Publications by authors named "Ingrid M Winship"

54Publications

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.

Genet Med 2020 Sep;22(9):1569

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

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http://dx.doi.org/10.1038/s41436-020-0892-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462742PMC
September 2020

A Genomic Test for Colorectal Cancer Risk: Is This Acceptable and Feasible in Primary Care?

Public Health Genomics 2020 20;23(3-4):110-121. Epub 2020 Jul 20.

Centre for Cancer Research, University of Melbourne, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1159/000508963DOI Listing
July 2020

Genetic resilience to Alzheimer's disease in APOE ε4 homozygotes: A systematic review.

Alzheimers Dement 2019 12 7;15(12):1612-1623. Epub 2019 Sep 7.

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/10.1016/j.jalz.2019.05.011DOI Listing
December 2019

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.

Genet Med 2020 01 24;22(1):15-25. Epub 2019 Jul 24.

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

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http://dx.doi.org/10.1038/s41436-019-0596-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371626PMC
January 2020

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

Mol Genet Genomic Med 2019 07 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

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
June 2020

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

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

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

Eur Heart J 2019 03;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

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

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

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

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

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

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

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

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

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

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

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

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

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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http://dx.doi.org/10.5694/mja13.10978DOI Listing
November 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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http://dx.doi.org/10.5694/mja13.10381DOI Listing
July 2013

FSH receptor gene variants are rarely associated with premature ovarian failure.

Reprod Biomed Online 2013 Apr 19;26(4):396-9. Epub 2013 Jan 19.

Discipline of Oncology, University of Auckland, Auckland, New Zealand.

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http://dx.doi.org/10.1016/j.rbmo.2013.01.004DOI Listing
April 2013

Renal tumors associated with germline SDHB mutation show distinctive morphology.

Am J Surg Pathol 2011 Oct;35(10):1578-85

Department of Anatomical Pathology, Royal North Shore Hospital, St Leonards, NSW, 2065, Australia.

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http://dx.doi.org/10.1097/PAS.0b013e318227e7f4DOI Listing
October 2011

Lessons from the skin--cutaneous features of familial cancer.

Lancet Oncol 2008 May;9(5):462-72

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

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http://linkinghub.elsevier.com/retrieve/pii/S147020450870126
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http://dx.doi.org/10.1016/S1470-2045(08)70126-8DOI Listing
May 2008

Genetic diversity and linkage disequilibrium in the Polynesian population of Niue Island.

Hum Biol 2006 Apr;78(2):131-45

New Zealand Liver Transplant Unit, Auckland Hospital, Private Bag 92-024, Auckland, New Zealand.

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http://dx.doi.org/10.1353/hub.2006.0031DOI Listing
April 2006

Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure.

Fertil Steril 2006 Oct;86(4):1009-12

Department of Obstetrics and Gynaecology, Faculty of Medical and Health Sciences, University of Auckland, New Zealand.

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http://dx.doi.org/10.1016/j.fertnstert.2006.02.107DOI Listing
October 2006

Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure.

Fertil Steril 2006 Nov 18;86(5):1518-21. Epub 2006 Sep 18.

Department of Obstetrics and Gynaecology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.

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http://dx.doi.org/10.1016/j.fertnstert.2006.03.054DOI Listing
November 2006

An investigation into FOXE1 polyalanine tract length in premature ovarian failure.

Mol Hum Reprod 2006 Mar 15;12(3):145-9. Epub 2006 Feb 15.

Department of Obstetrics and Gynaecology, Faculty of Medical and Health Sciences, University of Auckland, New Zealand.

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http://dx.doi.org/10.1093/molehr/gal017DOI Listing
March 2006

INHA promoter polymorphisms are associated with premature ovarian failure.

Mol Hum Reprod 2005 Nov 3;11(11):779-84. Epub 2006 Jan 3.

Department of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.

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http://dx.doi.org/10.1093/molehr/gah219DOI Listing
November 2005

Asthma phenotypes in Niue Islanders.

Respirology 2004 Nov;9(4):521-7

Department of Molecular Medicine, University of Auckland, Auckland, New Zealand.

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http://dx.doi.org/10.1111/j.1440-1843.2004.00601.xDOI Listing
November 2004