Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Henry Houlden, Prasanth Sivakumar et al.|Nature Genetics|2019Cited by 592
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Sabrina W. Yum, Yi Zhu et al.|Nature Genetics|2020Cited by 177
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
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Michael E. Shy, Yi Zhu et al.|Nature Genetics|2020Cited by 3