Thomas A. Ravenscroft

Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease

Cyril Pottier, Kevin F. Bieniek, Ni Cole A. Finch et al. · Acta Neuropathologica · 2015 · 314 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms

Hyung-Lok Chung, Michael F. Wangler, Paul C. Marcogliese et al. · Neuron · 2020 · 163 citations · Full text

Life Sciences, Genetics, Neuroscience +8

Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency

Bret M. Evers, Carlos Rodríguez‐Navas, Rachel Tesla et al. · Cell Reports · 2017 · 137 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

TYROBP genetic variants in early-onset Alzheimer's disease

Cyril Pottier, Thomas A. Ravenscroft, Patricia H. Brown et al. · Neurobiology of Aging · 2016 · 103 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

<i>C9ORF72</i> repeat expansions in cases with previously identified pathogenic mutations

Marka van Blitterswijk, Matthew Baker, Mariely DeJesus‐Hernandez et al. · Neurology · 2013 · 83 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17