Resultados da pesquisa - Mahanta, Lisa

The Translational Genomics Core at Partners Personalized Medicine: Facilitating the Transition of Research towards Personalized Medicine Por Blau, Ashley, Brown, Alison, Mahanta, Lisa, Amr, Sami S.

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Information Technology Support for Clinical Genetic Testing within an Academic Medical Center Por Aronson, Samuel, Mahanta, Lisa, Ros, Lei Lei, Clark, Eugene, Babb, Lawrence, Oates, Michael, Rehm, Heidi, Lebo, Matthew

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The Information Technology Infrastructure for the Translational Genomics Core and the Partners Biobank at Partners Personalized Medicine Por Boutin, Natalie, Holzbach, Ana, Mahanta, Lisa, Aldama, Jackie, Cerretani, Xander, Embree, Kevin, Leon, Irene, Rathi, Neeta, Vickers, Matilde

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VisCap: inference and visualization of germ-line copy-number variants from targeted clinical sequencing data Por Pugh, Trevor J., Amr, Sami S., Bowser, Mark J., Gowrisankar, Sivakumar, Hynes, Elizabeth, Mahanta, Lisa M., Rehm, Heidi L., Funke, Birgit, Lebo, Matthew S.

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Next generation sequencing‐based copy number analysis reveals low prevalence of deletions and duplications in 46 genes associated with genetic cardiomyopathies Por Ceyhan‐Birsoy, Ozge, Pugh, Trevor J., Bowser, Mark J., Hynes, Elizabeth, Frisella, Ashley L., Mahanta, Lisa M., Lebo, Matt S., Amr, Sami S., Funke, Birgit H.

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Analyzing and Reanalyzing the Genome: Findings from the MedSeq Project Por Machini, Kalotina, Ceyhan-Birsoy, Ozge, Azzariti, Danielle R., Sharma, Himanshu, Rossetti, Peter, Mahanta, Lisa, Hutchinson, Laura, McLaughlin, Heather, Green, Robert C., Lebo, Matthew, Rehm, Heidi L.

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Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test Por Brockman, Deanna G., Austin-Tse, Christina A., Pelletier, Renée C., Harley, Caroline, Patterson, Candace, Head, Holly, Leonard, Courtney Elizabeth, O’Brien, Kimberly, Mahanta, Lisa M., Lebo, Matthew S., Lu, Christine Y., Natarajan, Pradeep, Khera, Amit V., Aragam, Krishna G., Kathiresan, Sekar, Rehm, Heidi L., Udler, Miriam S.

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Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization Por Blout Zawatsky, Carrie L., Shah, Nidhi, Machini, Kalotina, Perez, Emma, Christensen, Kurt D., Zouk, Hana, Steeves, Marcie, Koch, Christopher, Uveges, Melissa, Shea, Janelle, Gold, Nina, Krier, Joel, Boutin, Natalie, Mahanta, Lisa, Rehm, Heidi L., Weiss, Scott T., Karlson, Elizabeth W., Smoller, Jordan W., Lebo, Matthew S., Green, Robert C.

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A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort Por Schwartz, Marci L.B., McCormick, Cara Zayac, Lazzeri, Amanda L., Lindbuchler, D’Andra M., Hallquist, Miranda L.G., Manickam, Kandamurugu, Buchanan, Adam H., Rahm, Alanna Kulchak, Giovanni, Monica A., Frisbie, Lauren, Flansburg, Carroll N., Davis, F. Daniel, Sturm, Amy C., Nicastro, Christine, Lebo, Matthew S., Mason-Suares, Heather, Mahanta, Lisa Marie, Carey, David J., Williams, Janet L., Williams, Marc S., Ledbetter, David H., Faucett, W. Andrew, Murray, Michael F.

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Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Ca... Por Morales, Ana, Ing, Alexander, Antolik, Christian, Austin-Tse, Christina, Baudhuin, Linnea M., Bronicki, Lucas, Cirino, Allison, Hawley, Megan H., Fietz, Michael, Garcia, John, Ho, Carolyn, Ingles, Jodie, Jarinova, Olga, Johnston, Tami, Kelly, Melissa A., Kurtz, C. Lisa, Lebo, Matt, Macaya, Daniela, Mahanta, Lisa, Maleszewski, Joseph, Manrai, Arjun K., Murray, Mitzi, Richard, Gabriele, Semsarian, Chris, Thomson, Kate L., Winder, Tom, Ware, James S., Hershberger, Ray E., Funke, Birgit H., Vatta, Matteo

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