Tracking the development of the Genetic Counsellor role In 2020 the Wellcome Connecting Science Engagement and Society team explored the … More
Category: Ethical issues of genetics
Global perspectives on health, research and trustworthiness
Trust is critical to virtually everything we do in life, wherever in the world we are. We trust that when … More
I:DNA – an immersive exploration into the view of people living with genetic conditions
This multi-sensory art installation moves online In 2019, the Imagining Futures research by Prof Felicity Boardman, a professor in medicine … More
So Much More Than Just a Test, the introductory film to the Voices of Genetic Counsellors short documentary series, is an official selection for the 2020 Imagine Science Film Festival
Placing the role of Genetic Counsellors in the Spotlight We are proud to share that So Much More Than Just … More
Wellcome Genome Campus Society and Ethics Research Lead on a UK Citizens Assembly.
Wellcome Genome Campus Society and Ethics lead of a UK citizens assembly for gene-editing
Future of Genomic Research at Risk Without Greater Public Trust in How Genetic Data is Shared, Survey Finds.
The largest ever survey on global public attitudes towards genomic research and data sharing suggests that work is needed to … More
Genetic Counsellors: Enabling Patients to Fostering Resilience
Turning patient stories into hope and resilience One of the main reasons people seek a genetic test is to establish … More
Addressing inclusion in genetic counselling
For patients receiving genetic counselling there is often a mixture of emotions and anxieties involved. The very purpose of this service is to help people make sense of who they are, what inherited risks they might face, or even come to terms with a difficult diagnosis.
“Informed Consent” to edit embryos: what consent?
Richard Milne and Anna Middleton from the Society and Ethics Research group provide a commentary on informed consent and its … More
Genetopia – The compelling stories and tensions behind genetic testing
What springs to mind when thinking about genetic testing? You would expect the answer to be something about families, heredity, … More
Human Embryo Editing: edging ever closer
“As scientific knowledge advances and societal views evolve, the clinical use of germline editing should be revisited on a regular … More
Articulating the contract between science and people: DNA data sharing
A new deal on data: are you with us? For most of us it is hard to unpick the various … More
Editing embryos – Could you? Would you? Should you? Views from Genetic Counsellors
Genetic counsellors sit on the front line of genomics – translating (literally) the science for people who are trying to … More
Legal duty to share genetic information goes to trial
By Vicky Chico and Anna Middleton Following on from our previous blog on the legal duty to share genetic information, … More
Legal duty to share genetic information? ABC v St George’s Healthcare NHS Trust
Guest blog by Dr Vicky Chico, Legal Consultant, Society and Ethics Research Group, Wellcome Genome Campus, Cambridge Yesterday myself and … More
Your Genome, Your Research Agenda
On 30th September 2016 we were part of a very exciting event to determine, from a patient perspective, what the … More
DNA and Big Data: be part of the conversation
The Global Alliance for Genomics and Health (GA4GH) and the Wellcome Genome Campus have launched a new project to explore … More
Largest survey of public attitudes shows perceived value of genomic data
We made it! Finally, the main set of results from our survey (opposite) have been published. Below is the press … More
“If you know it, I’d like to know it too” – involving participants in genomics research
This blog post is based on the talk I gave at the launch of the Nuffield Council of Bioethic’s report … More
Leading questions
“Why do we itch – what’s occurring in our bodies?” and “Do animals have belly buttons?” These are just a … More
Survey talk – guest blog by Dr Jenny Cham
This past Friday on the Genome Campus, Dr Anna Middleton of the Wellcome Trust Sanger Institute gave an interesting seminar … More
Attention The Times: Prince William’s DNA is not a toy
An ancestor of Prince William’s from the 19th century was half Indian, according to The Times. This claim is based … More
Dame Sally Davies, Chief Medical Officer comments on Genomethics
To date, 3000 people have completed our online survey exploring various ethical implications arising from the application of genome technology. … More
‘No choice for you’ according to the ACMG
The American College of Medical Genetics (ACMG) has recently published recommendations for reporting incidental findings (IFs) in clinical exome and … More
DNA Sequencing – Can You Handle the Truth?
Having your genes studied is cheap (about $99) and easy (just spit here). And according to 23andMe (one of the … More
Channel 4 news article on Genomethics survey
Channel 4 news ran a newspiece in 2014 on our research all about what people want to know from their … More
Should patients know that they are research subjects?
Accidental Research Subjects I read an article In the San Francisco Chronicle this week that raised a prickly question, namely … More