Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation

von Brand, Harrison, Collins, Ryan L., Hanscom, Carrie, Rosenfeld, Jill A., Pillalamarri, Vamsee, Stone, Matthew R., Kelley, Fontina, Mason, Tamara, Margolin, Lauren, Eggert, Stacey, Mitchell, Elyse, Hodge, Jennelle C., Gusella, James F., Sanders, Stephan J., Talkowski, Michael E.
Veröffentlicht in Am J Hum Genet (2015)

Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders

von Brand, Harrison, Pillalamarri, Vamsee, Collins, Ryan L., Eggert, Stacey, O’Dushlaine, Colm, Braaten, Ellen B., Stone, Matthew R., Chambert, Kimberly, Doty, Nathan D., Hanscom, Carrie, Rosenfeld, Jill A., Ditmars, Hillary, Blais, Jessica, Mills, Ryan, Lee, Charles, Gusella, James F., McCarroll, Steven, Smoller, Jordan W., Talkowski, Michael E., Doyle, Alysa E.
Veröffentlicht 2014

Genome-wide Linkage and Association Analyses Implicate FASN in Predisposition to Uterine Leiomyomata

von Eggert, Stacey L., Huyck, Karen L., Somasundaram, Priya, Kavalla, Raghava, Stewart, Elizabeth A., Lu, Ake T., Painter, Jodie N., Montgomery, Grant W., Medland, Sarah E., Nyholt, Dale R., Treloar, Susan A., Zondervan, Krina T., Heath, Andrew C., Madden, Pamela A.F., Rose, Lynda, Buring, Julie E., Ridker, Paul M., Chasman, Daniel I., Martin, Nicholas G., Cantor, Rita M., Morton, Cynthia C.
Veröffentlicht 2012