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Author Details
Full Name
Colin N A Palmer
Affiliation
Pat Macpherson Centre for Pharmacogenomics and Pharmacogenetics, University of Dundee
ORCID
Career Start Year
1987
Papers
367
H Index
105
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37690457
Environmental risk factors for respiratory infection and wheeze in young children: A multicentre birth cohort study.
Pediatr Pulmonol
2024
37690457
Environmental risk factors for respiratory infection and wheeze in young children: A multicentre birth cohort study.
Pediatr Pulmonol
2024
36355188
Development and external validation of multivariable risk models to predict incident and resolved neuropathic pain: a DOLORisk Dundee study.
J Neurol
2023
36355188
Development and external validation of multivariable risk models to predict incident and resolved neuropathic pain: a DOLORisk Dundee study.
J Neurol
2023
37253618
A gene risk score using missense variants in SLCO1B1 is associated with earlier onset statin intolerance.
Eur Heart J Cardiovasc Pharmacother
2023
36998609
The cholesterol-lowering effect of statins is modified by <i>LILRB5</i> intolerance genotype: Results from a recruit-by-genotype clinical trial.
Front Pharmacol
2023
37302544
Amino acid homeostasis is a target of metformin therapy.
Mol Metab
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
37253618
A gene risk score using missense variants in SLCO1B1 is associated with earlier onset statin intolerance.
Eur Heart J Cardiovasc Pharmacother
2023
37302544
Amino acid homeostasis is a target of metformin therapy.
Mol Metab
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
36998609
The cholesterol-lowering effect of statins is modified by <i>LILRB5</i> intolerance genotype: Results from a recruit-by-genotype clinical trial.
Front Pharmacol
2023
34562103
Diabetes status modifies the long-term effect of lipoprotein-associated phospholipase A2 on major coronary events.
Diabetologia
2022
36102151
Identification of 4 New Loci Associated With Primary Hyperparathyroidism (PHPT) and a Polygenic Risk Score for PHPT.
J Clin Endocrinol Metab
2022
36036237
Association of bronchial steroid inducible methylation quantitative trait loci with asthma and chronic obstructive pulmonary disease treatment response.
Clin Transl Allergy
2022
35763030
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease.
Diabetologia
2022
35949104
Mannose-binding lectin genotype is associated with respiratory disease in young children: A multicenter cohort study.
Pediatr Pulmonol
2022
35754128
Multi-ancestry genome-wide association study of asthma exacerbations.
Pediatr Allergy Immunol
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
36939796
A Meta-Analysis of the Genome-Wide Association Studies on Two Genetically Correlated Phenotypes Suggests Four New Risk Loci for Headaches.
Phenomics
2022
34562103
Diabetes status modifies the long-term effect of lipoprotein-associated phospholipase A2 on major coronary events.
Diabetologia
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
35763030
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease.
Diabetologia
2022
35754128
Multi-ancestry genome-wide association study of asthma exacerbations.
Pediatr Allergy Immunol
2022
36939796
A Meta-Analysis of the Genome-Wide Association Studies on Two Genetically Correlated Phenotypes Suggests Four New Risk Loci for Headaches.
Phenomics
2022
36102151
Identification of 4 New Loci Associated With Primary Hyperparathyroidism (PHPT) and a Polygenic Risk Score for PHPT.
J Clin Endocrinol Metab
2022
36036237
Association of bronchial steroid inducible methylation quantitative trait loci with asthma and chronic obstructive pulmonary disease treatment response.
Clin Transl Allergy
2022
35949104
Mannose-binding lectin genotype is associated with respiratory disease in young children: A multicenter cohort study.
Pediatr Pulmonol
2022
32948670
The Relationship between AKI and CKD in Patients with Type 2 Diabetes: An Observational Cohort Study.
J Am Soc Nephrol
2021
34128573
ADRB2 haplotypes and asthma exacerbations in children and young adults: An individual participant data meta-analysis.
Clin Exp Allergy
2021
33706416
Genome-wide association studies of exacerbations in children using long-acting beta2-agonists.
Pediatr Allergy Immunol
2021
34172468
The association between SARS-CoV-2 RT-PCR cycle threshold and mortality in a community cohort.
Eur Respir J
2021
33479111
Asthma prescribing according to Arg16Gly beta-2 genotype: a randomised trial in adolescents.
Eur Respir J
2021
33952538
Cohort profile: DOLORisk Dundee: a longitudinal study of chronic neuropathic pain.
BMJ Open
2021
34108472
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.
Nat Commun
2021
34050993
An FCER2 polymorphism is associated with increased oral leukotriene receptor antagonists and allergic rhinitis prescribing.
Clin Exp Allergy
2021
33998162
Neutrophil-to-lymphocyte ratio and outcomes in patients with new-onset or worsening heart failure with reduced and preserved ejection fraction.
ESC Heart Fail
2021
33731365
Erratum. Clinical Impact of Residual C-Peptide Secretion in Type 1 Diabetes on Glycemia and Microvascular Complications. Diabetes Care 2021;44:390-398.
Diabetes Care
2021
33727701
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
2021
33558525
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
2021
34249083
Polymorphism in <i>INSR</i> Locus Modifies Risk of Atrial Fibrillation in Patients on Thyroid Hormone Replacement Therapy.
Front Genet
2021
33547206
Erratum. Clinical Impact of Residual C-Peptide Secretion in Type 1 Diabetes on Glycemia and Microvascular Complications. Diabetes Care 2021;44:390-398.
Diabetes Care
2021
32989287
Genome-wide association study identifies 48 common genetic variants associated with handedness.
Nat Hum Behav
2021
33303639
Clinical Impact of Residual C-Peptide Secretion in Type 1 Diabetes on Glycemia and Microvascular Complications.
Diabetes Care
2021
33303529
Genome-wide association study of asthma exacerbations despite inhaled corticosteroid use.
Eur Respir J
2021
33334125
Phospholemman Phosphorylation Regulates Vascular Tone, Blood Pressure, and Hypertension in Mice and Humans.
Circulation
2021
32948670
The Relationship between AKI and CKD in Patients with Type 2 Diabetes: An Observational Cohort Study.
J Am Soc Nephrol
2021
32786158
Combined analysis of transcriptomic and genetic data for the identification of loci involved in glucocorticosteroid response in asthma.
Allergy
2021
33402679
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
2021
33385700
A review of machine learning methods for retinal blood vessel segmentation and artery/vein classification.
Med Image Anal
2021
1 - 50 of 734
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Nilesh J Samani
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Lars Lind
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Karen L Mohlke
Co-authored papers
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Eric Boerwinkle
Baylor College of Medicine
Co-authored papers
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Francis S Collins
University of Michigan ann arbor
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Anne U Jackson
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Tim D Spector
King's College London
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