Ingrid M. Winship

Medical Geneticist

Female📍 Parkville

About of Ingrid M. Winship

Ingrid M. Winship is a Medical Geneticist based in Parkville, VIC, at 305 Grattan Street. She works with people and families across Australia who are dealing with a possible inherited condition, or who want clearer answers about risk for the future.


Genetics can feel confusing and, at times, a bit confronting. Ingrid focuses on taking the time to explain what genetic results may mean in plain language. In many cases, that helps families make more informed choices about next steps, screening, and treatment options. She also supports people who are trying to connect health patterns across generations.


A big part of her work is looking at inherited cancer risk. This can include Lynch Syndrome and familial colorectal cancer, as well as syndromes linked with endometrial or ovarian cancer. She also helps when there are genes connected to polyps, breast cancer (including breast cancer in men), and other cancers that can run in families. Sometimes the concern is about a specific diagnosis. Other times it’s more about a family history that doesn’t quite fit together yet.


Ingrid also looks after people where the concern is broader than cancer alone. That can include conditions linked to skin, blood vessels, and other body systems. At times, referrals may be about mosaicism or other complex genetic changes. For some families, the focus is on understanding a rare condition and planning care with the rest of the health team.


Her clinic approach is practical. She listens first, then connects the dots using genetic information and family history. If further testing is needed, she helps explain why, what it can show, and what it might not show. Over time, that can reduce guesswork and bring some steadier direction to a hard situation.


Ingrid’s work sits across teamwork with local hospitals, specialist doctors, and allied health services. That matters, because genetic results often affect more than one part of care. She helps make sure the genetics side of things fits into the bigger plan.


For people who have been told “it runs in the family,” or who are unsure what their results mean, getting good, clear genetics support can make a real difference. Ingrid aims to keep the conversation calm and grounded, so families know where they are at and what happens next.

Services & Conditions Treated

Lynch SyndromeColorectal CancerFamilial Colorectal CancerTurcot SyndromeBirt-Hogg-Dube SyndromeEndometrial CancerFamilial Adenomatous PolyposisHereditary Hemorrhagic TelangiectasiaMosaicismNevoid Basal Cell Carcinoma SyndromePeutz-Jeghers SyndromePhacomatosis PigmentokeratoticaSalpingo-OophorectomySebaceous AdenomaTelangiectasiaAchondrogenesisAcrokeratoelastoidosis of CostaAcromesomelic DysplasiaAcromesomelic Dysplasia Campailla Martinelli TypeAcromesomelic Dysplasia Hunter Thompson TypeAcromesomelic Dysplasia Maroteaux TypeAdenine Phosphoribosyltransferase DeficiencyAlzheimer's DiseaseAplasia Cutis CongenitaArrhythmiasArteriovenous MalformationAsperger's SyndromeAutism Spectrum DisorderB-Cell LymphomaBannayan-Riley-Ruvalcaba SyndromeBasal Cell Skin CancerBrain TumorBreast CancerBreast Cancer in MenCardiac ArrestCardiomyopathyChondrodysplasia Punctata SyndromeClouston SyndromeColonoscopyColorectal PolypsCongenital Coronary Artery MalformationCowden SyndromeDementiaEctodermal DysplasiasEhlers-Danlos Syndrome (EDS)EndoscopyEpidermolysis Bullosa with Pyloric AtresiaErythropoietic ProtoporphyriaFamilial Dilated CardiomyopathyFamilial Hypertrophic CardiomyopathyFamilial Prostate CancerFamilial Ventricular TachycardiaFibromatosisHemangioblastomaHemangiomaHormone Replacement Therapy (HRT)Hypermobile JointsHypertrophic Cardiomyopathy (HCM)Hypothalamic TumorHysterectomyLhermitte-Duclos DiseaseLi-Fraumeni SyndromeLinear Nevus Sebaceous SyndromeMedulloblastomaMelanomaMelasmaMenopauseNeuroendocrine TumorOophorectomyOvarian CancerPalmoplantar KeratodermaPheochromocytomaPorphyriaPremature Ovarian FailurePrimary Lateral SclerosisProtoporphyriaRenal Cell Carcinoma (RCC)Ruvalcaba SyndromeSpontaneous Coronary Artery Dissection (SCAD)Uterine FibroidsVascular DementiaVascular Ehlers-Danlos Syndrome (VEDS)Ventricular TachycardiaVon Hippel-Lindau (VHL) SyndromeX-Linked Chondrodysplasia Punctata 2

Publications

1 total

Causes of DNA mismatch repair deficiency in sebaceous skin lesions demonstrating loss of MLH1 protein expression: constitutional over somatic MLH1 promoter methylation.

Familial cancer • January 21, 2025

Frequently Asked Questions

What services does Dr Ingrid M. Winship offer?
Dr Ingrid M. Winship is a medical geneticist who works with hereditary and familial cancer and related disorders. Her listed focus includes conditions such as Lynch syndrome, familial colorectal cancer, various hereditary cancer syndromes, and related genetic evaluation and management.
What conditions are commonly discussed with a medical geneticist like Dr Winship?
Common topics include hereditary colorectal cancer syndromes (like Lynch syndrome and familial colorectal cancer), other hereditary cancers, and genetic testing options. If you have a family history of cancer or genetic conditions, she can review your risk and options.
How do I book an appointment at the Parkville clinic?
To book an appointment, contact the Parkville clinic at 305 Grattan Street, Parkville, VIC 3010, Australia. If you’re unsure what you need, you can ask the receptionist for a medical genetics consultation.
What should I bring to my genetic appointment?
Bring any known family history of cancers or genetic conditions, any previous genetic test results, and a list of medications you’re taking. If you have referral notes, bring them as well.
Do you work with other specialists for patient care?
Yes. Genetic evaluation often involves a team approach. Depending on your situation, care may involve coordination with other doctors, such as oncologists, surgeons, and other genetics professionals.
Who is suitable for a genetic assessment or testing?
People with a strong family history of certain cancers or inherited conditions, or those who have been told they may be at risk based on family history, may be suitable for a genetic assessment. A clinician will assess whether genetic testing is appropriate for you.

Contact Information

305 Grattan Street, Parkville, VIC 3010, Australia

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