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Author Details

Andrew P Morris
The University of Manchester
1997
324
101
PMIDPaper TitleJournal TitlePublished Year
36273658Dog ownership in infancy is protective for persistent wheeze in 17q21 asthma-risk carriers.J Allergy Clin Immunol2023
36243888Do genetics contribute to TNF inhibitor response prediction in Psoriatic Arthritis?Pharmacogenomics J2023
36273658Dog ownership in infancy is protective for persistent wheeze in 17q21 asthma-risk carriers.J Allergy Clin Immunol2023
37949886Leveraging information between multiple population groups and traits improves fine-mapping resolution.Nat Commun2023
37669986Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry.Nat Commun2023
37749248Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.Nat Genet2023
37905000Genomic insights into the comorbidity between type 2 diabetes and schizophrenia.medRxiv2023
37639939Genome-wide association analysis of cystatin-C kidney function in continental Africa.EBioMedicine2023
37683633Integration of genetic fine-mapping and multi-omics data reveals candidate effector genes for hypertension.Am J Hum Genet2023
36835433Genome-Wide Gene-Set Analysis Identifies Molecular Mechanisms Associated with ALS.Int J Mol Sci2023
37321637The Effect of COVID-19 on Medication Adherence in a Rheumatoid Arthritis (BRAGGSS) and Psoriatic Arthritis (OUTPASS) UK Cohort.J Rheumatol2023
37448981Bridging the diversity gap: Analytical and study design considerations for improving the accuracy of trans-ancestry genetic prediction.HGG Adv2023
36804406Atopic Polygenic Risk Score Is Associated with Paradoxical Eczema Developing in Patients with Psoriasis Treated with Biologics.J Invest Dermatol2023
36693378Loci for insulin processing and secretion provide insight into type 2 diabetes risk.Am J Hum Genet2023
37433298Genetic underpinning of the comorbidity between type 2 diabetes and osteoarthritis.Am J Hum Genet2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37669986Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry.Nat Commun2023
37905000Genomic insights into the comorbidity between type 2 diabetes and schizophrenia.medRxiv2023
37749248Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.Nat Genet2023
37949886Leveraging information between multiple population groups and traits improves fine-mapping resolution.Nat Commun2023
37683633Integration of genetic fine-mapping and multi-omics data reveals candidate effector genes for hypertension.Am J Hum Genet2023
37639939Genome-wide association analysis of cystatin-C kidney function in continental Africa.EBioMedicine2023
37321637The Effect of COVID-19 on Medication Adherence in a Rheumatoid Arthritis (BRAGGSS) and Psoriatic Arthritis (OUTPASS) UK Cohort.J Rheumatol2023
37448981Bridging the diversity gap: Analytical and study design considerations for improving the accuracy of trans-ancestry genetic prediction.HGG Adv2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37433298Genetic underpinning of the comorbidity between type 2 diabetes and osteoarthritis.Am J Hum Genet2023
36693378Loci for insulin processing and secretion provide insight into type 2 diabetes risk.Am J Hum Genet2023
36835433Genome-Wide Gene-Set Analysis Identifies Molecular Mechanisms Associated with ALS.Int J Mol Sci2023
36804406Atopic Polygenic Risk Score Is Associated with Paradoxical Eczema Developing in Patients with Psoriasis Treated with Biologics.J Invest Dermatol2023
36243888Do genetics contribute to TNF inhibitor response prediction in Psoriatic Arthritis?Pharmacogenomics J2023
34523676Blood copper and risk of cardiometabolic diseases: a Mendelian randomization study.Hum Mol Genet2022
35393509Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.Commun Biol2022
35513483Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.Commun Biol2022
36035246Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations.HGG Adv2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35690124Kidney omics in hypertension: from statistical associations to biological mechanisms and clinical applications.Kidney Int2022
35377444Pre-defined gene co-expression modules in rheumatoid arthritis transition towards molecular health following anti-TNF therapy.Rheumatology (Oxford)2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35930604Investigating the prediction of CpG methylation levels from SNP genotype data to help elucidate relationships between methylation, gene expression and complex traits.Genet Epidemiol2022
36050321Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.Nat Commun2022
34523676Blood copper and risk of cardiometabolic diseases: a Mendelian randomization study.Hum Mol Genet2022
34893803Contributions of obesity to kidney health and disease: insights from Mendelian randomization and the human kidney transcriptomics.Cardiovasc Res2022
35131763ADAMTS5 as a therapeutic target for osteoarthritis: Mendelian randomisation study.Ann Rheum Dis2022
34999880Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease.Int J Epidemiol2022
35220425Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.Hum Mol Genet2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35377444Pre-defined gene co-expression modules in rheumatoid arthritis transition towards molecular health following anti-TNF therapy.Rheumatology (Oxford)2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
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Collaborators

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Co-authored papers 108
Lars Lind
Co-authored papers 97
Erik Ingelsson
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Co-authored papers 91
Mark I McCarthy
Co-authored papers 87
Anubha Mahajan
Co-authored papers 83
Nicholas J Wareham
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Ruth J F Loos
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Michael Boehnke
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Eleftheria Zeggini
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Markku Laakso
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Erasmus University Medical Center
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Claudia Langenberg
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Karen L Mohlke
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John C Chambers
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Jaakko Tuomilehto
Co-authored papers 53
Jaspal S Kooner
London NorthWest Healthcare NHS Trust
Co-authored papers 53
Tim D Spector
King's College London
Co-authored papers 53
Bruce M Psaty
Co-authored papers 52
Johanna Kuusisto
Co-authored papers 52
Tamara B Harris
National Institute on Aging
Co-authored papers 52
Release 1.2