iiinova — where your digital self keeps evolving

Inês Barroso @inesbarroso.bsky.social · 30/09/2025

Source: News Excited to share our results showing that in the UK G6PD deficiency is common in Black and South Asian men. It is associated with 4yr delay in diabetes diagnosis and increased risk of complications. We need to do better!

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Inês Barroso @inesbarroso.bsky.social · 04/04/2025

Deleted the old app and tried to delete my profile but realised it was linked to old email and couldn’t remember the password 🙄. So it’s stays frozen in time, maybe one day when we come out of current dystopia…

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Reposted by Inês Barroso

John Dennis @johndennis.bsky.social · 26/02/2025

5-drug precision prescribing for people with type 2 diabetes is here Our model for optimising glucose lowering therapy using low-cost routine clinical features published in the Lancet today Paper: thelancet.com/journals/lan... Try the web tool here: diabetesgenes.org/t2-treatment/

thelancet.com

A five-drug class model using routinely available clinical features to optimise prescribing in type 2 diabetes: a prediction model development and validation study

We have developed a five-drug class model that uses routine clinical data to identify optimal glucose-lowering therapies for people with type 2 diabetes. Individuals on model-predicted optimal therapy...

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Reposted by Inês Barroso

ezpearson.bsky.social @ezpearson.bsky.social · 26/02/2025

Fantastic to be involved in this work that will change the care of most people with T2D. We are presenting this tomorrow at #DUKPC25 in Glasgow

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Reposted by Inês Barroso

Dr Gareth Hawkes @drghawkes.bsky.social · 26/02/2025

Really excited to share our next population-scale WGS work preprint. Here, we analyse three anthropometric traits in nearly 700,000 individuals (discovery UKB ~450K, replication AoU). We show, for these traits, that common and rare variant heritability is convergent www.biorxiv.org/content/10.1...

biorxiv.org

Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations

Genetic association studies have mostly focussed on common variants from genotyping arrays or rare protein-coding variants from exome sequencing. Here, we used whole-genome sequence (WGS) data in 672,...

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Inês Barroso @inesbarroso.bsky.social · 10/02/2025

Would you like to eork in beautiful Devon with great collaborative colleages? We’re recruiting a new lecturer in Health Data Science ! Apply!! jobs.exeter.ac.uk/hrpr_webrecr...

jobs.exeter.ac.uk

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Inês Barroso @inesbarroso.bsky.social · 16/12/2024

jobs.exeter.ac.uk/hrpr_webrecr... Interested in data management? Want a permanent position working in beautiful Devon and work collaboratively to support the work of lots of genomics team? Apply!!

jobs.exeter.ac.uk

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Inês Barroso @inesbarroso.bsky.social · 13/12/2024

Explore fully-funded PhD studentships for Black British researchers at the University of Exeter, promoting diversity and excellence in postgraduate study.

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Inês Barroso @inesbarroso.bsky.social · 07/12/2024

Hello! I’ve made it over here the other place wasn’t so great to hang out anymore!!

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