C. Szu‐Tu

Alpha‐synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease

M. Farrer, A. Rajput, A. Rajput, 2013, Movement disorders : official journal of the Movement Disorder Society.

Double homozygous mutations (R275W and M432V) in the ParkinGene associated with late‐onset Parkinson's disease

S. Bardien, I. Guella, J. Carr, 2016, Movement disorders : official journal of the Movement Disorder Society.

DNAJC13 mutations in Parkinson disease.

Wyeth W Wasserman, Virginie Bernard, Silke Appel-Cresswell, 2014, Human molecular genetics.

Defining neurodegeneration on Guam by targeted genomic sequencing

D. Dickson, I. Guella, H. Morris, 2015, Annals of neurology.

α‐synuclein genetic variability: A biomarker for dementia in Parkinson disease

Ekaterina Nosova, Irene Litvan, Laura Parkkinen, 2016, Annals of neurology.

Genetic variability of the retromer cargo recognition complex in parkinsonism

Martin J. McKeown, A. Rajput, A. Rajput, 2015, Movement disorders : official journal of the Movement Disorder Society.

DCTN1 p.K56R in progressive supranuclear palsy.

Martin J. McKeown, M. Farrer, A. Rajput, 2016, Parkinsonism & related disorders.

STX6 rs1411478 is not associated with increased risk of Parkinson's disease.

Alan Donald, M. Farrer, A. Rajput, 2013, Parkinsonism & related disorders.

Novel LRRK2 mutations in Parkinsonism.

Martin J. McKeown, M. Farrer, A. Rajput, 2015, Parkinsonism & Related Disorders.