Wolcott-Rallison syndrome

Overview of attention for article published in Orphanet Journal of Rare Diseases, November 2010

Altmetric Badge

About this Attention Score

In the top 25% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (83rd percentile)
Good Attention Score compared to outputs of the same age and source (72nd percentile)

Mentioned by

twitter: 3 X users
patent: 3 patents

wikipedia: 4 Wikipedia pages

Citations

dimensions_citation: 172 Dimensions

Readers on

mendeley: 177 Mendeley

Summary X Patents Wikipedia Dimensions citations

So far, Altmetric has seen 3 X posts from 3 X users, with an upper bound of 4,328 followers.

@PedsGIChat Julier C, Nicolino M. Wolcott-Rallison syndrome. Orphanet J Rare Dis. 2010 Nov 4;5:29. doi: 10.1186/1750-1172-5-29. PMID: 21050479; PMCID: PMC2991281. https://t.co/5k38CVwxqy

14 Apr 2022

Reply Repost Favourite

Wolcott-Rallison syndrome is an autosomal receive disorder caused by a mutation in the gene EIF2AK3. https://t.co/EVW0pls5yH

28 Jul 2017

Reply Repost Favourite

@saif_abdullah_ @Al3noud_8 وهذه روابط أجنبية أكيد أنتم أدرى مني فيها لكني أحببت مشاركتكم بها http://t.co/SCQ8iuXHMo http://t.co/bSUPkWlOkt

05 Nov 2013

Reply Repost Favourite

This page shows the most recent X posts that mention this research output.

Click here to find out how to access more activity.