Publications by authors named "Mathew Sloane"

20Publications

Disruption of a -35 kb Enhancer Impairs CTCF Binding and Expression in Colorectal Cells.

Clin Cancer Res 2018 09 13;24(18):4602-4611. Epub 2018 Jun 13.

Adult Cancer Program, Lowy Cancer Research Centre and Prince of Wales Clinical School, UNSW Sydney, Sydney, New South Wales, Australia.

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September 2018

Pathogenic germline MCM9 variants are rare in Australian Lynch-like syndrome patients.

Cancer Genet 2016 Nov 11;209(11):497-500. Epub 2016 Oct 11.

Adult Cancer Program, Lowy Cancer Research Centre and Prince of Wales Clinical School, UNSW Australia, Sydney, New South Wales 2052, Australia. Electronic address:

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November 2016

The molecular characteristics of colonic neoplasms in serrated polyposis: a systematic review and meta-analysis.

J Pathol Clin Res 2016 Jul 22;2(3):127-37. Epub 2016 Apr 22.

Prince of Wales Clinical School, University of New South WalesSydney, Australia; Office of the Deputy Vice-Chancellor (Research), University of QueenslandBrisbane, Australia.

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July 2016

Defining the criteria for identifying constitutional epimutations.

Clin Epigenetics 2016 18;8:39. Epub 2016 Apr 18.

Adult Cancer Program, Lowy Cancer Research Centre and Prince of Wales Clinical School, UNSW Australia, Kensington, Sydney, New South Wales 2052 Australia.

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December 2016

Understanding the Pathogenicity of Noncoding Mismatch Repair Gene Promoter Variants in Lynch Syndrome.

Hum Mutat 2016 May 18;37(5):417-26. Epub 2016 Mar 18.

Adult Cancer Program, Lowy Cancer Research Centre and Prince of Wales Clinical School, UNSW Australia, Sydney, New South Wales, Australia.

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May 2016

A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.

Carcinogenesis 2016 Jan 24;37(1):10-17. Epub 2015 Oct 24.

Adult Cancer Program , Lowy Cancer Research Centre and Prince of Wales Clinical School, UNSW Australia , Sydney New South Wales 2052 , Australia.

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January 2016

The search for cis-regulatory driver mutations in cancer genomes.

Oncotarget 2015 Oct;6(32):32509-25

Prince of Wales Clinical School and Lowy Cancer Research Centre, UNSW Australia, Sydney, Australia.

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October 2015

Mosaic Epigenetic Inheritance as a Cause of Early-Onset Colorectal Cancer.

JAMA Oncol 2015 Oct;1(7):953-7

Adult Cancer Program, Lowy Cancer Research Centre and Prince of Wales Clinical School, University of New South Wales, Sydney, New South Wales, Australia4Brian Wilson Chancellery, University of Queensland, Brisbane, Queensland, Australia.

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October 2015

Lynch syndrome associated with two MLH1 promoter variants and allelic imbalance of MLH1 expression.

Hum Mutat 2015 Jun 17;36(6):622-30. Epub 2015 Apr 17.

Adult Cancer Program, Lowy Cancer Research Centre and Prince of Wales Clinical School, UNSW Australia, Sydney, New South Wales, Australia.

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June 2015

Nucleosome positioning is unaltered at MLH1 splice site mutations in cells derived from Lynch syndrome patients.

Clin Epigenetics 2014 13;6(1):32. Epub 2014 Dec 13.

Adult Cancer Program, Lowy Cancer Research Centre and Prince of Wales Clinical School, University of New South Wales, Sydney, NSW Australia.

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December 2014

Altered promoter nucleosome positioning is an early event in gene silencing.

Epigenetics 2014 Oct;9(10):1422-30

a Adult Cancer Program; Lowy Cancer Research Center and Prince of Wales Clinical School; UNSW ; Sydney , Australia.

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October 2014

Epigenetic inactivation of the candidate tumor suppressor USP44 is a frequent and early event in colorectal neoplasia.

Epigenetics 2014 Aug 16;9(8):1092-100. Epub 2014 May 16.

Adult Cancer Program; Lowy Cancer Research Centre and Prince of Wales Clinical School; Sydney, NSW Australia.

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August 2014

Reassembly of nucleosomes at the MLH1 promoter initiates resilencing following decitabine exposure.

PLoS Genet 2013 25;9(7):e1003636. Epub 2013 Jul 25.

Adult Cancer Program, Lowy Cancer Research Centre and Prince of Wales Clinical School, University of New South Wales, Sydney, New South Wales, Australia.

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January 2014

Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome.

Mol Cell 2007 Aug;27(3):353-66

CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Institute of Genetics, Max F. Perutz Laboratories, Vienna Biocenter, Dr. Bohr-Gasse 9/4, A-1030 Vienna, Austria.

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August 2007