JOANNE TRINH

 

PERSONAL INFORMATION

Position/Title: Research Group Leader (Institute of Neurogenetics)

Address: University of Lübeck; Ratzeburger Allee 160, 23538 Lübeck, Germany

Tel: +49-451-31018200; Fax: +49-451-31018204

@: joanne.trinh@neuro.uni-luebeck.de; www.neurogenetics-luebeck.de

 

EDUCATION/POSITIONS

2008-2012 Bachelor of Science (University of British Columbia, Vancouver, Canada)

2012-2017 PhD Thesis (Centre for Applied Neurogenetics, Department of Medical Genetics, University of British Columbia)

2015-2016 Visiting Scientist (VIB Department of Molecular Genetics, University of Antwerp)

2017-2018 Postdoctoral research (Institute of Neurogenetics, University of Lübeck)

2018-present Leader of research group “Integrative Omics approaches in Parkinson’s disease” (Institute of Neurogenetics, University of Lübeck) 

ACADEMIC ACTIVITIES

2010-present Member of the American Society of Human Genetics

2012-present Member of the Michael J. Fox Foundation LRRK2 modifier consortium

2013-present Member of the Michael J. Fox Foundation LRRK2 consortium

2012-present Ad Hoc Reviewer (Journals): Nature Communications, Nature Neurology Reviews, Annals of Neurology, Movement Disorders, European Journal of Neurology, Scientific Reports, Neuroscience Letters, Parkinsonism and Related Disorders, Frontiers of Neurology, Journal of Neurological Sciences, Neurobiology of Aging, Parkinson’s disease

AWARDS

2010-present International and National Travel Awards: >10 (e.g. MDS International Congress Travel Award, Colorado Keystone Meeting Travel Award, GeoPD Travel Award, Cold Spring Harbor Travel Award)

2010-present Poster Awards: 1st place (Life Sciences Institute, UBC), Honourable Mention (National Canadian Institutes of Health Research), Honourable Mention (CCMT/CFRI UBC Competition), Best Poster (NGS Symposium, Cancer Agency)

2014 UBC Four Year Fellowship Award and Tuition Award

2014 Simons Foundation Doctoral Award

2014 Canadian Institutes of Health Research Doctoral Award

2015 Michael Smith Foreign Exchange Supplement Award (CIHR)

2015 James Miller Memorial Award for Outstanding Translational Research (Department of Medical Genetics, UBC)

2015 Faculty of Medicine Graduate Student Award

2017 Alexander Von Humboldt Postdoctoral Fellowship

2017 CIHR Postdoctoral Fellowship (deferred)

2017 Joachim Herz Stiftung: Add-on Fellowship for Interdisciplinary Science

2019 Peter and Traudl Engelhorn Fellowship

 

SELECTED PUBLICATIONS

From 30 publications; total citations: 1,254; h-index: 13

    1. Vilariño-Güell C, Rajput A, Milnerwood AJ, Shah B, Szu-Tu C, Trinh J, Yu I, Encarnacion M, Munsie LN, Tapia L, Gustavsson EK, Chou P, Tatarnikov I, Evans DM, Pishotta FT, Volta M, Beccano-Kelly D, Thompson C, Lin MK, Sherman HE, Han HJ, Guenther BL, Wasserman WW, Bernard V, Ross CJ, Appel-Cresswell S, Stoessl AJ, Robinson CA, Dickson DW, Ross OA, Wszolek ZK, Aasly JO, Wu RM, Hentati F, Gibson RA, McPherson PS, Girard M, Rajput M, Rajput AH, Farrer MJ. DNAJC13 mutations in Parkinson disease. Hum Mol Genet 2014;23:1794-801. [IF: 6.4]
    2. Trinh J, Amouri R, Duda JE, Morley JF, Read M, Donald A, Vilariño-Güell C, Thompson C, Szu Tu C, Gustavsson EK, Sassi SB, Hentati E, Zouari M, Farhat E, Nabli F, Hentati F, Farrer MJ. A comparative study of Parkinson;s disease and LRRK2 p.G2019S parkinsonism. Neurobiology of Aging 2014;35:1125-31 [IF: 4.9]
    3. Hentati F, Trinh J (equally contributing first author), Thompson C, Nosova E, Farrer M, Aasly J. LRRK2 parkinsonism in Tunisia and Norway: A comparative study of disease penetrance. Neurology 2014; 83:568-9. [IF: 8.3]
    4. Trinh J, Guella I, Farrer M. Disease penetrance of late-onset parkinsonism: a meta-analyses. JAMA Neurol 2014;71:1535-9. [IF: 7.3]
    5. Trinh J, Gustavsson EK, Vilariño-Güell C, Latourelle J, McKenzie M, Szu Tu C, Nosova E, Khina J, Lesage S, Brice A, Aasly J, Parkkinen L, Foroud T, Myers RH, Milnerwood A, Sassi SB, Hentati E, Nabli F, Farhat E, Amouri R, Hentati F, Farrer MJ. DNM3 modifiers age of onset in LRRK2 parkinsonism: a linkage and association study. Lancet Neurol 2016;15:1248-1256. [IF: 26.3]
    6. Trinh J, Lohmann K (equally contributing first author), Baumann H, Balck A, Borsche M, Brüggemann N, Dure L, Tünc S, Prasuhn J, Pawlack H, Imhoff S, Lill CM, Kasten M, Bauer P, Rolfs A, Klein C. Utility and implications of exome sequencing in early-onset Parkinson’s disease. Mov Disord 2019;34:133-137. [IF: 8.1]
    7. Trinh J, Zeldenrust FMJ, Huang Jana, Kasten M, Petkovic S, Madoev H, Zorn I, Schaake S, König I, Bertram L, Lohmann K, Lill CM, Klein C, Marras C. Genotype-phenotype relations for the Parkinson’s disease genes: SNCA, LRRK2, VPS35: MDSGene systematic review. Mov Disord 2018;33:1857-1870. [IF: 8.1]
    8. Kia DA, Sabir MS, Ahmed S, Trinh J, Badres-Ciga S. Analysis of LRP10 in a large series of Parkinson’s disease. Lancet Neurol 2018;17:1032. [IF: 28.8]
    9. Dulovic Mahlow M, Trinh J (equally contributing first author), Kandaswamy KK, Braathen GJ, Werber M, Krajka V, Busk OL, Oprea G, DiDonato N, Vos M, Rolfs A, Lohmann K. De-novo mutations in TAOK1 cause neurodevelopmental disorders. Am J Hum Genet 2019105:213-220. [IF: 9.9]
    10. Ouzren N, Delcambre S, Ghelfi J, Seibler P, Farrer MJ, König I, Aasly JO, Trinh J, Klein C, Grünewald A. Somatic mtDNA major arc deletions discriminate manifesting from non-manifesting LRRK2 G2019S mutation carriers. Ann Neurol 2019;86:324-326. [IF: 9.5]