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Brain : a Journal of Neurology|May 31, 2022
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's diseaseWilliam Zhu, Xiaoping Huang, Esther Yoon, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 8, 2017
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern ItalyRosa Capozzo, Celeste Sassi, Monia B Hammer, et al.
Human Molecular Genetics|June 23, 2012
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathiesDaniah Trabzuni, Selina Wray, Jana Vandrovcova, et al.
Annals of Clinical and Translational Neurology|September 25, 2015
Genome-wide association study of neocortical Lewy-related pathologyTerhi Peuralinna, Liisa Myllykangas, Minna Oinas, et al.
Molecular Neurodegeneration|April 26, 2017
The PINK1 p.I368N mutation affects protein stability and ubiquitin kinase activityMaya Ando, Fabienne C Fiesel, Roman Hudec, et al.
Molecular Cell|February 20, 2018
PINK1 Phosphorylates MIC60/Mitofilin to Control Structural Plasticity of Mitochondrial Crista JunctionsPei-I Tsai, Chin-Hsien Lin, Chung-Han Hsieh, et al.
Parkinsonism & Related Disorders|July 6, 2020
GBA variation and susceptibility to multiple system atrophyAnna I Wernick, Ronald L Walton, Shunsuke Koga, et al.
Brain : a Journal of Neurology|June 6, 2023
Genetic risk scores enhance the diagnostic value of plasma biomarkers of brain amyloidosisVijay K Ramanan, Robel K Gebre, Jonathan Graff-Radford, et al.
Frontiers in Microbiomes|July 30, 2026
Shotgun metagenomic analysis reveals taxonomic and functional alterations in the gut microbiome across prodromal and symptomatic Lewy body diseaseXiaowei Zhao, Stuart J McCarter, Vinod K Gupta, et al.
Neurogenetics|January 17, 2007
Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's diseaseJulie P Taylor, Mary M Hulihan, Jennifer M Kachergus, et al.
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