Registered Genetic Counsellor @GenePeopleUK. working in the voluntary sector to support the Genetic community. @theAGNC EDI Sub-committee member.

Sheffield UK
Joined November 2015
Emily Clarke (she/her) 🧬🦮 retweeted
What does a clinical scientist do? In our latest blog, Nicola Marchbank, Clinical Scientist on the Generation Study, explains more about the vital role clinical scientists play in genomic testing, linked below. ow.ly/Won450ZZcCH
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Emily Clarke (she/her) 🧬🦮 retweeted
The Unique team have pulled out their denim for @jeansforgenes Week to help change the lives of the 1 in 25 Children in the UK affected by a genetic condition. Jeans for Genes UK are an incredible organisation so get on your jeans and help spread the word!
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Emily Clarke (she/her) 🧬🦮 retweeted
'Opening Doors’ is a suicide prevention learning resource to support NHS staff on how to recognise signs of suicidal distress in themselves and others. The training also signposts to the help that is available. ➡️learninghub.nhs.uk/catalogue… #WorldSuicidePreventionDay
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Emily Clarke (she/her) 🧬🦮 retweeted
Explore our free on-demand PPIE and EDI courses, open to all researchers Involving patients and the public boosts research quality and ethics. Engaging them in decision-making leads to innovative solutions and improved outcomes. 🔗 buff.ly/1qK8d2E #NIHR20 #EDI #PPIE
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Emily Clarke (she/her) 🧬🦮 retweeted
Today is Duchenne Muscular Dystrophy (DMD) Awareness Day! Did you know: Around 2,500 people are living with DMD in the UK, and 1 in 3,500 live male births are affected worldwide. Learn more at @DuchenneUK's website: duchenneuk.org
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Emily Clarke (she/her) 🧬🦮 retweeted
Applications are now open for the EURORDIS Open Academy x ERDERA Schools! 🎓 Build the skills and networks to engage with researchers, regulators & policymakers 📍 Barcelona, 7-10 June 2027 ⏰ Apply by 16 October 2026 🔗 Learn more: loom.ly/F3Ka2j8 #RareDiseases
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Emily Clarke (she/her) 🧬🦮 retweeted
Are you searching for support, information or connections in the rare disease community? Raremap helps you find charities, patient organisations and more: raremap.co.uk/
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Emily Clarke (she/her) 🧬🦮 retweeted
💜 Your experience can inspire change. We’re inviting individuals and families affected by rare genetic neurodevelopmental disorders to share their stories 🧬 Help raise awareness, build community, and inspire others. Share your story: bit.ly/ShareYourRareStory
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Emily Clarke (she/her) 🧬🦮 retweeted
#Genomic #newborn #screening is expanding worldwide, but policy decisions need rigorous evidence of clinical utility. bit.ly/4xJO9t0 #NBS #C-GUIDE #Clinicalutility
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Emily Clarke (she/her) 🧬🦮 retweeted
Do you find navigating the complicated benefits system difficult? @renaissance_uk are hosting several webinars that focus to help. You can register for each of these events direct from Renaissance Legal's webite here: renaissancelegal.co.uk/event…
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Emily Clarke (she/her) 🧬🦮 retweeted
#GeneticCounseling is the strongest predictor of genetic testing completion in Stargardt disease, while racial and socioeconomic disparities continue to limit access & clinical trial participation. bit.ly/4h5jZM2 #GIMO #ABCA4 #ClinicalTrialRecruitment #HealthDisparities
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Emily Clarke (she/her) 🧬🦮 retweeted
Raremap is a fantastic new resource designed to make it easier to discover, find and connect with others in the rare condition ecosystem.​ Find out more in the post below 👇
The rare disease landscape can be complex to navigate – that's why we've collaborated with @lifearc1 to launch Raremap. It's a searchable directory of rare disease organisations so you can find out who does what and how to connect. Visit Raremap now: tinyurl.com/3atbumrt
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Emily Clarke (she/her) 🧬🦮 retweeted
Could you help improve genomic diagnostic reports and the way genomic diagnoses are communicated to families? Take part in a short survey to see what could be improved: forms.cloud.microsoft/pages/…
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Emily Clarke (she/her) 🧬🦮 retweeted
While pride month may be ending the AGNC EDI subcommittee have been reflecting on how we can show up for our LGBTQIA+ colleagues and patients through out the year. Please see our statement in support of Transgender, Gender Diverse and Sex Diverse Patients. #pridemonth
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Emily Clarke (she/her) 🧬🦮 retweeted
In our latest participant story, Marnie's family shares their experience of receiving a "no condition suspected" result, and why taking part in the Generation Study was still an important part of their newborn's care. Read Marnie's story: genomicsengland.co.uk/patien…
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Emily Clarke (she/her) 🧬🦮 retweeted
There are 13 different types of Ehlers-Danlos syndrome (EDS), each with distinct features and risks. In this video, Dr. Clair Francomano, medical geneticist, clearly explains the key differences between EDS types, such as classical EDS, vascular EDS, and kyphoscoliotic EDS. Watch now: youtu.be/w62qVQvznYM?si=6IAV…
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Emily Clarke (she/her) 🧬🦮 retweeted
Discover how Dr. Jackie Cook and Dr. Frances Elmslie are pushing to streamline genomics adoption in the NHS. The article covers the push for faster rare disease diagnosis, the need for greater clinical literacy, and the role of AI and new technologies in this exciting field. rarerevolutionmagazine.com/r… #GenomicsInTheNHS #RareDiseaseUK #NHSGenomics #AIinHealthcare #TuberousSclerosis #DiagnosticOdyssey
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Emily Clarke (she/her) 🧬🦮 retweeted
What do we mean by de-identified data? Georgia Chan, Senior Data Wrangler at Genomics England, joins our latest Genomics 101 episode to explain. These bitesize podcast episodes explain genomics terms. Listen on your favourite podcast app or on our website: ow.ly/ukzu50YvH5Z
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Emily Clarke (she/her) 🧬🦮 retweeted
🚨Calling all Nurses and Healthcare Practitioners 🚨 On Tuesday 24th March, join Diogo Gomes ANP for a rapid introduction to genetic haemochromatosis, it's symptoms, treatment and ongoing care. haemochromatosis.org.uk/Even…
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