Mathias Toft

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Marcus Wahlqvist, Mathias Toft, Marcus Wahlqvist, 2011 .

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.

Timothy Lynch, Jan Aasly, Demetrius M Maraganore, 2005, American journal of human genetics.

Clinical features of LRRK2‐associated Parkinson's disease in central Norway

Mathias Toft, M. Farrer, J. Kachergus, 2005, Annals of neurology.

Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

Zafar Iqbal, Lasse Pihlstrøm, Mathias Toft, 2017, PloS one.

LRRK2 mutations and Parkinsonism

Mathias Toft, M. Farrer, J. Kachergus, 2005, The Lancet.

MAPK‐pathway activity, Lrrk2 G2019S, and Parkinson's disease

Mathias Toft, M. Farrer, L. White, 2007, Journal of neuroscience research.

Lrrk2 and Lewy body disease

Irene Litvan, Deborah C Mash, Dennis W Dickson, 2006, Annals of neurology.