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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 2
2006 4
2007 3
2008 1
2010 3
2011 2
2012 6
2013 2
2014 2
2015 6
2019 1
2024 0

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Page 1
Hypomorphic mutation of the mouse Huntington's disease gene orthologue.
Murthy V, Tebaldi T, Yoshida T, Erdin S, Calzonetti T, Vijayvargia R, Tripathi T, Kerschbamer E, Seong IS, Quattrone A, Talkowski ME, Gusella JF, Georgopoulos K, MacDonald ME, Biagioli M. Murthy V, et al. PLoS Genet. 2019 Mar 21;15(3):e1007765. doi: 10.1371/journal.pgen.1007765. eCollection 2019 Mar. PLoS Genet. 2019. PMID: 30897080 Free PMC article.
Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease.
Ramos EM, Gillis T, Mysore JS, Lee JM, Gögele M, D'Elia Y, Pichler I, Sequeiros J, Pramstaller PP, Gusella JF, MacDonald ME, Alonso I. Ramos EM, et al. Am J Med Genet B Neuropsychiatr Genet. 2015 Mar;168B(2):135-43. doi: 10.1002/ajmg.b.32289. Epub 2015 Feb 5. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 25656686 Free PMC article.
Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.
Ramos EM, Latourelle JC, Gillis T, Mysore JS, Squitieri F, Di Pardo A, Di Donato S, Gellera C, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Gomez-Tortosa E, Ayuso C, Suchowersky O, Trent RJ, McCusker E, Novelletto A, Frontali M, Jones R, Ashizawa T, Frank S, Saint-Hilaire MH, Hersch SM, Rosas HD, Lucente D, Harrison MB, Zanko A, Abramson RK, Marder K, Gusella JF, Lee JM, Alonso I, Sequeiros J, Myers RH, Macdonald ME. Ramos EM, et al. Neurogenetics. 2013 Nov;14(3-4):173-9. doi: 10.1007/s10048-013-0364-y. Epub 2013 May 4. Neurogenetics. 2013. PMID: 23644918 Free PMC article.
30 results