Ann‐Kathrin Hauser

<i>GBA</i> ‐associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study

Kathrin Brockmann, Karin Srulijes, Sylvia Pflederer et al. · Movement Disorders · 2014 · 268 citations

A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia

Niccolò E. Mencacci, Ignacio Rubio‐Agusti, Anselm A. Zdebik et al. · The American Journal of Human Genetics · 2015 · 139 citations · Full text

Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson’s disease and dementia with Lewy bodies

Kathrin Brockmann, Corinne Quadalti, Stefanie Lerche et al. · Acta Neuropathologica Communications · 2021 · 116 citations · Full text

A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease

Hui Liu, Christos Koros, Timo Strohäker et al. · Movement Disorders · 2021 · 106 citations · Full text

Clinical and brain imaging characteristics in leucine‐rich repeat kinase 2–associated PD and asymptomatic mutation carriers

Kathrin Brockmann, Adriane Gröger, Adriana Di Santo et al. · Movement Disorders · 2011 · 77 citations