Genetics Archives

Genetics

Podcasts

Angelman Syndrome – Gene Therapy | Tuberous sclerosis – Information for GPs

This special podcast features two episodes on the the future of genetics and gene therapy & the clinical manifestations of Tuberous Sclerosis Complex (TSC). See the valuable resources recommended by our experts for your clinical practice.

Expert/s: Prof David J. Segal, Dr Clara Chung

Genetics

Podcasts

Rare disease management in general practice – New resources to support GPs and their patients

Dr Elizabeth Palmer discusses rare disease and managing common and individual issues that make them difficult to identify. GP resources included for your clinical practice...

Expert/s: Dr Elizabeth Palmer

Genetics

Clinical Articles

New recommendations to improve diagnosis of rare diseases

Collectively, rare diseases are more common than diabetes. The first-ever national recommendations launched in March, outlining how GPs can help patients get timely diagnosis and effective support....

Expert/s: Lynnette Hoffman

Genetics

Podcasts

Reproductive screening – Your questions answered

Dr Samantha Sundercombe answers your most pressing questions regarding reproductive screening. These were compiled by GPs and health professionals around Australia.

Expert/s: Dr Samantha Sundercombe

Genetics

Clinical Articles

Eggs from men, sperm from women: how stem cell science may change how we reproduce

It may soon be possible to coax human skin cells into becoming functional eggs and sperm using a technique known as “in vitro gametogenesis”.

Expert/s: Julian Koplin, A/Prof Neera Bhatia

Genetics

Clinical Articles

The ‘weird’ male Y chromosome has finally been fully sequenced. Can we now understand how it works, and how it evolved?

The Y chromosome is a never-ending source of fascination (particularly to men) because it bears genes that determine maleness and make sperm. It’s also small and seriously weird; it carries few genes and is full of junk DNA that makes it horrendous to sequence.

Expert/s: Prof Jenny Graves

Genetics

Clinical Articles

At-home DNA tests just aren’t that reliable

The field of genomic science is rapidly advancing, with commercial genetic tests becoming affordable and popular

Genetics

Clinical Articles

Humans are 8% virus – how the ancient viral DNA in your genome plays a role in human disease and development

Remnants of ancient viral pandemics in the form of viral DNA sequences embedded in our genomes are still active in healthy people, according to new research my colleagues and I recently published.

Expert/s: Healthed

Genetics, Women's health

Podcasts

Clinical genetic services for GPs

The range of services provided in a clinical genetics centre, the patients who might benefit most from clinical genetic screening, the limitations of genetic screening

Expert/s: Dr Janan Karatas, A/Prof David Coman

Genetics, Neurology

Clinical Articles

Fetal brains at risk

The first 1000 days are the most important for brain development in the fetus and newborn. And adequate iodine intake and thyroid function are vital to this process.

Expert/s: Dr Linda Calabresi

Diagnostics, Genetics

Podcasts

Rare disease management in general practice

Rare diseases together are not rare! Collectively they affect 1:12 Australians

Expert/s: Dr Elizabeth Palmer

Genetics

Podcasts

Epigenetic testing

The reality of epigenetic tests in general practice may not be that far away

Expert/s: Prof Jeffrey Craig

Genetics

Angelman Syndrome – Gene Therapy | Tuberous sclerosis – Information for GPs

This special podcast features two episodes on the the future of genetics and gene therapy & the clinical manifestations of Tuberous Sclerosis Complex (TSC). See the valuable resources recommended by our experts for your clinical practice.

Rare disease management in general practice – New resources to support GPs and their patients

Dr Elizabeth Palmer discusses rare disease and managing common and individual issues that make them difficult to identify. GP resources included for your clinical practice...

New recommendations to improve diagnosis of rare diseases

Collectively, rare diseases are more common than diabetes. The first-ever national recommendations launched in March, outlining how GPs can help patients get timely diagnosis and effective support....

Reproductive screening – Your questions answered

Dr Samantha Sundercombe answers your most pressing questions regarding reproductive screening. These were compiled by GPs and health professionals around Australia.

Eggs from men, sperm from women: how stem cell science may change how we reproduce

It may soon be possible to coax human skin cells into becoming functional eggs and sperm using a technique known as “in vitro gametogenesis”.

The ‘weird’ male Y chromosome has finally been fully sequenced. Can we now understand how it works, and how it evolved?

The Y chromosome is a never-ending source of fascination (particularly to men) because it bears genes that determine maleness and make sperm. It’s also small and seriously weird; it carries few genes and is full of junk DNA that makes it horrendous to sequence.

At-home DNA tests just aren’t that reliable

The field of genomic science is rapidly advancing, with commercial genetic tests becoming affordable and popular

Humans are 8% virus – how the ancient viral DNA in your genome plays a role in human disease and development

Remnants of ancient viral pandemics in the form of viral DNA sequences embedded in our genomes are still active in healthy people, according to new research my colleagues and I recently published.

Clinical genetic services for GPs

The range of services provided in a clinical genetics centre, the patients who might benefit most from clinical genetic screening, the limitations of genetic screening

Fetal brains at risk

The first 1000 days are the most important for brain development in the fetus and newborn. And adequate iodine intake and thyroid function are vital to this process.

Rare disease management in general practice

Rare diseases together are not rare! Collectively they affect 1:12 Australians

Epigenetic testing

The reality of epigenetic tests in general practice may not be that far away

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Genetics

This special podcast features two episodes on the the future of genetics and gene therapy & the clinical manifestations of Tuberous Sclerosis Complex (TSC). See the valuable resources recommended by our experts for your clinical practice.

Dr Elizabeth Palmer discusses rare disease and managing common and individual issues that make them difficult to identify. GP resources included for your clinical practice...

Collectively, rare diseases are more common than diabetes. The first-ever national recommendations launched in March, outlining how GPs can help patients get timely diagnosis and effective support....

Dr Samantha Sundercombe answers your most pressing questions regarding reproductive screening. These were compiled by GPs and health professionals around Australia.

It may soon be possible to coax human skin cells into becoming functional eggs and sperm using a technique known as “in vitro gametogenesis”.

The Y chromosome is a never-ending source of fascination (particularly to men) because it bears genes that determine maleness and make sperm. It’s also small and seriously weird; it carries few genes and is full of junk DNA that makes it horrendous to sequence.

The field of genomic science is rapidly advancing, with commercial genetic tests becoming affordable and popular

Remnants of ancient viral pandemics in the form of viral DNA sequences embedded in our genomes are still active in healthy people, according to new research my colleagues and I recently published.

The range of services provided in a clinical genetics centre, the patients who might benefit most from clinical genetic screening, the limitations of genetic screening

The first 1000 days are the most important for brain development in the fetus and newborn. And adequate iodine intake and thyroid function are vital to this process.

Rare diseases together are not rare! Collectively they affect 1:12 Australians

The reality of epigenetic tests in general practice may not be that far away

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