Jacqueline M. Ogier

Geneticist

Female📍 Parkville

About of Jacqueline M. Ogier

Jacqueline M. Ogier is a Geneticist based at 50 Flemington Road, Parkville, VIC 3052, Australia. Her work sits at the point where genes meet real life health. She looks after families who want clearer answers about inherited conditions, and she helps people understand what the results can (and can’t) mean for day to day care.


Jacqueline focuses on genetic conditions linked to hearing and vision, as well as some broader inherited syndromes. This can include Grix Blankenship Peterson Syndrome, CHARGE Syndrome, Alport Syndrome, and hearing loss. She also works with cases involving Norrie Disease, Otitis, and Waardenburg Syndrome, including Waardenburg Syndrome Type 1. At times, these diagnoses can help explain symptoms that have been present for a while, and other times they can guide next steps when things are still a bit unclear.


In many cases, the first question families ask is simple: “What’s going on, and why?” Jacqueline’s approach is calm and practical. She helps organise the genetic picture and supports families through the process. This often means talking through likely patterns of inheritance and how genetic findings may affect children, siblings, or other relatives. It can also mean reviewing what’s already known from tests and medical history, then mapping out what might be worth checking next.


Because genetic information can be complex, it helps when the conversation stays clear. Jacqueline works with patients and carers to break things down into plain language, so the next decision feels more manageable. She also takes care to explain uncertainty where it exists, rather than pushing for easy answers. Over time, that way of working can make a real difference, especially for families dealing with ongoing health needs.


Jacqueline’s education and training are rooted in genetics and clinical care, which supports the way she reviews cases and plans follow up discussions. While she also considers new developments in the field through ongoing medical learning, the focus stays on what matters most for patients. For people in Parkville and across Victoria, she provides genetics support for a range of inherited conditions that affect hearing, growth, and overall health.

Services & Conditions Treated

Grix Blankenship Peterson SyndromeCHARGE SyndromeAlport SyndromeHearing LossNorrie DiseaseOtitisWaardenburg SyndromeWaardenburg Syndrome Type 1

Publications

1 total

Loss of KAT6B causes premature ossification and promotes osteoblast differentiation during development.

Developmental biology • October 30, 2024

Frequently Asked Questions

What services does Dr Jacqueline M. Ogier offer?
Dr Ogier provides genetic consultation and testing related to conditions such as Grix Blankenship Peterson Syndrome, CHARGE Syndrome, Alport Syndrome, Norrie Disease, Waardenburg Syndrome (including Type 1), and related hearing loss issues.
Which conditions related to genetics does she treat?
She focuses on genetic conditions including Grix Blankenship Peterson Syndrome, CHARGE Syndrome, Alport Syndrome, Norrie Disease, Waardenburg Syndrome (Type 1), and related hearing loss problems.
Who should consider a genetic consultation with Dr Ogier?
Anyone with a family history or personal concern about the genetic conditions listed, or with unexplained hearing loss or syndromic features, may benefit from a genetic consult.
Where is the clinic located?
The clinic is at 50 Flemington Road, Parkville, VIC 3052, Australia.
What should I bring to a genetic appointment?
Bring any medical records, family history of genetic conditions, and any relevant test results to help the consultation.
How can I learn more or book an appointment?
For details on services or to book, contact the clinic at the Parkville address. If you have questions, you can ask during the initial inquiry or appointment booking.

Contact Information

50 Flemington Road, Parkville, VIC 3052, Australia

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