Twitter Beğeni Hilesi

cashforkidsgive.co.uk/campaign/cash-…

Reminder of survey link - please share your experiences living with a rare disease(s) across Ireland, RoI and NI. Help us gather evidence to advocate for improvements for you. …althandagriscience.fra1.qualtrics.com/jfe/form/SV_8t…. #RareDiseaseNI

This book was one of the reasons I decided to do medicine & when I first fell in love with genetics 🧬. This copy was signed for my dad. Matt Ridley

.Monica Hsiung Wojcik was asked and wanted to know - Is genome sequencing just a fancy exome? Or should we pursue it for patients with rare disease who remain undiagnosed after clinical exome sequencing? So she and Gabrielle Lemire investigated… 1/

Opportunities for #carers of people with a #RareDisease to help design support tool(s) #RareDiseaseNI 👇🏻RAiN Cambridge Rare Disease Network (CamRARE) Fiona McLaughlin Christine Collins MBE Shane McKee Cmckenna Public Health Agency Beacon for Rare Diseases Rare Diseases Ireland RARE Ireland Office for Rare Conditions Glasgow Medics4RareDiseases

Delighted to be shortlisted for the AHAwards💙 award for service improvement. It is an honour to work alongside so many talented allied health professionals & healthcare scientists. Eamonn Holmes OBE here we come 🥂

Thank you AHAwards💙 & Eamonn Holmes OBE for a great night celebrating allied health professionals & lab scientists.

Northern Ireland Rare Disease Partnership & members of Magee University Rare Disease Student Society. #Rareawareness #1in17 #rarediseaseawareness

👇This is a super resource on selecting genetic tests & approaches in paediatric clinics 🧬developed by RCPCH Genomics Working Group in collab & partnership with colleagues Genomics Education. Plus downloadable pdf. Check it out! Cmckenna, Eleanor Dhanda & Melody Redman

Are you (or are you about to be) a Consultant in #ClinicalGenetics who would love to come and work in #Belfast? We have an opening! Great place, great staff, great music, great craic, but it's our patients and families who make the job so rewarding. jobs.hscni.net/Job/32870/7182…

Two Funded PhD studentships with our team - applications closing tomorrow!!! #RenalResearchNI #RareDiseaseNI QUB Public Health QUB MHLS Faculty findaphd.com/phds/project/i…. findaphd.com/phds/project/m…

Paediatricians! Register now for the RCPCH Genomics in Paediatrics in-person Study Day, in collab with Genomics Education This event programme incls the fundamentals of genomics, practicalities of testing, genomics education & a future look 🧬✨ 👇👇👇 rcpch.ac.uk/news-events/ev…

PowerPoint presenter mode + Microsoft Teams 😩

This is so cool - a remarkably frequent mutation in a non-protein-coding RNA gene, which causes around one in every 200 currently undiagnosed cases of developmental delay around the world (including 8 Australian families so far!). A couple of thoughts (1/3)

Today staff across the Trust are taking part in an encompass Go-Live Readiness Assessment to update on progress. Dr. Shane McKee, encompass Deputy Chief Clinical Information Officer, shares his excitement for the project and the benefits it offers service users. #encompassni

The book AI recommended for me, about AI 😎 #AIinMedicine

Our daughters’ DNA is helping other families bbc.com/news/articles/… Well done Shane McKee Great to see positive coverage of the department & Genomics England 100kGP. 🧬