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Author Details
Full Name
Duncan Sproul
Affiliation
Institute of Genetics and Cancer, University of Edinburgh
ORCID
Career Start Year
2004
Papers
37
H Index
24
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37336879
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
Nat Commun
2023
37782664
Genome-wide single-molecule analysis of long-read DNA methylation reveals heterogeneous patterns at heterochromatin that reflect nucleosome organisation.
PLoS Genet
2023
37380644
Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
Nat Commun
2023
35078341
Cluster mean-field theory accurately predicts statistical properties of large-scale DNA methylation patterns.
J R Soc Interface
2022
36253871
Local CpG density affects the trajectory and variance of age-associated DNA methylation changes.
Genome Biol
2022
35074757
In Vivo Modeling of Patient Genetic Heterogeneity Identifies New Ways to Target Cholangiocarcinoma.
Cancer Res
2022
31796892
An epigenetic predictor of death captures multi-modal measures of brain health.
Mol Psychiatry
2021
33514701
De novo DNA methyltransferase activity in colorectal cancer is directed towards H3K36me3 marked CpG islands.
Nat Commun
2021
33857425
Glioblastomas acquire myeloid-affiliated transcriptional programs via epigenetic immunoediting to elicit immune evasion.
Cell
2021
32585002
Activation of transcription factor circuity in 2i-induced ground state pluripotency is independent of repressive global epigenetic landscapes.
Nucleic Acids Res
2020
33230297
cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing.
Nat Genet
2020
32699299
Transition to naïve human pluripotency mirrors pan-cancer DNA hypermethylation.
Nat Commun
2020
30478443
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions.
Nat Genet
2019
31043600
Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
Nat Commun
2019
30918249
Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
Nat Commun
2019
29025912
Variable outcome and methylation status according to <i>CEBPA</i> mutant type in double-mutated acute myeloid leukemia patients and the possible implications for treatment.
Haematologica
2018
30348214
Genotype effects contribute to variation in longitudinal methylome patterns in older people.
Genome Med
2018
28465359
Elevated FOXG1 and SOX2 in glioblastoma enforces neural stem cell identity through transcriptional control of cell cycle and epigenetic regulators.
Genes Dev
2017
28351383
Diverse interventions that extend mouse lifespan suppress shared age-associated epigenetic changes at critical gene regulatory regions.
Genome Biol
2017
25531315
FOXA1 repression is associated with loss of BRCA1 and increased promoter methylation and chromatin silencing in breast cancer.
Oncogene
2015
26235388
Estrogen-induced chromatin decondensation and nuclear re-organization linked to regional epigenetic regulation in breast cancer.
Genome Biol
2015
24277643
DNA methylation reprogramming in cancer: does it act by re-configuring the binding landscape of Polycomb repressive complexes?
Bioessays
2014
25187560
Transcription factor binding predicts histone modifications in human cell lines.
Proc Natl Acad Sci U S A
2014
23341493
Genomic insights into cancer-associated aberrant CpG island hypermethylation.
Brief Funct Genomics
2013
23703216
Expression of a large LINE-1-driven antisense RNA is linked to epigenetic silencing of the metastasis suppressor gene TFPI-2 in cancer.
Nucleic Acids Res
2013
22106369
Tissue type is a major modifier of the 5-hydroxymethylcytosine content of human genes.
Genome Res
2012
23034185
Tissue of origin determines cancer-associated CpG island promoter hypermethylation patterns.
Genome Biol
2012
22689141
Targeting of Rac GTPases blocks the spread of intact human breast cancer.
Oncotarget
2012
22514623
Diversity of matriptase expression level and function in breast cancer.
PLoS One
2012
22323521
Lactate, a product of glycolytic metabolism, inhibits histone deacetylase activity and promotes changes in gene expression.
Nucleic Acids Res
2012
21368160
Transcriptionally repressed genes become aberrantly methylated and distinguish tumors of different lineages in breast cancer.
Proc Natl Acad Sci U S A
2011
21859834
Modelling genetic and clinical heterogeneity in epithelial ovarian cancers.
Carcinogenesis
2011
20471950
Ring1B compacts chromatin structure and represses gene expression independent of histone ubiquitination.
Mol Cell
2010
21070966
Analysis of active and inactive X chromosome architecture reveals the independent organization of 30 nm and large-scale chromatin structures.
Mol Cell
2010
18369458
Recruitment to the nuclear periphery can alter expression of genes in human cells.
PLoS Genet
2008
16160692
The role of chromatin structure in regulating the expression of clustered genes.
Nat Rev Genet
2005
14759252
Adenosine deaminases acting on RNA (ADARs): RNA-editing enzymes.
Genome Biol
2004
1 - 37 of 37
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