Featured news
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Empowering nurses and midwives: Spinal Muscular Atrophy session
Join us on 30 September for an online webinar which will give you the tools to improve care for people with Spinal Muscular Atrophy, also known as SMA.
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Norfolk service identifying people at highest risk of cardiovascular disease shortlisted for patient care award
Our Familial Hypercholesterolaemia (FH) service, based at NNUH, has been shortlisted for a Picker Experience Network Award, in the category of 'Commissioning for Better Experience of Care'.
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Baby's ALD gene discovery through genome sequencing leads to diagnosis for older brother
A baby whose rare genetic change was picked up by a major research study has helped diagnose the same change in his older brother - allowing vital early monitoring of both for a potentially life-limiting rare condition.
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"Participating in gut research found my womb cancer early"
Victoria, a member of our patient panel, shares the story of how taking part in IBD research saved her from womb cancer.
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Over 17,000 babies have been recruited into the Generation study in our region
Across the East region (East Midlands and East of England), participating hospital Trusts have recruited over 17,000 babies and families into the Generation Study as of this month.
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We're supporting BBC Radio Derby's Inherited Cancer Campaign
BBC Radio Derby are running their 'It Starts With You' awareness campaign focused on hereditary and genetic cancers, encouraging families to discuss medical histories, understand risks regarding mutations like BRCA and Lynch syndrome.
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Empowering nurses and midwives: Spinal Muscular Atrophy session
Join us on 30 September for an online webinar which will give you the tools to improve care for people with Spinal Muscular Atrophy, also known as SMA.
Norfolk service identifying people at highest risk of cardiovascular disease shortlisted for patient care award
Our Familial Hypercholesterolaemia (FH) service, based at NNUH, has been shortlisted for a Picker Experience Network Award, in the category of 'Commissioning for Better Experience of Care'.
Baby's ALD gene discovery through genome sequencing leads to diagnosis for older brother
A baby whose rare genetic change was picked up by a major research study has helped diagnose the same change in his older brother - allowing vital early monitoring of both for a potentially life-limiting rare condition.
"Participating in gut research found my womb cancer early"
Victoria, a member of our patient panel, shares the story of how taking part in IBD research saved her from womb cancer.
Over 17,000 babies have been recruited into the Generation study in our region
Across the East region (East Midlands and East of England), participating hospital Trusts have recruited over 17,000 babies and families into the Generation Study as of this month.
We're supporting BBC Radio Derby's Inherited Cancer Campaign
BBC Radio Derby are running their 'It Starts With You' awareness campaign focused on hereditary and genetic cancers, encouraging families to discuss medical histories, understand risks regarding mutations like BRCA and Lynch syndrome.
RareSummit 2026: Where RARE connections come to life
CamRARE’s RAREsummit is back for 2026 and this year is a hybrid event, providing you with the option to attend in person at Hinxton Hall Conference Centre, Cambridge or online on 7th October 2026.
Black women's experience of prenatal testing in England
Join the national Midwives in Genetics and Genomics (MiGGs) meeting this September to hear about 'Black women's experiences of prenatal testing in England'.
ctDNA for Cancer of Unknown Primary is coming! Webinar on 7 July 2026
From 13 July 2026, patients with CUP can be referred for circulating tumour DNA (ctDNA) testing via the NHS Genomic Test Directory.
East leads on equitable access to genomic testing for cancer patients
By finding a way to collect samples without the need for specialist technologies, we're helping more patient to benefit from genomic testing.
New study shows that broader DNA testing is needed to diagnose complex eye conditions
A new study by University of Leicester experts shows that complex eye conditions can be diagnosed much earlier through genome-wide testing.
Webinar: Empowering nurses and midwives - giving you the tools to improve the care of people with Down syndrome
Our national Genomics Lunch & Learn is series is back.
Upcoming Genomics Community of Practice sessions
Here at East Genomics we support 16 Genomics Communities of Practice across cancers and rare and inherited conditions. In 2025 we ran over 120 sessions attended by over 1,500 healthcare staff across our region. Our series continues in 2026...
DNA breakthrough ends 30-year mystery for family with life-threatening heart condition
A family from Nottingham have finally received the correct diagnosis for a dangerous inherited heart condition - after more than three decades of uncertainty - thanks to advances in genetic testing.
Lifesaving genetic stroke test launched in minor stroke clinic at Nottingham University Hospitals
Nottingham University Hospitals (NUH) has become one of a handful of hospitals across the UK to implement a rapid genetic test which could dramatically improve outcomes for thousands of stroke patients in the future.
Feedback sought for WGS in Cancer evaluation
In collaboration with the Cancer Alliances for the East Midlands and East of England we are conducting a formal service evaluation (audit) of the Cancer Whole Genome Sequencing (WGS) pathway.
International Day of the Midwife
Every year on 5 May we celebrate the incredible work of midwives, who play a vital role in supporting families through one of life’s most important journeys.
HNF1B support day, 4 July 2026
The University of Exeter Medical School are hosting an online HNF1B support day in July for patients, families, carers and clinicians.
East of England Cancer Alliance launch first in series of VR training videos
The East of England Regional Genomic Practitioner Service (RGPS) have launched a VR training module called 'Genomics – Mainstream Testing for Lynch Syndrome'.
Reflections on a career in NHS genetics
As she retires, Kim Oakhill, our inherited cancer lead, looks back on a career spanning almost 30 years.