The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands

Overview of attention for article published in European Journal of Human Genetics, December 2016

Altmetric Badge

About this Attention Score

Good Attention Score compared to outputs of the same age (73rd percentile)
Good Attention Score compared to outputs of the same age and source (70th percentile)

Mentioned by

policy: 1 policy source

twitter: 3 X users

Citations

dimensions_citation: 94 Dimensions

Readers on

mendeley: 82 Mendeley

Summary Policy documents X Dimensions citations

So far, Altmetric has seen 3 X posts from 3 X users, with an upper bound of 1,816 followers.

In 33% is er een erfelijke oorzaak (tot 50% bij congenitaal gehoorverlies; zie https://t.co/loyOLJhpdG). Dit kan uitsluitend gehoorverlies zijn maar er zijn ook vormen waarbij er meer speelt zoals blindheid (syndroom van Usher) #Usher @usher_syndroom

07 Nov 2020

Reply Repost Favourite

The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands. https://t.co/7ySnMokCTl

09 Jan 2017

Reply Repost Favourite

The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands https://t.co/vrIRFKDA3W

22 Dec 2016

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.