Alexandra M. Nicholson

TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics

Ian R. Mackenzie, Alexandra M. Nicholson, Mohona Sarkar et al. · Neuron · 2017 · 651 citations · Full text

Life Sciences, Neurology, Neuroscience +16

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

Rosa Rademakers, Matt Baker, Alexandra M. Nicholson et al. · Nature Genetics · 2011 · 579 citations · Full text

Life Sciences, Molecular Genetics, Neuroscience +5

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

<i>CSF1R</i> mutations link POLD and HDLS as a single disease entity

Alexandra M. Nicholson, Matt Baker, NiCole A. Finch et al. · Neurology · 2013 · 168 citations · Full text

Life Sciences, Genetics, Neurology +15

TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia

Marka van Blitterswijk, Bianca Mullen, Alexandra M. Nicholson et al. · Acta Neuropathologica · 2014 · 158 citations · Full text

Medicine, Molecular Genetics, Neurology +11