Intergenerational instability in Huntington disease: Extreme repeat changes among 134 transmissions - Ramos, E.M.; Cerqueira, J.; Lemos, C.; Pinto-Basto, J.; Alonso, I.; Sequeiros, J. (Movement Disorders, 2012)

Large normal and reduced penetrance alleles in Huntington disease: Instability in families and frequency at the laboratory, at the clinic and in the population - Sequeiros, J.; Ramos, E.M.; Cerqueira, J.; Costa, M.C.; Sousa, A.; Pinto-Basto, J.; Alonso, I. (Clinical Genetics, 2010)

Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype - Costa, M.D.C.; Teixeira-Castro, A.; Constante, M.; Magalhães, M.; Magalhães, P.; Cerqueira, J.; Vale, J.; Passão, V.; Barbosa, C.; Robalo, C.; Coutinho, P.; Barros, J.; et al. (Journal of Human Genetics, 2006)