Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Overview of attention for article published in Nature Genetics, August 2022

Altmetric Badge

About this Attention Score

In the top 5% of all research outputs scored by Altmetric
Among the highest-scoring outputs from this source (#30 of 8,762)
High Attention Score compared to outputs of the same age (99th percentile)
High Attention Score compared to outputs of the same age and source (98th percentile)

Mentioned by

news: 110 news outlets
blogs: 8 blogs
twitter: 160 X users
patent: 1 patent
facebook: 3 Facebook pages

reddit: 6 Redditors
q&a: 1 Q&A thread
bluesky: 2 Bluesky users
podcasts: 1 podcast

Readers on

mendeley: 430 Mendeley

So far, Altmetric has seen 197 X posts from 160 X users, with an upper bound of 3,732,328 followers.

RFX3 is also an autism gene implicated through rare variant burden (https://t.co/Ok2DxoABQH) and a regulator of activity-dependent transcription of immediate early genes (IEGs) (https://t.co/338mI0Ypdt).

@liz_churchill10 https://t.co/Sorw6Jk6Kz https://t.co/Wo0y5JPA7f https://t.co/b5Ez45sn4Q https://t.co/IoNBpAN6F3 https://t.co/7A6mOGmNNY https://t.co/lYNGylhaz9 https://t.co/wlB0vHkIpg https://t.co/xYGUh3aW2A https://t.co/MpCO1MTjpi https://t.co/HDUfbyjiUS

@wendy_frye @AgeofAutism There are multiple genes associated. https://t.co/qNth1sunTA

RT @IntegralAnswers: 12/ Fu JM, Satterstrom FK, Peng M, et al. (2022). Rare coding variation provides insight into the genetic architecture…

This page shows the most recent X posts that mention this research output. Click here to find out how to access more activity, including 193 additional X posts.