Sarah Wiethoff

机构：University Hospital Münster

发表论文 83 篇 · 总被引 5974 次 · h-index 35

代表论文

• The emerging spectrum of COVID-19 neurology: clinical, radiological and laboratory findings (2020 · Brain · 被引 1171)
• Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia (2016 · Nature Genetics · 被引 254)
• Loss‐of‐Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities (2020 · Annals of Neurology · 被引 113)
• Genetics of neurodegenerative diseases: an overview (2017 · Handbook of clinical neurology · 被引 113)
• Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial (2017 · Brain · 被引 111)
• FAHN/SPG35: a narrow phenotypic spectrum across disease classifications (2019 · Brain · 被引 77)