Articles with public access mandates - Jonathan Mill - UK Medical Research CouncilLearn more
NoteFor this mandate, articles should be available from specific locations.
Not available based on mandate: 19
From promises to practical strategies in epigenetic epidemiology
J Mill, BT Heijmans
Nature Reviews Genetics 14 (8), 585-594, 2013
Profiling regulatory variation in the brain: methods for exploring the neuronal epigenome
AR Jeffries, J Mill
Biological psychiatry 81 (2), 90-91, 2017
Whole blood DNA methylation changes are associated with anti-TNF drug concentration in patients with Crohn’s disease
S Lin, E Hannon, M Reppell, JF Waring, N Smaoui, V Pivorunas, H Guay, ...
Journal of Crohn's and Colitis, jjad133, 2023
Accelerated pace of aging in schizophrenia: five case-control studies
A Caspi, G Shireby, J Mill, TE Moffitt, K Sugden, E Hannon
Biological Psychiatry 95 (11), 1038-1047, 2024
Novel CYP1B1-RMDN2 Alzheimer’s disease locus identified by genome-wide association analysis of cerebral tau deposition on PET
K Nho, SL Risacher, L Apostolova, PJ Bice, J Brosch, R Deardorff, ...
medRxiv, 2023.02. 27.23286048, 2023
Naive pluripotent stem cell-based models capture FGF-dependent human hypoblast lineage specification
A Dattani, E Corujo-Simon, A Radley, T Heydari, Y Taheriabkenar, ...
Cell Stem Cell, 2024
A methylome-wide association study of major depression with out-of-sample case-control classification and trans-ancestry comparison
X Shen, M Barbu, D Caramaschi, R Arathimos, D Czamara, F David, ...
medRxiv, 2023.10. 27.23297630, 2023
Human naive stem cell models reveal the role of FGF signalling in hypoblast specification in the human embryo
A Dattani, EC Simon, A Radley, T Heydari, Y Taheriabkenar, F Carlisle, ...
bioRxiv, 2023.11. 30.569161, 2023
Long-read transcript sequencing identifies differential isoform expression in the entorhinal cortex in a transgenic model of tau pathology
SK Leung, AR Jeffries, I Castanho, RA Bamford, K Moore, EL Dempster, ...
bioRxiv, 2023.09. 20.558220, 2023
Novel epigenetic clock for fetal brain development predicts fetal epigenetic age for iPSCs and iPSC-derived neurons.
LC Steg, GL Shireby, J Imm, JP Davies, R Flynn, SC Namboori, A Bhinge, ...
Using organoids to model sex differences in the human brain
A Pavlinek, D Adhya, A Tsompanidis, V Warrier, AC Vernon, M Lancaster, ...
Biological Psychiatry Global Open Science, 100343, 2024
Antidepressant Exposure and DNA Methylation: Insights from a Methylome-Wide Association Study
E Davyson, X Shen, F Huider, M Adams, K Borges, D McCartney, L Barker, ...
medRxiv, 2024.05. 01.24306640, 2024
Leveraging epigenetic signatures to determine the cell-type of origin from long read sequencing data
E Hannon, J Mill
bioRxiv, 2024.06. 03.597114, 2024
An atlas of expressed transcripts in the prenatal and postnatal human cortex
R Bamford, SK Leung, VK Chundru, AR Jeffries, J Davies, A Franklin, ...
bioRxiv, 2024.05. 24.595768, 2024
DNA methylation patterns in the frontal lobe white matter of multiple system atrophy, Parkinson's disease, and progressive supranuclear palsy: A cross-comparative investigation
M Murthy, K Fodder, Y Miki, N Rambarack, E De Pablo Fernandez, J Mill, ...
bioRxiv, 2024.01. 10.574852, 2024
Longitudinal changes in DNA methylation associated with clozapine use in treatment-resistant schizophrenia from two international cohorts
A Gillespie, EM Walker, E Hannon, G McQueen, KV Sendt, A Avila, J Lally, ...
medRxiv, 2023.11. 17.23298669, 2023
Blood-based multivariate methylation risk score for cognitive impairment and dementia
J Koetsier, R Cavill, RA Reijnders, J Harvey, K Deckers, S Köhler, ...
medRxiv, 2023.09. 27.23296143, 2023
Epigenome-wide profiling in the dorsal raphe nucleus highlights cell-type-specific changes in TNXB in Alzheimer′s disease
RJM Riemens, E Pishva, A Iatrou, JAY Roubroeks, J Nolz, R Lardenoije, ...
bioRxiv, 2023.08. 28.555168, 2023
Uncertainty quantification of reference based cellular deconvolution algorithms
D Seiler Vellame, G Shireby, A MacCalman, EL Dempster, J Burrage, ...
bioRxiv, 2022.06. 15.496235, 2022
Available based on mandate: 165
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ...
Nature genetics 50 (5), 668-681, 2018
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