Výsledky vyhledávání - Hart, Ragan

The Impact of Body Mass Index and Genetics on Warfarin Major Bleeding Outcomes in a Community Setting Autor Hart, Ragan, Veenstra, David L., Boudreau, Denise M., Roth, Joshua A.

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Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium Autor Amendola, Laura M., Robinson, Jill O., Hart, Ragan, Biswas, Sawona, Lee, Kaitlyn, Bernhardt, Barbara A., East, Kelly, Gilmore, Marian J., Kauffman, Tia L., Lewis, Katie L., Roche, Myra, Scollon, Sarah, Wynn, Julia, Blout, Carrie

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Clinical Exome Sequencing vs. Usual Care for Hereditary Colorectal Cancer Diagnosis: A Pilot Comparative Effectiveness Study Autor Niu, Xin, Amendola, Laura M., Hart, Ragan, Bennette, Caroline S., Heagerty, Patrick, Horike-Pyne, Martha, Trinidad, Susan B., Rosenthal, Elisabeth A., Comstock, Bryan, Nefcy, Chris, Hisama, Fuki M, Bennett, Robin L., Grady, William M., Gallego, Carlos J., Tarczy-Hornoch, Peter, Fullerton, Stephanie M, Burke, Wylie, Regier, Dean A., Dorschner, Michael O., Shirts, Brian H., Robertson, Peggy D., Nickerson, Deborah A., Patrick, Donald L., Jarvik, Gail P., Veenstra, David L.

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The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research Autor Horowitz, Carol R., Orlando, Lori A., Slavotinek, Anne M., Peterson, Josh, Angelo, Frank, Biesecker, Barbara, Bonham, Vence L., Cameron, Linda D., Fullerton, Stephanie M., Gelb, Bruce D., Goddard, Katrina A.B., Hailu, Benyam, Hart, Ragan, Hindorff, Lucia A., Jarvik, Gail P., Kaufman, Dave, Kenny, Eimear E., Knight, Sara J., Koenig, Barbara A., Korf, Bruce R., Madden, Ebony, McGuire, Amy L., Ou, Jeffrey, Wasserstein, Melissa P., Robinson, Mimsie, Leventhal, Howard, Sanderson, Saskia C.

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Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium Autor Amendola, Laura M., Jarvik, Gail P., Leo, Michael C., McLaughlin, Heather M., Akkari, Yassmine, Amaral, Michelle D., Berg, Jonathan S., Biswas, Sawona, Bowling, Kevin M., Conlin, Laura K., Cooper, Greg M., Dorschner, Michael O., Dulik, Matthew C., Ghazani, Arezou A., Ghosh, Rajarshi, Green, Robert C., Hart, Ragan, Horton, Carrie, Johnston, Jennifer J., Lebo, Matthew S., Milosavljevic, Aleksandar, Ou, Jeffrey, Pak, Christine M., Patel, Ronak Y., Punj, Sumit, Richards, Carolyn Sue, Salama, Joseph, Strande, Natasha T., Yang, Yaping, Plon, Sharon E., Biesecker, Leslie G., Rehm, Heidi L.

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Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium Autor Amendola, Laura M., Jarvik, Gail P., Leo, Michael C., McLaughlin, Heather M., Akkari, Yassmine, Amaral, Michelle D., Berg, Jonathan S., Biswas, Sawona, Bowling, Kevin M., Conlin, Laura K., Cooper, Greg M., Dorschner, Michael O., Dulik, Matthew C., Ghazani, Arezou A., Ghosh, Rajarshi, Green, Robert C., Hart, Ragan, Horton, Carrie, Johnston, Jennifer J., Lebo, Matthew S., Milosavljevic, Aleksandar, Ou, Jeffrey, Pak, Christine M., Patel, Ronak Y., Punj, Sumit, Richards, Carolyn Sue, Salama, Joseph, Strande, Natasha T., Yang, Yaping, Plon, Sharon E., Biesecker, Leslie G., Rehm, Heidi L.

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The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations Autor Amendola, Laura M., Berg, Jonathan S., Horowitz, Carol R., Angelo, Frank, Bensen, Jeannette T., Biesecker, Barbara B., Biesecker, Leslie G., Cooper, Gregory M., East, Kelly, Filipski, Kelly, Fullerton, Stephanie M., Gelb, Bruce D., Goddard, Katrina A.B., Hailu, Benyam, Hart, Ragan, Hassmiller-Lich, Kristen, Joseph, Galen, Kenny, Eimear E., Koenig, Barbara A., Knight, Sara, Kwok, Pui-Yan, Lewis, Katie L., McGuire, Amy L., Norton, Mary E., Ou, Jeffrey, Parsons, Donald W., Powell, Bradford C., Risch, Neil, Robinson, Mimsie, Rini, Christine, Scollon, Sarah, Slavotinek, Anne M., Veenstra, David L., Wasserstein, Melissa P., Wilfond, Benjamin S., Hindorff, Lucia A., Plon, Sharon E., Jarvik, Gail P.

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Actionable exomic incidental findings in 6503 participants: challenges of variant classification Autor Amendola, Laura M., Dorschner, Michael O., Robertson, Peggy D., Salama, Joseph S., Hart, Ragan, Shirts, Brian H., Murray, Mitzi L., Tokita, Mari J., Gallego, Carlos J., Kim, Daniel Seung, Bennett, James T., Crosslin, David R., Ranchalis, Jane, Jones, Kelly L., Rosenthal, Elisabeth A., Jarvik, Ella R., Itsara, Andy, Turner, Emily H., Herman, Daniel S., Schleit, Jennifer, Burt, Amber, Jamal, Seema M., Abrudan, Jenica L., Johnson, Andrew D., Conlin, Laura K., Dulik, Matthew C., Santani, Avni, Metterville, Danielle R., Kelly, Melissa, Foreman, Ann Katherine M., Lee, Kristy, Taylor, Kent D., Guo, Xiuqing, Crooks, Kristy, Kiedrowski, Lesli A., Raffel, Leslie J., Gordon, Ora, Machini, Kalotina, Desnick, Robert J., Biesecker, Leslie G., Lubitz, Steven A., Mulchandani, Surabhi, Cooper, Greg M., Joffe, Steven, Richards, C. Sue, Yang, Yaoping, Rotter, Jerome I., Rich, Stephen S., O’Donnell, Christopher J., Berg, Jonathan S., Spinner, Nancy B., Evans, James P., Fullerton, Stephanie M., Leppig, Kathleen A., Bennett, Robin L., Bird, Thomas, Sybert, Virginia P., Grady, William M., Tabor, Holly K., Kim, Jerry H., Bamshad, Michael J., Wilfond, Benjamin, Motulsky, Arno G., Scott, C. Ronald, Pritchard, Colin C., Walsh, Tom D., Burke, Wylie, Raskind, Wendy H., Byers, Peter, Hisama, Fuki M., Rehm, Heidi, Nickerson, Debbie A., Jarvik, Gail P.

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