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Acta Neuropathologica Communications|December 8, 2020
MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical featuresRebecca R Valentino, Shunsuke Koga, Ronald L Walton, et al.
Parkinsonism & Related Disorders|July 8, 2022
PLA2G6-associated neurodegeneration in four different populations-case series and literature reviewRana Hanna Al-Shaikh, Lukasz M Milanowski, Vikram V Holla, et al.
Acta Neuropathologica|October 15, 2013
Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degenerationNaomi Kouri, Yari Carlomagno, Matthew Baker, et al.
Molecular Neurodegeneration|November 7, 2014
Analysis of COQ2 gene in multiple system atrophyKotaro Ogaki, Shinsuke Fujioka, Michael G Heckman, et al.
Neurobiology of Aging|February 6, 2018
Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variantsCristina Razquin, Sara Ortega-Cubero, Estefania Rojo-Bustamante, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North AfricaBarbara Jasinska-Myga, Jennifer Kachergus, Carles Vilariño-Güell, et al.
Acta Neuropathologica|April 26, 2022
APOE4 exacerbates α-synuclein seeding activity and contributes to neurotoxicity in Alzheimer's disease with Lewy body pathologyYunjung Jin, Fuyao Li, Berkiye Sonoustoun, et al.
Parkinsonism & Related Disorders|September 16, 2008
Genetic variation of Omi/HtrA2 and Parkinson's diseaseOwen A Ross, Alexandra I Soto, Carles Vilariño-Güell, et al.
Parkinsonism & Related Disorders|September 2, 2009
LINGO1 rs9652490 is associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Owen A Ross, Christian Wider, et al.
Neurobiology of Aging|April 2, 2014
Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's diseaseBarbara Shannon, Alexandra Soto-Ortolaza, Sruti Rayaprolu, et al.
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