatic Lipase).
Circulation. Genomic and precision medicine
2020
32822252
Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.
Circ Genom Precis Med
2020
33230300
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
2020
31148376
The association of genetic variants in the cholesteryl ester transfer protein gene with hemostatic factors and a first venous thrombosis.
Journal of Thrombosis and Haemostasis
2019
30478992
Glucose levels and diabetes are not associated with the risk of venous thrombosis: results from the MEGA case-control study.
British Journal of Haematology
2019
30420679
Mendelian randomization reveals unexpected effects of CETP on the lipoprotein profile.
European Journal of Human Genetics
2019
29988085
Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium.
Mol Psychiatry
2019
31491410
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.
Am J Hum Genet
2019
31220183
Assessment of reproducibility and biological variability of fasting and postprandial plasma metabolite concentrations using 1H NMR spectroscopy.
PLoS ONE
2019
31160809
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2019
31190057
Genome-wide association study of breakfast skipping links clock regulation with food timing.
Am J Clin Nutr
2019
27958378
Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.
Pharmacogenomics J
2018
28719597
Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology.
Pharmacogenomics J
2018
30175238
Meta-analysis of exome array data identifies six novel genetic loci for lung function.
Wellcome Open Res
2018
30012220
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.
Genome Biol
2018
29874175
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals.
Circ Genom Precis Med
2018
30429575
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Nat Genet
2018
30046734
Factor V levels and risk of venous thrombosis: The MEGA case-control study.
Research and Practice in Thrombosis and Haemostasis
2018
30224653
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Nat Genet
2018
29451423
Replication of Type 2 diabetes-associated variants in a Saudi Arabian population.
Physiological Genomics
2018
29098321
Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis.
Diabetologia
2018
29758381
Exploring the role of low-frequency and rare exonic variants in alcohol and tobacco use.
Drug Alcohol Depend
2018
29304378
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
Am J Hum Genet
2018
29748316
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval.
Circ Genom Precis Med
2018
29549330
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
29373077
Genetics of fasting and postprandial metabolite levels are overlapping.
Physiological Genomics
2018
29249917
Postprandial metabolite profiles associated with type 2 diabetes clearly stratify individuals with impaired fasting glucose.
Metabolomics
2018
29549329
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
29728394
CETP (Cholesteryl Ester Transfer Protein) Concentration: A Genome-Wide Association Study Followed by Mendelian Randomization on Coronary Artery Disease.
Circulation. Genomic and precision medicine
2018
1 - 50 of 76
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