Optimizing line-plot size for personal laser scanning: modeling distance-dependent tree detection probability along transects von Ritter, T, Tockner, A, Krassnitzer, R, Witzmann, S, Gollob, C, Nothdurft, A

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ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG) von Miller, David T., Lee, Kristy, Chung, Wendy K., Gordon, Adam S., Herman, Gail E., Klein, Teri E., Stewart, Douglas R., Amendola, Laura M., Adelman, Kathy, Bale, Sherri J., Gollob, Michael H., Harrison, Steven M., Hershberger, Ray E., McKelvey, Kent, Richards, C. Sue, Vlangos, Christopher N., Watson, Michael S., Martin, Christa Lese

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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomic... von Miller, David T., Lee, Kristy, Gordon, Adam S., Amendola, Laura M., Adelman, Kathy, Bale, Sherri J., Chung, Wendy K., Gollob, Michael H., Harrison, Steven M., Herman, Gail E., Hershberger, Ray E., Klein, Teri E., McKelvey, Kent, Richards, C. Sue, Vlangos, Christopher N., Stewart, Douglas R., Watson, Michael S., Martin, Christa Lese

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Role of Raf Kinase in Cancer: Therapeutic Potential of Targeting the Raf/MEK/ERK Signal Transduction Pathway von Gollob, Jared A., Wilhelm, Scott, Carter, Chris, Kelley, Susan L.

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An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome von Adler, Arnon, Novelli, Valeria, Amin, Ahmad S., Abiusi, Emanuela, Care, Melanie, Nannenberg, Eline A., Feilotter, Harriet, Amenta, Simona, Mazza, Daniela, Bikker, Hennie, Sturm, Amy C., Garcia, John, Ackerman, Michael J., Hershberger, Raymond E., Perez, Marco V., Zareba, Wojciech, Ware, James S., Wilde, Arthur A.M., Gollob, Michael H.

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ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG) von Miller, David T., Lee, Kristy, Abul-Husn, Noura S., Amendola, Laura M., Brothers, Kyle, Chung, Wendy K., Gollob, Michael H., Gordon, Adam S., Harrison, Steven M., Hershberger, Ray E., Klein, Teri E., Richards, C. Sue, Stewart, Douglas R., Martin, Christa Lese

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European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement... von Wilde, Arthur A M, Semsarian, Christopher, Márquez, Manlio F, Shamloo, Alireza Sepehri, Ackerman, Michael J, Ashley, Euan A, Sternick, Eduardo Back, Barajas-Martinez, Héctor, Behr, Elijah R, Bezzina, Connie R, Breckpot, Jeroen, Charron, Philippe, Chockalingam, Priya, Crotti, Lia, Gollob, Michael H, Lubitz, Steven, Makita, Naomasa, Ohno, Seiko, Ortiz-Genga, Martín, Sacilotto, Luciana, Schulze-Bahr, Eric, Shimizu, Wataru, Sotoodehnia, Nona, Tadros, Rafik, Ware, James S, Winlaw, David S, Kaufman, Elizabeth S, Aiba, Takeshi, Bollmann, Andreas, Choi, Jong Il, Dalal, Aarti, Darrieux, Francisco, Giudicessi, John, Guerchicoff, Mariana, Hong, Kui, Krahn, Andrew D, MacIntyre, Ciorsti, Mackall, Judith A, Mont, Lluís, Napolitano, Carlo, Ochoa, Juan Pablo, Peichl, Petr, Pereira, Alexandre C, Schwartz, Peter J, Skinner, Jon, Stellbrink, Christoph, Tfelt-Hansen, Jacob, Deneke, Thomas

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Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death von Walsh, Roddy, Adler, Arnon, Amin, Ahmad S, Abiusi, Emanuela, Care, Melanie, Bikker, Hennie, Amenta, Simona, Feilotter, Harriet, Nannenberg, Eline A, Mazzarotto, Francesco, Trevisan, Valentina, Garcia, John, Hershberger, Ray E, Perez, Marco V, Sturm, Amy C, Ware, James S, Zareba, Wojciech, Novelli, Valeria, Wilde, Arthur A M, Gollob, Michael H

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Immunoregulatory networks in human Chagas disease von Dutra, W. O., Menezes, C. A. S., Magalhães, L. M. D., Gollob, K. J.

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Retrospective study of a TTR FAP cohort to modify NIS + 7 for therapeutic trials von Suanprasert, N, Berk, J.L, Benson, M.D, Dyck, P.J.B, Klein, C.J, Gollob, J.A, Bettencourt, B.R, Karsten, V, Dyck, P.J

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Importance of genetic testing in unexplained cardiac arrest von Grondin, Steffany, Davies, Brianna, Cadrin-Tourigny, Julia, Steinberg, Christian, Cheung, Christopher C, Jorda, Paloma, Healey, Jeffrey S, Green, Martin S, Sanatani, Shubhayan, Alqarawi, Wael, Angaran, Paul, Arbour, Laura, Antiperovitch, Pavel, Khan, Habib, Leather, Richard, Guerra, Peter G, Rivard, Lena, Simpson, Christopher S, Gardner, Martin, MacIntyre, Ciorsti, Seifer, Colette, Fournier, Anne, Joza, Jacqueline, Gollob, Michael H, Lettre, Guillaume, Talajic, Mario, Laksman, Zachary W, Roberts, Jason D, Krahn, Andrew D, Tadros, Rafik

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Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome von Hosseini, S Mohsen, Kim, Raymond, Udupa, Sharmila, Costain, Gregory, Jobling, Rebekah, Liston, Eriskay, Jamal, Seema M, Szybowska, Marta, Morel, Chantal F, Bowdin, Sarah, Garcia, John, Care, Melanie, Sturm, Amy C, Novelli, Valeria, Ackerman, Michael J, Ware, James S, Hershberger, Ray E, Wilde, Arthur A.M, Gollob, Michael H

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

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Wall panel von GOLLOB NEAL C, KEATING STEPHEN

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Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation von Gollob, Michael H, Jones, Douglas L, Krahn, Andrew D, Danis, Lynne, Gong, Xiang-Qun, Shao, Qing, Liu, Xiaoqin, Veinot, John P, Tang, Anthony S.L, Stewart, Alexandre F.R, Tesson, Frederique, Klein, George J, Yee, Raymond, Skanes, Allan C, Guiraudon, Gerard M, Ebihara, Lisa, Bai, Donglin

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Wall panel von GOLLOB NEAL C, KEATING STEPHEN

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Lung cancer in never smokers: Tumor immunology and challenges for immunotherapy von de Alencar, Viviane Teixeira L., Figueiredo, Amanda B., Corassa, Marcelo, Gollob, Kenneth J., Cordeiro de Lima, Vladmir C.

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PORTABLE WALL BOARD SYSTEM AND METHOD FOR USING SAME von KEATING, STEPHEN, GOLLOB, NEAL C

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Derivation and Validation of a Simple Exercise-Based Algorithm for Prediction of Genetic Testing in Relatives of LQTS Probands von SY, Raymond W, VAN DER WERF, Christian, GULA, Lorne J, LEONG-SIT, Peter, VISKIN, Sami, KLEIN, George J, WILDE, Arthur A, KRAHN, Andrew D, CHATTHA, Ishvinder S, CHOCKALINGAM, Priya, ADLER, Arnon, HEALEY, Jeffrey S, PERRIN, Mark, GOLLOB, Michael H, SKANES, Allan C, YEE, Raymond

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Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia von Sy, Raymond W., MBBS, Gollob, Michael H., MD, Klein, George J., MD, Yee, Raymond, MD, Skanes, Allan C., MD, Gula, Lorne J., MD, Leong-Sit, Peter, MD, Gow, Robert M., MBBS, Green, Martin S., MD, Birnie, David H., MD, Krahn, Andrew D., MD

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