Dr. Laura Kilarski
Functions
- Resident at the department of psychiatry and psychotherapy, UKB
- Research associate at the section psychiatric genomics and epigenomics
Curriculum Vitae
- Since 2023: Research associate and resident at the department of psychiatry and psychotherapy, UKB
- 2022: Research associate and resident at the department of psychiatry and psychotherapy, Charité Universitätsmedizin Berlin
- 2021-2022: Research associate and resident at the department of psychiatry and psychotherapy, UKB
- 2013-2020: Study of human medicine at University of Cologne
- 2011-2013: Research associate at St. George’s, University of London, UK
- 2008-2012: Study of Genetics (PhD) at Cardiff University, UK
- 2006-2007: Study of Neuroscience (MSc) at University College London, UK
- 2002-2006: Study of Biochemy (BSc) at University of Warwick, UK
Clinical focus
- Genetic diagnostics in psychiatry
- Substance-use disorders
- Affective und psychotic disorders
Scientific focus
- Pharmacogenetics und -genomics
- Neuropsychiatric genetics (Association studies, polygenic risk scores)
- Genetic risk factors in connection with Long-Covid
Memberships
- Deutsche Gesellschaft für Psychiatrie und Psychotherapie, Psychosomatik und Nervenheilkunde (DGPPN)
Publications (excerpt)
- Pelgrim TAD, Philipsen A, Young AH, …, Kilarski LL et al. A New Intervention for Implementation of Pharmacogenetics in Psychiatry: A Description of the PSY-PGx Clinical Study. Pharmaceuticals. 2024; 17(2):151.
- Bschor T, Kilarski LL. Are antidepressants effective? A debate on their efficacy for the treatment of major depression in adults. Expert Rev Neurother 2016;16(4):367-74.
- Kilarski LL, Rutten-Jacobs LC, Bevan S, et al. Prevalence of CADASIL and Fabry Disease in a Cohort of MRI Defined Younger Onset Lacunar Stroke. PLoS One 2015;10(8):e0136352.
- Kilarski LL, Achterberg S, Devan WJ, et al. Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12. Neurology 2014; 83(8): 678-85.
- Simón-Sánchez J*, Kilarski LL*, Nalls MA, et al. Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease. PLoS One 2012;7(3):e28787.
For full reference list see ORCID: 0000-0003-0645-3134
GoogleScholar: https://scholar.google.com/citations?hl=en&user=VbfSSSYAAAAJ