Alexandra Durr

Neurofilament light protein in blood predicts regional atrophy in Huntington disease

Eileanoir B. Johnson, Lauren M. Byrne, Sarah Gregory et al. · Neurology · 2018 · 85 citations · Full text

Life Sciences, Genetics, Neurology +17

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Wouter van Rheenen, Rick van der Spek, Mark K. Bakker et al. · Research Square · 2021 · 56 citations · Full text

Life Sciences, Genetics, Neurology +17

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

Thomas Roux, Mathieu Barbier, Mélanie Papin et al. · Genetics in Medicine · 2020 · 49 citations · Full text

Life Sciences, Genetics, Neurology +12

SCA13 causes dominantly inherited non-progressive myoclonus ataxia

Solveig Montaut, Emmanuelle Apartis, Jean‐Baptiste Chanson et al. · Parkinsonism & Related Disorders · 2017 · 14 citations

Life Sciences, Genetics, Neurology +12