Dale, Russell C.

Top Publications

Top Publications Authored or Co-Authored by "Dale, Russell C."

• Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type i interferon signaling

  Nature Genetics, Volume 46, No. 5, Year 2014, Citations 494
• Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

  American Journal of Medical Genetics, Part A, Volume 167, No. 2, Year 2015, Citations 449
• Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia

  Nature Communications, Volume 7, Article 11601, Year 2016, Citations 212
• KMT2B-related disorders: Expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation

  Brain, Volume 143, No. 11, Year 2020, Citations 100
• Use and Safety of Immunotherapeutic Management of N -Methyl- d -Aspartate Receptor Antibody Encephalitis: A Meta-analysis

  JAMA Neurology, Volume 78, No. 11, Year 2021, Citations 73