Thomas A. Ravenscroft

机构：Howard Hughes Medical Institute, Janelia Research Campus · ORCID：0000-0003-3321-2619

发表论文 20 篇 · 总被引 1302 次 · h-index 15

代表论文

• Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease (2015 · Acta Neuropathologica · 被引 317)
• Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms (2020 · Neuron · 被引 166)
• Genetics of FTLD : overview and what else we can expect from genetic studies (2016 · Journal of Neurochemistry · 被引 153)
• Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency (2017 · Cell Reports · 被引 139)
• TYROBP genetic variants in early-onset Alzheimer's disease (2016 · Neurobiology of Aging · 被引 103)
• C9ORF72 repeat expansions in cases with previously identified pathogenic mutations (2013 · Neurology · 被引 83)