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PROF INGRID WINSHIP



Contact Details

Organization: Medicine - Royal Melbourne and Western Hospitals
Position: CHAIR IN ADULT CLINICAL GENETICS
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Qualifications, Honours, Fellowships and Other Awards

Qualifications

Title Institution Date Awarded Abbreviation
MBChB University of Cape Town 31-Dec-1981
Doctor of Medicine University of Cape Town 31-Dec-1986

Fellowships

Fellowship Date Awarded
Fellow of the Royal Australasian College of Physicians (FRACP) 31-Dec-2002

Government Research Classifications

Research Fields, Courses and Discipline Classifications

Socio-Economic Objective Classifications

Grants and Contracts

Research Grants, Contracts and Consultancies awarded to the University of Melbourne as the administering institution (since 2003) as recorded in Themis Agreements.

Grants

Title Role Funding Source Scheme Award Date
STUDIES INTO GYNAECOLOGICAL CANCERS ASSOCIATED WITH THE SYNDROME: HEREDITARY NONPOLYPOSIS COLON CANCER Chief Investigator CANCER COUNCIL VICTORIA Grants-in-Aid 27/11/2006
Breast cancer and fertility: Contributing to General Practitioners; management and support of their patients Chief Investigator HELEN MACPHERSON SMITH TRUST Research Grants 17/07/2009

Publications

Publications produced at the University of Melbourne and reported in the Annual Publications Collection and 'Research Report' since 2001. The Themis Publications module, released in November 2006, allows additional publications from previous institutions and publications from past years to be entered.

Publications in 2008

Journal Articles

  • Cultural enhancement of a clinical service to meet the needs of indigenous people; genetic service development in response to issues for New Zealand Maori
    Year: 2008
    Journal: Clinical Genetics
    Volume: 73
    Page numbers: 132-138
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  • Familial breast cancer: double heterozygosity for BRCA1 and BRCA2 mutations with differing phenotypes
    Year: 2008
    Journal: Familial Cancer
    Volume: 7
    Issue: 2
    Page numbers: 119-124
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  • Lessons from the skin--cutaneous features of familial cancer
    Year: 2008
    Journal: The Lancet
    Volume: 9
    Issue: 462-472
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  • The clinical phenotype of Lynch Syndrome due to germ-line PMS2 mutations
    Year: 2008
    Journal: Gastroenterology
    Volume: 135
    Page numbers: 419-428
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  • Towards more effective and equitable genetic testing for BRCA1 and BRCA2 mutation carriers
    Year: 2008
    Journal: Journal of Medical Genetics
    Volume: 45
    Page numbers: 409-410
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Publications in 2006

Journal Articles

  • An investigation into FOXE1 polyalanine tract length in premature ovarian failure
    Year: 2006
    Journal: Molecular Human Reproduction
    Volume: 12
    Page numbers: 145-149
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  • Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families
    Year: 2006
    Journal: Nephrology, Dialysis, Transplantation
    Volume: 21
    Page numbers: 665-671
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  • Confirming a diagnosis of hereditary colorectal cancer: the impact of a Familial Bowel Cancer Registry in New Zealand
    Year: 2006
    Journal: New Zealand Medical Journal
    Volume: 119
    Page numbers: U2168
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  • Genetic diversity and linkage disequilibrium in the Polynesian population of Niue Island
    Year: 2006
    Journal: Human Biology
    Volume: 78
    Page numbers: 131-145
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  • Hereditary diffuse gastric cancer: Diagnosis and management
    Year: 2006
    Journal: Clinical Gastroenterology and Hepatology
    Volume: 4
    Page numbers: 262-275
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  • Hyperplastic polyposis syndrome: Phenotypic presentations and the role of MBD4 and MYH
    Year: 2006
    Journal: Gastroenterology
    Volume: 131
    Page numbers: 30-39
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  • Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovaian failure
    Year: 2006
    Journal: Fertility and Sterility
    Volume: 86
    Page numbers: 1009-1012
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  • Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure
    Year: 2006
    Journal: Fertility and Sterility
    Volume: 86
    Page numbers: 1518-1521
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  • The Colorectal Cancer Family Registry: An international resource for studying the genetic and molecular epidemiology of colorectal cancer
    Year: 2006
    Journal: Gastrointestinal Cancer Update
    Volume: 46
    Page numbers: 14-20
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Publications in 2005

Journal Articles

  • INHA promoter polymorphisms are associated with premature ovarian failure
    Year: 2005
    Journal: Molecular Human Reproduction
    Volume: 11
    Page numbers: 779-784
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  • Blepharocheilodontic syndrome or lagophthalmos: a child with overlapping features
    Year: 2005
    Journal: Clinical Dysmorphology
    Volume: 14
    Issue: 3
    Page numbers: 151-153
    Publisher: Lippincott Williams & Wilkins
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  • Controversies and ethical issues in cancer-genetics clinics
    Year: 2005
    Journal: Lancet Oncology
    Volume: 6
    Issue: 5
    Page numbers: 301-310
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  • Further case report of a child with a 9q34 deletion and a review of the reported cases
    Year: 2005
    Journal: American Journal of Medical Genetics
    Volume: 133A
    Issue: 2
    Page numbers: 219-221
    Publisher: Wiley-Liss(New York)
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Publications in 2004

Journal Articles

  • Asthma phenotypes in Niue Islanders
    Year: 2004
    Journal: Respirology
    Volume: 9
    Page numbers: 521-527
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Publications in 2003

Journal Articles

  • Autosomal dominant velopharyngeal insufficienty: father-to-son transmission confirmed
    Year: 2003
    Journal: Clinical Genetics
    Volume: 64
    Page numbers: 522-523
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  • False-positive diagnosis of trisomy 21 using fluorescence in situ hybridisation (FISH) on uncultured amniotic fluid cells
    Year: 2003
    Journal: Prenatal Diagnosis
    Volume: 23
    Page numbers: 302-305
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  • Paternal uniparental disomy in monozygotic twins discordant for hemihypertrophy
    Year: 2003
    Journal: Journal of Medical Genetics
    Volume: 40
    Page numbers: 223-226
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Publications in 2002

Journal Articles

  • Attitudes about genetic testing for breast cancer susceptibility: A survey of general practitioners, medical students, and women in the northern region of New Zealand


    Year: 2002
    Journal: New Zealand Family Physician
    Volume: 29
    Page numbers: 234-239
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  • Identification of novel mutations in FOXL2 associated with premature ovarian failure
    Year: 2002
    Journal: Molecular Human Reproduction
    Volume: 8
    Page numbers: 729-733
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  • Novel germline CDH1 mutations in hereditary diffuse gastric cancer families
    Year: 2002
    Journal: Human Mutation
    Volume: 19
    Page numbers: 518-525
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  • Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype
    Year: 2002
    Journal: American Journal of Medical Genetics
    Volume: 111
    Page numbers: 19-26
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Publications in 2001

Journal Articles

  • Analysis of the TGFß functional pathway in epithelial ovarian carcinoma
    Year: 2001
    Journal: British Journal of Cancer
    Volume: 85
    Page numbers: 687-691
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  • Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia
    Year: 2001
    Journal: New England Journal of Medicine
    Volume: 245
    Page numbers: 325-334
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  • Clinical phenotypes of nine cases of Kabuki syndrome from New Zealand
    Year: 2001
    Journal: Clinical Dysmorphology
    Volume: 10
    Page numbers: 257-262
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