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2016
Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9.Shin, JW, Kim KH, Chao MJ, Atwal RS, Gillis T., Macdonald ME, Gusella JF, and Lee JM Human molecular genetics, 2016/09/15, (2016) Read More / View Supplemental Materials
Abstract
The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease.Keum, JW, Shin A., Gillis T., Mysore JS, Abu Elneel K., Lucente D., Hadzi T., Holmans P., Jones L., Orth M., Kwak S., Macdonald ME, Gusella JF, and Lee JM American journal of human genetics, 2016/02/04, Volume 98, Issue 2, p.287-98, (2016) Read More / View Supplemental Materials
Abstract
2015
The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease.Correia, K., Harold D., Kim KH, Holmans P., Jones L., Orth M., Myers RH, Kwak S., Wheeler VC, Macdonald ME, Gusella JF, and Lee JM Journal of Huntington's disease, 2015/09/29, Volume 4, Issue 3, p.279-84, (2015) Read More / View Supplemental Materials
Abstract
Sequence-Level Analysis of the Major European Huntington Disease Haplotype.Lee, JM, Kim KH, Shin A., Chao MJ, Abu Elneel K., Gillis T., Mysore JS, Kaye JA, Zahed H., Kratter IH, Daub AC, Finkbeiner S., Li H., Roach JC, Goodman N., Hood L., Myers RH, Macdonald ME, and Gusella JF American journal of human genetics, 2015/09/03, Volume 97, Issue 3, p.435-44, (2015) Read More / View Supplemental Materials
Abstract
Htt CAG repeat expansion confers pleiotropic gains of mutant huntingtin function in chromatin regulation.Biagioli, M., Ferrari F., Mendenhall EM, Zhang Y., Erdin S., Vijayvargia R., Vallabh SM, Solomos N., Manavalan P., Ragavendran A., Ozsolak F., Lee JM, Talkowski ME, Gusella JF, Macdonald ME, Park PJ, and Seong IS Human molecular genetics, 2015/01/08, (2015) Read More / View Supplemental Materials
Abstract
2013
Stroke Genetics Network (SiGN) Study: Design and Rationale for a Genome-Wide Association Study of Ischemic Stroke Subtypes.Meschia, JF, Arnett DK, Ay H., Brown RD Jr, Benavente OR, Cole JW, de Bakker PI, Dichgans M., Doheny KF, Fornage M., Grewal RP, Gwinn K., Jern C., Conde JJ, Johnson JA, Jood K., Laurie CC, Lee JM, Lindgren A., Markus HS, et al. Stroke; a journal of cerebral circulation, 2013/10/01, Volume 44, Issue 10, p.2694-702, (2013) Read More / View Supplemental Materials
Abstract
2012
Common SNP-Based Haplotype Analysis of the 4p16.3 Huntington Disease Gene Region.Lee, JM, Gillis T., Mysore JS, Ramos EM, Myers RH, Hayden MR, Morrison PJ, Nance M., Ross CA, Margolis RL, Squitieri F., Griguoli A., Di Donato S., Gomez-Tortosa E., Ayuso C., Suchowersky O., Trent RJ, McCusker E., Novelletto A., Frontali M., et al. American journal of human genetics, 2012/03/09, Volume 90, Issue 3, p.434-444, (2012) Read More / View Supplemental Materials
Abstract
  • Showing 1-7 of 7 Results