Trust is critical to virtually everything we do in life, wherever in the world we are. We trust that when … More
Genomics, Public Trust and Engagement “Genomics” – a scientific term previously considered most relevant to scientific research, is now a … More
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 lead of a UK citizens assembly for gene-editing
Turning patient stories into hope and resilience One of the main reasons people seek a genetic test is to establish … More
The art of caring in clinical practice For genetic counsellors it’s not simply enough to impart scientific knowledge, or to … More
The Music of Life: What is a Gene? short-film selected to appear in the 2020 Raw Science Film Festival (Los Angeles, California).
Receiving a confirmed diagnosis of a genetic condition can have a ripple effect, potentially affecting multiple generations of a single family.
Genomethics discusses how genetic counsellors can help their colleagues learn about genetics
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.
Genomic data is being produced in ever greater quantities, whether within our health services, in academic research projects, or by … More
A major new report based on a public dialogue around genomic medicine was launched last week. A Public Dialogue on … More
Are we heading towards a future where genetic conditions are ‘screened-out’? Who gets to decide which conditions are screened for? … More
The Topol Review, led by cardiologist, geneticist, and digital medicine researcher Dr Eric Topol and facilitated by Health Education England, … More
“As scientific knowledge advances and societal views evolve, the clinical use of germline editing should be revisited on a regular … More
On 30th September 2016 we were part of a very exciting event to determine, from a patient perspective, what the … More
How easy is it to strike up a conversation about genomics? Geno-what? Does the average person on the street know … More
We made it! Finally, the main set of results from our survey (opposite) have been published. Below is the press … More
This blog post is based on the talk I gave at the launch of the Nuffield Council of Bioethic’s report … More
The genomic era is upon us. From the Government’s pledge to sequence 100,000 genomes to the launch of 23andMe, a … More
This past Friday on the Genome Campus, Dr Anna Middleton of the Wellcome Trust Sanger Institute gave an interesting seminar … More
To date, 3000 people have completed our online survey exploring various ethical implications arising from the application of genome technology. … More
A paper published in the Lancet on 28th Feb showed that there were shared genetic causes behind autism spectrum disorder, … More