Michael A. Gitcho

<i>TDP‐43</i> A315T mutation in familial motor neuron disease

Michael A. Gitcho, Robert H. Baloh, Sumi Chakraverty et al. · Annals of Neurology · 2008 · 608 citations · Full text

TDP-43 in Familial and Sporadic Frontotemporal Lobar Degeneration with Ubiquitin Inclusions

Nigel J. Cairns, Manuela Neumann, Eileen H. Bigio et al. · American Journal Of Pathology · 2007 · 525 citations · Full text

Ubiquitin Inclusions, Mendelian Disorder, Genetic Disorder +9

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin

Odity Mukherjee, Pau Pástor, Nigel J. Cairns et al. · Annals of Neurology · 2006 · 188 citations · Full text

TARDBP 3′-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

Michael A. Gitcho, Eileen H. Bigio, Manjari Mishra et al. · Acta Neuropathologica · 2009 · 163 citations · Full text

Genetic Disorder, Genetics, Molecular Biology +6

TDP-43 interacts with mitochondrial proteins critical for mitophagy and mitochondrial dynamics

Stephani A. Davis, Sheed Itaman, Christopher Janney et al. · Neuroscience Letters · 2018 · 146 citations · Full text