Associated Papers
Analyses of Human Genetic Data to Identify Clinically Relevant Domains of Neuroligins.
Lehr AW et al.
Genes, 2024
Using structural analysis to clarify the impact of single nucleotide variants in neurexin/neuroligin revealed in clinical genomic sequencing.
Xue K et al.
Journal of Biomolecular Structure & Dynamics, 2022
An Autism-Associated Mutation Impairs Neuroligin-4 Glycosylation and Enhances Excitatory Synaptic Transmission in Human Neurons.
Cast TP et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2021
The neuroligins and the synaptic pathway in Autism Spectrum Disorder.
Trobiani L et al.
Neuroscience and Biobehavioral Reviews, 2020
Autism-associated variants of neuroligin 4X impair synaptogenic activity by various molecular mechanisms.
Yumoto T et al.
Molecular Autism, 2020
Neuroligins and Neurodevelopmental Disorders: X-Linked Genetics.
Nguyen TA et al.
Frontiers in Synaptic Neuroscience, 2020
Not all neuroligin 3 and 4X missense variants lead to significant functional inactivation.
Xu X et al.
Brain and Behavior, 2017
Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort.
Landini M et al.
International Journal of Molecular Sciences, 2016
Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.
Xu X et al.
Molecular Biology Reports, 2014
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