Výsledky vyhledávání - Kate M. Orland

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  1. 1
    Psychosocial Consequences of False-Positive Newborn Screens for Cystic Fibrosis

    Psychosocial Consequences of False-Positive Newborn Screens for Cystic Fibrosis Autor Audrey Tluczek, Kate M. Orland, Laura Cavanagh

    Vydáno 2010
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  2. 2
    Newborn Screening

    Newborn Screening Autor Audrey Tluczek, Kate M. Orland, Sara Wolfgram Nick, Roger Brown

    Vydáno 2009
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  3. 3
    A PAS-targeting hERG1 activator reduces arrhythmic events in Jervell and Lange-Nielsen syndrome patient-derived hiPSC-CMs

    A PAS-targeting hERG1 activator reduces arrhythmic events in Jervell and Lange-Nielsen syndrome patient-derived hiPSC-CMs Autor Chiamaka U. Ukachukwu, Eric N. Jiménez‐Vázquez, Shreya Salwi, Mark S. Goodrich, Francisco G. Sanchez-Conde, Kate M. Orland, Abhilasha Jain, Lee L. Eckhardt, Timothy J. Kamp, David Jones

    Vydáno 2025
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  4. 4
    A Case for Inclusion of Genetic Counselors in Cardiac Care

    A Case for Inclusion of Genetic Counselors in Cardiac Care Autor Patricia Arscott, Colleen Caleshu, Katrina E. Kotzer, Sarah Kreykes, Teresa Kruisselbrink, Kate M. Orland, Christina Rigelsky, Emily Smith, Katherine G. Spoonamore, Joy Larsen Haidle, Monica Marvin, Michael J. Ackerman, Azam Hadi, Arya Mani, Steven R. Ommen, Sara Cherny

    Vydáno 2015
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  5. 5
    Clinical and Functional Characterization of Ryanodine Receptor 2 Variants Implicated in Calcium-Release Deficiency Syndrome

    Clinical and Functional Characterization of Ryanodine Receptor 2 Variants Implicated in Calcium-Release Deficiency Syndrome Autor Thomas M. Roston, Jinhong Wei, Wenting Guo, Yanhui Li, Xiaowei Zhong, Ruiwu Wang, John Paul Estillore, Puck J. Peltenburg, Ferran Rosés‐Noguer, Jan Till, Lee L. Eckhardt, Kate M. Orland, Robert M. Hamilton, Martin J. LaPage, Andrew D. Krahn, Rafik Tadros, Jeffrey M. Vinocur, Dania Kallas, Sonia Franciosi, Jason D. Roberts, Arthur A.M. Wilde, Henrik Kjærulf Jensen, Shubhayan Sanatani, S.R. Wayne Chen

    Vydáno 2021
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  6. 6
    Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel

    Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Exp... Autor Melissa Kelly, Colleen Caleshu, Ana Morales, Jillian G. Buchan, Zena Wolf, Steven M. Harrison, Stuart A. Cook, Mitchell W. Dillon, John Garcia, Eden Haverfield, Jan D.H. Jongbloed, Daniela Macaya, Arjun K. Manrai, Kate M. Orland, Gabriele Richard, Katherine G. Spoonamore, Matthew Thomas, Kate Thomson, Lisa M. Vincent, Roddy Walsh, Hugh Watkins, Nicola Whiffin, Jodie Ingles, J. Peter van Tintelen, Christopher Semsarian, James S. Ware, Ray E. Hershberger, Birgit Funke

    Vydáno 2018
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  7. 7
    An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of <i>CASQ2</i> -Catecholaminergic Polymorphic Ventricular Tachycardia

    An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of <i>CASQ2</i> -Catecholaminergic Polymorphic Ventricular Tachycardia Autor Kevin Ng, Erron W. Titus, Krystien V.V. Lieve, Thomas M. Roston, Andrea Mazzanti, Fred Deiter, Isabelle Denjoy, Jodie Ingles, Jan Till, Tomas Robyns, Sean P. Connors, Christian Steinberg, Dominic J. Abrams, B. Pang, Melvin M. Scheinman, J. Martijn Bos, Stephen A. Duffett, Christian van der Werf, Alice Maltret, Martin S. Green, Julie Rutberg, Seshadri Balaji, Julia Cadrin‐Tourigny, Kate M. Orland, Linda M. Knight, Caitlin Brateng, Jeremy Wu, Anthony Tang, Allan C. Skanes, Jaimie Manlucu, Jeff S. Healey, Craig T. January, Andrew D. Krahn, Kathryn K. Collins, Kathleen R. Maginot, Peter Fischbach, Susan P. Etheridge, Lee L. Eckhardt, Robert M. Hamilton, Michael J. Ackerman, Ferran Rosés‐Noguer, Christopher Semsarian, Natalia Jura, Antoine Leenhardt, Michael H. Gollob, Silvia G. Priori, Shubhayan Sanatani, Arthur A.M. Wilde, Rahul C. Deo, Jason D. Roberts

    Vydáno 2020
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  8. 8
    The impact of common and rare genetic variants on bradyarrhythmia development

    The impact of common and rare genetic variants on bradyarrhythmia development Autor Lu‐Chen Weng, Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall, Valerie N. Morrill, Xin Wang, Victor Nauffal, Yan V. Sun, Dominik Beer, Simon S. K. Lee, Girish N. Nadkarni, ThuyVy Duong, Biqi Wang, Tomasz Czuba, Thomas R. Austin, Zachary T. Yoneda, Daniel J. Friedman, Anne Clayton, Matthew C. Hyman, Renae Judy, Allan C. Skanes, Kate M. Orland, Timothy Treu, Matthew T. Oetjens, Álvaro Alonso, Elsayed Z. Soliman, Honghuang Lin, Kathryn L. Lunetta, Jesper van der Pals, Tariq Z. Issa, Navid A. Nafissi, Heidi T May, Peter Leong‐Sit, Carolina Roselli, Seung Hoan Choi, Goncalo Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Xiaodong Bai, Suganthi Balasubramanian, Andrew Blumenfeld, Boris Boutkov, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Adam J. Mansfield, Evan K. Maxwell, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Razvan Panea, Tommy Polanco, Ayesha Rasool, William Salerno, Jeffrey Staples, Marcus B. Jones, Lyndon J. Mitnaul, Habib Khan, Stacey Knight, Richard Karlsson Linnér, Connie R. Bezzina, Samuli Ripatti, Susan R. Heckbert, J. Michael Gaziano, Ruth J. F. Loos, Bruce M. Psaty, J. Gustav Smith, Emelia J. Benjamin, Dan E. Arking, Daniel J. Rader, Svati H. Shah, Dan M. Roden, Scott M. Damrauer, Lee L. Eckhardt, Jason D. Roberts, Michael J. Cutler

    Vydáno 2025
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