| 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 | 836 | 2013 |
| Advances in the genetics of Parkinson disease J Trinh, M Farrer Nature Reviews Neurology 9 (8), 445-454, 2013 | 568 | 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 | 371 | 2014 |
| 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 | 195 | 2018 |
| 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 | 158 | 2018 |
| Disease Penetrance of Late-Onset Parkinsonism: A Meta-analysis J Trinh, I Guella, M Farrer JAMA Neurology, 2014 | 140 | 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 | 101 | 2014 |
| Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease JJ Kim, D Vitale, DV Otani, MM Lian, K Heilbron, H Iwaki, J Lake, ... Nature genetics 56 (1), 27-36, 2024 | 98 | 2024 |
| 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 | 89 | 2016 |
| Nonsteroidal Anti‐inflammatory Use and LRRK2 Parkinson's Disease Penetrance M San Luciano, CM Tanner, C Meng, C Marras, SM Goldman, AE Lang, ... Movement Disorders 35 (10), 1755-1764, 2020 | 86 | 2020 |
| 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 | 74 | 2014 |
| DNAJC13 genetic variants in parkinsonism EK Gustavsson, J Trinh, I Guella, C Vilarino-Guell, S Appel-Cresswell, ... Movement Disorders, 2014 | 63 | 2014 |
| Detecting somatic mosaicism: considerations and clinical implications ASA Cohen, SL Wilson, J Trinh, XC Ye Clinical genetics 87 (6), 554-562, 2015 | 57 | 2015 |
| Parkin deficiency impairs mitochondrial DNA dynamics and propagates inflammation K Wasner, S Smajic, J Ghelfi, S Delcambre, CA Prada‐Medina, E Knappe, ... Movement Disorders 37 (7), 1405-1415, 2022 | 50 | 2022 |
| Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders J Trinh, KK Kandaswamy, M Werber, MER Weiss, G Oprea, S Kishore, ... Journal of neurodevelopmental disorders 11, 1-6, 2019 | 49 | 2019 |
| Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease D Lai, B Alipanahi, P Fontanillas, TH Schwantes‐An, J Aasly, RN Alcalay, ... Annals of neurology 90 (1), 76-88, 2021 | 48 | 2021 |
| Variants in Miro1 cause alterations of ER-mitochondria contact sites in fibroblasts from Parkinson’s disease patients C Berenguer-Escuder, D Grossmann, F Massart, P Antony, LF Burbulla, ... Journal of clinical medicine 8 (12), 2226, 2019 | 48 | 2019 |
| Genotype–phenotype relations for the atypical parkinsonism genes: MDSGene systematic review C Wittke, S Petkovic, V Dobricic, S Schaake, ... Movement Disorders 36 (7), 1499-1510, 2021 | 47 | 2021 |
| Age at onset of LRRK2 p. Gly2019Ser is related to environmental and lifestyle factors T Lüth, IR König, A Grünewald, M Kasten, C Klein, F Hentati, M Farrer, ... Movement Disorders 35 (10), 1854-1858, 2020 | 47 | 2020 |
| 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 | 45 | 2019 |
Christine KleinUniversity of LuebeckEmail yang diverifikasi di neuro.uni-luebeck.de