QOL-13. FROM SURVIVING TO THRIVING WITH A BRAIN TUMOR: THE UNIVERSITY OF CALIFORNIA, SAN FRANCISCO NEUROONCOLOGY MODEL FOR AN EMPOWERED AND ENGAGED PEER VOLUNTEER SUPPORT COMMUNITY by Hoffer, Naomi, Rodriguez-Almaraz, Eduardo, Fetting, Mary Lacy, Choi, Elizabeth, Destri, Mary, Taylor, Jennie, Chang, Susan

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INNV-29. PATIENT BARRIERS AND PREFERENCES FOR EXERCISE FOLLOWING A BRAIN TUMOR DIAGNOSIS by Fogh, Shannon, Mishra, Kavita, Hoffer, Naomi, Destri, Mary, Chang, Susan, Taylor, Jennie

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INNV-34. A NOVEL APPROACH TO ADDRESSING THE UNIQUE NEEDS OF ADOLESCENT AND YOUNG ADULT (AYA) BRAIN TUMOR PATIENTS: A FRAMEWORK FOR A VIRTUAL PEER-LED YOUNG ADULT SUPPORT GROUP by Hines, Dace, Scotford, Katie, Bryson-Cahn, Phoebe, Hoffer, Naomi, Destri, Mary, Greenstein, Alexa, Chang, Susan, Schulte, Jessica

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QOL-17. UNDERSTANDING MULTIDISCIPLINARY PROVIDER PERSPECTIVES AND PREFERENCES FOR INCORPORATING EXERCISE INTO PRIMARY BRAIN TUMOR MANAGEMENT by Fogh, Shannon, Hernandez, Yanel, Ambati, Vardhaan, Collis, Sophia, Tawil, Michael, Zhang, Lucy, Greenstein, Alexa, Frederic, Regan, Destri, Mary, Hoffer, Naomi, Mishra, Kavita, Marshall, Natalie, Chang, Susan M, Taylor, Jennie

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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism by Chopra, Maya, McEntagart, Meriel, Clayton-Smith, Jill, Platzer, Konrad, Shukla, Anju, Girisha, Katta M., Kaur, Anupriya, Kaur, Parneet, Pfundt, Rolph, Veenstra-Knol, Hermine, Mancini, Grazia M.S., Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Kortüm, Fanny, Hempel, Maja, Denecke, Jonas, Lehman, Anna, Kleefstra, Tjitske, Stuurman, Kyra E., Wilke, Martina, Thompson, Michelle L., Bebin, E. Martina, Bijlsma, Emilia K., Hoffer, Mariette J.V., Peeters-Scholte, Cacha, Slavotinek, Anne, Weiss, William A., Yip, Tiffany, Hodoglugil, Ugur, Whittle, Amy, diMonda, Janette, Neira, Juanita, Yang, Sandra, Kirby, Amelia, Pinz, Hailey, Lechner, Rosan, Sleutels, Frank, Helbig, Ingo, McKeown, Sarah, Helbig, Katherine, Willaert, Rebecca, Juusola, Jane, Semotok, Jennifer, Hadonou, Medard, Short, John, Yachelevich, Naomi, Lala, Sajel, Fernández-Jaen, Alberto, Pelayo, Janvier Porta, Klöckner, Chiara, Kamphausen, Susanne B., Abou Jamra, Rami, Arelin, Maria, Innes, A. Micheil, Niskakoski, Anni, Amin, Sam, Williams, Maggie, Evans, Julie, Smithson, Sarah, Smedley, Damian, de Burca, Anna, Kini, Usha, Delatycki, Martin B., Gallacher, Lyndon, Yeung, Alison, Pais, Lynn, Field, Michael, Martin, Ellenore, Charles, Perrine, Courtin, Thomas, Keren, Boris, Iascone, Maria, Cereda, Anna, Poke, Gemma, Abadie, Véronique, Chalouhi, Christel, Parthasarathy, Padmini, Halliday, Benjamin J., Robertson, Stephen P., Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher T.

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Critical care admission following elective surgery was not associated with survival benefit: prospective analysis of data from 27 countries by Kahan, Brennan C., Koulenti, Desponia, Arvaniti, Kostoula, Beavis, Vanessa, Campbell, Douglas, Chan, Matthew, Moreno, Rui, Pearse, Rupert M.

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Refining the Phenotypic Spectrum of KMT5B -Associated Developmental Delay by Eliyahu, Aviva, Barel, Ortal, Greenbaum, Lior, Zaks Hoffer, Gal, Goldberg, Yael, Raas-Rothschild, Annick, Singer, Amihood, Bar-Joseph, Ifat, Kunik, Vered, Javasky, Elisheva, Staretz-Chacham, Orna, Pode-Shakked, Naomi, Bazak, Lily, Ruhrman-Shahar, Noa, Pras, Elon, Frydman, Moshe, Shohat, Mordechai, Pode-Shakked, Ben

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Prospective observational cohort study on grading the severity of postoperative complications in global surgery research by Haddow, J., Moreno, Rui, Fang, Xiangming, Shulman, Mark, Rehak, Adam, Roels, Nathalie, Vanluchene, Ann, Silva, Joao, Maia, Bernardo, Suen, Andrew, Bernard, Andre, Ami, Noam, Du, Xindan, Luo, Hong, Zhang, Xiaolin, Zhen, Jungang, Bao, Qi, Chen, Yaqiu, Sun, Yu, Shi, Yugang, Li, Jing, Yu, Shuchun, Guo, Zheng, Jing, Yan, Zhang, Baoling, Ekelund, Kim, Wallet, Florent, Maudet, Valerie Serra, Sojod, Ghassan, Nau, Carla, Veroniki, Fotini, Papailia, Aspasia, Katsika, Eleni, Iasonidou, Christina, Malliotakis, Polychronis, Nyktari, Vasileia, Papaioannou, Alexandra, Lam, Tracy, Lai, Man Ling, Kulkarni, Atul, Aribawa, Mahaalit Alit, Cannavo, Maurizio, Dzulkipli, Norizawati, Kuan, Pei Xuan, Rojas, Eder, Urias, Emma, Choi, Hyun‐min David, McAllister, Davina, Moores, Mark, Polakovich, Daniel, Freschini, David, McAllister, Davina, Gbolahan, Olalere, Faria, Filomena, Ursu, Irina, Hagau, Natalia, Chilinciuc, Ion, Dutu, Madalina, Rhaden, Richard, Conradie, Alae, Wilscott‐Davids, Candice, Govender, Komalan, Ferrando, Carlos, Delgado García, David R, Aldecoa, Cesar, Garcia‐Saiz, Irene, Nystrom, Lena, Schiltz, Boris, Kirya, Fred, Daniel, Gayatri Daniel, Trodd, Dawn, Freitas, Katie, Hesketh, Sue, Bland, Martin, Patrick, Abigail, Browning, Julie, Boshier, Piers, Smith, Neil, Anderson, Colette, Mawdsley, Matthew, Weatherill, J, Andreou, Prematie, Saad, Hesham, Dudgeon, Lucy, Hall, Kathryn, Scholefield, John, Wong, Tony, Bell, Gillian, Graves, Lynne, Hutchings, Melanie, Minik, Orsolya, Thomas, Richard, Craig, Jayne, Baldwin, Jacqueline, Kerslake, Ian, Cornell, Jonathan, Too, Lingxi, Arumugam, Swarna, Lawson, Simon, Bodansky, Daniella

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eP148 - Heterozygous ANKRD17 loss of function variants cause a syndrome with intellectual disability, speech delay and dysmorphism by Chopra, Maya, McEntagart, Meriel, Clayton-Smith, Jill, Platzer, Konrad, Shukla, Anju, Girisha, Katta, Kaur, Anupriya, Kaur, Parmeet, Pfundt, Rolph, Veenstra-Knol, Hermine, Mancini, Grazia, Capuccio, Gerarda, Brunetti-Pierri, Nicola, Kortüm, Fanny, Hempel, Maja, Denecke, Jonas, Lehman, Anna, Kleefstra, Tjitske, Stuurman, Kyra, Wilke, Martina, Thompson, Michelle, Bebin, Martina, Bijlsma, Emilia, Hoffer, Mariette, Peters-Scholte, Cacha, Slavotinek, Anne, Weiss, William, Yip, Tiffany, Hodoglugil, Ugur, Whittle, Amy, diMonda, Janette, Neira, Juanita, Yang, Sandra, Kirby, Amelia, Pinz, Hailey, Lechner, Rosan, Sleutels, Frank, Helbig, Ingo, McKeown, Sarah, Helbig, Katherine, Yachelevich, Naomi, Wilaert, Rebecca, Juusola, Jane, Semotok, Jennifer, Hadonou, Medard, Short, John, Lala, Sajel, Fernández-Jaen, Alberto, Pelayo, Janvier Porta, Kloechner, Chiara, Kamphausen, Susanne, Jamra, Rami, Arelin, Maria, Innes, Micheil, Niskakoski, Anni, Amin, Sam, Williams, Maggie, Evans, Julie, Smithson, Sarah, Smedley, Damien, de Burca, Anna, Kini, Usha, Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher

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Heterozygous ANKRD17 loss of function variants cause a syndrome with intellectual disability, speech delay and dysmorphism by Chopra, Maya, McEntagart, Meriel, Clayton-Smith, Jill, Platzer, Konrad, Shukla, Anju, Girisha, Katta, Kaur, Anupriya, Kaur, Parmeet, Pfundt, Rolph, Veenstra-Knol, Hermine, Mancini, Grazia, Capuccio, Gerarda, Brunetti-Pierri, Nicola, Kortüm, Fanny, Hempel, Maja, Denecke, Jonas, Lehman, Anna, Kleefstra, Tjitske, Stuurman, Kyra, Wilke, Martina, Thompson, Michelle, Bebin, Martina, Bijlsma, Emilia, Hoffer, Mariette, Peters-Scholte, Cacha, Slavotinek, Anne, Weiss, William, Yip, Tiffany, Hodoglugil, Ugur, Whittle, Amy, diMonda, Janette, Neira, Juanita, Yang, Sandra, Kirby, Amelia, Pinz, Hailey, Lechner, Rosan, Sleutels, Frank, Helbig, Ingo, McKeown, Sarah, Helbig, Katherine, Yachelevich, Naomi, Wilaert, Rebecca, Juusola, Jane, Semotok, Jennifer, Hadonou, Medard, Short, John, Lala, Sajel, Fernández-Jaen, Alberto, Pelayo, Janvier Porta, Kloechner, Chiara, Kamphausen, Susanne, Jamra, Rami, Arelin, Maria, Innes, Micheil, Niskakoski, Anni, Amin, Sam, Williams, Maggie, Evans, Julie, Smithson, Sarah, Smedley, Damien, de Burca, Anna, Kini, Usha, Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher

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Partial loss of USP9X function leads to a male neurodevelopmental and behavioural disorder converging on TGFβ signalling by Johnson, Brett V., Kumar, Raman, Oishi, Sabrina, Alexander, Suzy, Kasherman, Maria, Vega, Michelle Sanchez, Ivancevic, Atma, Gardner, Alison, Domingo, Deepti, Corbett, Mark, Parnell, Euan, Yoon, Sehyoun, Oh, Tracey, Lines, Matthew, Lefroy, Henrietta, Kini, Usha, Van Allen, Margot, Grønborg, Sabine, Mercier, Sandra, Küry, Sébastien, Bézieau, Stéphane, Pasquier, Laurent, Raynaud, Martine, Afenjar, Alexandra, de Villemeur, Thierry Billette, Keren, Boris, Désir, Julie, Van Maldergem, Lionel, Marangoni, Martina, Dikow, Nicola, Koolen, David A., VanHasselt, Peter M., Weiss, Marjan, Zwijnenburg, Petra, Sa, Joaquim, Reis, Claudia Falcao, López-Otín, Carlos, Santiago-Fernández, Olaya, Fernández-Jaén, Alberto, Rauch, Anita, Steindl, Katharina, Joset, Pascal, Goldstein, Amy, Madan-Khetarpal, Suneeta, Infante, Elena, Zackai, Elaine, Mcdougall, Carey, Narayanan, Vinodh, Ramsey, Keri, Mercimek-Andrews, Saadet, Pena, Loren, Shashi, Vandana, Schoch, Kelly, Sullivan, Jennifer A., Pinto e Vairo, Filippo, Pichurin, Pavel N., Ewing, Sarah A., Barnett, Sarah S., Klee, Eric W., Perry, M. Scott, Koenig, Mary Kay, Keegan, Catherine E., Schuette, Jane L., Asher, Stephanie, Perilla-Young, Yezmin, Smith, Laurie D., Rosenfeld, Jill A., Bhoj, Elizabeth, Kaplan, Paige, Li, Dong, Oegema, Renske, van Binsbergen, Ellen, van der Zwaag, Bert, Smeland, Marie Falkenberg, Cutcutache, Ioana, Page, Matthew, Armstrong, Martin, Lin, Angela E., Steeves, Marcie A., den Hollander, Nicolette, Hoffer, Mariëtte J V, Reijnders, Margot R.F., Demirda, Serwet, Koboldt, Daniel C., Bartholomew, Dennis, Mosher, Theresa Mihalic, Hickey, Scott E., Shieh, Christine, Sanchez-Lara, Pedro A., Graham, John M., Tezcan, Kamer, Schaefer, G. B., Danylchuk, Noelle R., Asamoah, Alexander, Jackson, Kelly E., Yachelevich, Naomi, Au, Margaret, Pérez-Jurado, Luis A., Kleefstra, Tjitske

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The Tinnitus Retraining Therapy Trial (TRTT): study protocol for a randomized controlled trial by Scherer, Roberta W, Formby, Craig, Gold, Susan, Erdman, Sue, Rodhe, Charles, Carlson, Michele, Shade, Dave, Tucker, Melanie, Sensinger, Lee McCaffrey, Hughes, Gordon, Conley, George S, Downey, Naomi, Eades, Cynthia, Jylkka, Margaret, Haber-Perez, Ada, Harper, Courtney, Russell, Shoshannah Kantor, Sierra-Irizarry, Benigno, Sullivan, Mark

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Rationale for the tinnitus retraining therapy trial by Formby, Craig, Scherer, Roberta

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