Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Henry Houlden, Roberto Simone et al.|Nature Genetics|2019Cited by 592
MIR-NATs repress MAPT translation and aid proteostasis in neurodegenerationRoberto Simone, Rohan de Silva, Faiza Javad et al.|Nature|2021Cited by 74
Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsyRaffaele Ferrari, Rohan de Silva, Mina Ryten et al.|Neurobiology of Aging|2014Cited by 50
Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Henry Houlden, Roberto Simone et al.|Nature Genetics|2019Cited by 14
Corrigendum to “Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.” [Neurobiol. Aging 35 (2014) 1514.e1–1514.e12]Raffaele Ferrari, Rohan de Silva, Mina Ryten et al.|Neurobiology of Aging|2015Cited by 3