Bart P. van de Warrenburg

Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease

Marialuisa Quadri, Antonio Federico, Tianna Zhao et al. · The American Journal of Human Genetics · 2012 · 415 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts

Hirotaka Iwaki, Cornelis Blauwendraat, Hampton L. Leonard et al. · Movement Disorders · 2019 · 190 citations · Full text

Life Sciences, Genetics, Neurology +17

Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

Janneke Schuurs-Hoeijmakers, Michael T. Geraghty, Erik‐Jan Kamsteeg et al. · The American Journal of Human Genetics · 2012 · 182 citations · Full text

Medicine, Genetics, Molecular Genetics +6

Genetic risk of Parkinson disease and progression:

Hirotaka Iwaki, Cornelis Blauwendraat, Hampton L. Leonard et al. · Neurology Genetics · 2019 · 162 citations · Full text

Life Sciences, Genetics, Neurology +17

Genotype–phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort

Koen L.I. van Gassen, Charlotte D.C.C. van der Heijden, Susanne T. de Bot et al. · Brain · 2012 · 140 citations · Full text

Life Sciences, Genetics, Neurology +17