Reproductive genetic carrier screening (RCS) is increasingly being offered more widely,
including to people with no family history or otherwise elevated chance of having a baby …

In health and medical research, guidelines are a set of statements and recommendations,
whereby experts or stakeholders assess published literature to generate practical advice for …

There is a well-recognized need to include diverse populations in genetic studies, but
several obstacles continue to be prohibitive, including (but are not limited to) the difficulty of …

The probability an individual is a carrier for a recessive disorder despite a negative carrier
test, referred to as residual risk, has been part of carrier screening for over 2 decades …

Abstract Background Aboriginal and Torres Strait Islander people do not enjoy equal access
to specialist health services that adequately meet their needs. Clinical genetics services are …

(1) Background: Genomic precision medicine (PM) utilises people's genomic data to inform
the delivery of preventive and therapeutic health care. PM has not been well-established for …

Background Biobanks are vital resources for genetics and genomics, and it is broadly
recognised that for maximal benefit it is essential that they include samples and data from …

The purpose of this report is to assist the Indigenous Australian Genomics Committee of the
Commonwealth Department of Health in identifying current research, clinical services and …

This chapter provides a critical review of the contemporary state of the field of bioethics
within the Western, English-language context. It outlines the main current areas of activity in …

Background Human genomics research is growing rapidly. More effective methods are
required for co-design and involving people, especially those sub-populations which are …