AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disordersVincenzo Salpietro, Alison M. Muir, Christine L. Dixon et al.|Nature Communications|2019Cited by 249
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathiesBo Yuan, Pengfei Liu, Xiaofei Song et al.|Genetics in Medicine|2018Cited by 88