Kathrin Müller
Novartis (Switzerland)(CH)Universität Ulm(DE)
Publications by Year
Research Areas
Amyotrophic Lateral Sclerosis Research, Neurogenetic and Muscular Disorders Research, Parkinson's Disease Mechanisms and Treatments, Functional Brain Connectivity Studies, Neurological diseases and metabolism
Most-Cited Works
- → Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia(2015)775 cited
- → Correlated gene expression supports synchronous activity in brain networks(2015)679 cited
- → Hot-spot KIF5A mutations cause familial ALS(2017)229 cited
- → Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis(2015)219 cited
- → Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis(2013)149 cited
- → Peripheral monocytes are functionally altered and invade the CNS in ALS patients(2016)144 cited
- → Different neuroinflammatory profile in amyotrophic lateral sclerosis and frontotemporal dementia is linked to the clinical phase