Friedrich Asmus

Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

Alexander Zimprich, Saskia Biskup, Petra Leitner et al. · Neuron · 2004 · 3K citations · Full text

Mendelian Disorder, Genetic Disorder, Parkinson Disease +5

Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome

Alexander Zimprich, Monika Grabowski, Friedrich Asmus et al. · Nature Genetics · 2001 · 474 citations

Mendelian Disorder, Genetic Disorder, Medicine +5

EFNS guidelines on diagnosis and treatment of primary dystonias

Alberto Albanese, Friedrich Asmus, Kailash P. Bhatia et al. · European Journal of Neurology · 2010 · 425 citations · Full text

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

Hreinn Stefánsson, Stacy Steinberg, Hjörvar Pétursson et al. · Nature Genetics · 2009 · 225 citations · Full text

Essential Tremor, Developmental Biology, Molecular Neuroscience +7

The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing Interval

Alexander Zimprich, Bertram Müller-Myhsok, Matthew J. Farrer et al. · The American Journal of Human Genetics · 2004 · 222 citations · Full text

Parkinson Disease, Genetics, Experimental Neuropathology +9