A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia - Seixas, A.I.; Loureiro, J.R.; Costa, C.; Ordóñez-Ugalde, A.; Marcelino, H.; Oliveira, C.L.; Loureiro, J.L.; Dhingra, A.; Brandão, E.; Cruz, V.T.; Timóteo, A.; Quintáns, B.; et al. (American Journal of Human Genetics, 2017)

'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization - García-Murias, M.; Quintáns, B.; Arias, M.; Seixas, A.I.; Cacheiro, P.; Tarrío, R.; Pardo, J.; Millán, M. J.; Arias-Rivas, S.; Blanco-Arias, P.; Dapena, D.; Moreira, R.; et al. (Brain, 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)

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)

Haplotype diversity and somatic instability in normal and expanded SCA8 alleles - Martins, S.; Seixas, A.I.; Magalhães, P.; Coutinho, P.; Sequeiros, J.; Silveira, I. (American Journal of Medical Genetics - Neuropsychiatric Genetics, 2005)

A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14 - Alonso, I.; Costa, C.; Gomes, A.; Ferro, A.; Seixas, A.I.; Silva, S.; Cruz, V.T.; Coutinho, P.; Sequeiros, J.; Silveira, I. (Journal of Human Genetics, 2005)