Andreas Puschmann

发表

GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.

Timothy Lynch, Magdalena Boczarska-Jedynak, D. Serie, 2013, American journal of neurodegenerative disease.

Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research

Martin N. Rossor, Margaret Sutherland, Colin J. Mahoney, 2012, PloS one.

Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke

Sofie Samuelsson, Arne Lindgren, Ulf Kristoffersson, 2020, Stroke.

Nationwide prevalence of primary dystonia, progressive ataxia and hereditary spastic paraplegia.

A. Puschmann, Clara Hellberg, Andreas Puschmann, 2019, Parkinsonism & related disorders.