Barnes, Michael R.
Queen Mary University of London · National Institute for Health and Care Research · The Alan Turing Institute · William Harvey Research Institute
15 papers on CoChatORCID 0000-0001-9097-7381
Most cited papers
- Verified
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Program, T. M. V., Evangelou, E., Warren, H. R., Mosen-Ansorena, D., Mifsud, B., Pazoki, R., Gao, H., Ntritsos, G., Dimou, N., Cabrera, C. P., et al. (2018) · Nature Genetics
Genetic Associations and EpidemiologyBlood Pressure and Hypertension Studies
Cited by 1,381
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A mega-analysis of genome-wide association studies for major depressive disorder
Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Ripke, S., Wray, N. R., Lewis, C. M., Hamilton, S. P., Weissman, M. M., Breen, G., Byrne, E. M., Blackwood, D. H. R., Boomsma, D. I., et al. (2013) · Molecular Psychiatry
Genetic Associations and EpidemiologyBipolar Disorder and Treatment
Cited by 1,120
- Verified
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease
Li, H., Wetten, S., Li, L., St. Jean, P. L., Upmanyu, R., Surh, L., Hosford, D., Barnes, M. R., Briley, J. D., Borrie, M., et al. (2008) · Archives of Neurology
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 499
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Disruption of the neurexin 1 gene is associated with schizophrenia
Rujescu, D., Ingason, A., Cichon, S., Pietiläinen, O. P. H., Barnes, M. R., Toulopoulou, T., Picchioni, M., Vassos, E., Ettinger, U., Bramon, E., et al. (2009) · Human Molecular Genetics
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 471
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Clinical applications of machine learning algorithms: beyond the black box
Watson, D. S., Krutzinna, J., Bruce, I. N., Griffiths, C. E., McInnes, I. B., Barnes, M. R., & Floridi, L. (2019) · BMJ
Explainable Artificial Intelligence (XAI)Artificial Intelligence in Healthcare and Education
Cited by 450
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Pathway and network-based analysis of genome-wide association studies in multiple sclerosis
Baranzini, S. E., Galwey, N. W., Wang, J., Khankhanian, P., Lindberg, R., Pelletier, D., Wu, W., Uitdehaag, B. M. J., Kappos, L., GeneMSA Consortium, et al. (2009) · Human Molecular Genetics
Multiple Sclerosis Research StudiesBioinformatics and Genomic Networks
Cited by 383
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Health and population effects of rare gene knockouts in adult humans with related parents
Narasimhan, V. M., Hunt, K. A., Mason, D., Baker, C. L., Karczewski, K. J., Barnes, M. R., Barnett, A. H., Bates, C., Bellary, S., Bockett, N. A., et al. (2016) · Science
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 286
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Reaching the end-game for GWAS: Machine learning approaches for the prioritization of complex disease loci
Nicholls, H. L., John, C. R., Watson, D. S., Munroe, P. B., Barnes, M. R., & Cabrera, C. P. (2020) · Frontiers in Genetics
Genetic Associations and EpidemiologyBioinformatics and Genomic Networks
Cited by 155
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Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders
Arloth, J., Bogdan, R., Weber, P., Frishman, G., Menke, A., Wagner, K. V., Balsevich, G., Schmidt, M. V., Karbalai, N., Czamara, D., et al. (2015) · Neuron
Stress Responses and CortisolGenetic Associations and Epidemiology
Cited by 142
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Whole-genome sequence-based analysis of thyroid function
Taylor, P. N., Porcu, E., Chew, S., Campbell, P. J., Traglia, M., Brown, S. J., Mullin, B. H., Shihab, H. A., Min, J., Walter, K., et al. (2015) · Nature Communications
Genetic Associations and EpidemiologyThyroid Disorders and Treatments
Cited by 104
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Genomics implicates adaptive and innate immunity in Alzheimer’s and Parkinson’s diseases
Gagliano, S. A., Pouget, J. G., Hardy, J., Knight, J., Barnes, M. R., Ryten, M., & Weale, M. E. (2016) · Annals of Clinical and Translational Neurology
Neuroinflammation and Neurodegeneration MechanismsAlzheimer's disease research and treatments
Cited by 85
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The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects
Peyrot, W. J., Lee, S. H., Milaneschi, Y., Abdellaoui, A., Byrne, E. M., Esko, T., de Geus, E. J. C., Hemani, G., Hottenga, J. J., Kloiber, S., et al. (2015) · Molecular Psychiatry
Genetic Associations and EpidemiologyNeurotransmitter Receptor Influence on Behavior
Cited by 84
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Common Genetic Variants and Gene-Expression Changes Associated with Bipolar Disorder Are Over-Represented in Brain Signaling Pathway Genes
Pedroso, I., Lourdusamy, A., Rietschel, M., Nöthen, M. M., Cichon, S., McGuffin, P., Al-Chalabi, A., Barnes, M. R., & Breen, G. (2012) · Biological Psychiatry
Bipolar Disorder and TreatmentGenetic Associations and Epidemiology
Cited by 59
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Genome-wide association analysis of copy number variation in recurrent depressive disorder
Rucker, J. J. H., Breen, G., Pinto, D., Pedroso, I., Lewis, C. M., Cohen-Woods, S., Uher, R., Schosser, A., Rivera, M., Aitchison, K. J., et al. (2013) · Molecular Psychiatry
Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology
Cited by 51
- Verified
ADAMTSL3 as a candidate gene for schizophrenia: gene sequencing and ultra-high density association analysis by imputation
Dow, D. J., Huxley-Jones, J., Hall, J. M., Francks, C., Maycox, P. R., Kew, J. N. C., Gloger, I. S., Mehta, N. A. L., Kelly, F. M., Muglia, P., et al. (2011) · Schizophrenia Research
Schizophrenia research and treatmentGenetic Associations and Epidemiology
Cited by 48
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