GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel BlockersDong Li, Marni J. Falk, Gabrielle J. Kosobucki et al.|The American Journal of Human Genetics|2016Cited by 183
AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-AcetylaspartateMarni J. Falk, Håkon Håkonarson, Dong Li et al.|JIMD Reports|2014Cited by 80
The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning systemKenneth D. Mandl, Gabor Korodi, Tracy A. Glauser et al.|Genetics in Medicine|2019Cited by 46