Ingrid Winship

Ingrid Winship

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Ingrid Winship

Publications by authors named "Ingrid Winship"

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Arrhythmogenic Right Ventricular Cardiomyopathy: A Review of Living and Deceased Probands.

Heart Lung Circ 2019 Jul 11;28(7):1034-1041. Epub 2018 Aug 11.

Department of Cardiology, The Royal Melbourne Hospital, Melbourne, Vic, Australia; Genomic Medicine Department, The Royal Melbourne Hospital, Melbourne, Vic, Australia; Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, Vic, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.hlc.2018.07.017DOI Listing
July 2019

Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene.

Fam Cancer 2019 07;18(3):311-315

Parkville Familial Cancer Centre, The Royal Melbourne Hospital and Peter MacCallum Cancer Centre, Parkville, VIC, Australia.

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http://link.springer.com/10.1007/s10689-019-00120-0
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http://dx.doi.org/10.1007/s10689-019-00120-0DOI Listing
July 2019

Tumor mutational signatures in sebaceous skin lesions from individuals with Lynch syndrome.

Mol Genet Genomic Med 2019 Jul 4;7(7):e00781. Epub 2019 Jun 4.

Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, Parkville, Vic., Australia.

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http://dx.doi.org/10.1002/mgg3.781DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625139PMC
July 2019

Response to Veenstra et al.

Genet Med 2019 Jul 15. Epub 2019 Jul 15.

Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.

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http://dx.doi.org/10.1038/s41436-019-0581-3DOI Listing
July 2019

Chondrodysplasia punctata (CDPX2) in a male caused by single-gene mosaicism: A 20-year follow-up.

Australas J Dermatol 2019 May 7;60(2):e160-e162. Epub 2018 Oct 7.

Department of Genetic Medicine, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://doi.wiley.com/10.1111/ajd.12938
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http://dx.doi.org/10.1111/ajd.12938DOI Listing
May 2019

Clinico-pathological predictors of mismatch repair deficiency in sebaceous neoplasia: A large case series from a single Australian private pathology service.

Australas J Dermatol 2019 May 2;60(2):126-133. Epub 2018 Dec 2.

Department of Clinical Pathology, Colorectal Oncogenomics Group, The University of Melbourne, Parkville, Victoria, Australia.

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http://doi.wiley.com/10.1111/ajd.12958
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http://dx.doi.org/10.1111/ajd.12958DOI Listing
May 2019

Loss-of-Function in SMAD4 Might Not Be Critical for Human Natural Killer Cell Responsiveness to TGF-β.

Front Immunol 2019 1;10:904. Epub 2019 May 1.

Division of Immunology/Molecular Immunology, Department of Medical Biology, The Walter and Eliza Hall Institute of Medical Research, University of Melbourne, Parkville, VIC, Australia.

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http://dx.doi.org/10.3389/fimmu.2019.00904DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506781PMC
May 2019

Correction: Population genomic screening of all young adults in a health-care system: a cost-effectiveness analysis.

Genet Med 2019 Apr 4. Epub 2019 Apr 4.

Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.

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http://dx.doi.org/10.1038/s41436-019-0515-0DOI Listing
April 2019

Insights into sudden cardiac death: exploring the potential relevance of non-diagnostic autopsy findings.

Eur Heart J 2019 Mar;40(10):831-838

Department of Cardiology, Royal Melbourne Hospital, 300 Grattan Street, Melbourne, VIC, Australia.

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http://dx.doi.org/10.1093/eurheartj/ehy654DOI Listing
March 2019

Warfarin ineffective as symptomatic therapy for erythropoietic protoporphyria.

Australas J Dermatol 2019 Mar 27. Epub 2019 Mar 27.

Department of Medicine, The University of Melbourne, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/ajd.13033DOI Listing
March 2019

Living with Hereditary Haemorrhagic Telangiectasia: stigma, coping with unpredictable symptoms, and self-advocacy.

Psychol Health 2019 Mar 31:1-20. Epub 2019 Mar 31.

a Genomic Medicine , Royal Melbourne Hospital , Parkville , Victoria, Australia.

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http://dx.doi.org/10.1080/08870446.2019.1583341DOI Listing
March 2019

Phacomatosis pigmentokeratotica: Postzygotic HRAS mutation with malignant degeneration of the sebaceous naevus.

Australas J Dermatol 2019 Feb 14. Epub 2019 Feb 14.

Adult Genetic Medicine, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/ajd.13007DOI Listing
February 2019

Population genomic screening of all young adults in a health-care system: a cost-effectiveness analysis.

Genet Med 2019 Feb 18. Epub 2019 Feb 18.

Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.

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http://dx.doi.org/10.1038/s41436-019-0457-6DOI Listing
February 2019

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.

Hered Cancer Clin Pract 2019 28;17. Epub 2019 Feb 28.

4Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, part of Oslo University Hospital, Olso, Norway.

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https://hccpjournal.biomedcentral.com/articles/10.1186/s1305
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http://dx.doi.org/10.1186/s13053-019-0106-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394091PMC
February 2019

Hemangioblastoma in Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome: a phenotypic overlap between VHL and HLRCC Syndromes.

Fam Cancer 2019 01;18(1):91-95

Genetic Medicine and Family Cancer Clinic, Royal Melbourne Hospital, Parkville, Australia.

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http://dx.doi.org/10.1007/s10689-018-0081-7DOI Listing
January 2019

The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study.

Authors:
Mattias Johansson Robert Carreras-Torres Ghislaine Scelo Mark P Purdue Daniela Mariosa David C Muller Nicolas J Timpson Philip C Haycock Kevin M Brown Zhaoming Wang Yuanqing Ye Jonathan N Hofmann Matthieu Foll Valerie Gaborieau Mitchell J Machiela Leandro M Colli Peng Li Jean-Guillaume Garnier Helene Blanche Anne Boland Laurie Burdette Egor Prokhortchouk Konstantin G Skryabin Meredith Yeager Sanja Radojevic-Skodric Simona Ognjanovic Lenka Foretova Ivana Holcatova Vladimir Janout Dana Mates Anush Mukeriya Stefan Rascu David Zaridze Vladimir Bencko Cezary Cybulski Eleonora Fabianova Viorel Jinga Jolanta Lissowska Jan Lubinski Marie Navratilova Peter Rudnai Simone Benhamou Geraldine Cancel-Tassin Olivier Cussenot Elisabete Weiderpass Börje Ljungberg Raviprakash Tumkur Sitaram Christel Häggström Fiona Bruinsma Susan J Jordan Gianluca Severi Ingrid Winship Kristian Hveem Lars J Vatten Tony Fletcher Susanna C Larsson Alicja Wolk Rosamonde E Banks Peter J Selby Douglas F Easton Gabriella Andreotti Laura E Beane Freeman Stella Koutros Satu Männistö Stephanie Weinstein Peter E Clark Todd L Edwards Loren Lipworth Susan M Gapstur Victoria L Stevens Hallie Carol Matthew L Freedman Mark M Pomerantz Eunyoung Cho Kathryn M Wilson J Michael Gaziano Howard D Sesso Neal D Freedman Alexander S Parker Jeanette E Eckel-Passow Wen-Yi Huang Richard J Kahnoski Brian R Lane Sabrina L Noyes David Petillo Bin Tean Teh Ulrike Peters Emily White Garnet L Anderson Lisa Johnson Juhua Luo Julie Buring I-Min Lee Wong-Ho Chow Lee E Moore Timothy Eisen Marc Henrion James Larkin Poulami Barman Bradley C Leibovich Toni K Choueiri G Mark Lathrop Jean-Francois Deleuze Marc Gunter James D McKay Xifeng Wu Richard S Houlston Stephen J Chanock Caroline Relton J Brent Richards Richard M Martin George Davey Smith Paul Brennan

PLoS Med 2019 01 3;16(1):e1002724. Epub 2019 Jan 3.

International Agency for Research on Cancer (IARC), Lyon, France.

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http://dx.doi.org/10.1371/journal.pmed.1002724DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317776PMC
January 2019

Utility of immunohistochemistry for mismatch repair proteins on colorectal polyps in the familial cancer clinic.

Intern Med J 2018 Nov;48(11):1325-1330

Genetic Medicine and Family Cancer Clinic, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/imj.13953DOI Listing
November 2018

Correction: Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1.

Genet Med 2018 10;20(10):1299

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Victoria, Australia.

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http://dx.doi.org/10.1038/gim.2017.265DOI Listing
October 2018

Cancer Risks for PMS2-Associated Lynch Syndrome.

J Clin Oncol 2018 Oct 30;36(29):2961-2968. Epub 2018 Aug 30.

Sanne W. ten Broeke, Heleen M. van der Klift, Carli M.J. Tops, Manon Suerink, Frederik J. Hes, Hans F.A. Vasen, Juul T. Wijnen, and Maartje Nielsen, Leiden University Medical Center, Leiden; Encarna Gomez Garcia, Maastricht University Medical Center, Maastricht; Nicoline Hoogerbrugge, Arjen R. Mensenkamp, and Liesbeth Spruijt, Radboud University Medical Center, Nijmegen; Tom G.W. Letteboer, University Medical Center, Utrecht; Theo A.M. van Os and Egbert J.W. Redeker, Academic Medical Center, Amsterdam; Maran J.W. Olderode-Berends and Yvonne J. Vos, University of Groningen; University Medical Center Groningen, Groningen; Anja Wagner, Erasmus Medical Center, Rotterdam, the Netherlands; Stefan Aretz, University of Bonn; University Hospital Bonn, Bonn; Christoph Engel, Leipzig University; Medizinisch Genetisches Zentrum Bayerstr, Leipzig; Magnus von Knebel Doeberitz, University of Heidelberg; German Cancer Research Center, Heidelberg; Pål Møller, University of Witten-Herdecke, Wuppertal; Nils Rahner, Heinrich-Heine-University, Düsseldorf; Hans K. Schackert, Technische Universität Dresden, Dresden; Verena Steinke-Lange, Medizinische Klinik und Poliklinik IV Campus Innenstadt, Klinikum der Universität München, Munich, Germany; Pål Møller, The Norwegian Radium Hospital; Oslo University Hospital, Oslo, Norway; Inge Bernstein, Hvidovre Hospital, Hvidovre, and Aalborg University Hospital, Aalborg, Denmark; Daniel D. Buchanan, Mark Clendenning, John L. Hopper, Mark A. Jenkins, Christophe Rosty, Ingrid Winship, and Aung Ko Win, The University of Melbourne; Daniel D. Buchanan, Ingrid Winship, and Aung Ko Win, Royal Melbourne Hospital, Parkville, Melbourne, Victoria; Rodney Scott, University of Newcastle, Newcastle, New South Wales, Australia; Albert de la Chapelle, Heather L. Hampel, Rachel Pearlman, and Leigha Senter, The Ohio State University Comprehensive Cancer Center, Columbus, OH; Gabriel Capella and Marta Pineda, Institut d'Investigació Biomédica de Bellvitge, Barcelona, Spain; Steven Gallinger, Mount Sinai Hospital, Toronto, Ontario, Canada; Jane C. Figueiredo and Robert Haile, Cedars-Sinai Medical Center, Los Angeles, CA; Loic Le Marchand, University of Hawaii Cancer Center, Honolulu, HI; Annika Lindblom, Karolinska Institutet; Karolinska University Hospital, Stockholm, Sweden; Noralane M. Lindor, Mayo Clinic Arizona, Scottsdale, AZ; Polly A. Newcomb, Fred Hutchinson Cancer Research Center; University of Washington, Seattle, WA; and Stephen Thibodeau, Mayo Clinic, Rochester, MN.

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http://ascopubs.org/doi/10.1200/JCO.2018.78.4777
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http://dx.doi.org/10.1200/JCO.2018.78.4777DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349460PMC
October 2018

Absence of renal phenotype in hereditary haemorrhagic telangiectasia.

Intern Med J 2018 Oct;48(10):1255-1257

Department of Genomic Medicine, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://doi.wiley.com/10.1111/imj.14059
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http://dx.doi.org/10.1111/imj.14059DOI Listing
October 2018

APRT deficiency: the need for early diagnosis.

BMJ Case Rep 2018 Oct 23;2018. Epub 2018 Oct 23.

Clinical Genetics, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://casereports.bmj.com/lookup/doi/10.1136/bcr-2018-22574
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http://dx.doi.org/10.1136/bcr-2018-225742DOI Listing
October 2018

Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1.

Genet Med 2018 08 9;20(8):890-895. Epub 2017 Nov 9.

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Victoria, Australia.

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http://www.nature.com/articles/gim2017185
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http://dx.doi.org/10.1038/gim.2017.185DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943186PMC
August 2018

Family history-based colorectal cancer screening in Australia: A modelling study of the costs, benefits, and harms of different participation scenarios.

PLoS Med 2018 08 16;15(8):e1002630. Epub 2018 Aug 16.

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Victoria, Australia.

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http://dx.doi.org/10.1371/journal.pmed.1002630DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095490PMC
August 2018

Update on Hereditary Colorectal Cancer: Improving the Clinical Utility of Multigene Panel Testing.

Clin Colorectal Cancer 2018 06 11;17(2):e293-e305. Epub 2018 Jan 11.

Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, Parkville, Victoria, Australia; Genetic Medicine and Family Cancer Clinic, Royal Melbourne Hospital, Parkville, Victoria, Australia; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Carlton, Victoria, Australia; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Parkville, Victoria, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.clcc.2018.01.001DOI Listing
June 2018

A rapid scoring tool to assess mutation probability in patients with inherited cardiac disorders.

Eur J Med Genet 2018 Feb 2;61(2):61-67. Epub 2017 Nov 2.

Department of Genomic Medicine, Royal Melbourne Hospital, Australia; Department of Pathology, University of Melbourne, Australia.

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http://dx.doi.org/10.1016/j.ejmg.2017.10.020DOI Listing
February 2018

Multiple cutaneous leiomyomas leading to discovery of novel splice mutation in the fumarate hydratase gene associated with HLRCC.

Australas J Dermatol 2017 Nov 7;58(4):e246-e248. Epub 2017 Mar 7.

Department of Medicine, Royal Melbourne Hospital, University of Melbourne, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/ajd.12605DOI Listing
November 2017

Penetrance and the Healthy Elderly.

Genet Test Mol Biomarkers 2017 Nov 6;21(11):637-640. Epub 2017 Sep 6.

1 Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia .

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http://dx.doi.org/10.1089/gtmb.2017.0126DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695739PMC
November 2017

Pathogenic variants in the healthy elderly: unique ethical and practical challenges.

J Med Ethics 2017 10 24;43(10):714-722. Epub 2017 Mar 24.

Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, ASPREE - Monash University, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1136/medethics-2016-103967DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629947PMC
October 2017

Rare disease registries: a call to action.

Intern Med J 2017 Sep;47(9):1075-1079

Centre for Comparative Genomics (CCG), Murdoch University, Perth, Western Australia, Australia.

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http://dx.doi.org/10.1111/imj.13528DOI Listing
September 2017

Consent Processes for Mobile App Mediated Research: Systematic Review.

JMIR Mhealth Uhealth 2017 Aug 30;5(8):e126. Epub 2017 Aug 30.

Sage Bionetworks, Seattle, WA, United States.

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http://dx.doi.org/10.2196/mhealth.7014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597795PMC
August 2017

Mutation screening of ACKR3 and COPS8 in kidney cancer cases from the CONFIRM study.

Fam Cancer 2017 07;16(3):411-416

Department of Medicine, The Universityof Melbourne, Melbourne, Australia.

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http://dx.doi.org/10.1007/s10689-016-9961-xDOI Listing
July 2017

Lack of evidence for germline mutations in patients with serrated polyposis syndrome from a large multinational study.

Gut 2017 06 31;66(6):1170-1172. Epub 2016 Aug 31.

Colorectal Oncogenomics Group, Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Parkville, Victoria, Australia.

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http://dx.doi.org/10.1136/gutjnl-2016-312773DOI Listing
June 2017

Cohort study of Gorlin syndrome with emphasis on standardised phenotyping and quality of life assessment.

Intern Med J 2017 Jun;47(6):664-673

Department of Genetic Medicine, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/imj.13429DOI Listing
June 2017

Genome-wide association study identifies multiple risk loci for renal cell carcinoma.

Authors:
Ghislaine Scelo Mark P Purdue Kevin M Brown Mattias Johansson Zhaoming Wang Jeanette E Eckel-Passow Yuanqing Ye Jonathan N Hofmann Jiyeon Choi Matthieu Foll Valerie Gaborieau Mitchell J Machiela Leandro M Colli Peng Li Joshua N Sampson Behnoush Abedi-Ardekani Celine Besse Helene Blanche Anne Boland Laurie Burdette Amelie Chabrier Geoffroy Durand Florence Le Calvez-Kelm Egor Prokhortchouk Nivonirina Robinot Konstantin G Skryabin Magdalena B Wozniak Meredith Yeager Gordana Basta-Jovanovic Zoran Dzamic Lenka Foretova Ivana Holcatova Vladimir Janout Dana Mates Anush Mukeriya Stefan Rascu David Zaridze Vladimir Bencko Cezary Cybulski Eleonora Fabianova Viorel Jinga Jolanta Lissowska Jan Lubinski Marie Navratilova Peter Rudnai Neonila Szeszenia-Dabrowska Simone Benhamou Geraldine Cancel-Tassin Olivier Cussenot Laura Baglietto Heiner Boeing Kay-Tee Khaw Elisabete Weiderpass Borje Ljungberg Raviprakash T Sitaram Fiona Bruinsma Susan J Jordan Gianluca Severi Ingrid Winship Kristian Hveem Lars J Vatten Tony Fletcher Kvetoslava Koppova Susanna C Larsson Alicja Wolk Rosamonde E Banks Peter J Selby Douglas F Easton Paul Pharoah Gabriella Andreotti Laura E Beane Freeman Stella Koutros Demetrius Albanes Satu Männistö Stephanie Weinstein Peter E Clark Todd L Edwards Loren Lipworth Susan M Gapstur Victoria L Stevens Hallie Carol Matthew L Freedman Mark M Pomerantz Eunyoung Cho Peter Kraft Mark A Preston Kathryn M Wilson J Michael Gaziano Howard D Sesso Amanda Black Neal D Freedman Wen-Yi Huang John G Anema Richard J Kahnoski Brian R Lane Sabrina L Noyes David Petillo Bin Tean Teh Ulrike Peters Emily White Garnet L Anderson Lisa Johnson Juhua Luo Julie Buring I-Min Lee Wong-Ho Chow Lee E Moore Christopher Wood Timothy Eisen Marc Henrion James Larkin Poulami Barman Bradley C Leibovich Toni K Choueiri G Mark Lathrop Nathaniel Rothman Jean-Francois Deleuze James D McKay Alexander S Parker Xifeng Wu Richard S Houlston Paul Brennan Stephen J Chanock

Nat Commun 2017 06 9;8:15724. Epub 2017 Jun 9.

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department Health and Human Services, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1038/ncomms15724DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472706PMC
June 2017

The role of STK 11 gene testing in individuals with oral pigmentation.

Australas J Dermatol 2017 May 14;58(2):135-138. Epub 2016 Jan 14.

Royal Melbourne Hospital, Familial Cancer Centre, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/ajd.12443DOI Listing
May 2017

Meanings of abortion in context: accounts of abortion in the lives of women diagnosed with breast cancer.

BMC Womens Health 2017 04 5;17(1):26. Epub 2017 Apr 5.

Jean Hailes Research Unit, School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, Melbourne, 3004, Australia.

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http://dx.doi.org/10.1186/s12905-017-0383-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382471PMC
April 2017

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

Authors:
Melissa C Southey David E Goldgar Robert Winqvist Katri Pylkäs Fergus Couch Marc Tischkowitz William D Foulkes Joe Dennis Kyriaki Michailidou Elizabeth J van Rensburg Tuomas Heikkinen Heli Nevanlinna John L Hopper Thilo Dörk Kathleen Bm Claes Jorge Reis-Filho Zhi Ling Teo Paolo Radice Irene Catucci Paolo Peterlongo Helen Tsimiklis Fabrice A Odefrey James G Dowty Marjanka K Schmidt Annegien Broeks Frans B Hogervorst Senno Verhoef Jane Carpenter Christine Clarke Rodney J Scott Peter A Fasching Lothar Haeberle Arif B Ekici Matthias W Beckmann Julian Peto Isabel Dos-Santos-Silva Olivia Fletcher Nichola Johnson Manjeet K Bolla Elinor J Sawyer Ian Tomlinson Michael J Kerin Nicola Miller Federik Marme Barbara Burwinkel Rongxi Yang Pascal Guénel Thérèse Truong Florence Menegaux Marie Sanchez Stig Bojesen Sune F Nielsen Henrik Flyger Javier Benitez M Pilar Zamora Jose Ignacio Arias Perez Primitiva Menéndez Hoda Anton-Culver Susan Neuhausen Argyrios Ziogas Christina A Clarke Hermann Brenner Volker Arndt Christa Stegmaier Hiltrud Brauch Thomas Brüning Yon-Dschun Ko Taru A Muranen Kristiina Aittomäki Carl Blomqvist Natalia V Bogdanova Natalia N Antonenkova Annika Lindblom Sara Margolin Arto Mannermaa Vesa Kataja Veli-Matti Kosma Jaana M Hartikainen Amanda B Spurdle kConFab Investigators Els Wauters Dominiek Smeets Benoit Beuselinck Giuseppe Floris Jenny Chang-Claude Anja Rudolph Petra Seibold Dieter Flesch-Janys Janet E Olson Celine Vachon Vernon S Pankratz Catriona McLean Christopher A Haiman Brian E Henderson Fredrick Schumacher Loic Le Marchand Vessela Kristensen Grethe Grenaker Alnæs Wei Zheng David J Hunter Sara Lindstrom Susan E Hankinson Peter Kraft Irene Andrulis Julia A Knight Gord Glendon Anna Marie Mulligan Arja Jukkola-Vuorinen Mervi Grip Saila Kauppila Peter Devilee Robert A E M Tollenaar Caroline Seynaeve Antoinette Hollestelle Montserrat Garcia-Closas Jonine Figueroa Stephen J Chanock Jolanta Lissowska Kamila Czene Hatef Darabi Mikael Eriksson Diana M Eccles Sajjad Rafiq William J Tapper Sue M Gerty Maartje J Hooning John W M Martens J Margriet Collée Madeleine Tilanus-Linthorst Per Hall Jingmei Li Judith S Brand Keith Humphreys Angela Cox Malcolm W R Reed Craig Luccarini Caroline Baynes Alison M Dunning Ute Hamann Diana Torres Hans Ulrich Ulmer Thomas Rüdiger Anna Jakubowska Jan Lubinski Katarzyna Jaworska Katarzyna Durda Susan Slager Amanda E Toland Christine B Ambrosone Drakoulis Yannoukakos Anthony Swerdlow Alan Ashworth Nick Orr Michael Jones Anna González-Neira Guillermo Pita M Rosario Alonso Nuria Álvarez Daniel Herrero Daniel C Tessier Daniel Vincent Francois Bacot Jacques Simard Martine Dumont Penny Soucy Rosalind Eeles Kenneth Muir Fredrik Wiklund Henrik Gronberg Johanna Schleutker Børge G Nordestgaard Maren Weischer Ruth C Travis David Neal Jenny L Donovan Freddie C Hamdy Kay-Tee Khaw Janet L Stanford William J Blot Stephen Thibodeau Daniel J Schaid Joseph L Kelley Christiane Maier Adam S Kibel Cezary Cybulski Lisa Cannon-Albright Katja Butterbach Jong Park Radka Kaneva Jyotsna Batra Manuel R Teixeira Zsofia Kote-Jarai Ali Amin Al Olama Sara Benlloch Stefan P Renner Arndt Hartmann Alexander Hein Matthias Ruebner Diether Lambrechts Els Van Nieuwenhuysen Ignace Vergote Sandrina Lambretchs Jennifer A Doherty Mary Anne Rossing Stefan Nickels Ursula Eilber Shan Wang-Gohrke Kunle Odunsi Lara E Sucheston-Campbell Grace Friel Galina Lurie Jeffrey L Killeen Lynne R Wilkens Marc T Goodman Ingo Runnebaum Peter A Hillemanns Liisa M Pelttari Ralf Butzow Francesmary Modugno Robert P Edwards Roberta B Ness Kirsten B Moysich Andreas du Bois Florian Heitz Philipp Harter Stefan Kommoss Beth Y Karlan Christine Walsh Jenny Lester Allan Jensen Susanne Krüger Kjaer Estrid Høgdall Bernard Peissel Bernardo Bonanni Loris Bernard Ellen L Goode Brooke L Fridley Robert A Vierkant Julie M Cunningham Melissa C Larson Zachary C Fogarty Kimberly R Kalli Dong Liang Karen H Lu Michelle A T Hildebrandt Xifeng Wu Douglas A Levine Fanny Dao Maria Bisogna Andrew Berchuck Edwin S Iversen Jeffrey R Marks Lucy Akushevich Daniel W Cramer Joellen Schildkraut Kathryn L Terry Elizabeth M Poole Meir Stampfer Shelley S Tworoger Elisa V Bandera Irene Orlow Sara H Olson Line Bjorge Helga B Salvesen Anne M van Altena Katja K H Aben Lambertus A Kiemeney Leon F A G Massuger Tanja Pejovic Yukie Bean Angela Brooks-Wilson Linda E Kelemen Linda S Cook Nhu D Le Bohdan Górski Jacek Gronwald Janusz Menkiszak Claus K Høgdall Lene Lundvall Lotte Nedergaard Svend Aage Engelholm Ed Dicks Jonathan Tyrer Ian Campbell Iain McNeish James Paul Nadeem Siddiqui Rosalind Glasspool Alice S Whittemore Joseph H Rothstein Valerie McGuire Weiva Sieh Hui Cai Xiao-Ou Shu Rachel T Teten Rebecca Sutphen John R McLaughlin Steven A Narod Catherine M Phelan Alvaro N Monteiro David Fenstermacher Hui-Yi Lin Jennifer B Permuth Thomas A Sellers Y Ann Chen Ya-Yu Tsai Zhihua Chen Aleksandra Gentry-Maharaj Simon A Gayther Susan J Ramus Usha Menon Anna H Wu Celeste L Pearce David Van Den Berg Malcolm C Pike Agnieszka Dansonka-Mieszkowska Joanna Plisiecka-Halasa Joanna Moes-Sosnowska Jolanta Kupryjanczyk Paul Dp Pharoah Honglin Song Ingrid Winship Georgia Chenevix-Trench Graham G Giles Sean V Tavtigian Doug F Easton Roger L Milne

J Med Genet 2016 12 5;53(12):800-811. Epub 2016 Sep 5.

Centre for Epidemiology and Biostatistics, School of Population and Global Health, The University of Melbourne, Melbourne, Australia.

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http://dx.doi.org/10.1136/jmedgenet-2016-103839DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5200636PMC
December 2016

Renal angiomyolipoma in Birt-Hogg-Dube syndrome: A case study supporting overlap with tuberous sclerosis complex.

Am J Med Genet A 2016 12 19;170(12):3323-3326. Epub 2016 Sep 19.

Genetic Medicine and Family Cancer Clinic, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1002/ajmg.a.37952DOI Listing
December 2016

A Prospective Study of Sudden Cardiac Death among Children and Young Adults.

N Engl J Med 2016 Jun;374(25):2441-52

From the Agnes Ginges Center for Molecular Cardiology, Centenary Institute, University of Sydney (R.D.B., J.I., L.Y., L.L., C.S.), Sydney Medical School, University of Sydney (R.D.B., J.I., J.D., R.P., C.S.), Department of Forensic Medicine, NSW Health Pathology (J.D.), and Department of Cardiology, Royal Prince Alfred Hospital (J.I., L.Y., R.P., C.S.), Sydney, the Department of Cardiology, Royal Children's Hospital, Murdoch Children's Research Institute and University of Melbourne (R.G.W., A.M.D., V.C., D.S.), Departments of Pediatrics (A.M.D.) and Pathology (P.J.), University of Melbourne, Genetic Medicine, Royal Melbourne Hospital (T.T., P.J., J.V., I.W.), Department of Medicine, Royal Melbourne Hospital, University of Melbourne (J.V., I.W.), and Victorian Institute of Forensic Medicine (M.L., N.M.), Melbourne, VIC, Forensic and Scientific Services, Archerfield, QL (J.W., C.N.), University of Queensland (J.W., C.N.), and Royal Brisbane and Women's Hospital (J.A., J.M.), Brisbane, QL, Department of Forensic Pathology, PathWest, Fremantle, WA (J.W.), ACT Pathology, Canberra Hospital, Canberra, ACT (L.H.), Royal Hobart Hospital, University of Tasmania, Hobart, TAS (C.L.), and the Attorney General's Department, University of Adelaide, Adelaide, SA (N.L.) - all in Australia; and Green Lane Pediatric and Congenital Cardiac Services, Starship Children's Hospital (J.C., J.R.S.), LabPLUS, Auckland City Hospital (D.L.), and the Department of Child Health, University of Auckland (J.R.S.), Auckland, New Zealand.

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http://dx.doi.org/10.1056/NEJMoa1510687DOI Listing
June 2016

Tributes.

S Afr Med J 2016 05 25;106(6 Suppl 1):S59-64. Epub 2016 May 25.

Emeritus Professor of Otolaryngology, University of Cape Town, South Africa.

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http://dx.doi.org/10.7196/SAMJ.2016.v106i6.10996DOI Listing
May 2016

PALB2: research reaching to clinical outcomes for women with breast cancer.

Hered Cancer Clin Pract 2016 19;14. Epub 2016 Apr 19.

Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Parkville, VIC 3010 Australia.

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http://dx.doi.org/10.1186/s13053-016-0049-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837522PMC
April 2016

Gene panel testing for hereditary breast cancer.

Med J Aust 2016 Mar;204(5):188-90

Department of Pathology, University of Melbourne, Melbourne, VIC.

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March 2016

Mal de Meleda in Indonesia: Mutations in the SLURP1 gene appear to be ubiquitous.

Australas J Dermatol 2016 Feb 30;57(1):e11-3. Epub 2014 Dec 30.

Genetic Medicine, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/ajd.12239DOI Listing
February 2016

Multiple familial pilomatrixomas in the absence of other clinical features: a case of familial benign pilomatrixoma.

Australas J Dermatol 2016 Feb;57(1):75-6

Genetic Medicine and Familial Cancer Clinic, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/ajd.12233DOI Listing
February 2016

Incidental diagnosis of HLRCC following investigation for Asperger Syndrome: actionable and actioned.

Fam Cancer 2016 Jan;15(1):25-9

Genetics Medicine and Familial Cancer Centre, The Royal Melbourne Hospital, Parkville, Victoria, Australia.

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http://dx.doi.org/10.1007/s10689-015-9829-5DOI Listing
January 2016

Lynch syndrome and cervical cancer.

Int J Cancer 2015 Dec 14;137(11):2757-61. Epub 2015 Jul 14.

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, VIC, Australia.

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http://dx.doi.org/10.1002/ijc.29641DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573262PMC
December 2015

Halo naevi and café au lait macule regression in a renal transplant patient on immunosuppression.

Australas J Dermatol 2015 Nov 1;56(4):e88-90. Epub 2014 Sep 1.

Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/ajd.12188DOI Listing
November 2015

Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndrome.

Genes Cancer 2015 Nov;6(11-12):445-51

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Victoria, Australia; Colorectal Oncogenomics Group, Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Parkville, Victoria, Australia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701223PMC
http://dx.doi.org/10.18632/genesandcancer.85DOI Listing
November 2015

Implementing a telephone based peer support intervention for women with a BRCA1/2 mutation.

Fam Cancer 2015 Sep;14(3):373-82

Centre for Behavioural Research in Cancer, Cancer Council Victoria, 615 St Kilda Road, Melbourne, VIC, 3004, Australia.

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http://dx.doi.org/10.1007/s10689-015-9797-9DOI Listing
September 2015

Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome.

J Natl Cancer Inst 2015 Sep 24;107(9). Epub 2015 Jun 24.

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Victoria, Australia (DAO, SGD, RC, DDB, GGG, JLH, MAJ, AKW); Oncogenomics Group, Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Parkville, Victoria, Australia (DDB, MC, CR); University of Queensland, School of Medicine, Herston, Queensland, Australia (CR); Department of Medicine, Royal Melbourne Hospital, The University of Melbourne, Parkville, Victoria, Australia (IMW, FAM); Genetic Medicine and Family Cancer Clinic, Royal Melbourne Hospital, Parkville, Australia (IMW, FAM); Departments of Haematology and Oncology, The Queen Elizabeth Hospital, Woodville, South Australia, Australia (JPY); SAHMRI Colorectal Node, Basil Hetzel Institute for Translational Research, Woodville, South Australia, Australia (JPY); School of Medicine, University of Adelaide, South Australia, Australia (JPY); Cancer Epidemiology Centre, Cancer Council Victoria, Melbourne, Victoria, Australia (GGG); QIMR Berghofer Medical Research Institute, Royal Brisbane Hospital, Herston, Queensland, Australia (BL); Colorectal Medicine and Genetics, The Royal Melbourne Hospital, Parkville, Victoria, Australia (FAM); Department of Medicine, University of Colorado School of Medicine, Denver, CO (DJA); Department of Preventive Medicine, Keck School of Medicine and Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA (GC); Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada (SG); Department of Medicine, Division of Oncology, Stanford Cancer Institute, Stanford University, CA (RWH); University of Hawaii Cancer Center, Honolulu, HI (LLM); Molecular Genetics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN (SNT); Department of Health Science Research, Mayo Clinic Arizona, Scottsdale, AZ (NML); Public Health Science

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http://dx.doi.org/10.1093/jnci/djv170DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4651105PMC
September 2015

Precision medicine: are we there?

Authors:
Ingrid Winship

Med J Aust 2015 Aug;203(3):132-3, 133e.1

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August 2015

Interpretation of genomic variation and disease association: the great missense mutation challenge!

Breast Cancer Res Treat 2015 Jun 22;151(2):475-6. Epub 2015 Apr 22.

Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Melbourne, VIC, 3010, Australia.

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http://dx.doi.org/10.1007/s10549-015-3394-3DOI Listing
June 2015

Is cardiac rhabdomyoma a feature of Birt Hogg Dubé syndrome?

Am J Med Genet A 2015 Apr 5;167A(4):802-4. Epub 2015 Feb 5.

Genetic Medicine and Family Cancer Clinic, Royal Melbourne Hospital, Melbourne, Australia; Department of Medicine, Royal Melbourne Hospital, University of Melbourne, Melbourne, Australia; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal Child Health, Section of Medical Genetics, University of Genoa, Genoa, Italy.

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http://dx.doi.org/10.1002/ajmg.a.36917DOI Listing
April 2015

Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome.

Fam Cancer 2015 Mar;14(1):151-5

Genetic Medicine and Familial Cancer Centre, Royal Melbourne Hospital, Grattan Street, Parkville, VIC, 3050, Australia,

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http://dx.doi.org/10.1007/s10689-014-9752-1DOI Listing
March 2015

Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review.

Fam Cancer 2015 Mar;14(1):157-60

Clinical Genetics and Familial Cancer Centre, The Royal Melbourne Hospital, University of Melbourne, Parkville, Australia,

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http://dx.doi.org/10.1007/s10689-014-9763-yDOI Listing
March 2015

Red cells from ferrochelatase-deficient erythropoietic protoporphyria patients are resistant to growth of malarial parasites.

Blood 2015 Jan 20;125(3):534-41. Epub 2014 Nov 20.

Australian School of Advanced Medicine, Macquarie University, North Ryde, NSW, Australia; The John Curtin School of Medical Research, Australian National University, Canberra, ACT, Australia.

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http://dx.doi.org/10.1182/blood-2014-04-567149DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296013PMC
January 2015

Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry.

Breast Cancer Res Treat 2015 Jan 10;149(2):547-54. Epub 2015 Jan 10.

Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Melbourne, VIC, 3010, Australia,

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http://dx.doi.org/10.1007/s10549-014-3260-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542063PMC
January 2015

Randomized controlled trial of a telephone-based peer-support program for women carrying a BRCA1 or BRCA2 mutation: impact on psychological distress.

J Clin Oncol 2014 Dec 17;32(36):4073-80. Epub 2014 Nov 17.

Victoria M. White, Ashley Farrelly, and Michael Jefford, Cancer Council Victoria; Elizabeth Williamson and Ingrid Winship, The University of Melbourne; Ingrid Winship, Royal Melbourne Hospital; Elizabeth Williamson, Monash University, Melbourne; Mary-Anne Young and Michael Jefford, Peter MacCallum Cancer Centre, East Melbourne; Sandra Ieropoli, Early in Life Mental Health Service, Monash Health Mental Health Program, Clayton, Victoria; Bettina Meiser, Prince of Wales Clinical School, The University of New South Wales, Sydney; and Jessica Duffy, Hereditary Cancer Clinic, Prince of Wales Hospital, Randwick, New South Wales, Australia.

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http://jco.ascopubs.org/content/early/2014/11/12/JCO.2013.54
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http://jco.ascopubs.org/cgi/doi/10.1200/JCO.2013.54.1607
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http://dx.doi.org/10.1200/JCO.2013.54.1607DOI Listing
December 2014

Should the grading of colorectal adenocarcinoma include microsatellite instability status?

Hum Pathol 2014 Oct 17;45(10):2077-84. Epub 2014 Jul 17.

Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Carlton 3010, VIC, Australia; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, VIC 3010, Australia.

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http://dx.doi.org/10.1016/j.humpath.2014.06.020DOI Listing
October 2014

Fertility and apparent genetic anticipation in Lynch syndrome.

Fam Cancer 2014 Sep;13(3):369-74

Deakin University Department of Surgery, Geelong Hospital, Ryrie Street, Geelong, VIC, 3227, Australia,

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http://dx.doi.org/10.1007/s10689-014-9714-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357528PMC
September 2014

Re: Microsatellite instability and BRAF mutation testing in colorectal cancer prognostication.

J Natl Cancer Inst 2014 Aug 11;106(8). Epub 2014 Aug 11.

Cancer and Population Studies Group, QIMR Berghofer Medical Research Institute, Australia (CR, MC, RJW, MDW, DDB); Oncogenomics Group, Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Parkville, Australia (MC, DDB); University of Queensland, School of Medicine, Herston, Australia (CR); Envoi Pathology, Herston, Australia (CR); Centre for Molecular, Environmental, Genetic and Analytic Epidemiology, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Australia (EJW, AKW, MAJ, JLH, GGG, DRE, DDB); Department of Histopathology, Sullivan Nicolaides Pathology, Taringa, Australia (MDW); Seoul National University, Seoul, Korea (JLH); Department of Medicine, The University of Melbourne, Parkville, Australia (IW); Genetic Medicine, The Royal Melbourne Hospital, Parkville, Australia (IW); Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Carlton, Australia (MCS); Cancer Epidemiology Centre, Cancer Council Victoria, Carlton, Australia (GGG, DRE).

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http://dx.doi.org/10.1093/jnci/dju180DOI Listing
August 2014

Succinate dehydrogenase deficiency is rare in pituitary adenomas.

Am J Surg Pathol 2014 Apr;38(4):560-6

*Department of Anatomical Pathology, Royal North Shore Hospital ‡University of Sydney, Sydney †Cancer Diagnosis and Pathology Research Group, Kolling Institute of Medial Research #Cancer Genetics, Kolling Institute of Medical Research, Royal North Shore Hospital, St Leonards §Histopath Pathology, North Ryde ∥Department of Anatomical Pathology, St Vincents Hospital, Darlinghurst, NSW ¶Department of Medicine, University of Melbourne, Royal Melbourne Hospital, Melbourne, Vic., Australia.

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http://dx.doi.org/10.1097/PAS.0000000000000149DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966922PMC
April 2014

Dermatitis artefacta presenting as a recurrent skin eruption in a patient with 1p36 deletion syndrome.

Australas J Dermatol 2014 Feb;55(1):90

Royal Melbourne Hospital, Parkville, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/ajd.12131DOI Listing
February 2014

Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy.

Genet Med 2013 Dec 18;15(12):972-7. Epub 2013 Apr 18.

1] Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, Australia [2] School of Medicine, University of Sydney, Sydney, Australia.

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http://dx.doi.org/10.1038/gim.2013.44DOI Listing
December 2013

Dynamic consent in the digital age of biology: online initiatives and regulatory considerations.

J Prim Health Care 2013 Dec 1;5(4):341-7. Epub 2013 Dec 1.

Faculty of Law, University of Otago, PO Box 56, Dunedin 9054, New Zealand.

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December 2013

Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes.

Heart Rhythm 2013 Nov 22;10(11):1653-60. Epub 2013 Aug 22.

Department of Cardiology, The Royal Melbourne Hospital, Parkville, Victoria, Australia; Department of Medicine, University of Melbourne, Parkville, Victoria, Australia.

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http://dx.doi.org/10.1016/j.hrthm.2013.08.022DOI Listing
November 2013

The utility of genetics in inherited cancer.

Med J Aust 2013 Nov;199(10):644

University of Melbourne, Royal Melbourne Hospital, Melbourne, VIC, Australia.

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November 2013

Deficiency in complement factor B.

N Engl J Med 2013 Oct;369(17):1667-9

Royal Melbourne Hospital, Melbourne, VIC, Australia

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http://dx.doi.org/10.1056/NEJMc1306326DOI Listing
October 2013

PALB2 and breast cancer: ready for clinical translation!

Appl Clin Genet 2013 19;6:43-52. Epub 2013 Jul 19.

Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Victoria, Australia.

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http://www.dovepress.com/palb2-and-breast-cancer-ready-for-c
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http://dx.doi.org/10.2147/TACG.S34116DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735037PMC
August 2013

A funding model for public-good clinical trials.

Med J Aust 2013 Jul;199(2):90-1

Melbourne Health, Melbourne, VIC, Australia.

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July 2013

Familial SDHA mutation associated with pituitary adenoma and pheochromocytoma/paraganglioma.

J Clin Endocrinol Metab 2013 Jun 30;98(6):E1103-8. Epub 2013 Apr 30.

Cancer Genetics, Hormones and Cancer Group, Kolling Institute of Medical Research, Royal North Shore Hospital, Sydney, New South Wales 2065, Australia.

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http://dx.doi.org/10.1210/jc.2013-1400DOI Listing
June 2013