Life-Long Learning for Psychologists: Current Status and a Vision for the Future von Wise, Erica H, Sturm, Cynthia A, Nutt, Roberta L, Rodolfa, Emil, Schaffer, Jack B, Webb, Carol

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Determination and Documentation of the Need for Practice Guidelines von Sturm, Cynthia A, Hancock, Kristin A, Cerbone, Armand R, de La Cancela, Victor, Connell, Mary A, Foote, William E, Galietta, Michele M, James, Larry C, Jerome, Leigh W, Knight, Sara J, Mohr, David C, West, Carolyn M, Witt, Phillip H

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TREATMENT ACCEPTABILITY OF ALTERNATIVE MARITAL THERAPIES: A COMPARATIVE ANALYSIS von Bornstein, Philip H., Ballweg, Bernard J., Weisser, Charles E., Fox, Steven G., Kirby, Kristie L., Andre, John C., Sturm, Cynthia A., Wilson, Gregory L., McLellarn, Robert W.

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Paradoxical instruction in the treatment of encopresis and chronic constipation: An experimental analysis von Bornstein, Philip H., Sturm, Cynthia A., Retzlaff, Paul D., Kirby, Kristie L., Chong, Hoili

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K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas von Khuong-Quang, Dong-Anh, Buczkowicz, Pawel, Rakopoulos, Patricia, Liu, Xiao-Yang, Fontebasso, Adam M., Bouffet, Eric, Bartels, Ute, Albrecht, Steffen, Schwartzentruber, Jeremy, Letourneau, Louis, Bourgey, Mathieu, Bourque, Guillaume, Montpetit, Alexandre, Bourret, Genevieve, Lepage, Pierre, Fleming, Adam, Lichter, Peter, Kool, Marcel, von Deimling, Andreas, Sturm, Dominik, Korshunov, Andrey, Faury, Damien, Jones, David T., Majewski, Jacek, Pfister, Stefan M., Jabado, Nada, Hawkins, Cynthia

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Clinical, Radiologic, Pathologic, and Molecular Characteristics of Long-Term Survivors of Diffuse Intrinsic Pontine Glioma (DIPG): A Collaborative Report From the International and... von Hoffman, Lindsey M, Veldhuijzen van Zanten, Sophie E M, Colditz, Niclas, Baugh, Joshua, Chaney, Brooklyn, Hoffmann, Marion, Lane, Adam, Fuller, Christine, Miles, Lili, Hawkins, Cynthia, Bartels, Ute, Bouffet, Eric, Goldman, Stewart, Leary, Sarah, Foreman, Nicholas K, Packer, Roger, Warren, Katherine E, Broniscer, Alberto, Kieran, Mark W, Minturn, Jane, Comito, Melanie, Broxson, Emmett, Shih, Chie-Schin, Khatua, Soumen, Chintagumpala, Murali, Carret, Anne Sophie, Escorza, Nancy Yanez, Hassall, Timothy, Ziegler, David S, Gottardo, Nicholas, Dholaria, Hetal, Doughman, Renee, Benesch, Martin, Drissi, Rachid, Nazarian, Javad, Jabado, Nada, Boddaert, Nathalie, Varlet, Pascale, Giraud, Géraldine, Castel, David, Puget, Stephanie, Jones, Chris, Hulleman, Esther, Modena, Piergiorgio, Giagnacovo, Marzia, Antonelli, Manila, Pietsch, Torsten, Gielen, Gerrit H, Jones, David T W, Sturm, Dominik, Pfister, Stefan M, Gerber, Nicolas U, Grotzer, Michael A, Pfaff, Elke, von Bueren, André O, Hargrave, Darren, Solanki, Guirish A, Jadrijevic Cvrlje, Filip, Kaspers, Gertjan J L, Vandertop, William P, Grill, Jacques, Bailey, Simon, Biassoni, Veronica, Massimino, Maura, Calmon, Raphaël, Sanchez, Esther, Bison, Brigitte, Warmuth-Metz, Monika, Leach, James, Jones, Blaise, van Vuurden, Dannis G, Kramm, Christof M, Fouladi, Maryam

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Paediatric and adult glioblastoma: multiform (epi)genomic culprits emerge von Sturm, Dominik, Bender, Sebastian, Jones, David T. W., Lichter, Peter, Grill, Jacques, Becher, Oren, Hawkins, Cynthia, Majewski, Jacek, Jones, Chris, Costello, Joseph F., Iavarone, Antonio, Aldape, Kenneth, Brennan, Cameron W., Jabado, Nada, Pfister, Stefan M.

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Abstract 13583: Secondary Findings of Loss-of-function Variants in FLNC Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes in a General Clinical Population von Haggerty, Christopher M, Kelly, Melissa, Tichnell, Crystal, Murray, Brittney, Sturm, Amy C, Fornwalt, Brandon, James, Cynthia

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Dysfunction in the βII spectrin-dependent cytoskeleton underlies human arrhythmia von Smith, Sakima A, Sturm, Amy C, Curran, Jerry, Kline, Crystal F, Little, Sean C, Bonilla, Ingrid M, Long, Victor P, Makara, Michael, Polina, Iuliia, Hughes, Langston D, Webb, Tyler R, Wei, Zhiyi, Wright, Patrick, Voigt, Niels, Bhakta, Deepak, Spoonamore, Katherine G, Zhang, Chuansheng, Weiss, Raul, Binkley, Philip F, Janssen, Paul M, Kilic, Ahmet, Higgins, Robert S, Sun, Mingzhai, Ma, Jianjie, Dobrev, Dobromir, Zhang, Mingjie, Carnes, Cynthia A, Vatta, Matteo, Rasband, Matthew N, Hund, Thomas J, Mohler, Peter J

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Dissecting the genomic complexity underlying medulloblastoma von Jones, David T. W., Jäger, Natalie, Kool, Marcel, Zichner, Thomas, Hutter, Barbara, Sultan, Marc, Cho, Yoon-Jae, Pugh, Trevor J., Hovestadt, Volker, Stütz, Adrian M., Rausch, Tobias, Warnatz, Hans-Jörg, Ryzhova, Marina, Bender, Sebastian, Sturm, Dominik, Pleier, Sabrina, Cin, Huriye, Pfaff, Elke, Sieber, Laura, Wittmann, Andrea, Remke, Marc, Witt, Hendrik, Hutter, Sonja, Tzaridis, Theophilos, Weischenfeldt, Joachim, Raeder, Benjamin, Avci, Meryem, Amstislavskiy, Vyacheslav, Zapatka, Marc, Weber, Ursula D., Wang, Qi, Lasitschka, Bärbel, Bartholomae, Cynthia C., Schmidt, Manfred, von Kalle, Christof, Ast, Volker, Lawerenz, Chris, Eils, Jürgen, Kabbe, Rolf, Benes, Vladimir, van Sluis, Peter, Koster, Jan, Volckmann, Richard, Shih, David, Betts, Matthew J., Russell, Robert B., Coco, Simona, Paolo Tonini, Gian, Schüller, Ulrich, Hans, Volkmar, Graf, Norbert, Kim, Yoo-Jin, Monoranu, Camelia, Roggendorf, Wolfgang, Unterberg, Andreas, Herold-Mende, Christel, Milde, Till, Kulozik, Andreas E., von Deimling, Andreas, Witt, Olaf, Maass, Eberhard, Rössler, Jochen, Ebinger, Martin, Schuhmann, Martin U., Frühwald, Michael C., Hasselblatt, Martin, Jabado, Nada, Rutkowski, Stefan, von Bueren, André O., Williamson, Dan, Clifford, Steven C., McCabe, Martin G., Peter Collins, V., Wolf, Stephan, Wiemann, Stefan, Lehrach, Hans, Brors, Benedikt, Scheurlen, Wolfram, Felsberg, Jörg, Reifenberger, Guido, Northcott, Paul A., Taylor, Michael D., Meyerson, Matthew, Pomeroy, Scott L., Yaspo, Marie-Laure, Korbel, Jan O., Korshunov, Andrey, Eils, Roland, Pfister, Stefan M., Lichter, Peter

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The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network von Leppig, Kathleen A., Kulchak Rahm, Alanna, Appelbaum, Paul, Aufox, Sharon, Bland, Harris T., Buchanan, Adam, Christensen, Kurt D., Chung, Wendy K., Clayton, Ellen Wright, Crosslin, David, Denny, Josh, DeVange, Shannon, Gordon, Adam, Green, Robert C., Hakonarson, Hakon, Harr, Margaret H., Henrikson, Nora, Hoell, Christin, Holm, Ingrid A., Kullo, Iftikhar J., Jarvik, Gail P., Lammers, Philip E., Larson, Eric B., Lindor, Noralane M., Marasa, Maddalena, Myers, Melanie F., Perez, Emma, Peterson, Josh F., Pratap, Siddharth, Prows, Cynthia A., Ralston, James D., Rasouly, Hila Milo, Roden, Dan M., Sharp, Richard R., Singh, Rajbir, Shaibi, Gabriel, Smith, Maureen E., Sturm, Amy, Thiese, Heidi A., Van Driest, Sara L., Williams, Janet, Williams, Marc S., Wynn, Julia, Blout Zawatsky, Carrie L., Wiesner, Georgia L.

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HF-566-02 PREDICTED RISK OF VENTRICULAR ARRHYTHMIA IN INDIVIDUALS WITH DESMOSOME GENE VARIANTS IDENTIFIED VIA POPULATION GENOMIC SCREENING von Carruth, Eric, Alsaid, Amro, Murray, Brittney, Tichnell, Crystal, Sturm, Amy C., James, Cynthia A., Haggerty, Christopher M.

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Prevalence and Electronic Health Record-Based Phenotype of Loss-of-Function Genetic Variants in Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Genes von Carruth, Eric D., Young, Wilson, Beer, Dominik, James, Cynthia A., Calkins, Hugh, Jing, Linyuan, Raghunath, Sushravya, Hartzel, Dustin N., Leader, Joseph B., Kirchner, H. Lester, Smelser, Diane T., Carey, David J., Kelly, Melissa A., Sturm, Amy C., Alsaid, Amro, Fornwalt, Brandon K., Haggerty, Christopher M.

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Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy von Roberts, Jason D, Murphy, Nathaniel P, Hamilton, Robert M, Lubbers, Ellen R, James, Cynthia A, Kline, Crystal F, Gollob, Michael H, Krahn, Andrew D, Sturm, Amy C, Musa, Hassan, El-Refaey, Mona, Koenig, Sara, Aneq, Meriam Åström, Hoorntje, Edgar T, Graw, Sharon L, Davies, Robert W, Rafiq, Muhammad Arshad, Koopmann, Tamara T, Aafaqi, Shabana, Fatah, Meena, Chiasson, David A, Taylor, Matthew Rg, Simmons, Samantha L, Han, Mei, van Opbergen, Chantal Jm, Wold, Loren E, Sinagra, Gianfranco, Mittal, Kirti, Tichnell, Crystal, Murray, Brittney, Codima, Alberto, Nazer, Babak, Nguyen, Duy T, Marcus, Frank I, Sobriera, Nara, Lodder, Elisabeth M, van den Berg, Maarten P, Spears, Danna A, Robinson, John F, Ursell, Philip C, Green, Anna K, Skanes, Allan C, Tang, Anthony S, Gardner, Martin J, Hegele, Robert A, van Veen, Toon Ab, Wilde, Arthur Am, Healey, Jeff S, Janssen, Paul Ml, Mestroni, Luisa, van Tintelen, J Peter, Calkins, Hugh, Judge, Daniel P, Hund, Thomas J, Scheinman, Melvin M, Mohler, Peter J

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Loss-of-Function FLNC Variants Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes When Identified Through Exome Sequencing of a General Clinical Population von Carruth, Eric D., Qureshi, Maria, Alsaid, Amro, Kelly, Melissa A., Calkins, Hugh, Murray, Brittney, Tichnell, Crystal, Sturm, Amy C., Baras, Aris, Lester Kirchner, H., Fornwalt, Brandon K., James, Cynthia A., Haggerty, Christopher M.

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Association of CYP2D6 genotype predicted phenotypes with oxycodone requirements and side effects in children undergoing surgery von Merchant, Soroush, Prows, Cynthia A, Yang, Fang, Ding, Lili, MacDonald, Jacob, Zhang, Xue, Sadhasivam, Senthilkumar, Garcia, Victor, Sturm, Peter, Chidambaran, Vidya

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HGG-39. CLINICAL CHARACTERISTICS AND SURVIVAL OUTCOMES OF DIFFUSE HEMISPHERIC GLIOMA, H3 G34-MUTANT: INTERIM RESULTS OF A MULTICENTRE INTERNATIONAL STUDY von Crowell, Cameron, Bennett, Julie, Bandopadhayay, Pratiti, Sturm, Dominik, Green, Adam L, MacNeil, Mary, Vanan, Magimairajan Issai, Larouche, Valérie, Renzi, Samuele, Imber, Brandon, Jones, Jacquelyn, Perreault, Sébastien, Mata-Mbemba, Daddy, Feddersen, Charlotte, Vizzini, Olivia, Zápotocký, Michal, Cheng, Sylvia, Harrison, Rebecca, Popovacki, Aimee, Klawinski, Darren, Hansford, Jordan R, Lapointe, Sarah, Cayrol, Romain, Mankuzhy, Nikhil, Coleman, Christina, Wright-Nadkarni, Mariah, Salloum, Ralph, Karajannis, Matthias, Hawkins, Cynthia, Jones, David T W, Ligon, Keith L, Jabado, Nada, Erker, Craig

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Use of Whole Exome Sequencing for the Identification of Ito‐Based Arrhythmia Mechanism and Therapy von Sturm, Amy C., Kline, Crystal F., Glynn, Patric, Johnson, Benjamin L., Curran, Jerry, Kilic, Ahmet, Higgins, Robert S. D., Binkley, Philip F., Janssen, Paul M. L., Weiss, Raul, Raman, Subha V., Fowler, Steven J., Priori, Silvia G., Hund, Thomas J., Carnes, Cynthia A., Mohler, Peter J.

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Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study von von Hoff, Katja, Haberler, Christine, Schmitt-Hoffner, Felix, Schepke, Elizabeth, de Rojas, Teresa, Jacobs, Sandra, Zapotocky, Michal, Sumerauer, David, Perek-Polnik, Marta, Dufour, Christelle, van Vuurden, Dannis, Slavc, Irene, Gojo, Johannes, Pickles, Jessica C, Gerber, Nicolas U, Massimino, Maura, Gil-da-Costa, Maria Joao, Garami, Miklos, Kumirova, Ella, Sehested, Astrid, Scheie, David, Cruz, Ofelia, Moreno, Lucas, Cho, Jaeho, Zeller, Bernward, Bovenschen, Niels, Grotzer, Michael, Alderete, Daniel, Snuderl, Matija, Zheludkova, Olga, Golanov, Andrey, Okonechnikov, Konstantin, Mynarek, Martin, Juhnke, Björn Ole, Rutkowski, Stefan, Schüller, Ulrich, Pizer, Barry, von Zezschwitz, Barbara, Kwiecien, Robert, Wechsung, Maximilian, Konietschke, Frank, Hwang, Eugene I, Sturm, Dominik, Pfister, Stefan M, von Deimling, Andreas, Rushing, Elisabeth J, Ryzhova, Marina, Hauser, Peter, Łastowska, Maria, Wesseling, Pieter, Giangaspero, Felice, Hawkins, Cynthia, Figarella-Branger, Dominique, Eberhart, Charles, Burger, Peter, Gessi, Marco, Korshunov, Andrey, Jacques, Tom S, Capper, David, Pietsch, Torsten, Kool, Marcel

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EPID-10. CNSONTRK STUDY: CLINICAL CHARACTERISTICS AND OUTCOME OF CENTRAL NERVOUS SYSTEM TUMORS HARBORING NTRK GENE FUSIONS von Lamoureux, Audrey-Anne, Fisher, Michael, Lemelle, Lauriane, Pfaff, Elke, De Wilde, Bram, Pfister, Stefan, Sturm, Dominik, Orbach, Daniel, Raskin, Scott, Drilon, Alexander, Zapotocky, Michal, Barritault, Marc, Leblond, Pierre, Tabori, Uri, Hawkins, Cynthia, Hansford, Jordan, Erker, Craig, Gottardo, Nicholas, Nørøxe, Dorte, Goto, Hiroaki, Ziegler, David, Liu, Yen-Lin, Hwang, Eugene, Aguilar-Bonilla, Ana, Cheng, Sylvia, Cacciotti, Chantel, Massimino, Maura, Wood, Paul, Hoffman, Lindsey, Lassaletta, Alvaro, Gerber, Nicolas, Ceruso, Mariella Spalato, Bendel, Anne, Abadi, Christina Coleman, Mueller, Sabine, Aguilera, Dolly, Robison, Nathan, O’Halloran, Katrina, Abbou, Samuel, Geoerger, Birgit, Øra, Ingrid, Moertel, Christopher, Razis, Evangelia, Seizeur, Romuald, Clarke, Matthew, Doz, François, Laetsch, Theodore, Perreault, Sébastien, Ellezam, Benjamin, Alves, Mélanie

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