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Current Opinion in Neurology|November 20, 2012
How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?Marka van Blitterswijk, Mariely DeJesus-Hernandez, Rosa Rademakers
Muscle & Nerve|June 15, 2010
Fus gene mutations in familial and sporadic amyotrophic lateral sclerosisRosa Rademakers, Heather Stewart, Mariely Dejesus-Hernandez, et al.
American Journal of Neurodegenerative Disease|February 6, 2013
C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo ClinicAleksandra Wojtas, Kristin A Heggeli, Nicole Finch, et al.
Molecular Neurodegeneration|October 11, 2012
Expression of Fused in sarcoma mutations in mice recapitulates the neuropathology of FUS proteinopathies and provides insight into disease pathogenesisChristophe Verbeeck, Qiudong Deng, Mariely Dejesus-Hernandez, et al.
Acta Neuropathologica|January 10, 2012
Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9pHeather Stewart, Nicola J Rutherford, Hannah Briemberg, et al.
Neurobiology of Aging|November 16, 2010
Pathogenicity of exonic indels in fused in sarcoma in amyotrophic lateral sclerosisNicola J Rutherford, Nicole A Finch, Mariely DeJesus-Hernandez, et al.
Acta Neuropathologica|October 12, 2012
Tau pathology in frontotemporal lobar degeneration with C9ORF72 hexanucleotide repeat expansionKevin F Bieniek, Melissa E Murray, Nicola J Rutherford, et al.
Archives of Neurology|May 29, 2012
Characterization of a family with c9FTD/ALS associated with the GGGGCC repeat expansion in C9ORF72Rodolfo Savica, Anahita Adeli, Prashanthi Vemuri, et al.
Human Mutation|March 17, 2010
De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosisMariely DeJesus-Hernandez, Jannet Kocerha, NiCole Finch, et al.
BMC Genomics|October 29, 2011
Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutationsJannet Kocerha, Naomi Kouri, Matt Baker, et al.
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