Inactivation of Magel2 suppresses oxytocin neurons through synaptic excitation-inhibition imbalance

Overview of attention for article published in Neurobiology of Disease, September 2018

Altmetric Badge

About this Attention Score

Good Attention Score compared to outputs of the same age (67th percentile)
Average Attention Score compared to outputs of the same age and source

Mentioned by

twitter: 2 X users

wikipedia: 2 Wikipedia pages

Readers on

mendeley: 61 Mendeley

So far, Altmetric has seen 2 citations on 2 Wikipedia pages.

MAGEL2

Cited by user Boghog on 08 Mar 2025

MAGE family member L2 (MAGEL2) is a protein that in human is encoded by the MAGEL2 gene.

Schaaf-Yang syndrome

Cited by user Citation bot on 01 Mar 2025

Schaaf-Yang syndrome is a rare genetic disorder that is caused by a heterozygous mutation in a paternal-expressed gene MAGEL2.

This page shows the most recent Wikipedia articles that mention this research output. Click here to find out how to access more activity.