Bart van de Warrenburg

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

Laurie Robak, Iris E. Jansen, Jeroen van Rooij et al. · Brain · 2017 · 451 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

Alexandria Beilina, Iakov N. Rudenko, Alice Kaganovich et al. · Proceedings of the National Academy of Sciences · 2014 · 367 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6

Jörg B. Schulz, Johannes Borkert, Stefanie Wolf et al. · NeuroImage · 2009 · 189 citations

Medicine, Neurology, Neuroscience +16

Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

Birte Zurek, Kornelia Ellwanger, Lisenka E.L.M. Vissers et al. · European Journal of Human Genetics · 2021 · 103 citations · Full text

Life Sciences, Bioinformatics, Biomedical Informatics +15

Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice

Carlo Wilke, Eva Haas, Kathrin Reetz et al. · EMBO Molecular Medicine · 2020 · 102 citations · Full text

Life Sciences, Neurology, Neuroscience +17