Arn van den Maagdenberg

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 423 citations · Full text

Life Sciences, Genetics, Neurology +9

Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

Julien Bryois, Nathan Skene, Thomas Folkmann Hansen et al. · Nature Genetics · 2020 · 387 citations · Full text

Life Sciences, Genetics, Neuroscience +14

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

Padhraig Gormley, Mitja Kurki, Marjo Hiekkala et al. · Neuron · 2018 · 99 citations · Full text

Life Sciences, Genetics, Neurology +14

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Bendik S. Winsvold, Christopher P. Nelson, Rainer Malik et al. · Neurology Genetics · 2015 · 74 citations · Full text

Life Sciences, Cardiology, Genetics +17

The S218L familial hemiplegic migraine mutation promotes deinhibition of Cav2.1 calcium channels during direct G-protein regulation

Norbert Weiss, Alejandro Sandoval, Ricardo Felix et al. · Pflügers Archiv - European Journal of Physiology · 2008 · 51 citations · Full text

Life Sciences, Neurology, Neuroscience +15