Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery

Overview of attention for article published in EBioMedicine, May 2022

Altmetric Badge

About this Attention Score

Good Attention Score compared to outputs of the same age (69th percentile)
Average Attention Score compared to outputs of the same age and source

Mentioned by

twitter: 8 X users

Readers on

mendeley: 46 Mendeley

So far, Altmetric has seen 10 X posts from 8 X users, with an upper bound of 15,194 followers.

RT @IngoHelbig: ...and here is our blog post on polygenic risk scores in families. Knowing that epilepsy has a strong contribution of com…

...and here is our blog post on polygenic risk scores in families. Knowing that epilepsy has a strong contribution of common variants, polygenic risk should run in families, right? ...it's not that simple. https://t.co/exJ36b0meu

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery https://t.co/NbVx6lj04B

RT @MelanieBahlo: Another awesome epilepsy collaboration! Congratulations Karen (@oliverkarenl)&;Colin: excellent work. Something we had su…

This page shows the most recent X posts that mention this research output. Click here to find out how to access more activity, including 6 additional X posts.