Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome

Overview of attention for article published in American Journal of Human Genetics, 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 (98th percentile)
High Attention Score compared to outputs of the same age and source (93rd percentile)

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news: 27 news outlets
blogs: 1 blog

twitter: 18 X users
facebook: 1 Facebook page

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@hectorsalas @NeuroscienceNew @wetbee_ @BalzaClarita @BelzaClarita @xai @elonmusk Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome https://t.co/4pBKgIYlYI …

Medicina del Aprendizaje @AAPninossanos @FundacionHOMI Descubierta una nueva enfermedad genética que retrasa el desarrollo del cerebro en población infantil Identification and functional evaluation of...variants... with ID: An...neurodevelopmental syndrom…

‘GRIA1 encodes the GluA1 subunit of α-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptors, which are ligand-gated ion channels that act as excitatory receptors for the neurotransmitter L-glutamate (Glu).’ https://t.co/8RVoiVkdsu!

Scientists discover new genetic #disease that delays brain development in children @AJHGNews https://t.co/cVWH1NcudM https://t.co/YrUp6JbnnB

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