Associated Papers
Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization.
Kopp N et al.
American Journal of Medical Genetics. Part A, 2021
The neuroligins and the synaptic pathway in Autism Spectrum Disorder.
Trobiani L et al.
Neuroscience and Biobehavioral Reviews, 2020
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder.
Schmitz-Abe K et al.
Scientific Reports, 2020
32820185 (PubMed )
Supplement: 41598_2020_70656_MOESM1_ESM.pdf
Neuroligins and Neurodevelopmental Disorders: X-Linked Genetics.
Nguyen TA et al.
Frontiers in Synaptic Neuroscience, 2020
Autism Spectrum Disorder and miRNA: An Overview of Experimental Models.
Schepici G et al.
Brain Sciences, 2019
Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era.
Jiang YH et al.
Critical Reviews in Clinical Laboratory Sciences, 2014
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