Aleksandra Wojtas

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 · 566 citations · Full text

Inflammation, Disease Mechanism, Pathogenesis +8

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

Adam L. Boxer, Ian R. Mackenzie, B. F. Boeve et al. · Journal of Neurology Neurosurgery & Psychiatry · 2010 · 185 citations

De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis

Mariely DeJesus‐Hernandez, Jannet Kocerha, NiCole A. Finch et al. · Human Mutation · 2010 · 149 citations · Full text

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Somatic Variant +14

Loss of clusterin shifts amyloid deposition to the cerebrovasculature via disruption of perivascular drainage pathways

Aleksandra Wojtas, Silvia S. Kang, Benjamin M. Olley et al. · Proceedings of the National Academy of Sciences · 2017 · 145 citations · Full text

<scp>TMEM</scp>106B p.T185S regulates <scp>TMEM</scp>106B protein levels: implications for frontotemporal dementia

Alexandra M. Nicholson, NiCole A. Finch, Aleksandra Wojtas et al. · Journal of Neurochemistry · 2013 · 127 citations

Ftld-tdp Risk, Genetics, Genetic Epidemiology +18