Associated Papers
Prime editing-installed suppressor tRNAs for disease-agnostic genome editing.
Pierce SE et al.
Nature, 2025
41261131 (PubMed )
Supplement: 41586_2025_9732_MOESM17_ESM.xlsx › Sequence_Context_Screen
Tissue-specific DNase I footprint analysis confirms the association of GATAD2B Q470* variant with intellectual disability.
Nikam V et al.
Journal of Genetics, 2021
GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder.
Shieh C et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2020
The NuRD complex and macrocephaly associated neurodevelopmental disorders.
Pierson TM et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2019
Whole exome sequencing in patients with white matter abnormalities.
Vanderver A et al.
Annals of Neurology, 2016
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