Bryony Thompson

Bryony Thompson

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Bryony Thompson

Bryony Thompson

Publications by authors named "Bryony Thompson"

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26Publications

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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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http://dx.doi.org/10.1002/humu.22971DOI Listing
May 2016

Microsatellite instability use in mismatch repair gene sequence variant classification.

Genes (Basel) 2015 Mar 30;6(2):150-62. Epub 2015 Mar 30.

Genetics and Computational Biology Department, QIMR Berghofer Medical Research Institute, 300 Herston Road, Brisbane, QLD 4006, Australia.

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http://dx.doi.org/10.3390/genes6020150DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488658PMC
March 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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http://dx.doi.org/10.1186/s13148-014-0032-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272815PMC
December 2014

Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.

J Clin Oncol 2014 Jan 9;32(2):90-100. Epub 2013 Dec 9.

Daniel D. Buchanan, Yen Y. Tan, Michael D. Walsh, Mark Clendenning, Alexander M. Metcalf, Kaltin Ferguson, Sven T. Arnold, Bryony A. Thompson, Felicity A. Lose, Michael T. Parsons, Rhiannon J. Walters, Sally-Ann Pearson, Joanne P. Young, Penelope M. Webb, and Amanda B. Spurdle, QIMR Berghofer Medical Research Institute, Herston; Yen Y. Tan and Andreas Obermair, University of Queensland School of Medicine, Brisbane; Margaret Cummings, University of Queensland Centre for Clinical Research, Herston, Queensland; Martin K. Oehler, Royal Adelaide Hospital, Adelaide, South Australia; Michael A. Quinn, Royal Women's Hospital, Melbourne, Victoria; Judy A. Kirk, Westmead Institute for Cancer Research, Westmead Millennium Institute, University of Sydney, Sydney, New South Wales; Colin J. Stewart, King Edward Memorial Hospital, Perth, Western Australia, Australia; and Penelope B. Blomfield, Royal Hobart Hospital, Hobart, Tasmania.

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http://jco.ascopubs.org/content/early/2013/12/09/JCO.2013.51
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http://jco.ascopubs.org/cgi/doi/10.1200/JCO.2013.51.2129
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http://dx.doi.org/10.1200/JCO.2013.51.2129DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876359PMC
January 2014

Pancreatic cancer and a novel MSH2 germline alteration.

Pancreas 2011 Oct;40(7):1138-40

Department of Medical Genetics and †Department of Health Science Research, Mayo Clinic, Rochester, MN 55905, USA.

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https://insights.ovid.com/crossref?an=00006676-201110000-000
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http://dx.doi.org/10.1097/MPA.0b013e318220c217DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425611PMC
October 2011

Mutation deep within an intron of MSH2 causes Lynch syndrome.

Fam Cancer 2011 Jun;10(2):297-301

Familial Cancer Laboratory, Queensland Institute of Medical Research, 300 Herston Road, Herston, QLD, Australia.

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http://dx.doi.org/10.1007/s10689-011-9427-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4580736PMC
June 2011

Use of DNA-damaging agents and RNA pooling to assess expression profiles associated with BRCA1 and BRCA2 mutation status in familial breast cancer patients.

PLoS Genet 2010 Feb 19;6(2):e1000850. Epub 2010 Feb 19.

Genetics and Population Health Division, Queensland Institute of Medical Research, Brisbane, Australia.

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http://dx.doi.org/10.1371/journal.pgen.1000850DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824809PMC
February 2010