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21.
Flinn, L.J.* et al.: TigarB causes mitochondrial dysfunction and neuronal loss in PINK1 deficiency. Ann. Neurol. 74, 837-847 (2013)
22.
Elstner, M. et al.: Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene. Ann. Neurol. 66, 792-798 (2009)
23.
Gschwendtner, A.* et al.: Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. Ann. Neurol. 65, 531-539 (2009)
24.
Scholz, S.W.* et al.: SNCA variants are associated with increased risk for multiple system atrophy. Ann. Neurol. 65, 610-614 (2009)
25.
Gretarsdottir, S.* & Gieger, C.: Risk Variants for Atrial Fibrillation on Chromosome 4q24 Associate with Ischemic Stroke. Ann. Neurol. 64, 402-409 (2008)
26.
Hartig, M.B. et al.: Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation. Ann. Neurol. 59, 248-256 (2006)
27.
Biskup, S. et al.: Common variants of LRRK2 are not associated with sporadic parkinson's disease. Ann. Neurol. 58, 905-908 (2005)
28.
Mueller, J.C. et al.: Multiple regions of alpha-synuclein are associated with parkinson's disease. Ann. Neurol. 57, 535-541 (2005)
29.
Asmus, F.* et al.: Myoclonus-Dystonia Syndrome : e-Sarcoglycan Mutations and Phenotype. Ann. Neurol. 52, 489-492 (2002)
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