Effects of an Ex Vivo Pediatric Extracorporeal Membrane Oxygenation Circuit on the Sequestration of Mycophenolate Mofetil, Tacrolimus, Hydromorphone, and Fentanyl von Heith, Catherine S, Hansen, Lizbeth A, Bakken, Rhonda M, Ritter, Sharon L, Long, Breeanna R, Hume, Janet R, Zhang, Lei, Amundsen, Danielle B, Steiner, Marie E, Fischer, Gwenyth A

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Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consort... von Horak, Peter, Griffith, Malachi, Danos, Arpad M., Pitel, Beth A., Madhavan, Subha, Liu, Xuelu, Chow, Cynthia, Williams, Heather, Carmody, Leigh, Barrow-Laing, Lisa, Rieke, Damian, Kreutzfeldt, Simon, Stenzinger, Albrecht, Tamborero, David, Benary, Manuela, Rajagopal, Padma Sheila, Ida, Cristiane M., Lesmana, Harry, Satgunaseelan, Laveniya, Merker, Jason D., Tolstorukov, Michael Y., Campregher, Paulo Vidal, Warner, Jeremy L., Rao, Shruti, Natesan, Maya, Shen, Haolin, Venstrom, Jeffrey, Roy, Somak, Tao, Kayoko, Kanagal-Shamanna, Rashmi, Xu, Xinjie, Ritter, Deborah I., Pagel, Kym, Krysiak, Kilannin, Dubuc, Adrian, Akkari, Yassmine M., Li, Xuan Shirley, Lee, Jennifer, King, Ian, Raca, Gordana, Wagner, Alex H., Li, Marylin M., Plon, Sharon E., Kulkarni, Shashikant, Griffith, Obi L., Chakravarty, Debyani, Sonkin, Dmitriy

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The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics von Popejoy, Alice B., Ritter, Deborah I., Crooks, Kristy, Currey, Erin, Fullerton, Stephanie M., Hindorff, Lucia A., Koenig, Barbara, Ramos, Erin M., Sorokin, Elena P., Wand, Hannah, Wright, Mathew W., Zou, James, Gignoux, Christopher R., Bonham, Vence L., Plon, Sharon E., Bustamante, Carlos D.

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Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants von Fortuno, Cristina, Lee, Kristy, Olivier, Magali, Pesaran, Tina, Mai, Phuong L., Andrade, Kelvin C., Attardi, Laura D., Crowley, Stephanie, Evans, D. Gareth, Feng, Bing‐Jian, Foreman, Ann K. M., Frone, Megan N., Huether, Robert, James, Paul A., McGoldrick, Kelly, Mester, Jessica, Seifert, Bryce A., Slavin, Thomas P., Witkowski, Leora, Zhang, Liying, Plon, Sharon E., Spurdle, Amanda B., Savage, Sharon A.

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Examining differences in prescription opioid use behaviors among U.S. adults with and without disabilities von Reif, Sharon, Lauer, Eric A., Adams, Rachel Sayko, Brucker, Debra L., Ritter, Grant A., Mitra, Monika

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Teaching a new mouse old tricks: Humanized mice as an infection model for Variola virus von Hutson, Christina L, Kondas, Ashley V, Ritter, Jana M, Reed, Zachary, Ostergaard, Sharon Dietz, Morgan, Clint N, Gallardo-Romero, Nadia, Tansey, Cassandra, Mauldin, Matthew R, Salzer, Johanna S, Hughes, Christine M, Goldsmith, Cynthia S, Carroll, Darin, Olson, Victoria A

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Design and implementation of an action plan for justice, equity, diversity, and inclusion within the Clinical Genome Resource von Popejoy, Alice B., Ritter, Deborah I., Azzariti, Danielle, Berg, Jonathan S., Bulkley, Joanna E., Cho, Mildred, Gonzaga-Jauregui, Claudia, Klein, Teri E., Martschenko, Daphne O., Oni-Orisan, Akinyemi, Ramos, Erin M., Rehm, Heidi L., Riggs, Erin R., Wright, Matthew W., Yudell, Michael, Plon, Sharon E., Morales, Joannella

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Somatic cancer variant curation and harmonization through consensus minimum variant level data von Ritter, Deborah I, Roychowdhury, Sameek, Roy, Angshumoy, Rao, Shruti, Landrum, Melissa J, Sonkin, Dmitriy, Shekar, Mamatha, Davis, Caleb F, Hart, Reece K, Micheel, Christine, Weaver, Meredith, Van Allen, Eliezer M, Parsons, Donald W, McLeod, Howard L, Watson, Michael S, Plon, Sharon E, Kulkarni, Shashikant, Madhavan, Subha

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Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework von Seifert, Bryce A., McGlaughon, Jennifer L., Jackson, Sarah A., Ritter, Deborah I., Roberts, Maegan E., Schmidt, Ryan J., Thompson, Bryony A., Jimenez, Sharisse, Trapp, Mackenzie, Lee, Kristy, Plon, Sharon E., Offit, Kenneth, Stadler, Zsofia K., Zhang, Liying, Greenblatt, Marc S., Ferber, Matthew J.

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Parallel transmit pulse design for saturation homogeneity (PUSH) for magnetization transfer imaging at 7T von Leitão, David, Tomi‐Tricot, Raphael, Bridgen, Pip, Wilkinson, Tom, Liebig, Patrick, Gumbrecht, Rene, Ritter, Dieter, Giles, Sharon L., Baburamani, Ana, Sedlacik, Jan, Hajnal, Joseph V., Malik, Shaihan J.

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Initial findings from a novel population-based child mortality surveillance approach: a descriptive study von Taylor, Allan W, Blau, Dianna M, Bassat, Quique, Onyango, Dickens, Kotloff, Karen L, Arifeen, Shams El, Mandomando, Inacio, Chawana, Richard, Baillie, Vicky L, Akelo, Victor, Tapia, Milagritos D, Salzberg, Navit T, Keita, Adama Mamby, Morris, Timothy, Nair, Shailesh, Assefa, Nega, Seale, Anna C, Scott, J Anthony G, Kaiser, Reinhard, Jambai, Amara, Barr, Beth A Tippet, Gurley, Emily S, Ordi, Jaume, Zaki, Sherif R, Sow, Samba O, Islam, Farzana, Rahman, Afruna, Dowell, Scott F, Koplan, Jeffrey P, Raghunathan, Pratima L, Madhi, Shabir A, Breiman, Robert F

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New Australian guidelines for the treatment of alcohol problems: an overview of recommendations von Haber, Paul S, Riordan, Benjamin C, Winter, Daniel T, Barrett, Liz, Saunders, John, Hides, Leanne, Gullo, Matthew, Manning, Victoria, Day, Carolyn A, Bonomo, Yvonne, Burns, Lucinda, Assan, Robert, Curry, Ken, Mooney‐Somers, Julie, Demirkol, Apo, Monds, Lauren, McDonough, Mike, Baillie, Andrew J, Clark, Paul, Ritter, Alison, Quinn, Catherine, Cunningham, John, Lintzeris, Nicholas, Rombouts, Susan, Savic, Michael, Norman, Amanda, Reid, Sharon, Hutchinson, Delyse, Zheng, Catherine, Iese, Yasmine, Black, Nicola, Draper, Brian, Ridley, Nicole, Gowing, Linda, Stapinski, Lexine, Taye, Belaynew, Lancaster, Kari, Stjepanović, Daniel, Kay‐Lambkin, Frances, Jamshidi, Nazila, Lubman, Dan, Pastor, Adam, White, Natalie, Wilson, Scott, Jaworski, Alison L, Memedovic, Sonja, Logge, Warren, Mills, Katherine, Seear, Kate, Freeburn, Bradley, Lea, Toby, Withall, Adrienne, Marel, Christina, Boffa, John, Roxburgh, Amanda, Purcell‐Khodr, Gemma, Doyle, Michael, Conigrave, Kate, Teesson, Maree, Butler, Kerryn, Connor, Jason, Morley, Kirsten C

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Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consort... von Horak, Peter, Griffith, Malachi, Danos, Arpad M., Pitel, Beth A., Madhavan, Subha, Liu, Xuelu, Chow, Cynthia, Williams, Heather, Carmody, Leigh, Barrow-Laing, Lisa, Rieke, Damian, Kreutzfeldt, Simon, Stenzinger, Albrecht, Tamborero, David, Benary, Manuela, Rajagopal, Padma Sheila, Ida, Cristiane M., Lesmana, Harry, Satgunaseelan, Laveniya, Merker, Jason D., Tolstorukov, Michael Y., Campregher, Paulo Vidal, Warner, Jeremy L., Rao, Shruti, Natesan, Maya, Shen, Haolin, Venstrom, Jeffrey, Roy, Somak, Tao, Kayoko, Kanagal-Shamanna, Rashmi, Xu, Xinjie, Ritter, Deborah I., Pagel, Kym, Krysiak, Kilannin, Dubuc, Adrian, Akkari, Yassmine M., Li, Xuan Shirley, Lee, Jennifer, King, Ian, Raca, Gordana, Wagner, Alex H., Li, Marylin M., Plon, Sharon E., Kulkarni, Shashikant, Griffith, Obi L., Chakravarty, Debyani, Sonkin, Dmitriy

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Incidence of Retinoblastoma Has Increased: Results from 40 European Countries von Stacey, Andrew W., Bowman, Richard, Foster, Allen, Kivelä, Tero T., Munier, Francis L., Cassoux, Nathalie, Fabian, Ido Didi, Harby, Lamis Al, Portabella, Silvia Alarcón, Alia, Donjeta B., All-Eriksson, Charlotta, Antonino, Romanzo, Astbury, Nicholas J., Balaguer, Julia, Balwierz, Walentyna, Barranco, Honorio, Bascaran, Covadonga, Popovic, Maja Beck, Biewald, Eva M., Bobrova, Nadia, Bornfeld, Norbert, Brichard, Bénédicte G., Blum, Sharon, Capra, Michael, Castela, Guilherme, Català-Mora, Jaume, Chantada, Guillermo L., Chernodrinska, Violeta S., Cieslik, Krzysztof, Comsa, Codruta, Correa Llano, Maria G., Csóka, Monika, De Potter, Patrick, Desjardins, Laurence, Dragomir, Monica D., Fernández-Teijeiro, Ana, Aldana, David García, Gregersen, Pernille A., Gomel, Nir, Hadjistilianou, Theodora, Hederova, Stanislava, Hummlen, Marlies, Husakova, Kristina, Ida, Russo, Ilic, Vesna R., Jenkinson, Helen, Kapelushnik, Noa, Kardava, Tamar, Keren-Froim, Naama, Kepak, Tomas, Khotenashvili, Zaza, Klett, Artur, Krivaitiene, Dalia, Latinović, Slobodanka, Lumbroso, Livia, Lysytsia, Lesia, Maka, Erika, Begue, Nieves Martín, Midena, Edoardo, Moll, Annette C., Murgoi, Gabriela, Naumenko, Larisa, Neroev, Vladimir, Nikitovic, Marina, Olechowski, Andrzej, Papyan, Ruzanna, Parrozzani, Raffaele, Parulekar, Manoj V., Pawinska-Wasikowska, Katarzyna, Perić, Sanja, Pochop, Pavel, Polyakov, Vladimir G., Reddy, M. Ashwin, Ritter-Sovinz, Petra, Saakyan, Svetlana, Sagoo, Mandeep S., San Román Pacheco, Sonsoles, Seregard, Stefan, Silva, Sónia, Sorochynska, Tetyana, Stathopoulos, Christina, Kranjc, Branka Stirn, Svojgr, Karel, Tamamyan, Gevorg, Tandili, Alketa, Tateshi, Bekim, Pompe, Manca Tekavcic, Urbak, Steen F., Ushakova, Tatiana L., Valeina, Sandra, van Hoefen Wijsard, Milo, Veleva-Krasteva, Nevyana V., Viksnins, Maris, Wackernagel, Werner, Dod, Charlotte Wolley, Yarovaya, Vera A., Yarovoy, Andrey A., Zhilyaeva, Katsiaryna, Zondervan, Marcia

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ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines von Preston, Christine G, Wright, Matt W, Madhavrao, Rao, Harrison, Steven M, Goldstein, Jennifer L, Luo, Xi, Wand, Hannah, Wulf, Bryan, Cheung, Gloria, Mandell, Mark E, Tong, Howard, Cheng, Shaung, Iacocca, Michael A, Pineda, Arturo Lopez, Popejoy, Alice B, Dalton, Karen, Zhen, Jimmy, Dwight, Selina S, Babb, Lawrence, DiStefano, Marina, O'Daniel, Julianne M, Lee, Kristy, Riggs, Erin R, Zastrow, Diane B, Mester, Jessica L, Ritter, Deborah I, Patel, Ronak Y, Subramanian, Sai Lakshmi, Milosavljevic, Aleksander, Berg, Jonathan S, Rehm, Heidi L, Plon, Sharon E, Cherry, J Michael, Bustamante, Carlos D, Costa, Helio A

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Ancestry and genetic associations with bronchopulmonary dysplasia in preterm infants von Torgerson, Dara G, Ballard, Philip L, Keller, Roberta L, Oh, Sam S, Huntsman, Scott, Hu, Donglei, Eng, Celeste, Burchard, Esteban G, Ballard, Roberta A

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The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation von Andersen, Erica F., Azzariti, Danielle R., Babb, Larry, Berg, Jonathan S., Biesecker, Leslie G., Bly, Zo, Buchanan, Adam H., DiStefano, Marina T., Gong, Li, Harrison, Steven M., Hunter, Jessica Ezzell, Kattman, Brandi, Klein, Teri E., Landrum, Melissa J., Manickam, Kandamurugu, Marroquin, Alessandra Serrano, Martin, Christa L., Milko, Laura V., Milosavljevic, Aleksandar, Morales, Joannella, Nelson, Tristan H., Plon, Sharon E., Powell, Bradford C., Ramos, Erin M., Rehm, Heidi L., Riggs, Erin R., Ritter, Deborah, Shah, Neethu, Thaxton, Courtney L., Thorland, Erik C., Weaver, Meredith A., Weller, Phillip L., Wright, Matt W.

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Internet-delivered cognitive behavioural therapy programme to reduce depressive symptoms in patients with multiple sclerosis: a multicentre, randomised, controlled, phase 3 trial von Gold, Stefan M, Friede, Tim, Meyer, Björn, Moss-Morris, Rona, Hudson, Joanna, Asseyer, Susanna, Bellmann-Strobl, Judith, Leisdon, Andreas, Ißels, Leonie, Ritter, Kristin, Schymainski, David, Pomeroy, Hayley, Lynch, Sharon G, Cozart, Julia S, Thelen, Joan, Román, Cristina A F, Cadden, Margaret, Guty, Erin, Lau, Stephanie, Pöttgen, Jana, Ramien, Caren, Seddiq-Zai, Susan, Kloidt, Anna-Maria, Wieditz, Johannes, Penner, Iris-Katharina, Paul, Friedemann, Sicotte, Nancy L, Bruce, Jared M, Arnett, Peter A, Heesen, Christoph

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Maternal Black Race and Persistent Wheezing Illness in Former Extremely Low Gestational Age Newborns: Secondary Analysis of a Randomized Trial von Wai, Katherine C., Hibbs, Anna M., Steurer, Martina A., Black, Dennis M., Asselin, Jeanette M., Eichenwald, Eric C., Strong, Suzanne Hamilton, Immamura-Ching, Jill, Orfanos-Villalobos, Margaret, Williams, Cassandra, Durand, David J., Merrill, Jeffrey D., Horton, Dolia, Willard, April, Truog, William E., Gauldin, Cheryl, Holmes, Anne, Johnson, Patrice, Meinert, Kerrie, Reynolds, Anne Marie, Conway, Patrick, Leadersdorff, Michael, Orbank, Pam, Wynn, Karen, Steinhorn, Robin H., deUngria, Maria, Khan, Janine Yasmin, Hamann, Karin, Schau, Molly, Hopkins, Brad, Shariff, Jila, McGovern, Rose, Adelman, Jeff, Combs, Adrienne, Tjersland, Mary, Mayock, Dennis E., Howland, Elizabeth, Longoria, Jim, Meo, Holly, McDavid, Georgia, Burson, Katrina, Hinojosa, Richard, Johnson, Christopher, Martin, Sarah, Rogers, Shawna, Wright, Sharon, Hudak, Mark L., Barnette, Kimberly, Kellum, Amanda, Burcke, Michelle, Hayes, Christie, Chadwick, Stephanie, Howard, Danielle, Kennedy, Carla, O'Shea, T. Michael, Stefanescu, Beatrice, Brown, Patty, Bendel, Catherine M., Davern, Bridget, Mills, Marla, Ritter, Sharon, Wagner, Carol, Ryan, Rita M., Roberson, Jimmy, Mammel, Mark C., Lampland, Andrea, Meyers, Pat, Brey, Angela, Bendel-Stenzel, Ellen M., Mulrooney, Neil, Worwa, Cathy, Dixon, Pam, Ebert, Gerald, Hejl, Cathy, Maxwell, Molly, Dhanireddy, Ramasubbareddy, El Abiad, Mohammed T., Talati, Ajay, Dempsey, Sheila, Gammage, Kathy, Gower, Gayle, James, Kathy, LeNoue, Pam, Bell, Suzi, Bruton, Dawn, Beaulieu, Michelle, Williams, Richard, Barron-Nelson, Robin, Taylor, Shane, Lowe, Gary, Rogers, Elizabeth E., Chapin, Cheryl, Hamann, Karin, Kelley, Susan, Knowles, Karin, Newton, Nancy, Hietpas, Jean, Denton, Laurie, Palermo, Lisa, Wu, Lucy

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112. ClinGen Somatic Cancer Variant Interpretation (CVI) committee and the Somatic Cancer expert panel process von Ritter, Deborah, Duncavage, Eric, Elvin, Julia, Garrett, Frampton, Griffith, Obi L., Griffith, Malachi, Janeway, Katherine, MacConaill, Laura, McCoy, Matthew, Meric-Bernstam, Funda, Merker, Jason, Mullighan, Charles, Parsons, Donald, Patel, Keyur, Raca, Gordana, Ramos, Erin, Rosenbaum, Jason, Roy, Somak, Roy, Angshumoy, Sonkin, Dmitriy, Wagner, Alex, Warner, Jeremy, Plon, Sharon, Li, Marilyn, Kulkarni, Shashikant

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