Karina Banasik

Subgrouping patients with ischemic heart disease by means of the Markov cluster algorithm - Communications Medicine Haue, Holm et al. use unsupervised clustering to subgroup a large set of ischemic heart disease patients from their pre-existing diseases, covering the entire multimorbidity spectrum. They identify subgroups that have different risk profiles and are characterized by different patterns when looking at patient blood tests and genetic profiles.

🚨 NEW RESEARCH! ⚕️ 🩺

Haue, Holm et al. use unsupervised clustering to subgroup a large set of ischemic heart disease patients from their pre-existing diseases, covering the entire multimorbidity spectrum.

https://bit.ly/47bW6M7

#IschemicHeartDisease

Learn more and apply via this link 👇
www.regionh.dk/job/s%C3%B8g...

#WomensHealth #StatisticalGenetics #Genomics #Hiring #Denmark #DataScience #GeneticEpidemiology 6/6

Our team is passionate about translating complex multi-omics and clinical data into actionable insights. If you have a PhD and proven experience with large-scale genetic datasets, we need you to help us advance this mission! 🚀
5/6

The role offers plenty of perks, including access to state-of-the-art computational resources at the Danish national supercomputer for AI, Gefion, amazing biobanks with multi-omics data, and a unique opportunity to contribute to a collaborative, friendly, international team. 💻🌍 4/6

We’re seeking an expert to lead large-scale analyses, identify genetic risk factors for complex reproductive health conditions, and build predictive models that advance precision women’s health. 🧬 3/6

Do you have a background in genetic epidemiology or statistical genetics, a passion for women’s health, and want to work in a highly interdisciplinary team? 2/6

We’re hiring! 📣 We are looking for a Researcher in Statistical Genetics to join our team at Hvidovre Hospital in Copenhagen. #womenshealth 1/6

These malaria drugs treat the mosquitoes — not the people Hear the biggest stories from the world of science | 21 May 2025

This week on the pod 🔊

🦟 Treating mosquitoes for malaria
🧬 The genetics that can lead to pregnancy loss

https://go.nature.com/4dLLUgp

Sequence diversity lost in early pregnancy - Nature Around 1 in 136 pregnancies is lost due to a pathogenic small sequence variant genotype in the fetus.

Our paper @hakonjon.bsky.social (missing other colleagues from Bluesky!), Sequence diversity lost in early pregnancy, was published in Nature (@nature.com) today

www.nature.com/articles/s41...

Sequence diversity lost in early pregnancy - Nature Around 1 in 136 pregnancies is lost due to a pathogenic small sequence variant genotype in the fetus.

Nature research paper: Sequence diversity lost in early pregnancy

https://go.nature.com/4dDftAv

Sequence diversity lost in early pregnancy - Nature Around 1 in 136 pregnancies is lost due to a pathogenic small sequence variant genotype in the fetus.

And if that makes you want to know more: www.nature.com/articles/s41...

Today, I had the honor of presenting a poster on the Copenhagen Pregnancy Loss study at #GenomicMechanisms25

At the same time, somewhere else in the world, the final touches were made on our manuscript, which is now online in Nature 🎉

In this podcast you can learn more about our study 👇 (13.02)

Translational genomics of osteoarthritis in 1,962,069 individuals - Nature A genome-wide association study meta-analysis combined with multiomics data of osteoarthritis identifies 700 effector genes as well as biological processes with a convergent involvement of multiple effector genes; 10% of these genes express the target of approved drugs.

Nature research paper: Translational genomics of osteoarthritis in 1,962,069 individuals

https://go.nature.com/4juvSsT