S. McKeown

A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation

Alex S. Felmeister, Colin A. Ellis, I. Helbig, 2020, Genetics in Medicine.

Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies

Colin A. Ellis, R. Krause, Manuela Pendziwiat, 2020, American journal of human genetics.

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

Michael T. Zimmermann, Rebecca C. Spillmann, Q. K. Tan, 2020, Nature Genetics.

Correction: A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation

Alex S. Felmeister, Colin A. Ellis, I. Helbig, 2020, Genetics in Medicine.