@article {4721,
	title = {Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington{\textquoteright}s disease motor onset},
	journal = {Neurogenetics},
	volume = {14},
	year = {2013},
	note = {Cited By (since 1996):2Export Date: 8 April 2014Source: Scopus},
	month = {2013},
	pages = {173 - 179},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84888063832\&partnerID=40\&md5=10b47c0fd5922805d754454404213459},
	author = {Ramos, E.M. and Latourelle, J.C. and Gillis, T. and Mysore, J. S. and Squitieri, F. and Di Pardo, A. and Di Donato, S. and Gellera, C. and Hayden, M. R. and Morrison, P. J. and Nance, M. and Ross, C.A. and Margolis, R.L. and Gomez-Tortosa, E. and Ayuso, C. and Suchowersky, O. and Trent, R. J. and McCusker, E. and Novelletto, A. and Frontali, M. and Jones, R. and Ashizawa, T. and Frank, S. and Saint-Hilaire, M. -H. and Hersch, S. M. and Rosas, H. D. and Lucente, D. and Harrison, M. B. and Zanko, A. and Abramson, R. K. and Marder, K. and Gusella, J. F. and Lee, J. -M. and Alonso, I. and Sequeiros, J. and Myers, R. H. and MacDonald, M. E.}
}
@article {4745,
	title = {Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant},
	journal = {Chromosome Research},
	volume = {21},
	year = {2013},
	note = {Cited By (since 1996):5Export Date: 8 April 2014Source: Scopus},
	month = {2013},
	pages = {101 - 106},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84880573233\&partnerID=40\&md5=e2ed1aca4487687e780ee2b0a2979c19},
	author = {Earnshaw, W.C. and Allshire, R.C. and Black, B.E. and Bloom, K. and Brinkley, B.R. and Brown, W. and Cheeseman, I.M. and Choo, K.H.A. and Copenhaver, G.P. and Deluca, J.G. and Desai, A. and Diekmann, S. and Erhardt, S. and Fitzgerald-Hayes, M. and Foltz, D. and Fukagawa, T. and Gassmann, R. and Gerlich, D.W. and Glover, D.M. and Gorbsky, G.J. and Harrison, S.C. and Heun, P. and Hirota, T. and Jansen, L.E.T. and Karpen, G. and Kops, G.J.P.L. and Lampson, M.A. and Lens, S.M. and Losada, A. and Luger, K. and Maiato, H. and Maddox, P.S. and Margolis, R.L. and Masumoto, H. and McAinsh, A.D. and Mellone, B.G. and Meraldi, P. and Musacchio, A. and Oegema, K. and O{\textquoteright}Neill, R.J. and Salmon, E.D. and Scott, K.C. and Straight, A.F. and Stukenberg, P.T. and Sullivan, B.A. and Sullivan, K.F. and Sunkel, C.E. and Swedlow, J.R. and Walczak, C.E. and Warburton, P.E. and Westermann, S. and Willard, H.F. and Wordeman, L. and Yanagida, M. and Yen, T.J. and Yoda, K. and Cleveland, D.W.}
}
@article {2976,
	title = {CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion},
	journal = {Neurology},
	volume = {78},
	year = {2012},
	note = {Cited By (since 1996): 12Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {690 - 695},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84858074593\&partnerID=40\&md5=e2e076dc1b33ef446094982342633861},
	author = {Lee, J. -M. and Ramos, E.M. and Lee, J. -H. and Gillis, T. and Mysore, J. S. and Hayden, M. R. and Warby, S. C. and Morrison, P. and Nance, M. and Ross, C.A. and Margolis, R.L. and Squitieri, F. and Orobello, S. and Di Donato, S. and Gomez-Tortosa, E. and Ayuso, C. and Suchowersky, O. and Trent, R. J. A. and McCusker, E. and Novelletto, A. and Frontali, M. and Jones, R. and Ashizawa, T. and Frank, S. and Saint-Hilaire, M. H. and Hersch, S. M. and Rosas, H. D. and Lucente, D. and Harrison, M. B. and Zanko, A. and Abramson, R. K. and Marder, K. and Sequeiros, J. and Paulsen, J. S. and Landwehrmeyer, G. B. and Myers, R. H. and MacDonald, M. E. and Gusella, J. F.}
}
@article {2974,
	title = {Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region},
	journal = {American Journal of Human Genetics},
	volume = {90},
	year = {2012},
	note = {Cited By (since 1996): 1Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {434 - 444},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84862831145\&partnerID=40\&md5=78917e3524aa125b61a52b87c44f68f1},
	author = {Lee, J. -M. and Gillis, T. and Mysore, J. S. and Ramos, E.M. and Myers, R. H. and Hayden, M. R. and Morrison, P. J. and Nance, M. and Ross, C.A. and Margolis, R.L. and Squitieri, F. and Griguoli, A. and Di Donato, S. and Gomez-Tortosa, E. and Ayuso, C. and Suchowersky, O. and Trent, R. J. and McCusker, E. and Novelletto, A. and Frontali, M. and Jones, R. and Ashizawa, T. and Frank, S. and Saint-Hilaire, M. -H. and Hersch, S. M. and Rosas, H. D. and Lucente, D. and Harrison, M. B. and Zanko, A. and Abramson, R. K. and Marder, K. and Sequeiros, J. and MacDonald, M. E. and Gusella, J. F.}
}
@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 {2878,
	title = {TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington{\textquoteright}s disease},
	journal = {Biochemical and Biophysical Research Communications},
	volume = {424},
	year = {2012},
	note = {Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {404 - 408},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84864757021\&partnerID=40\&md5=472b3f1e56a13963b3f6b7e441a54d83},
	author = {Lee, J. -H. and Lee, J. -M. and Ramos, E.M. and Gillis, T. and Mysore, J. S. and Kishikawa, S. and Hadzi, T. and Hendricks, A. E. and Hayden, M. R. and Morrison, P. J. and Nance, M. and Ross, C.A. and Margolis, R.L. and Squitieri, F. and Gellera, C. and Gomez-Tortosa, E. and Ayuso, C. and Suchowersky, O. and Trent, R. J. and McCusker, E. and Novelletto, A. and Frontali, M. and Jones, R. and Ashizawa, T. and Frank, S. and Saint-Hilaire, M. -H. and Hersch, S. M. and Rosas, H. D. and Lucente, D. and Harrison, M. B. and Zanko, A. and Abramson, R. K. and Marder, K. and Sequeiros, J. and Bernhard Landwehrmeyer, G. and Shoulson, I. and Myers, R. H. and MacDonald, M. E. and Gusella, J. F.}
}
@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.}
}
