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BMC Bioinformatics|April 18, 2018
Identification of missing variants by combining multiple analytic pipelinesYingxue Ren, Joseph S Reddy, Cyril Pottier, et al.
Plos One|November 7, 2014
Analysis of nuclear export sequence regions of FUS-Related RNA-binding proteins in essential tremorOswaldo Lorenzo-Betancor, Kotaro Ogaki, Alexandra Soto-Ortolaza, et al.
Neurogenetics|October 19, 2013
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystoniaMatt Baker, Audrey J Strongosky, Monica Y Sanchez-Contreras, et al.
Neuroscience Letters|February 18, 2021
Investigating ELOVL7 coding variants in multiple system atrophyAnna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2016
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degenerationMonica Sanchez-Contreras, Michael G Heckman, Pawel Tacik, et al.
Acta Neuropathologica|January 26, 2026
Spatially resolved molecular signatures of Lewy body dementiaYunjung Jin, Kai Chen, Alexander Q Wixom, et al.
Neuroscience Letters|May 12, 2009
Phactr2 and Parkinson's diseaseChristian Wider, Sarah J Lincoln, Michael G Heckman, et al.
Plos One|April 16, 2021
Impact of variant-level batch effects on identification of genetic risk factors in large sequencing studiesDaniel P Wickland, Yingxue Ren, Jason P Sinnwell, et al.
Acta Neuropathologica|June 22, 2018
Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtypeShunsuke Koga, Naomi Kouri, Ronald L Walton, et al.
Acta Neuropathologica|March 3, 2026
Association of mitochondrial genetic background with pS65-Ub in Lewy body diseaseNgan Le Kim Tran, Xu Hou, Michael G Heckman, et al.
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