Anja Schirmacher
Ludwig-Maximilians-Universität München(DE)Polish Academy of Sciences(PL)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurological diseases and metabolism, Genetic Neurodegenerative Diseases, Cerebrovascular and genetic disorders, Sleep and Wakefulness Research
Most-Cited Works
- → Mutations in SEPT9 cause hereditary neuralgic amyotrophy(2005)260 cited
- → Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women(2004)158 cited
- → Interaction of BDNF and COMT Polymorphisms on Paired-Associative Stimulation-Induced Cortical Plasticity(2012)107 cited
- → Electromagnetic fields (1.8 GHz) increase the permeability to sucrose of the blood-brain barrier in vitro(2000)100 cited
- → Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies(2017)78 cited
- → Not Only Sleepwalking But NREM Parasomnia Irrespective of the Type Is Associated with HLA DQB1*05:01(2016)78 cited