Rare Metabolic Diseases: Advancing Understanding, Improving Outcomes
Dr Jess Buxton attended PET's most recent event, which discussed how to improve diagnosis, treatment and support for people affected by rare and inherited metabolic diseases...
PET Adviser
Dr Jess Buxton is an Adviser to PET (the Progress Educational Trust), and a Volunteer Writer at its flagship publication BioNews. Jess was previously Genetics Editor of BioNews, and together with Professors Kirsty Horsey and Marcus Pembrey, she developed the BioNews writing scheme to provide practical science writing training and experience for PhD students. Jess has a PhD in Human Genetics, awarded for her work on the genetic condition myotonic dystrophy, and carried out postdoctoral research on the genetics of human disease at Imperial College London and University College London. Following her last academic role as a senior lecturer at Kingston University, Jess is now working in medical communications at Aspire Scientific.
Dr Jess Buxton attended PET's most recent event, which discussed how to improve diagnosis, treatment and support for people affected by rare and inherited metabolic diseases...
This latest PET event explored the importance of representing diversity in health research datasets. This is the second in a series of three events exploring large-scale biomedical databases and research resources...
The latest PET event focused on access to and funding for preimplantation genetic testing, specifically in relation to monogenic conditions and chromosomal structural rearrangements...
The Progress Educational Trust, in partnership with the Scottish Government, brought together a group of experts to cut through the hype and jargon and explain the latest developments in genetics/genomics in the context of assisted conception...
Genomics England's Newborn Genomes Programme is a pilot study exploring the potential benefits, practicalities, and challenges of offering whole genome sequencing (WGS) for all newborn babies...
A new pilot study embedded in the NHS will explore whether and how to offer whole genome sequencing to newborn babies...
The past few years have seen a huge increase in the identification of rare and common genetic variants associated with disease, advances made possible through ever cheaper and faster genome sequencing technologies...
by Professor Marcus Pembrey and 1 others
Professor Marcus Pembrey and Dr Jess Buxton reflect on 20 years of BioNews and its unrivalled coverage of scientific, legal and ethical developments in the fields of human genetics and assisted conception...
Being an unashamed enthusiast for genetics and genomics research and its potential to improve human health, I was delighted when an email announcing the unveiling of the Personal Genome Project (PGP) UK pilot study arrived in my inbox...
We are already into the second month of 2018, so if you made New Year's resolutions then the chances are that, like me, you've long ditched them — especially any regarding your health. It seems that changing old habits is hard, even those that we know w
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