Associated Papers
Developmental convergence and divergence in human stem cell models of autism.
Gordon A et al.
Nature, 2026
Novel copy number variations and phenotypes of infantile epileptic spasms syndrome.
Cheng M et al.
Clinical Genetics, 2024
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T et al.
Nature Communications, 2020
33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM10_ESM.xlsx › Supplementary_Data_8
Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.
Posey JE et al.
The New England Journal of Medicine, 2017
PRRT2 mutations and paroxysmal disorders.
Méneret A et al.
European Journal of Neurology, 2013
Select a paper to view details