Let’s Talk Genomics & Midwifery

The understanding and development of genetics and genomics is accelerating. 24-28 June is Genomics conversation week and the regional Lead…

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Genomics News – June Edition Now Live

The second 2024 issue of our Genomics News newsletter for June/Summer is now live! You can find links to genomics…

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Pharmacogenomics in Focus

Read all about the latest developments in Pharmacogenomics here, along with opportunities for e-learning and development.

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Developments for Patients with Inherited Cardiac Conditions

Julie Goodfellow, Lead Nurse for the NEY GMS (recently retired), has led a project within the region to review equity…

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Genomics… it’s in the Blood (and Bone Marrow)!

The NEY Podcast team recently interviewed Dr. Polly Talley and found out all about the important role of genomics for…

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NEY GLH at the forefront of research to help validate pathogenicity of variants in Mitochondrial Disease

Making a definitive genetic cause is important to families as it means that they can find out what is wrong…

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New testing pilot to help thousands more lung cancer patients receive earlier treatment

The North East & Yorkshire and North Thames Genomic Medicine Services (GMS) are leading a national pilot to integrate circulating…

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Genomics News – March Edition Now Live

The first 2024 issue for our Genomics News newsletter for March/Spring is now live! You can find links to genomics…

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Genomics in Pharmacy Practice – Meet Neil Masters

Meet Neil Masters, Highly Specialist Advanced Oncology Pharmacist at Sheffield Teaching Hospitals, and find out more about his professional development,…

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Patient Perspectives on Genomics

Angela Watt, a member of our Patient and Community Forum – a group of patients and members of the public…

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The Uncommonly Common Nature of Rare Disease

This year, Rare Disease Day fell on the rarest of days – 29th of February. A rather appropriate convergence of…

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Latest on Lynch

As Lynch Syndrome Awareness Day approaches on the 22 March, we reflect on the great progress made in Lynch syndrome…

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