Emil K Gustavsson
Emil K Gustavsson
Verified email at can.ubc.ca
TitleCited byYear
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
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 Vilariño‐Güell, S Appel‐Cresswell, ...
Movement Disorders 30 (2), 273-278, 2015
The influence of mitonuclear genetic variation on personality in seed beetles
H Løvlie, E Immonen, E Gustavsson, E Kazancioğlu, G Arnqvist
Proceedings of the Royal Society B: Biological Sciences 281 (1796), 20141039, 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 28, 56-61, 2016
Altered dopamine release and monoamine transporters in Vps35 p. D620N knock-in mice
S Cataldi, J Follett, JD Fox, I Tatarnikov, C Kadgien, EK Gustavsson, ...
NPJ Parkinson's disease 4 (1), 1-11, 2018
Parkinson's disease, genetic variability and the Faroe Islands
MS Petersen, I Guella, S Bech, E Gustavsson, MJ Farrer
Parkinsonism & related disorders 21 (1), 75-78, 2015
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
A case of Parkinson’s disease with no Lewy body pathology due to a homozygous exon deletion in Parkin
KK Johansen, SH Torp, MJ Farrer, EK Gustavsson, JO Aasly
Case reports in neurological medicine 2018, 2018
Novel LRRK2 mutations in Parkinsonism
J Trinh, I Guella, M McKenzie, EK Gustavsson, C Szu-Tu, MS Petersen, ...
Parkinsonism & related disorders 21 (9), 1119-1121, 2015
The role of SNCA and MAPT in Parkinson disease and LRRK2 parkinsonism in the Tunisian Arab‐Berber population
J Trinh, EK Gustavsson, I Guella, C Vilariño‐Güell, D Evans, ...
European journal of neurology 21 (11), e91-e92, 2014
DNAJC13 p. Asn855Ser, implicated in familial parkinsonism, alters membrane dynamics of sorting nexin 1
J Follett, JD Fox, EK Gustavsson, C Kadgien, LN Munsie, LP Cao, ...
Neuroscience letters 706, 114-122, 2019
SNCA multiplication consortium: Clinicogenetic analysis of SNCA multiplication probands and families.
A Book, M Farrer, T Candido, I Guella, D Evans, E Gustavsson
DNAJC13 in Parkinson's disease; characterization of the p. N855S knock-in mouse model: 1761
J Follett, J Fox, E Gustavsson, M Farrrer
Movement Disorders 34, 2019
Family with primary periodic paralysis and a mutation in MCM3AP, a gene implicated in mRNA transport
EK Gustavsson, J Follett, MJ Farrer, JO Aasly
Muscle & nerve 60 (3), 311-314, 2019
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