@article {6421,
	title = {A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia},
	journal = {American Journal of Human Genetics},
	volume = {101},
	year = {2017},
	note = {Cited By :2Export Date: 19 March 2018},
	month = {2017},
	pages = {87 - 103},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021415706\&doi=10.1016\%2fj.ajhg.2017.06.007\&partnerID=40\&md5=84985cdc99a86734726baafd72a2cdc3},
	author = {Seixas, A.I. and Loureiro, J.R. and Costa, C. and Ord{\'o}{\~n}ez-Ugalde, A. and Marcelino, H. and Oliveira, C.L. and Loureiro, J.L. and Dhingra, A. and Brand{\~a}o, E. and Cruz, V.T. and Tim{\'o}teo, A. and Quint{\'a}ns, B. and Rouleau, G.A. and Rizzu, P. and Carracedo, A. and Bessa, J. and Heutink, P. and Sequeiros, J. and Sobrido, M.J. and Coutinho, P. and Silveira, I.}
}
@article {2941,
	title = {{\textquoteright}Costa da Morte{\textquoteright} ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization},
	journal = {Brain},
	volume = {135},
	year = {2012},
	note = {Cited By (since 1996): 2Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {1423 - 1435},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84860608331\&partnerID=40\&md5=69fbec9a4cf46680a5fc7a003f7a82f9},
	author = {Garc{\'\i}a-Murias, M. and Quint{\'a}ns, B. and Arias, M. and Seixas, A.I. and Cacheiro, P. and Tarr{\'\i}o, R. and Pardo, J. and Mill{\'a}n, M. J. and Arias-Rivas, S. and Blanco-Arias, P. and Dapena, D. and Moreira, R. and Rodr{\'\i}guez-Trelles, F. and Sequeiros, J. and Carracedo, A. and Silveira, I. and Sobrido, M. J.}
}
@article {2994,
	title = {Loss of junctophilin-3 contributes to huntington disease-like 2 pathogenesis},
	journal = {Annals of Neurology},
	volume = {71},
	year = {2012},
	note = {Cited By (since 1996): 2Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {245 - 257},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84857520653\&partnerID=40\&md5=d5662606f1fa602e818eb9b20884abaf},
	author = {Seixas, A.I. and Holmes, S.E. and Takeshima, H. and Pavlovich, A. and Sachs, N. and Pruitt, J. L. and Silveira, I. and Ross, C.A. and Margolis, R.L. and Rudnicki, D. D.}
}
@article {3111,
	title = {FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes},
	journal = {Behavioral and Brain Functions},
	volume = {7},
	year = {2011},
	note = {Export Date: 18 March 2013Source: ScopusArt. No.: 19},
	month = {2011///},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-79957829884\&partnerID=40\&md5=2be467541a40dac8980e300ecb23245a},
	author = {Seixas, A.I. and Vale, J. and Jorge, P. and Marques, I. and Santos, R. and Alonso, I. and Fortuna, A.M. and Pinto-Basto, J. and Coutinho, P. and Margolis, R.L. and Sequeiros, J. and Silveira, I.}
}
@article {4002,
	title = {A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array},
	journal = {Human Genetics},
	volume = {120},
	year = {2006},
	note = {Export Date: 18 March 2013Source: Scopus},
	month = {2006///},
	pages = {193 - 200},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-33747014342\&partnerID=40\&md5=8a2550a68049cb933a76a8f7dbd13268},
	author = {Holmes, S.E. and Wentzell, J.S. and Seixas, A.I. and Callahan, C. and Silveira, I. and Ross, C.A. and Margolis, R.L.}
}
@article {4169,
	title = {FXTAS, SCA10, and SCA17 in American patients with movement disorders [1]},
	journal = {American Journal of Medical Genetics},
	volume = {136 A},
	year = {2005},
	note = {Cited By (since 1996): 19Export Date: 18 March 2013Source: Scopus},
	month = {2005///},
	pages = {87 - 89},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-21644486998\&partnerID=40\&md5=be44c3f11c9988a6f826c7e0dc731cdb},
	author = {Seixas, A.I. and Maurer, M.H. and Lin, M. and Callahan, C. and Ahuja, A. and Matsuura, T. and Ross, C.A. and Hisama, F.M. and Silveira, I. and Margolis, R.L.}
}
@article {4114,
	title = {Haplotype diversity and somatic instability in normal and expanded SCA8 alleles},
	journal = {American Journal of Medical Genetics - Neuropsychiatric Genetics},
	volume = {139 B},
	year = {2005},
	note = {Cited By (since 1996): 5Export Date: 18 March 2013Source: Scopus},
	month = {2005///},
	pages = {109 - 114},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-27644506104\&partnerID=40\&md5=9f6d5bca13ae59b20f3a8f8a0d1f02f5},
	author = {Martins, S. and Seixas, A.I. and Magalh{\~a}es, P. and Coutinho, P. and Sequeiros, J. and Silveira, I.}
}
@article {4133,
	title = {A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14},
	journal = {Journal of Human Genetics},
	volume = {50},
	year = {2005},
	note = {Cited By (since 1996): 21Export Date: 18 March 2013Source: Scopus},
	month = {2005///},
	pages = {523 - 529},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-27644562111\&partnerID=40\&md5=240f114c28312907498c1576c7a34fd9},
	author = {Alonso, I. and Costa, C. and Gomes, A. and Ferro, A. and Seixas, A.I. and Silva, S. and Cruz, V.T. and Coutinho, P. and Sequeiros, J. and Silveira, I.}
}
