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Author Details

Andrew D Morris
University of Edinburgh
1992
291
96
PMIDPaper TitleJournal TitlePublished Year
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37190903Cancer incidence and mortality in 23â¿¿000 patients with type 1 diabetes in the UK: Long-term follow-up.Int J Cancer2023
37190903Cancer incidence and mortality in 23â¿¿000 patients with type 1 diabetes in the UK: Long-term follow-up.Int J Cancer2023
34480422The genomics of heart failure: design and rationale of the HERMES consortium.ESC Heart Fail2021
34480422The genomics of heart failure: design and rationale of the HERMES consortium.ESC Heart Fail2021
30487263Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.Diabetes2019
30487263Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.Diabetes2019
31160809Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2019
31377205The Ig superfamily protein PTGFRN coordinates survival signaling in glioblastoma multiforme.Cancer Lett2019
31377205The Ig superfamily protein PTGFRN coordinates survival signaling in glioblastoma multiforme.Cancer Lett2019
31160809Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2019
29025058Cohort Profile: Genetics of Diabetes Audit and Research in Tayside Scotland (GoDARTS).Int J Epidemiol2018
29025058Cohort Profile: Genetics of Diabetes Audit and Research in Tayside Scotland (GoDARTS).Int J Epidemiol2018
30297969Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.Nat Genet2018
30429575Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30178632A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes.Acta Ophthalmol2018
30224653Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
29623345Lp-PLA<sub>2</sub> activity is associated with increased risk of diabetic retinopathy: a longitudinal disease progression study.Diabetologia2018
29549330Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
29549329Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
29632382Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.Nat Genet2018
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
29273807Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
30178632A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes.Acta Ophthalmol2018
30224653Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30429575Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30297969Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.Nat Genet2018
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
29549330Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
29549329Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
29632382Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.Nat Genet2018
29623345Lp-PLA<sub>2</sub> activity is associated with increased risk of diabetic retinopathy: a longitudinal disease progression study.Diabetologia2018
29273807Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
28790154<i>CKM</i> Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia.Circ Cardiovasc Genet2017
29020356A common missense variant of LILRB5 is associated with statin intolerance and myalgia.Eur Heart J2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
28379579Discovery of novel heart rate-associated loci using the Exome Chip.Hum Mol Genet2017
28790154<i>CKM</i> Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia.Circ Cardiovasc Genet2017
28566273An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Diabetes2017
28739976Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.Hypertension2017
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
28270201Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.Genome Med2017
28146470Rare and low-frequency coding variants alter human adult height.Nature2017
28209224Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.J Am Coll Cardiol2017
28379579Discovery of novel heart rate-associated loci using the Exome Chip.Hum Mol Genet2017
28270201Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.Genome Med2017
28209224Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.J Am Coll Cardiol2017
28146470Rare and low-frequency coding variants alter human adult height.Nature2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
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Collaborators

Colin N A Palmer
Pat Macpherson Centre for Pharmacogenomics and Pharmacogenetics, University of Dundee
Co-authored papers 110
Alex S F Doney
University of Dundee. Ninewells Hospital
Co-authored papers 76
Mark I McCarthy
Co-authored papers 69
Nicholas J Wareham
Co-authored papers 53
Andrew T Hattersley
Co-authored papers 53
Timothy M Frayling
Co-authored papers 51
Cecilia M Lindgren
Co-authored papers 48
Michael Boehnke
Co-authored papers 46
Markku Laakso
Co-authored papers 44
Francis S Collins
University of Michigan ann arbor
Co-authored papers 43
Claudia Langenberg
Co-authored papers 43
Ruth J F Loos
Co-authored papers 42
Jaakko Tuomilehto
Co-authored papers 42
Johanna Kuusisto
Co-authored papers 41
Eleftheria Zeggini
Co-authored papers 40
Karen L Mohlke
Co-authored papers 39
Anne U Jackson
Co-authored papers 39
Erik Ingelsson
Stanford University School of Medicine
Co-authored papers 39
Andrew P Morris
The University of Manchester
Co-authored papers 39
Leif Groop
Co-authored papers 39
Lars Lind
Co-authored papers 38
Veikko Salomaa
Co-authored papers 37
Inês Barroso
Co-authored papers 37
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 36
Tim D Spector
King's College London
Co-authored papers 35
Cornelia M van Duijn
University of Oxford
Co-authored papers 35
Unnur Thorsteinsdottir
University of Iceland
Co-authored papers 34
Kari Stefansson
University of Iceland
Co-authored papers 34
Gudmar Thorleifsson
deCODE genetics/Amgen Inc.
Co-authored papers 34
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 34
Release 1.2