Outcomes of Congenital Diaphragmatic Hernia in the Modern Era of Management von Wynn, Julia, MS, Krishnan, Usha, MD, Aspelund, Gudrun, MD, Zhang, Yuan, PhD, Duong, Jimmy, PhD, Stolar, Charles J.H., MD, Hahn, Eunice, MD, Pietsch, John, MD, Chung, Dai, MD, Moore, Donald, MD, Austin, Eric, MD, Mychaliska, George, MD, Gajarski, Robert, MD, Foong, Yen-Lim, MD, Michelfelder, Erik, MD, Potolka, Douglas, MD, Bucher, Brian, MD, Warner, Brad, MD, Grady, Mark, MD, Azarow, Ken, MD, Fletcher, Scott E., MD, Kutty, Shelby, MD, Delaney, Jeff, MD, Crombleholme, Timothy, MD, Rosenzweig, Erika, MD, Chung, Wendy, MD, PhD, Arkovitz, Marc S., MD

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The usefulness of whole-exome sequencing in routine clinical practice von Iglesias, Alejandro, Anyane-Yeboa, Kwame, Wynn, Julia, Wilson, Ashley, Truitt Cho, Megan, Guzman, Edwin, Sisson, Rebecca, Egan, Claire, Chung, Wendy K.

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Congenital diaphragmatic hernias: from genes to mechanisms to therapies von Kardon, Gabrielle, Ackerman, Kate G, McCulley, David J, Shen, Yufeng, Wynn, Julia, Shang, Linshan, Bogenschutz, Eric, Sun, Xin, Chung, Wendy K

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De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders von Qi, Hongjian, Yu, Lan, Zhou, Xueya, Wynn, Julia, Zhao, Haoquan, Guo, Yicheng, Zhu, Na, Kitaygorodsky, Alexander, Hernan, Rebecca, Aspelund, Gudrun, Lim, Foong-Yen, Crombleholme, Timothy, Cusick, Robert, Azarow, Kenneth, Danko, Melissa E, Chung, Dai, Warner, Brad W, Mychaliska, George B, Potoka, Douglas, Wagner, Amy J, ElFiky, Mahmoud, Wilson, Jay M, Nickerson, Debbie, Bamshad, Michael, High, Frances A, Longoni, Mauro, Donahoe, Patricia K, Chung, Wendy K, Shen, Yufeng

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Validation of a non-invasive prenatal test for fetal RhD, C, c, E, K and Fya antigens von Alford, Brian, Landry, Brian P., Hou, Sarah, Bower, Xavier, Bueno, Anna M., Chen, Drake, Husic, Brooke, Cantonwine, David E., McElrath, Thomas F., Carozza, Jacqueline A., Wynn, Julia, Hoskovec, Jennifer, Gray, Kathryn J.

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Researchers’ views on return of incidental genomic research results: qualitative and quantitative findings von Klitzman, Robert, Appelbaum, Paul S., Fyer, Abby, Martinez, Josue, Buquez, Brigitte, Wynn, Julia, Waldman, Cameron R., Phelan, Jo, Parens, Erik, Chung, Wendy K.

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Clinical providers' experiences with returning results from genomic sequencing: an interview study von Wynn, Julia, Lewis, Katie, Amendola, Laura M, Bernhardt, Barbara A, Biswas, Sawona, Joshi, Manasi, McMullen, Carmit, Scollon, Sarah

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SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice von El Chehadeh, Salima, Han, Kyung Ah, Kim, Dongwook, Jang, Gyubin, Bakhtiari, Somayeh, Lim, Dongseok, Kim, Hee Young, Kim, Jinhu, Kim, Hyeonho, Wynn, Julia, Chung, Wendy K., Vitiello, Giuseppina, Cutcutache, Ioana, Page, Matthew, Gecz, Jozef, Harper, Kelly, Han, Ah-reum, Kim, Ho Min, Wessels, Marja, Bayat, Allan, Jaén, Alberto Fernández, Selicorni, Angelo, Maitz, Silvia, de Brouwer, Arjan P. M., Silfhout, Anneke Vulto-van, Armstrong, Martin, Symonds, Joseph, Küry, Sébastien, Isidor, Bertrand, Cogné, Benjamin, Nizon, Mathilde, Feger, Claire, Muller, Jean, Torti, Erin, Grange, Dorothy K., Willems, Marjolaine, Kruer, Michael C., Ko, Jaewon, Piton, Amélie, Um, Ji Won

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Participant choices for return of genomic results in the eMERGE Network von Hoell, Christin, Wynn, Julia, Rasmussen, Luke V., Marsolo, Keith, Aufox, Sharon A., Chung, Wendy K., Connolly, John J., Freimuth, Robert R., Kochan, David, Hakonarson, Hakon, Harr, Margaret, Holm, Ingrid A., Kullo, Iftikhar J., Lammers, Philip E., Leppig, Kathleen A., Leslie, Nancy D., Myers, Melanie F., Sharp, Richard R., Smith, Maureen E., Prows, Cynthia A.

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Comparative outcomes of right versus left congenital diaphragmatic hernia: A multicenter analysis von Abramov, Alexey, Fan, Weijia, Hernan, Rebecca, Zenilman, Ariela L., Wynn, Julia, Aspelund, Gudrun, Khlevner, Julie, Krishnan, Usha, Lim, Foong-Yen, Mychaliska, George B., Warner, Brad W., Cusick, Robert, Crombleholme, Timothy, Chung, Dai, Danko, Melissa E., Wagner, Amy J., Azarow, Kenneth, Schindel, David, Potoka, Douglas, Soffer, Sam, Fisher, Jason, McCulley, David, Farkouh-Karoleski, Christiana, Chung, Wendy K., Duron, Vincent

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Correspondence on "Current Controversy in Prenatal Diagnosis: The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use" von Wynn, Julia, Hoskovec, Jennifer

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Research Participants’ Preferences for Hypothetical Secondary Results from Genomic Research von Wynn, Julia, Martinez, Josue, Duong, Jimmy, Chiuzan, Codruta, Phelan, Jo C., Fyer, Abby, Klitzman, Robert L., Appelbaum, Paul S., Chung, Wendy K.

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GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing von Milo Rasouly, Hila, Cuneo, Nicole, Marasa, Maddalena, DeMaria, Natalia, Chatterjee, Debanjana, Thompson, Jacqueline J., Fasel, David A., Wynn, Julia, Chung, Wendy K., Appelbaum, Paul, Weng, Chunhua, Bakken, Suzanne, Gharavi, Ali G.

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Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia von Yu, Lan, Wynn, Julia, Cheung, Yee Him, Shen, Yufeng, Mychaliska, George B., Crombleholme, Timothy M., Azarow, Kenneth S., Lim, Foong Yen, Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc S., Chung, Wendy K.

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Impact of Receiving Secondary Results from Genomic Research: A 12-Month Longitudinal Study von Wynn, Julia, Martinez, Josue, Bulafka, Jessica, Duong, Jimmy, Zhang, Yuan, Chiuzan, Codruta, Preti, Jain, Cremona, Maria L., Jobanputra, Vaidehi, Fyer, Abby J., Klitzman, Robert L., Appelbaum, Paul S., Chung, Wendy K.

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Newborn screening for Duchenne muscular dystrophy: A two‐year pilot study von Tavakoli, Norma P., Gruber, Dorota, Armstrong, Niki, Chung, Wendy K., Maloney, Breanne, Park, Sunju, Wynn, Julia, Koval‐Burt, Carrie, Verdade, Lorraine, Tegay, David H., Cohen, Lilian L., Shapiro, Natasha, Kennedy, Annie, Noritz, Garey, Ciafaloni, Emma, Weinberger, Barry, Ellington, Marty, Schleien, Charles, Spinazzola, Regina, Sood, Sunil, Brower, Amy, Lloyd‐Puryear, Michele, Caggana, Michele, Laureta, Emma Cecilia M., Rochelson, Burton L, Hogan, Katherine A.

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Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot von Hartnett, Michael J, Lloyd-Puryear, Michele A, Tavakoli, Norma P, Wynn, Julia, Koval-Burt, Carrie L, Gruber, Dorota, Trotter, Tracy, Caggana, Michele, Chung, Wendy K, Armstrong, Niki, Brower, Amy M

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Genomic Testing: a Genetic Counselor’s Personal Reflection on Three Years of Consenting and Testing von Wynn, Julia

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Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias von Bogenschutz, Eric L., Fox, Zac D., Farrell, Andrew, Wynn, Julia, Moore, Barry, Yu, Lan, Aspelund, Gudrun, Marth, Gabor, Yandell, Mark, Shen, Yufeng, Chung, Wendy K., Kardon, Gabrielle

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O35: Feasibility of expanded newborn screening using genome sequencing for early actionable conditions in a diverse city von Chung, Wendy, Ziegler, Alban, Koval-Burt, Carrie, Kay, Denise, Suchy, Sharon, Bergtrup, Amber, Langley, Katherine, Amendola, Laura, Boyd, Brenna, Bradley, Jennifer, Brandt, Tracy, Cohen, Lilian, Coffey, Alison, Devaney, Joseph, Dygulska, Beata, Friedman, Bethany, Fuleihan, Ramsey, Gyimah, Awura, Hernan, Rebecca, Hofherr, Sean, Hruska, Kathleen, Hu, Zhanzhi, Jeanne, Mederic, Jin, Guanjun, Johnson, Aaron, Kavus, Haluk, Leibel, Rudolph, McWalter, Kirsty, Monaghan, Kristin, Soler, Nicole Pimentel, Quevedo, Yeyson, Ratner, Samantha, Retterer, Kyle, Shapiro, Natasha, Sicko, Robert, Storm, Samuel, Torene, Rebecca, Williams, Olatundun, Wynn, Julia, Taft, Ryan, Kruszka, Paul, Caggana, Michele

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