
Professional journeys into genomics: Delving deeper
In the second part of our blog series for this year’s Genomics Conversation, our group of NHS healthcare professionals explains the power of genomics education in their practice

Professional journeys into genomics: Taking the first step
In this blog series for the 2024 Genomics Conversation, NHS healthcare professionals from medicine, nursing, pharmacy and midwifery share their inspiring genomics journeys

Genomics on the front line: GLHs and GMSAs
The scientific and clinical arms of the Genomic Medicine Service have made a huge contribution to the journey of genomics in the NHS

Genomic technologies: where are we now?
Our ambitions for our patients are only as good as our methodologies. We take a look at the technology that underpins the revolution

How far we’ve come, how far we’ll go: 10 years of the GEP
The Genomics Education Programme (GEP) began in the summer of 2014 with big dreams, a small team, and a lot of work to do

Career tips for clinical geneticists: a conversation with Dr Alex Murray and Dr Rhian Thomas
Dr Alex Murray and Dr Rhian Thomas – GTAC clinical genetics professional lead and education specialist, respectively – offer advice for early-career practitioners

New bowel cancer screening launches for Lynch syndrome patients
Thousands of people in England at risk of bowel cancer will benefit from world-first preventative programme

Three career tips for genetic counsellors: a conversation with Dr Laura Boyes
Dr Laura Boyes, consultant genetic counsellor and GTAC genomic counselling professional lead, shares advice for new and aspiring practitioners

Rethinking insurance and genomic testing: the evidence
The DHSC's recent call for evidence received 57 responses from organisations and individuals, who voiced concerns and offered suggestions for future amendments

Post-stroke and mini-stroke prescribing: NICE calls for comments
NICE is inviting comments around genomic testing for post-stroke prescriptions of clopidogrel ahead of its treatment-influencing July publication

New Lynch syndrome registry ‘game-changing’ for patients
England’s latest Lynch syndrome patient database may transform the disease’s detection and monitoring, becoming a blueprint for other genomic diseases

Mind the gap: Five initiatives to boost genomic data diversity
White-ancestry genomes dominate genomic projects; here are five notable biobanks recruiting from under-represented populations to bridge the genomic gap