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Author Details

Michael R Barnes
William Harvey Research Institute, Queen Mary University of London
1997
121
41
PMIDPaper TitleJournal TitlePublished Year
36566926Local delivery of nitric oxide prevents endothelial dysfunction in periodontitis.Pharmacol Res2023
37498390The benefits and pitfalls of machine learning for biomarker discovery.Cell Tissue Res2023
37113250nestedcv: an R package for fast implementation of nested cross-validation with embedded feature selection designed for transcriptomics and high-dimensional data.Bioinform Adv2023
36684605Bayesian network analysis of panomic biological big data identifies the importance of triglyceride-rich LDL in atherosclerosis development.Front Cardiovasc Med2023
36051279Predicting post-contrast information from contrast agent free cardiac MRI using machine learning: Challenges and methods.Front Cardiovasc Med2022
35680389Interferon-α-mediated therapeutic resistance in early rheumatoid arthritis implicates epigenetic reprogramming.Ann Rheum Dis2022
35609980GEOexplorer: a webserver for gene expression analysis and visualisation.Nucleic Acids Res2022
34758253100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.N Engl J Med2021
33771529Meeting Report: Psoriasis Stratification to Optimize Relevant Therapy Showcase.J Invest Dermatol2021
33727701Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2021
34930920Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty.NPJ Genom Med2021
31501851Spectrum: fast density-aware spectral clustering for single and multi-omic data.Bioinformatics2020
32020004M3C: Monte Carlo reference-based consensus clustering.Sci Rep2020
31988455Polycomb-mediated repression of EphrinA5 promotes growth and invasion of glioblastoma.Oncogene2020
33230300Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2020
32945072Enzymatic degradation of RNA causes widespread protein aggregation in cell and tissue lysates.EMBO Rep2020
32439900Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.Nat Commun2020
32493844LGR4 deficiency results in delayed puberty through impaired Wnt/β-catenin signaling.JCI Insight2020
32351543Reaching the End-Game for GWAS: Machine Learning Approaches for the Prioritization of Complex Disease Loci.Front Genet2020
30662418Characterizing Nature and Participant Experience in Studies of Nature Exposure for Positive Mental Health: An Integrative Review.Front Psychol2019
30030151A Framework for Multi-Omic Prediction of Treatment Response to Biologic Therapy for Psoriasis.J Invest Dermatol2019
31411675Over 1000 genetic loci influencing blood pressure with multiple systems and tissues implicated.Hum Mol Genet2019
31554410Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated With Cardiac Morphogenesis and Heart Failure Development.Circulation2019
31461658Molecular Portraits of Early Rheumatoid Arthritis Identify Clinical and Treatment Response Phenotypes.Cell Rep2019
30862612Clinical applications of machine learning algorithms: beyond the black box.BMJ2019
30878974Synovial cellular and molecular signatures stratify clinical response to csDMARD therapy and predict radiographic progression in early rheumatoid arthritis patients.Ann Rheum Dis2019
30608578EAP1 regulation of GnRH promoter activity is important for human pubertal timing.Hum Mol Genet2019
30345732Oncometabolite induced primary cilia loss in pheochromocytoma.Endocr Relat Cancer2019
29161441Contributions of Function-Altering Variants in Genes Implicated in Pubertal Timing and Body Mass for Self-Limited Delayed Puberty.J Clin Endocrinol Metab2018
29931354HS6ST1 Insufficiency Causes Self-Limited Delayed Puberty in Contrast With Other GnRH Deficiency Genes.J Clin Endocrinol Metab2018
30224653Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30031863Sex differences in the nitrate-nitrite-NO<sup>â¿¢</sup> pathway: Role of oral nitrate-reducing bacteria.Free Radic Biol Med2018
30429575Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30311271Prediction of treatment response in rheumatoid arthritis patients using genome-wide SNP data.Genet Epidemiol2018
30379817Correction: Signatures of inflammation and impending multiple organ dysfunction in the hyperacute phase of trauma: A prospective cohort study.PLoS Med2018
30354342Druggability of Coronary Artery Disease Risk Loci.Circ Genom Precis Med2018
29362468Corrigendum: The RA-MAP Consortium: a working model for academia-industry collaboration.Nat Rev Rheumatol2018
29752460RNA sequencing and machine learning as molecular scalpels.Nat Rev Rheumatol2018
29523565Feasibility of real-time capture of routine clinical data in the electronic health record: a hospital-based, observational service-evaluation study.BMJ Open2018
29795407Genome-wide association study of response to methotrexate in early rheumatoid arthritis patients.Pharmacogenomics J2018
29274079Bioinformatics for dermatology: why we should learn about code.Br J Dermatol2018
29213124The RA-MAP Consortium: a working model for academia-industry collaboration.Nat Rev Rheumatol2018
27533743An ectopically expressed serum miRNA signature is prognostic, diagnostic, and biologically related to liver allograft rejection.Hepatology2017
28329392Evaluation of splenic switch off in a tertiary imaging centre: validation and assessment of utility.Eur Heart J Cardiovasc Imaging2017
29030403New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475â¿¿000 Individuals.Circ Cardiovasc Genet2017
28951623Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.Nat Genet2017
28739976Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.Hypertension2017
28715416Signatures of inflammation and impending multiple organ dysfunction in the hyperacute phase of trauma: A prospective cohort study.PLoS Med2017
28843296Research Techniques Made Simple: Bioinformatics for Genome-Scale Biology.J Invest Dermatol2017
28735850Enhanced Energetic State and Protection from Oxidative Stress in Human Myoblasts Overexpressing BMI1.Stem Cell Reports2017
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Collaborators

Patricia B Munroe
Co-authored papers 18
Mark J Caulfield
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 16
Helen R Warren
Co-authored papers 15
Daniel I Chasman
Harvard Medical School, Harvard University
Co-authored papers 12
Xiuqing Guo
Co-authored papers 11
Gerome Breen
Institute of Psychiatry, King's College London
Co-authored papers 11
Nilesh J Samani
Co-authored papers 11
Bruce M Psaty
Co-authored papers 11
Paul M Ridker
Co-authored papers 10
Jerome I Rotter
Co-authored papers 10
Vilmundur Gudnason
Co-authored papers 10
Daniel Levy
and Blood Institute, National Institutes of Health
Co-authored papers 10
Christopher Newton-Cheh
Co-authored papers 10
Eric Boerwinkle
Baylor College of Medicine
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Andrew P Morris
The University of Manchester
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Albert V Smith
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Kent D Taylor
Co-authored papers 10
Tim D Spector
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Joshua C Bis
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Andrew D Johnson
and Blood Institute
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Colin N A Palmer
Pat Macpherson Centre for Pharmacogenomics and Pharmacogenetics, University of Dundee
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Pim van der Harst
Co-authored papers 9
Brendan J Keating
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 8
Jaspal S Kooner
London NorthWest Healthcare NHS Trust
Co-authored papers 8
Paul Elliott
Co-authored papers 8
Evangelos Evangelou
University of Ioannina
Co-authored papers 8
Jo Knight
Data Science Institute and Lancaster University Medical School
Co-authored papers 8
Kenneth Rice
Co-authored papers 8
Walter Palmas
Co-authored papers 8
Veikko Salomaa
Co-authored papers 8
Release 1.2