Ella Thompson

Ella Thompson

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Ella Thompson

Ella Thompson

Publications by authors named "Ella Thompson"

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Characterization of a novel venetoclax resistance mutation (BCL2 Phe104Ile) observed in follicular lymphoma.

Br J Haematol 2019 Sep 24;186(6):e188-e191. Epub 2019 Jun 24.

Clinical Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Australia.

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http://dx.doi.org/10.1111/bjh.16069DOI Listing
September 2019

Developing home-based telemental health services for youth: Practices from the SUAY Study.

J Telemed Telecare 2019 Jul 25:1357633X19863208. Epub 2019 Jul 25.

2 Kaiser Permanente Washington Health Research Institute; Seattle, WA USA.

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http://dx.doi.org/10.1177/1357633X19863208DOI Listing
July 2019

Molecular Drivers of Breast Implant-Associated Anaplastic Large Cell Lymphoma.

Plast Reconstr Surg 2019 03;143(3S A Review of Breast Implant-Associated Anaplastic Large Cell Lymphoma):59S-64S

Parkville and East Melbourne, Victoria, Australia From the Department of Pathology, Peter MacCalllum Cancer Centre, and the Sir Peter MacCallum Department of Oncology, University of Melbourne; and Molecular Oncology and Cancer Immunology, Epworth Healthcare.

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http://dx.doi.org/10.1097/PRS.0000000000005570DOI Listing
March 2019

Sensitive NPM1 Mutation Quantitation in Acute Myeloid Leukemia Using Ultradeep Next-Generation Sequencing in the Diagnostic Laboratory.

Arch Pathol Lab Med 2018 May 9;142(5):606-612. Epub 2018 Feb 9.

From the Department of Pathology, Peter MacCallum Cancer Centre, Melbourne, Australia (Drs Blombery, Jones, Ryland, Thompson, Yannakou, and Westerman; Mr Doig; and Ms McBean); and the Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia (Drs Blombery, Thompson, Yannakou, and Westerman). Drs Blombery and Jones contributed equally to this work.

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http://dx.doi.org/10.5858/arpa.2017-0229-OADOI Listing
May 2018

Oral Health Promotion and Smoking Cessation Program Delivered via Tobacco Quitlines: The Oral Health 4 Life Trial.

Am J Public Health 2018 05 22;108(5):689-695. Epub 2018 Mar 22.

Jennifer B. McClure, Melissa L. Anderson, Paula Blasi, Ella Thompson, and Jennifer Nelson are with the Kaiser Permanente Washington Health Research Institute, Seattle, WA. Terry Bush is with the Optum Center for Wellbeing Research, Seattle. Sheryl L. Catz is with the Betty Irene Moore School of Nursing, University of California, Davis.

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http://dx.doi.org/10.2105/AJPH.2017.304279DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5888045PMC
May 2018

Canary: an atomic pipeline for clinical amplicon assays.

BMC Bioinformatics 2017 Dec 15;18(1):555. Epub 2017 Dec 15.

Department of Pathology, Peter MacCallum Cancer Centre, East Melbourne, VIC, Australia.

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http://dx.doi.org/10.1186/s12859-017-1950-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732437PMC
December 2017

Compromized DNA repair as a basis for identification of cancer radiotherapy patients with extreme radiosensitivity.

Cancer Lett 2016 12 28;383(2):212-219. Epub 2016 Sep 28.

Molecular Radiation Biology Laboratory, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, 3000, Australia; The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, VIC, 3010, Australia; Division of Radiation Oncology and Cancer Imaging, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, 3000, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.canlet.2016.09.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5159273PMC
December 2016

Reevaluation of RINT1 as a breast cancer predisposition gene.

Breast Cancer Res Treat 2016 09 20;159(2):385-92. Epub 2016 Aug 20.

Cancer Genetics Laboratory, Research Division, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.

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http://dx.doi.org/10.1007/s10549-016-3944-3DOI Listing
September 2016

Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.

J Clin Oncol 2016 May 19;34(13):1455-9. Epub 2016 Jan 19.

Ella R. Thompson, Simone M. Rowley, Na Li, Simone McInerny, Lisa Devereux, Alison H. Trainer, Gillian Mitchell, Paul A. James, and Ian G. Campbell, Peter MacCallum Cancer Centre, East Melbourne; Ella R. Thompson, Alison H. Trainer, Gillian Mitchell, Paul A. James, and Ian G. Campbell, University of Melbourne, Melbourne, Victoria; Michelle W. Wong-Brown and Rodney J. Scott, The University of Newcastle and Hunter Medical Research Institute; Rodney J. Scott, Hunter Area Pathology Service, Newcastle, New South Wales, Australia; Na Li, Huazhong University of Science and Technology, Wuhan, Hubei, China; and Gillian Mitchell, BC Cancer Agency, Vancouver, Canada.

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http://dx.doi.org/10.1200/JCO.2015.63.7454DOI Listing
May 2016

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.

Authors:
Douglas F Easton Fabienne Lesueur Brennan Decker Kyriaki Michailidou Jun Li Jamie Allen Craig Luccarini Karen A Pooley Mitul Shah Manjeet K Bolla Qin Wang Joe Dennis Jamil Ahmad Ella R Thompson Francesca Damiola Maroulio Pertesi Catherine Voegele Noura Mebirouk Nivonirina Robinot Geoffroy Durand Nathalie Forey Robert N Luben Shahana Ahmed Kristiina Aittomäki Hoda Anton-Culver Volker Arndt Caroline Baynes Matthias W Beckman Javier Benitez David Van Den Berg William J Blot Natalia V Bogdanova Stig E Bojesen Hermann Brenner Jenny Chang-Claude Kee Seng Chia Ji-Yeob Choi Don M Conroy Angela Cox Simon S Cross Kamila Czene Hatef Darabi Peter Devilee Mikael Eriksson Peter A Fasching Jonine Figueroa Henrik Flyger Florentia Fostira Montserrat García-Closas Graham G Giles Gord Glendon Anna González-Neira Pascal Guénel Christopher A Haiman Per Hall Steven N Hart Mikael Hartman Maartje J Hooning Chia-Ni Hsiung Hidemi Ito Anna Jakubowska Paul A James Esther M John Nichola Johnson Michael Jones Maria Kabisch Daehee Kang Veli-Matti Kosma Vessela Kristensen Diether Lambrechts Na Li Annika Lindblom Jirong Long Artitaya Lophatananon Jan Lubinski Arto Mannermaa Siranoush Manoukian Sara Margolin Keitaro Matsuo Alfons Meindl Gillian Mitchell Kenneth Muir Ines Nevelsteen Ans van den Ouweland Paolo Peterlongo Sze Yee Phuah Katri Pylkäs Simone M Rowley Suleeporn Sangrajrang Rita K Schmutzler Chen-Yang Shen Xiao-Ou Shu Melissa C Southey Harald Surowy Anthony Swerdlow Soo H Teo Rob A E M Tollenaar Ian Tomlinson Diana Torres Thérèse Truong Celine Vachon Senno Verhoef Michelle Wong-Brown Wei Zheng Ying Zheng Heli Nevanlinna Rodney J Scott Irene L Andrulis Anna H Wu John L Hopper Fergus J Couch Robert Winqvist Barbara Burwinkel Elinor J Sawyer Marjanka K Schmidt Anja Rudolph Thilo Dörk Hiltrud Brauch Ute Hamann Susan L Neuhausen Roger L Milne Olivia Fletcher Paul D P Pharoah Ian G Campbell Alison M Dunning Florence Le Calvez-Kelm David E Goldgar Sean V Tavtigian Georgia Chenevix-Trench

J Med Genet 2016 05 26;53(5):298-309. Epub 2016 Feb 26.

Department of Genetics, QIMR Berghofer Medical Research Institute, Brisbane, Australia.

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http://dx.doi.org/10.1136/jmedgenet-2015-103529DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938802PMC
May 2016

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.

Authors:
Paolo Peterlongo Irene Catucci Mara Colombo Laura Caleca Eliseos Mucaki Massimo Bogliolo Maria Marin Francesca Damiola Loris Bernard Valeria Pensotti Sara Volorio Valentina Dall'Olio Alfons Meindl Claus Bartram Christian Sutter Harald Surowy Valérie Sornin Marie-Gabrielle Dondon Séverine Eon-Marchais Dominique Stoppa-Lyonnet Nadine Andrieu Olga M Sinilnikova Gillian Mitchell Paul A James Ella Thompson Marina Marchetti Cristina Verzeroli Carmen Tartari Gabriele Lorenzo Capone Anna Laura Putignano Maurizio Genuardi Veronica Medici Isabella Marchi Massimo Federico Silvia Tognazzo Laura Matricardi Simona Agata Riccardo Dolcetti Lara Della Puppa Giulia Cini Viviana Gismondi Valeria Viassolo Chiara Perfumo Maria Antonietta Mencarelli Margherita Baldassarri Bernard Peissel Gaia Roversi Valentina Silvestri Piera Rizzolo Francesca Spina Caterina Vivanet Maria Grazia Tibiletti Maria Adelaide Caligo Gaetana Gambino Stefania Tommasi Brunella Pilato Carlo Tondini Chiara Corna Bernardo Bonanni Monica Barile Ana Osorio Javier Benitez Luisa Balestrino Laura Ottini Siranoush Manoukian Marco A Pierotti Alessandra Renieri Liliana Varesco Fergus J Couch Xianshu Wang Peter Devilee Florentine S Hilbers Christi J van Asperen Alessandra Viel Marco Montagna Laura Cortesi Orland Diez Judith Balmaña Jan Hauke Rita K Schmutzler Laura Papi Miguel Angel Pujana Conxi Lázaro Anna Falanga Kenneth Offit Joseph Vijai Ian Campbell Barbara Burwinkel Anders Kvist Hans Ehrencrona Sylvie Mazoyer Sara Pizzamiglio Paolo Verderio Jordi Surralles Peter K Rogan Paolo Radice

Hum Mol Genet 2015 Sep 30;24(18):5345-55. Epub 2015 Jun 30.

IFOM, the FIRC Institute of Molecular Oncology, Milan, Italy, Unit of Molecular Bases of Genetic Risk and Genetic Testing, Department of Preventive and Predictive Medicine.

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http://dx.doi.org/10.1093/hmg/ddv251DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550823PMC
September 2015

Copy number analysis of ductal carcinoma in situ with and without recurrence.

Mod Pathol 2015 Sep 19;28(9):1174-84. Epub 2015 Jun 19.

Cancer Genetics Laboratory, Peter MacCullum Cancer Centre, East Melbourne, VIC, Australia.

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http://dx.doi.org/10.1038/modpathol.2015.75DOI Listing
September 2015

Sustaining Research Networks: the Twenty-Year Experience of the HMO Research Network.

EGEMS (Wash DC) 2014 9;2(2):1067. Epub 2014 Jun 9.

Group Health Research Institute.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371441PMC
April 2015

Embedded research to improve health: the 20th annual HMO Research Network conference, March 31-April 3, 2014, Phoenix, Arizona.

Clin Med Res 2014 Sep;12(1-2):73-6

Institute for Health Research, Kaiser Permanente Colorado, Denver, CO, USA

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http://dx.doi.org/10.3121/cmr.2014.1251DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453312PMC
September 2014

Analysis of KLLN as a high-penetrance breast cancer predisposition gene.

Breast Cancer Res Treat 2012 Jul 13;134(2):543-7. Epub 2012 May 13.

VBCRC Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, Locked Bag 1, A'Beckett St, East Melbourne, VIC 8006, Australia.

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http://dx.doi.org/10.1007/s10549-012-2088-3DOI Listing
July 2012

Identification of copy number alterations associated with the progression of DCIS to invasive ductal carcinoma.

Breast Cancer Res Treat 2012 Jun 4;133(3):889-98. Epub 2011 Nov 4.

VBCRC Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, Locked Bag 1, A'Beckett St, East Melbourne, Victoria, VIC 8006, Australia.

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http://link.springer.com/content/pdf/10.1007/s10549-011-1835
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http://link.springer.com/10.1007/s10549-011-1835-1
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http://dx.doi.org/10.1007/s10549-011-1835-1DOI Listing
June 2012

CONTRA: copy number analysis for targeted resequencing.

Bioinformatics 2012 May 2;28(10):1307-13. Epub 2012 Apr 2.

Bioinformatics Core Facility, Peter MacCallum Cancer Centre, VIC 3002, Australia.

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http://dx.doi.org/10.1093/bioinformatics/bts146DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348560PMC
May 2012

BRCA and beyond: a genome-first approach to familial breast cancer risk assessment.

Discov Med 2011 Nov;12(66):433-43

Familial Cancer Service, Peter MacCallum Cancer Institute, East Melbourne, Australia.

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November 2011

Streamlining research by using existing tools.

Clin Transl Sci 2011 Aug;4(4):266-7

Group Health Cooperative, Group Health Research Institute, Seattle, Washington, USA.

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http://dx.doi.org/10.1111/j.1752-8062.2011.00296.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170080PMC
August 2011

Frequent somatic mutations of GATA3 in non-BRCA1/BRCA2 familial breast tumors, but not in BRCA1-, BRCA2- or sporadic breast tumors.

Breast Cancer Res Treat 2010 Jan 3;119(2):491-6. Epub 2009 Feb 3.

Queensland Institute of Medical Research, Royal Brisbane Hospital, Herston, QLD, Australia 4029.

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http://dx.doi.org/10.1007/s10549-008-0269-xDOI Listing
January 2010

High-resolution single nucleotide polymorphism array analysis of epithelial ovarian cancer reveals numerous microdeletions and amplifications.

Clin Cancer Res 2007 Aug;13(16):4731-9

Victorian Breast Cancer Research Consortium Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1158/1078-0432.CCR-07-0502DOI Listing
August 2007

Changes in health care costs before and after smoking cessation.

Nicotine Tob Res 2006 Jun;8(3):393-401

Center for Health Studies, Group Health Cooperative, Seattle, WA 98101, USA.

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http://ntr.oxfordjournals.org/content/8/3/393.full.pdf
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http://dx.doi.org/10.1080/14622200600670314DOI Listing
June 2006

Whole genome SNP arrays using DNA derived from formalin-fixed, paraffin-embedded ovarian tumor tissue.

Hum Mutat 2005 Oct;26(4):384-9

VBCRC Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1002/humu.20220DOI Listing
October 2005

A novel duplication polymorphism in the FANCA promoter and its association with breast and ovarian cancer.

BMC Cancer 2005 Apr 29;5:43. Epub 2005 Apr 29.

Department of Pathology, Peter MacCallum Cancer Centre, Locked Bag 1 A'Beckett St, Melbourne, Victoria 8006, Australia.

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http://dx.doi.org/10.1186/1471-2407-5-43DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1112586PMC
April 2005

Health care costs among smokers, former smokers, and never smokers in an HMO.

Health Serv Res 2003 Apr;38(2):733-49

Center for Health Studies, Group Health Cooperative of Puget Sound, Seattle, WA 98101, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1360912PMC
http://dx.doi.org/10.1111/1475-6773.00142DOI Listing
April 2003