NiCole A. Finch

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

Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis

Nicola J. Rutherford, Yong‐Jie Zhang, Matt Baker et al. · PLoS Genetics · 2008 · 463 citations · Full text

Life Sciences, Genetics, Neurology +16

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

NiCole A. Finch, Matthew B. Baker, Richard Crook et al. · Brain · 2009 · 382 citations · Full text

Life Sciences, Genetics, Neurology +17

<i>TMEM106B</i> regulates progranulin levels and the penetrance of FTLD in <i>GRN</i> mutation carriers

NiCole A. Finch, Minerva M. Carrasquillo, Matthew Baker et al. · Neurology · 2010 · 247 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

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