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The MRCC aims to improve the lives of people with rare conditions, across all ages, by providing a platform for the coordination of clinical care. research, education and engagement. Website:
mrcc.org.uk 
Researching somatic evolution at the University of Cambridge and Wellcome Sanger Institute. Also a scientific illustrator.
The FT’s team of reporters, statisticians, illustrators, cartographers, designers, and developers work with colleagues across our newsrooms, using graphics and data to find, investigate and explain stories.
ft.com/visual-and-data-jou…
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Publishing reviews and commentaries across the fields of genetics and genomics. Part of Springer Nature and Nature Portfolio.
nature.com/nrg/
Happy European human geneticist enjoying life in the United Kingdom. Love everything genomics, even married a genomicist..;)
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A national collaboration supporting the translation of genomic research into clinical practice.
chair of stanford dept of medicine
author of the genome odyssey
founder of biotechnology companies
Prof Genomic Medicine, UoOxford
Director Centre for Personalised Medicine
cpm.ox.ac.uk
Interested in how we bring together ethics, social, molecular and clinical sciences to make sense of genomics.
@annekeluc at the other place
Co-Founder and Chief Scientist | Venture Partner | Professor | Mentor | Proud mom of 3 ✨
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Functional Genomics, Rare Diseases and Cardiovascular Disease @ Exeter University
ORCID 0000-0001-8074-6299
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Endocrinologist. Physican scientist. Director of MRC Metabolic Diseases Unit, University of Cambridge. Expressing my own opinions here, not my employers
One of the world’s largest community-based genetics studies, aiming to improve health among Pakistani & Bangladeshi people 🧬
Based at Queen Mary University London.
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Professor of Epigenomics at the University of Exeter. Director of the UK Functional Genomics Initiative.
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Consultant Clinical Scientist in Genomics & Rare Disease Lead for NHS North East Yorkshire GLH. ACGS & CanVIG variant classification & HBOC best practice guidelines author.
linkedin.com/in/miranda-durkie
Group Leader
The Genome Function Laboratory
The Francis Crick Institute, London
We are a think tank focused on the policy challenges of implementing genomics and related technologies to improve population health
The UCSC Genome Browser is a public, freely available, open-source web-based graphical viewer for displaying genome sequences and their annotations.
Data scientist at Nightingale Health, associate professor at University of Oxford
Independent expert voice of biomedical and health research in the UK, fostering good health for all supported by the best research.
Visit
bit.ly/acmedsci for more info.
Exeter is a leading UK university and member of the Russell Group, which combines world-leading research with high levels of student satisfaction.
UK Doctor specialising in Clinical Genetics and Genomics. Researcher investigating Wiedemann-Steiner syndrome, chromatin disorders and genetics of orofacial clefting. All views are my own.
Head of Human Genetics & Senior Group Leader @ Wellcome Sanger Institute. Statistical geneticist working on complex diseases
#ibd #firstgen.
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Developing macromolecular structure resources and tools for life science.
- Founding partner of the wwPDB.
- Manage the community-led PDBe-KB resource and the AlphaFold Protein Structure Database, a collaboration with Google DeepMind.
- Part of EMBL-EBI
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Unique supports & informs anyone born w/a rare chromosome or gene disorder, their families & carers. Eurordis Patient Organisation Award winner.
http://rarechromo.org