Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset - Ramos, E.M.; Latourelle, J.C.; Gillis, T.; Mysore, J. S.; Squitieri, F.; Di Pardo, A.; Di Donato, S.; Gellera, C.; Hayden, M. R.; Morrison, P. J.; Nance, M.; Ross, C.A.; et al. (Neurogenetics, 2013)

Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant - Earnshaw, W.C.; Allshire, R.C.; Black, B.E.; Bloom, K.; Brinkley, B.R.; Brown, W.; Cheeseman, I.M.; Choo, K.H.A.; Copenhaver, G.P.; Deluca, J.G.; Desai, A.; Diekmann, S.; et al. (Chromosome Research, 2013)

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion - Lee, J. -M.; Ramos, E.M.; Lee, J. -H.; Gillis, T.; Mysore, J. S.; Hayden, M. R.; Warby, S. C.; Morrison, P.; Nance, M.; Ross, C.A.; Margolis, R.L.; Squitieri, F.; et al. (Neurology, 2012)

Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region - Lee, J. -M.; Gillis, T.; Mysore, J. S.; Ramos, E.M.; Myers, R. H.; Hayden, M. R.; Morrison, P. J.; Nance, M.; Ross, C.A.; Margolis, R.L.; Squitieri, F.; Griguoli, A.; et al. (American Journal of Human Genetics, 2012)

Loss of junctophilin-3 contributes to huntington disease-like 2 pathogenesis - Seixas, A.I.; Holmes, S.E.; Takeshima, H.; Pavlovich, A.; Sachs, N.; Pruitt, J. L.; Silveira, I.; Ross, C.A.; Margolis, R.L.; Rudnicki, D. D. (Annals of Neurology, 2012)

TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease - Lee, J. -H.; Lee, J. -M.; Ramos, E.M.; Gillis, T.; Mysore, J. S.; Kishikawa, S.; Hadzi, T.; Hendricks, A. E.; Hayden, M. R.; Morrison, P. J.; Nance, M.; Ross, C.A.; et al. (Biochemical and Biophysical Research Communications, 2012)

FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes - Seixas, A.I.; Vale, J.; Jorge, P.; Marques, I.; Santos, R.; Alonso, I.; Fortuna, A.M.; Pinto-Basto, J.; Coutinho, P.; Margolis, R.L.; Sequeiros, J.; Silveira, I. (Behavioral and Brain Functions, 2011)

A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array - Holmes, S.E.; Wentzell, J.S.; Seixas, A.I.; Callahan, C.; Silveira, I.; Ross, C.A.; Margolis, R.L. (Human Genetics, 2006)

FXTAS, SCA10, and SCA17 in American patients with movement disorders [1] - Seixas, A.I.; Maurer, M.H.; Lin, M.; Callahan, C.; Ahuja, A.; Matsuura, T.; Ross, C.A.; Hisama, F.M.; Silveira, I.; Margolis, R.L. (American Journal of Medical Genetics, 2005)