What can we learn from common variants associated with unexpected phenotypes in rare genetic diseases?

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2021

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In the top 25% of all research outputs scored by Altmetric
Good Attention Score compared to outputs of the same age (73rd percentile)
Good Attention Score compared to outputs of the same age and source (79th percentile)

So far, Altmetric has seen 13 X posts from 10 X users, with an upper bound of 22,087 followers.

RT @cardiogenetics: Congrats to @JeanetteErdmann for publishing "What can we learn from common variants associated with unexpected phenotyp…

@lisa_bastarache And if you haven't seen it already be sure to check out @JeanetteErdmann recent article: https://t.co/BwKRilvjJM

RT @JamesRPriestMD: .@JeanetteErdmann extrapolates from BioBank level data to explore the potential sequelae of her own neuromuscular condi…

Wow, this is great! Nice work @JeanetteErdmann 👏🏻 #cardiogen

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