Author details

Full Name

Oliver M Dovey

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34638130	The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11.	Blood Adv	2022
35701672	Publisher Correction: UTX-mediated enhancer and chromatin remodeling suppresses myeloid leukemogenesis through noncatalytic inverse regulation of ETS and GATA programs.	Nat Genet	2022
34556857	Mutational synergy during leukemia induction remodels chromatin accessibility, histone modifications and three-dimensional DNA topology to alter gene expression.	Nat Genet	2021
33956058	SETBP1 overexpression acts in the place of class-defining mutations to drive FLT3-ITD-mutant AML.	Blood advances	2021
32728019	Author Correction: The long non-coding RNA HOXB-AS3 regulates ribosomal RNA transcription in NPM1-mutated acute myeloid leukemia.	Nat Commun	2020
31911614	Publisher Correction: The long non-coding RNA HOXB-AS3 regulates ribosomal RNA transcription in NPM1-mutated acute myeloid leukemia.	Nat Commun	2020
31827282	HBO1 is required for the maintenance of leukaemia stem cells.	Nature	2020
31235852	SOCS2 is part of a highly prognostic 4-gene signature in AML and promotes disease aggressiveness.	Scientific Reports	2019
31767858	The long non-coding RNA HOXB-AS3 regulates ribosomal RNA transcription in NPM1-mutated acute myeloid leukemia.	Nat Commun	2019
29364867	Evolutionary routes and KRAS dosage define pancreatic cancer phenotypes.	Nature	2018
29282219	Mutant calreticulin knockin mice develop thrombocytosis and myelofibrosis without a stem cell self-renewal advantage.	Blood	2018
29736013	UTX-mediated enhancer and chromatin remodeling suppresses myeloid leukemogenesis through noncatalytic inverse regulation of ETS and GATA programs.	Nat Genet	2018
28835438	Molecular synergy underlies the co-occurrence patterns and phenotype of <i>NPM1</i>-mutant acute myeloid leukemia.	Blood	2017
28794285	Preventing chemotherapy-induced myelosuppression by repurposing the FLT3 inhibitor quizartinib.	Science Translational Medicine	2017
27757418	Promiscuous targeting of bromodomains by bromosporine identifies BET proteins as master regulators of primary transcription response in leukemia.	Sci Adv	2016
27175030	Identification of a germline F692L drug resistance variant in cis with Flt3-internal tandem duplication in knock-in mice.	Haematologica	2016
27760321	A CRISPR Dropout Screen Identifies Genetic Vulnerabilities and Therapeutic Targets in Acute Myeloid Leukemia.	Cell Rep	2016
24958871	Histone deacetylase (HDAC) 1 and 2 are essential for accurate cell division and the pluripotency of embryonic stem cells.	Proceedings of the National Academy of Sciences of the United States of America	2014
23287868	Histone deacetylase 1 and 2 are essential for normal T-cell development and genomic stability in mice.	Blood	2013
23478666	A powerful molecular synergy between mutant Nucleophosmin and Flt3-ITD drives acute myeloid leukemia in mice.	Leukemia	2013
20647764	Emphasizing the positive: A role for histone deacetylases in transcriptional activation.	Cell Cycle	2010
20713442	Lysine-specific demethylase 1 regulates the embryonic transcriptome and CoREST stability.	Mol Cell Biol	2010
20404188	Histone deacetylase 1 (HDAC1), but not HDAC2, controls embryonic stem cell differentiation.	Proceedings of the National Academy of Sciences of the United States of America	2010
18391979	Loss of Rassf1a cooperates with Apc(Min) to accelerate intestinal tumourigenesis.	Oncogene	2008
17571346	Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.	Nature	2007
17567991	Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes.	Genome Res	2007
17567990	The landscape of histone modifications across 1% of the human genome in five human cell lines.	Genome Res	2007
16823893	Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse.	J Pathol	2006
17122085	Accurate and reliable high-throughput detection of copy number variation in the human genome.	Genome Res	2006
16710414	The DNA sequence and biological annotation of human chromosome 1.	Nature	2006
16221759	Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays.	Hum Mol Genet	2005