Joanne Trinh
Joanne Trinh
Group Leader
Verified email at - Homepage
TitleCited byYear
Alpha‐synuclein p. H50Q, a novel pathogenic mutation for Parkinson's disease
S Appel‐Cresswell, C Vilarino‐Guell, M Encarnacion, H Sherman, I Yu, ...
Movement disorders 28 (6), 811-813, 2013
Advances in the genetics of Parkinson disease
J Trinh, M Farrer
Nature Reviews Neurology 9 (8), 445, 2013
DNAJC13 mutations in Parkinson disease
C Vilariño-Güell, A Rajput, AJ Milnerwood, B Shah, C Szu-Tu, J Trinh, I Yu, ...
Human molecular genetics 23 (7), 1794-1801, 2014
Disease Penetrance of Late-Onset Parkinsonism: A Meta-analysis
J Trinh, I Guella, M Farrer
JAMA Neurology, 2014
A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p. G2019S parkinsonism
J Trinh, R Amouri, JE Duda, JF Morley, M Read, A Donald, ...
Neurobiology of aging 35 (5), 1125-1131, 2014
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study
J Trinh, EK Gustavsson, C Vilariño-Güell, S Bortnick, J Latourelle, ...
The Lancet Neurology 15 (12), 1248-1256, 2016
DNAJC13 genetic variants in parkinsonism
EK Gustavsson, J Trinh, I Guella, C Vilarino-Guell, S Appel-Cresswell, ...
Movement Disorders, 2014
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects
E Seong, R Insolera, M Dulovic, EJ Kamsteeg, J Trinh, N Brüggemann, ...
Annals of neurology 83 (6), 1075-1088, 2018
Detecting somatic mosaicism: considerations and clinical implications
ASA Cohen, SL Wilson, J Trinh, XC Ye
Clinical genetics 87 (6), 554-562, 2015
Genotype‐phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review
J Trinh, FMJ Zeldenrust, J Huang, M Kasten, S Schaake, S Petkovic, ...
Movement Disorders 33 (12), 1857-1870, 2018
LRRK2 parkinsonism in Tunisia and Norway: a comparative analysis of disease penetrance
F Hentati, J Trinh, C Thompson, E Nosova, MJ Farrer, JO Aasly
Neurology 83 (6), 568-569, 2014
Genetic variability of the retromer cargo recognition complex in parkinsonism
EK Gustavsson, I Guella, J Trinh, C Szu‐Tu, A Rajput, AH Rajput, ...
Movement Disorders 30 (4), 580-584, 2015
DCTN1 p.K56R in progressive supranuclear palsy
EK Gustavsson, J Trinh, I Guella, C Szu-Tu, J Khinda, CH Lin, RM Wu, ...
Parkinsonism & related disorders, 2016
STX6 rs1411478 is not associated with increased risk of Parkinson's disease
J Trinh, C Vilariño-Güell, A Donald, B Shah, I Yu, C Szu-Tu, JO Aasly, ...
Parkinsonism & related disorders 19 (5), 563-565, 2013
Fine tuning of RFX/DAF-19-regulated target gene expression through binding to multiple sites in Caenorhabditis elegans
JSC Chu, M Tarailo-Graovac, D Zhang, J Wang, B Uyar, D Tu, J Trinh, ...
Nucleic acids research 40 (1), 53-64, 2012
A novel de novo mutation in CSNK2A1: reinforcing the link to neurodevelopmental abnormalities and dysmorphic features
J Trinh, I Hüning, N Budler, V Hingst, K Lohmann, G Gillessen-Kaesbach
Journal of human genetics 62 (11), 1005, 2017
LRRK2-related Parkinson disease
J Trinh, M Farrer, OA Ross, I Guella
GeneReviews®[Internet], 2014
De novo variants in TAOK1 cause neurodevelopmental disorders
M Dulovic-Mahlow, J Trinh, KK Kandaswamy, GJ Braathen, N Di Donato, ...
The American Journal of Human Genetics 105 (1), 213-220, 2019
LRP10 in α-synucleinopathies
DA Kia, MS Sabir, S Ahmed, J Trinh, S Bandres-Ciga, AJ Noyce, ...
The Lancet Neurology 17 (12), 1032, 2018
Genetic Identification in Early Onset Parkinsonism among Norwegian Patients
EK Gustavsson, J Trinh, M McKenzie, S Bortnick, MS Petersen, MJ Farrer, ...
Movement disorders clinical practice 4 (4), 499-508, 2017
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