Mutations disrupting neuritogenesis genes confer risk for cerebral palsySheng Chih Jin, Ali Fatemi, Sandra M. Nordlie et al.|Nature Genetics|2020Cited by 174
Variability in Cerebral Palsy DiagnosisBhooma R. Aravamuthan, Michael C. Kruer, Darcy Fehlings et al.|PEDIATRICS|2021Cited by 47
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing lossÉlodie M. Richard, Michele Pinelli, Somayeh Bakhtiari et al.|The American Journal of Human Genetics|2021Cited by 42