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  • Genomics in Healthcare
FREE COURSE

Genomics in Healthcare

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Free course

START DATE

 Start anytime

MODE

 Online

DURATION

 Self paced
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Meet the Expert

Jane Maguire

Jane Maguire
Professor

Jane’s research in exploring the genetics of stroke risk and stroke outcome is internationally acknowledged. She is an academic, a registered nurse in paediatric and child health, and a member of the leadership committee for the Global Genomics Nurses Alliance who are actively engaged in genomics education across the globe.

Jane is an ongoing leader within the International Stroke Genetics Consortium, working on multiple collaborative international research projects. She has recently joined a new international partnership, Stroke Recovery Research Roundtable, which draws together leading stroke experts in stroke recovery and rehabilitation. Jane is recognised internationally as one of the leading nurse stroke genetics researchers in the world.

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Stroke. Diabetes. Asthma. Schizophrenia. Heart attack. These are just some of the debilitating and sometimes fatal complex diseases that the field of genomics is unlocking the secrets to. This course will help you discover the way genomics is contributing to and impacting on medical science, from prenatal checks to end-of-life care, along with its ethical, pharmaceutical and clinical implications.

About this course

This is a free, self-paced online course.

Twenty years ago, experiencing a stroke was especially distressing if you were fit and healthy. Today, we have the potential to predict which people  may be more likely to experience these types of common diseases. Treatments can be targeted in more precise, patient-centred ways. That’s because we have finally unlocked the secrets of our DNA.

Genomics is transforming healthcare by allowing practitioners access to additional biological information about disease. This means a more targeted and relevant disease management plan for patients. Such change, however, naturally brings ethical complications. Imagine knowing, for example, that a mother’s unborn child is more likely to develop breast cancer or some other rare disease.

In this course you will be introduced to the way that genomic information is informing our knowledge about health conditions through the entire patient lifespan, from prenatal, through to end-of-life care. You will understand its implications from both a healthcare professional and patient perspective. By adapting to genomics and harnessing its potential, you will place yourself at the forefront of healthcare practitioners.

Through this course, you will be guided by academics, researchers and practitioners from healthcare facilities and Australian genomics centres. You will also hear from patients impacted by rare diseases. You will be able to share their expertise and experience to develop the ability to engage with the broad relevance of genomics in healthcare.

Course structure

  • Genomics and the promise of clinical utility
  • Ethics and challenges of access to personal information
  • Actionable pharmacogenomics
  • Risk and diagnostic testing.

 

Why you should do this course

  • Increase your genomic literacy through a succinct and clinically relevant course
  • Understand how recent advances in genomics will influence your clinical practice
  • Stay ahead of a trend that health professionals worldwide are embracing
  • Learn about new treatment options
  • Gain the foundation for undertaking an accredited CPD course or postgraduate qualification such as the UTS Master of Advanced Nursing.

Who is this course for?

This course is for passionate industry professionals who want to understand the effects of genomics and its implications on public life. 

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