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Author Details
Full Name
Dawn M Waterworth
Affiliation
ORCID
Career Start Year
1994
Papers
144
H Index
64
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36829046
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.
Nature
2023
36048866
Genetically proxied therapeutic prolyl-hydroxylase inhibition and cardiovascular risk.
Hum Mol Genet
2023
36653562
FinnGen provides genetic insights from a well-phenotyped isolated population.
Nature
2023
34562103
Diabetes status modifies the long-term effect of lipoprotein-associated phospholipase A2 on major coronary events.
Diabetologia
2022
35697829
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Commun Biol
2022
36055212
Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies.
Am J Hum Genet
2022
33137338
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Kidney Int
2021
33748830
Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality.
Eur Heart J
2021
32989287
Genome-wide association study identifies 48 common genetic variants associated with handedness.
Nat Hum Behav
2021
32605384
Meta-Analysis of 26 638 Individuals Identifies Two Genetic Loci Associated With Left Ventricular Ejection Fraction.
Circ Genom Precis Med
2020
31104631
Risks and clinical predictors of cirrhosis and hepatocellular carcinoma diagnoses in adults with diagnosed NAFLD: real-world study of 18 million patients in four European cohorts.
BMC Med
2019
30495974
Factors influencing longitudinal changes of circulating liver enzyme concentrations in subjects randomized to placebo in four clinical trials.
American Journal of Physiology - Gastrointestinal and Liver Physiology
2019
30760496
Integrated Functional Genomic Analysis Enables Annotation of Kidney Genome-Wide Association Study Loci.
J Am Soc Nephrol
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
30897999
Cardiovascular and Lifestyle Risk Factors and Cognitive Function in Patients With Stable Coronary Heart Disease.
Journal of the American Heart Association
2019
31152163
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Nat Genet
2019
29771307
Assessment of rosacea symptom severity by genome-wide association study and expression analysis highlights immuno-inflammatory and skin pigmentation genes.
Hum Mol Genet
2018
30099968
Real-world data reveal a diagnostic gap in non-alcoholic fatty liver disease.
BMC Med
2018
30289950
Lp-PLA2, scavenger receptor class B type I gene (SCARB1) rs10846744 variant, and cardiovascular disease.
PLoS One
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
29549329
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
29422496
Opioid Antagonists and the A118G Polymorphism in the μ-Opioid Receptor Gene: Effects of GSK1521498 and Naltrexone in Healthy Drinkers Stratified by OPRM1 Genotype.
2018
29273807
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
29313844
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.
Nat Commun
2017
28724990
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.
Nat Commun
2017
28753643
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
PLoS ONE
2017
29091937
Phenome-wide association study using research participants' self-reported data provides insight into the Th17 and IL-17 pathway.
PLoS One
2017
29116125
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.
Nat Commun
2017
27535281
The epigenetic signature of systemic insulin resistance in obese women.
Diabetologia
2016
27346689
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.
Am J Hum Genet
2016
27346686
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.
Am J Hum Genet
2016
27346685
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
Am J Hum Genet
2016
27301456
A phenome-wide association study of a lipoprotein-associated phospholipase A2 loss-of-function variant in 90 000 Chinese adults.
Int J Epidemiol
2016
27109624
Opioid Antagonists and the A118G Polymorphism in the μ-Opioid Receptor Gene: Effects of GSK1521498 and Naltrexone in Healthy Drinkers Stratified by OPRM1 Genotype.
2016
26972588
The genetics of drug efficacy: opportunities and challenges.
Nature Reviews Genetics
2016
26833098
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.
Nat Commun
2016
26791069
Lipoprotein-Associated Phospholipase A2 Loss-of-Function Variant and Risk of Vascular Diseases in 90,000 Chinese Adults.
J Am Coll Cardiol
2016
27252175
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease.
Sci Transl Med
2016
26672639
Body Mass Index and Risk of Nonalcoholic Fatty Liver Disease: Two Electronic Health Record Prospective Studies.
Journal of Clinical Endocrinology and Metabolism
2016
27695898
Erratum to: The epigenetic signature of systemic insulin resistance in obese women.
Diabetologia
2016
27788146
A Systematic Review of Biomarkers and Risk of Incident Type 2 Diabetes: An Overview of Epidemiological, Prediction and Aetiological Research Literature.
PLoS One
2016
26494809
Definitions of Metabolic Health and Risk of Future Type 2 Diabetes in BMI Categories: A Systematic Review and Network Meta-analysis.
Diabetes Care
2015
25673413
Genetic studies of body mass index yield new insights for obesity biology.
Nature
2015
25631608
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
Nat Commun
2015
25164947
A low-frequency variant in MAPK14 provides mechanistic evidence of a link with myeloperoxidase: a prognostic cardiovascular risk marker.
Journal of the American Heart Association
2014
24586186
Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links.
PLoS Genet
2014
23541341
The benefits of using genetic information to design prevention trials.
Am J Hum Genet
2013
23824729
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
Am J Clin Nutr
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
1 - 50 of 144
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