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Acta Neuropathologica|February 14, 2013
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?Aoife P Kiely, Yasmine T Asi, Eleanna Kara, et al.
The Lancet. Neurology|February 5, 2008
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRASarah Camargos, Sonja Scholz, Javier Simón-Sánchez, et al.
Plos One|September 28, 2011
Gene signatures derived from a c-MET-driven liver cancer mouse model predict survival of patients with hepatocellular carcinomaIrena Ivanovska, Chunsheng Zhang, Angela M Liu, et al.
Neurobiology of Disease|June 6, 2006
Kinase activity is required for the toxic effects of mutant LRRK2/dardarinElisa Greggio, Shushant Jain, Ann Kingsbury, et al.
Neurology. Genetics|October 5, 2018
Protein network analysis reveals selectively vulnerable regions and biological processes in FTDLuke W Bonham, Natasha Z R Steele, Celeste M Karch, et al.
Scientific Reports|July 28, 2019
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasiaLuke W Bonham, Natasha Z R Steele, Celeste M Karch, et al.
Research Square|June 10, 2024
p.L1795F LRRK2 variant is a common cause of Parkinson's disease in Central EuropeMiriam Ostrozovicova, Gertrud Tamas, Petr Dušek, et al.
Movement Disorders Clinical Practice|March 22, 2025
Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early-Onset and Familial Parkinson's DiseaseMiriam Ostrozovicova, Gertrud Tamas, Agsha Atputhavadivel, et al.
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