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2015
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
2012
Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities.Talkowski, ME, Maussion G., Crapper L., Rosenfeld JA, Blumenthal I., Hanscom C., Chiang C., Lindgren A., Pereira S., Ruderfer D., Diallo AB, Lopez JP, Turecki G., Chen ES, Gigek C., Harris DJ, Lip V., An Y., Biagioli M., Macdonald ME, et al. American journal of human genetics, 2012/12/07, Volume 91, Issue 6, p.1128-34, (2012) Read More / View Supplemental Materials
Abstract
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
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