Assessing Genetic Variants in Matched Biocompartments From Patients With Serous Ovarian Cancer von Sanders, Brooke E., Ku, Lisa, Walker, Paul, Bitler, Benjamin G.

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Small cell carcinoma of the ovary hypercalcemic type (SCCOHT): A review and novel case with dual germline SMARCA4 and BRCA2 mutations von Sanders, Brooke E., Wolsky, Rebecca, Doughty, Elizabeth S., Wells, Kristen L., Ghosh, Debashis, Ku, Lisa, Pressey, Joseph G., Bitler, Benjamin G., Brubaker, Lindsay W.

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Returning actionable genetic results to participants in the biobank at the Colorado Center for Personalized Medicine and UCHealth von Lowery, Jan T., Axell, Lisen, Ku, Lisa, Todd, Emily B., Kao, Dave, Rafaels, Nick, Taylor, Matt R.G., Kudron, Elizabeth, Wicks, Stephen, Jirikowic, Jean, Shalowitz, Elise, Crooks, Kristy R.

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Prevalence of desmin mutations in dilated cardiomyopathy von TAYLOR, Matthew R. G, SLAVOV, Dobromir, XIAO ZHU, CAVANAUGH, Jean, SUCHAROV, Carmen C, LONG, Carlin S, BRISTOW, Michael R, LAVORI, Philip, MESTRONI, Luisa, KU, Lisa, DI LENARDA, Andrea, SINAGRA, Gianfranco, CARNIEL, Elisa, HAUBOLD, Kurt, BOUCEK, Mark M, FERGUSON, Debra, GRAW, Sharon L

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Assessing somatic mutations in matched biospecimens from patients with serous ovarian cancer von Sanders, Brooke, Bitler, Benjamin, Ku, Lisa

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Danon disease presenting with dilated cardiomyopathy and a complex phenotype von Taylor, Matthew R G, Ku, Lisa, Slavov, Dobromir, Cavanaugh, Jean, Boucek, Mark, Zhu, Xiao, Graw, Sharon, Carniel, Elisa, Barnes, Carl, Quan, Dianna, Prall, Ryan, Lovell, Mark A, Mierau, Gary, Ruegg, Patsy, Mandava, Naresh, Bristow, Michael R, Towbin, Jeffrey A, Mestroni, Luisa

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Massive air embolism from continuous venovenous haemofiltration causing electromechanical dissociation in a cardiac surgical patient von Ku, Lisa, Weinberg, Laurence, Seevanayagam, Siven, Baldwin, Ian, Opdam, Helen, Doolan, Laurie

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SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia von MCNAIR, William P, KU, Lisa, TAYLOR, Matthew R. G, FAIN, Pam R, DAO, Dmi, WOLFEL, Eugene, MESTRONI, Luisa

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Building a vertically integrated genomic learning health system: The biobank at the Colorado Center for Personalized Medicine von Wiley, Laura K., Shortt, Jonathan A., Roberts, Emily R., Lowery, Jan, Kudron, Elizabeth, Lin, Meng, Mayer, David, Wilson, Melissa, Brunetti, Tonya M., Chavan, Sameer, Phang, Tzu L., Pozdeyev, Nikita, Lesny, Joseph, Wicks, Stephen J., Moore, Ethan T., Morgenstern, Joshua L., Roff, Alanna N., Shalowitz, Elise L., Stewart, Adrian, Williams, Cole, Edelmann, Michelle N., Hull, Madelyne, Patton, J. Tacker, Axell, Lisen, Ku, Lisa, Lee, Yee Ming, Jirikowic, Jean, Tanaka, Anna, Todd, Emily, White, Sarah, Peterson, Brett, Hearst, Emily, Zane, Richard, Greene, Casey S., Mathias, Rasika, Coors, Marilyn, Taylor, Matthew, Ghosh, Debashis, Kahn, Michael G., Brooks, Ian M., Aquilante, Christina L., Kao, David, Rafaels, Nicholas, Crooks, Kristy R., Hess, Steve, Barnes, Kathleen C., Gignoux, Christopher R.

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α-myosin heavy chain : A sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy von CARNIEL, Elisa, TAYLOR, Matthew R. G, GRAW, Sharon L, FEIGER, Jennie, XIAO ZHONG ZHU, DAO, Dmi, FERGUSON, Debra A, BRISTOW, Michael R, MESTRONI, Luisa, SINAGRA, Gianfranco, DI LENARDA, Andrea, KU, Lisa, FAIN, Pamela R, BOUCEK, Mark M, CAVANAUGH, Mi Jean, MIOCIC, Snjezana, SLAVOV, Dobromir

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Ophthalmic Manifestations of Danon Disease von Prall, F. Ryan, Drack, Arlene, Taylor, Matthew, Ku, Lisa, Olson, Jeffrey L., Gregory, Darren, Mestroni, Luisa, Mandava, Naresh

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Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy von Taylor, Matthew R.G., Slavov, Dobromir, Gajewski, Andreas, Vlcek, Sylvia, Ku, Lisa, Fain, Pamela R., Carniel, Elisa, Di Lenarda, Andrea, Sinagra, Gianfranco, Boucek, Mark M., Cavanaugh, Jean, Graw, Sharon L., Ruegg, Patsy, Feiger, Jennie, Zhu, Xiao, Ferguson, Debra A., Bristow, Michael R., Gotzmann, Josef, Foisner, Roland, Mestroni, Luisa

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Natural history of dilated cardiomyopathy due to lamin A/C gene mutations von Taylor, Matthew R.G, Fain, Pamela R, Sinagra, Gianfranco, Robinson, Misi L, Robertson, Alastair D, Carniel, Elisa, Di Lenarda, Andrea, Bohlmeyer, Teresa J, Ferguson, Debra A, Brodsky, Gary L, Boucek, Mark M, Lascor, Jean, Moss, Andrew C, Li, Wai-Lun P, Stetler, Gary L, Muntoni, Francesco, Bristow, Michael R, Mestroni, Luisa

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The impact of direct-to-consumer marketing of cancer genetic testing on women according to their genetic risk von Lowery, Jan T., Byers, Tim, Axell, Lisen, Ku, Lisa, Jacobellis, Jillian

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Cardiology patient page. Familial dilated cardiomyopathy von Ku, Lisa, Feiger, Jennie, Taylor, Matthew, Mestroni, Luisa

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Genetic Counseling Practice Analysis von Hampel, Heather, Grubs, Robin E., Walton, Carol S., Nguyen, Emma, Breidenbach, Daniel H., Nettles, Steve, Corliss, Meagan, Fox, Stephanie, Hiraki, Susan, Ku, Lisa, Neufeld-Kaiser, Whitney, Riley, Bronson, Taylor, Jamie, Weik, LuAnn

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Familial Dilated Cardiomyopathy von Ku, Lisa, Feiger, Jennie, Taylor, Matthew, Mestroni, Luisa

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Ophthalmic Manifestations of Danon Disease von Prall, F. Ryan, Drack, Arlene, Taylor, Matthew, Ku, Lisa, Olson, Jeff, Mandava, Naresh

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Small cell carcinoma of the ovary hypercalcemic type (SCCOHT): A review and novel case with dual germline SMARCA4 and BRCA2 mutations von Sanders, Brooke E, Wolsky, Rebecca, Doughty, Elizabeth S, Wells, Kristen L, Ghosh, Debashis, Ku, Lisa, Pressey, Joseph G, Bitler, Benjamin B, Brubaker, Lindsay W

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Grad‐seq in a Gram‐positive bacterium reveals exonucleolytic sRNA activation in competence control von Hör, Jens, Garriss, Geneviève, Di Giorgio, Silvia, Hack, Lisa‐Marie, Vanselow, Jens T, Förstner, Konrad U, Schlosser, Andreas, Henriques‐Normark, Birgitta, Vogel, Jörg

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