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  • Showing 1-7 of 7 Results
2014
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.Sugathan, A., Biagioli M., Golzio C., Erdin S., Blumenthal I., Manavalan P., Ragavendran A., Brand H., Lucente D., Miles J., Sheridan SD, Stortchevoi A., Kellis M., Haggarty SJ, Katsanis N., Gusella JF, and Talkowski ME Proceedings of the National Academy of Sciences of the United States of America, 2014/10/07, (2014) Read More / View Supplemental Materials
Abstract
Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders.Brand, H., Pillalamarri V., Collins RL, Eggert S., O'Dushlaine C., Braaten EB, Stone MR, Chambert K., Doty ND, Hanscom C., Rosenfeld JA, Ditmars H., Blais J., Mills R., Lee C., Gusella JF, McCarroll S., Smoller JW, Talkowski ME, and Doyle AE American journal of human genetics, 2014/10/02, Volume 95, Issue 4, p.454-61, (2014) Read More / View Supplemental Materials
Abstract
Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing.Veres, A., Gosis BS, Ding Q., Collins R., Ragavendran A., Brand H., Erdin S., Talkowski ME, and Musunuru K. Cell stem cell, 2014/07/03, Volume 15, Issue 1, p.27-30, (2014) Read More / View Supplemental Materials
Abstract
Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.Blumenthal, I., Ragavendran A., Erdin S., Klei L., Sugathan A., Guide JR, Manavalan P., Zhou JQ, Wheeler VC, Levin JZ, Ernst C., Roeder K., Devlin B., Gusella JF, and Talkowski ME American journal of human genetics, 2014/06/05, Volume 94, Issue 6, p.870-83, (2014) Read More / View Supplemental Materials
Abstract
Describing Sequencing Results of Structural Chromosome Rearrangements with a Suggested Next-Generation Cytogenetic Nomenclature.Ordulu, Z., Wong KE, Currall BB, Ivanov AR, Pereira S., Althari S., Gusella JF, Talkowski ME, and Morton CC American journal of human genetics, 2014/04/16, (2014) 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
Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries.Talkowski, ME, Rosenfeld JA, Blumenthal I., Pillalamarri V., Chiang C., Heilbut A., Ernst C., Hanscom C., Rossin E., Lindgren AM, Pereira S., Ruderfer D., Kirby A., Ripke S., Harris DJ, Lee JH, Ha K., Kim HG, Solomon BD, Gropman AL, et al. Cell, 2012/04/27, Volume 149, Issue 3, p.525-37, (2012) Read More / View Supplemental Materials
Abstract
  • Showing 1-7 of 7 Results