Author: Andrew P Morris

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Preprints

Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Genomic evaluation of circulating proteins for drug target characterisation and precision medicine

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Identification of type 2 diabetes loci in 433,540 East Asian individuals

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry

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New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

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Integrative cross tissue analysis of gene expression identifies novel type 2 diabetes genes

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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Genome-wide association study of susceptibility to idiopathic pulmonary fibrosis

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The genetic architecture of sporadic and recurrent miscarriage

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Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

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Analysis of chromatin organization and gene expression in T cells identifies functional genes for rheumatoid arthritis

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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MR-TRYX: A Mendelian randomization framework that exploits horizontal pleiotropy to infer novel causal pathways

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies

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Genome Wide Association Scan identifies new variants associated with a cognitive predictor of dyslexia.

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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Hypertension and renin-angiotensin system blockers are not associated with expression of Angiotensin Converting Enzyme 2 (ACE2) in the kidney

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Meta-analysis of exome array data identifies six novel genetic loci for lung function

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Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans

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Functional genomics atlas of synovial fibroblasts defining rheumatoid arthritis heritability

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methylSCOPA and META-methylSCOPA: software for the analysis and aggregation of epigenome-wide association studies of multiple correlated phenotypes

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Chromatin-based techniques map DNA interaction landscapes in psoriasis susceptibility loci and highlight KLF4 as a target gene in 9q31

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Obesity as a cause of kidney disease - insights from Mendelian randomisation studies

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