Hauke Baumann
Hauke Baumann, MS
PhD student
Phone number:+49 451 3101 8201

Current Position:

PhD student

Research focus:

Identification and characterization of novel genetic causes of movement disorders

Curriculum vitae

Education & Scientific training:

10/2010 - 09/2013 Studies of Biology at the University of Würzburg

04/2013 - 07/2013 Bachelor thesis, University of Würzburg, Institute of Physiological Chemistry (Director: Prof. M. Schartl), research group Melanoma Signal Transduction (PD S. Meierjohann), topic „PI3K signaling in melanoma“
Bachelor of Science

10/2013 - 04/2016 Studies of Biology at the University of Kiel

04/2015 - 10/2016 Master thesis, Leibniz-Center for Medicine and Biosciences, Borstel (Director: Prof. S. Ehlers), Priority Research Area Infection, research group Microbial Interface Biology (PD N. Reiling), topic „Influence of fatty acid supplementation on the mycobacteria-induced inflammatory and metabolic response of murine macrophages“
Master of Science

05/2016 - present PhD thesis, University of Lübeck, Institute of Neurogenetics (Director: Prof. C. Klein), research section “Genetics of Rare Diseases” supervised by Prof. K. Lohmann

Other Advanced Training

10/2018 - Whole Transcriptome Data Analysis, EMBL Course, Heidelberg, Germany

Memberships

Movement Disorder Society (MDS)

European Society of Human Genetics (ESHG)

Publications

Trinh J, Lohmann K, Baumann H, Balck A, Borsche M, Brüggemann N, Dure L, Dean M, Volkmann J, Tunc S, Prasuhn J, Pawlack H, Imhoff S, Lill CM, Kasten M, Bauer P, Rolfs A; International Parkinson's Disease Genomics Consortium (IPDGC), Klein C. Utility and implications of exome sequencing in early-onset Parkinson's disease. Mov Disord. 2019 34(1):133-137.

Baumann H, Jahn M, Muenchau A, Trilck-Winkler M, Lohmann K, Seibler P. Generation and characterization of eight human-derived iPSC lines from affected and unaffected THAP1 mutation carriers. Stem Cell Res. 2018 33:60-64.

Lohmann K, Masuho I, Patil DN, Baumann H, Hebert E, Steinrücke S, Trujillano D, Skamangas NK, Dobricic V, Hüning I, Gillessen-Kaesbach G, Westenberger A, Savic-Pavicevic D, Münchau A, Oprea G, Klein C, Rolfs A, Martemyanov KA. Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans. Hum Mol Genet. 2017 15;26(6):1078-1086.

Baumann H, Wolff S, Münchau A, Hagenah JM, Lohmann K, Klein C. Evaluating the role of TMEM230 variants in Parkinson's disease. Parkinsonism Relat Disord. 2017 35:100-101.

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