Lunch and Learn: Think Patient Care, Think Genomics
Online , United KingdomSession One: Cystic Fibrosis screening and diagnosis Join us for our first edition of Lunch and learn, a session for nurses and midwives focused on Cystic Fibrosis. Speakers and topics covered: Carrier testing Cathryn Moss, Principle Genetic Counsellor, St George’s Hospital This session will offer nurses and midwives a practical guide to Cystic Fibrosis […]
RCPCH Conference 2022
We are thrilled to be returning to a face-to-face conference this year. Taking place in Liverpool from 28 to 30 June, this is a great opportunity to network with colleagues once again, hear from leading voices and catch up on the latest innovations in child health at a wide range of specialty sessions. As the […]
Facing up to the genomic gap: Tackling equality and diversity in genomics
Online Webinar , United KingdomAbout this event This webinar is part of the popular Genetics of webinar series and will discuss the challenge of equality and diversity in genomic research and clinical settings and strategies to address this. Genomic research has traditionally been focused on Caucasian populations, which leads to inherent biases in genomic findings translated into clinical research. Underrepresentation of other populations in genomic […]
Lunch and Learn: Think Patient Care, Think Genomics
Online , United KingdomSession Two: Monogenic Diabetes in pregnancy Join us for our second edition of Lunch and learn, a session for nurses and midwives focused on Monogenic Diabetes. Monogenic diabetes is a rare form of diabetes caused by a mutation in a single gene and can often be misdiagnosed as type 1 diabetes. Accurate diagnosis and […]
Clinical Genomics Service Specification Consultation Webinar
Online , United KingdomNHS England are currently seeking feedback on the way clinical genomics services are delivered in England. The public consultation is open from 1 September until midnight on 30 September. Click here to view the consultation documents and access the online questionnaire to provide feedback. Join an information webinar to find out more NHS England is […]
SE Genomics Autumn Festival
via Microsoft Teams , United KingdomWe are keen to promote our second upcoming virtual event - SE Genomics Autumn Festival. Speakers will provide an overview of how the latest developments in genomics are impacting cancer care and share their expertise on different cancer genomics pathways and the tests available. Register now via Eventbrite and please share with your networks as […]
“Everything you want to know about genomics but are afraid to ask”
Online Webinar , United KingdomThe NHS North Thames GLH and NHS South East GLH are delighted to organise and co-host this Bayer sponsored educational meeting and welcome healthcare professional attendees from our regional cancer clinical teams. With the aim to explore the benefits and challenges of mainstreaming genomic profiling and precision oncology pathways in the management of patients with […]
Lunch and Learn: Think Patient Care, Think Genomics
Online , United KingdomSession Three: Lynch Syndrome Join us for our third edition of Lunch and learn, a series of webinars for nurses and midwives to gain insight into how genomic testing is used across different areas of healthcare. Professionals will share their expertise of genomic tests available for patients through different patient pathways. Speakers and topics […]
Whole Genome Sequencing drop-in session
Online , United KingdomWhole Genome Sequencing Drop In Session: Tuesday 11th October, 14:30-15:30 Are you a clinician looking to find out more about Whole Genome Sequencing (WGS)? Then this drop-in session is for you! During the session you will find out more information on this new testing, how it can be used for your patients and have the […]
Virtual Prenatal Genetics Short Course 2022
Online , United KingdomThis skills based course is designed to give midwives and other health professionals working in a prenatal testing setting tools to help them to enable patients to access appropriate onwards referral. These include obtaining a family history, identify high risk family histories, approaches to genetic testing, consent taking and counselling skills associated with providing information […]