T. Acharya

Tapping linked to function and structure in premanifest and symptomatic Huntington disease

S J Tabrizi, R I Scahill, H. D. Rosas, 2010, Neurology.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

Early atrophy of pallidum and accumbens nucleus in Huntington’s disease

Jeroen van der Grond, Douglas R. Langbehn, Rachael I. Scahill, 2010, Journal of Neurology.

MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1

Nick C Fox, T. Heskes, C. Kennard, 2019, Brain : a journal of neurology.