Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice

Overview of attention for article published in Proceedings of the National Academy of Sciences of the United States of America, June 2022

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In the top 5% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (97th percentile)
Good Attention Score compared to outputs of the same age and source (75th percentile)

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news: 9 news outlets
blogs: 1 blog

twitter: 18 X users

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mendeley: 15 Mendeley

So far, Altmetric has seen 18 X posts from 18 X users, with an upper bound of 1,755,440 followers.

Dysfunctional gene discovery leads to potentially treatable hearing loss https://t.co/wdo6F84rao https://t.co/rLCGWuWFAW https://t.co/5hm3CS6Ac5

RT @medical_xpress: Dysfunctional gene discovery leads to potentially treatable ##hearingloss @PNASNews https://t.co/nxHlgBt9vz https://t.c…

“Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice” by Mustafa Tekin et al. PNAS https://t.co/vjKrEF8k6z https://t.co/wOFTeED0Zd

RT @MariaLachgar: Our paper on MINAR2 mutations causing #deafness in humans and mice is finally out in @PNASNews ! https://t.co/57aNwZoQk2

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