Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy

Overview of attention for article published in American Journal of Human Genetics, December 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 (97th percentile)
High Attention Score compared to outputs of the same age and source (80th percentile)

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news: 10 news outlets
blogs: 1 blog

twitter: 28 X users
reddit: 3 Redditors

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mendeley: 41 Mendeley

So far, Altmetric has seen 10 news stories from 10 outlets.

Genetic cause behind novel DEE syndrome discovered

AZO Life Sciences, 20 Dec 2022

Autism and epilepsy are two highly prevalent conditions that fall under the umbrella of neurodevelopmental disorders (NDD)…

Descubierto un nuevo trastorno epiléptico del neurodesarrollo y su causa genética

Diario Siglo XXI, 19 Dec 2022

MADRID, 19 (EUROPA PRESS) Un estudio del Baylor College of Medicine, el Texas Children's Hospital, la Harvard Medical School y…

Descubierto un nuevo trastorno epiléptico del neurodesarrollo y su causa genética

NoticiasDe.es, 19 Dec 2022

MADRID, 19 (EUROPA PRESS) Un estudio del Baylor College of Medicine, el Texas Children’s Hospital, la Harvard Medical School y…

Descubierto un nuevo trastorno epiléptico del neurodesarrollo y su causa genética

Infosalus.com, 19 Dec 2022

MADRID, 19 Dic. (EUROPA PRESS) - Un estudio del Baylor College of Medicine, el Texas Children's Hospital, la Harvard Medical…

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