Search Results - Ragan Hart

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  1. 1
    Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium

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

    Published 2018
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  2. 2
    The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation

    The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation by Meng Li, Caroline S. Bennette, Laura M. Amendola, Ragan Hart, Patrick J. Heagerty, Bryan A. Comstock, Peter Tarczy‐Hornoch, Stephanie M. Fullerton, Dean A. Regier, Wylie Burke, Susan Brown Trinidad, Gail P. Jarvik, David L. Veenstra, Donald L. Patrick

    Published 2018
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  3. 3
    Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies

    Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies by Jill O. Robinson, Julia Wynn, Barbara B. Biesecker, Leslie G. Biesecker, Barbara A. Bernhardt, Kyle B. Brothers, Wendy K. Chung, Kurt D. Christensen, Robert C. Green, Amy L. McGuire, M. Ragan Hart, Ida Griesemer, Donald L. Patrick, Christine Rini, David L. Veenstra, Angel M. Cronin, Stacy W. Gray

    Published 2019
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    Revisão
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  4. 4
    The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research

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

    Published 2019
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  5. 5
    Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium

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

    Published 2016
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  6. 6
    Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium

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

    Published 2016
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  7. 7
    The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations

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

    Published 2018
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  8. 8
    Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

    Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study by Ragan Hart, Barbara B. Biesecker, Carrie L. Blout Zawatsky, Kurt D. Christensen, Laura M. Amendola, Katie Bergstrom, Sawona Biswas, Kevin M. Bowling, Kyle B. Brothers, Laura K. Conlin, Gregory M. Cooper, Matthew C. Dulik, Kelly M. East, Jessica N. Everett, Candice R. Finnila, Arezou A. Ghazani, Marian J. Gilmore, Katrina A.B. Goddard, Gail P. Jarvik, Jennifer J. Johnston, Tia L. Kauffman, Whitley V. Kelley, Joel B. Krier, Katie L. Lewis, Amy L. McGuire, Carmit K. McMullen, Jeffrey Ou, Sharon E. Plon, Heidi L. Rehm, C. Sue Richards, Edward J. Romasko, Ane Miren Sagardia, Nancy B. Spinner, Michelle L. Thompson, Erin Turbitt, Jason L. Vassy, Benjamin S. Wilfond, David L. Veenstra, Jonathan S. Berg, Robert C. Green, Leslie G. Biesecker, Lucia A. Hindorff

    Published 2018
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  9. 9
    Actionable exomic incidental findings in 6503 participants: challenges of variant classification

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

    Published 2015
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