Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects von Loges, Niki T., Antony, Dinu, Maver, Ales, Deardorff, Matthew A., Güleç, Elif Yýlmaz, Gezdirici, Alper, Nöthe-Menchen, Tabea, Höben, Inga M., Jelten, Lena, Frank, Diana, Werner, Claudius, Tebbe, Johannes, Wu, Kaman, Goldmuntz, Elizabeth, Čuturilo, Goran, Krock, Bryan, Ritter, Alyssa, Hjeij, Rim, Bakey, Zeineb, Pennekamp, Petra, Dworniczak, Bernd, Brunner, Han, Peterlin, Borut, Tanidir, Cansaran, Olbrich, Heike, Omran, Heymut, Schmidts, Miriam

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Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data von Glessner, Joseph T, Bick, Alexander G, Ito, Kaoru, Homsy, Jason G, Rodriguez-Murillo, Laura, Fromer, Menachem, Mazaika, Erica, Vardarajan, Badri, Italia, Michael, Leipzig, Jeremy, DePalma, Steven R, Golhar, Ryan, Sanders, Stephan J, Yamrom, Boris, Ronemus, Michael, Iossifov, Ivan, Willsey, A Jeremy, State, Matthew W, Kaltman, Jonathan R, White, Peter S, Shen, Yufeng, Warburton, Dorothy, Brueckner, Martina, Seidman, Christine, Goldmuntz, Elizabeth, Gelb, Bruce D, Lifton, Richard, Seidman, Jonathan, Hakonarson, Hakon, Chung, Wendy K

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CANOES: detecting rare copy number variants from whole exome sequencing data von Backenroth, Daniel, Homsy, Jason, Murillo, Laura R, Glessner, Joe, Lin, Edwin, Brueckner, Martina, Lifton, Richard, Goldmuntz, Elizabeth, Chung, Wendy K, Shen, Yufeng

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Tricuspid Annular Plane Systolic Excursion in the Assessment of Right Ventricular Function in Children and Adolescents after Repair of Tetralogy of Fallot von Mercer-Rosa, Laura, MD, MSCE, Parnell, Aimee, MD, MSCE, Forfia, Paul R., MD, Yang, Wei, PhD, Goldmuntz, Elizabeth, MD, Kawut, Steven M., MD, MS

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The Congenital Heart Disease Genetic Network Study: Cohort description von Hoang, Thanh T, Goldmuntz, Elizabeth, Roberts, Amy E, Chung, Wendy K, Kline, Jennie K, Deanfield, John E, Giardini, Alessandro, Aleman, Adolfo, Gelb, Bruce D, Mac Neal, Meghan, Porter, Jr, George A, Kim, Richard, Brueckner, Martina, Lifton, Richard P, Edman, Sharon, Woyciechowski, Stacy, Mitchell, Laura E, Agopian, A J

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De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes von Watkins, W. Scott, Hernandez, E. Javier, Wesolowski, Sergiusz, Bisgrove, Brent W., Sunderland, Ryan T., Lin, Edwin, Lemmon, Gordon, Demarest, Bradley L., Miller, Thomas A., Bernstein, Daniel, Brueckner, Martina, Chung, Wendy K., Gelb, Bruce D., Goldmuntz, Elizabeth, Newburger, Jane W., Seidman, Christine E., Shen, Yufeng, Yost, H. Joseph, Yandell, Mark, Tristani-Firouzi, Martin

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22q11.2 Deletion syndrome is associated with perioperative outcome in tetralogy of Fallot von Mercer-Rosa, Laura, MD, MSCE, Pinto, Nelangi, MD, Yang, Wei, PhD, Tanel, Ronn, MD, Goldmuntz, Elizabeth, MD

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DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia von Li, You, Yagi, Hisato, Onuoha, Ezenwa Obi, Damerla, Rama Rao, Francis, Richard, Furutani, Yoshiyuki, Tariq, Muhammad, King, Stephen M, Hendricks, Gregory, Cui, Cheng, Saydmohammed, Manush, Lee, Dong Min, Zahid, Maliha, Sami, Iman, Leatherbury, Linda, Pazour, Gregory J, Ware, Stephanie M, Nakanishi, Toshio, Goldmuntz, Elizabeth, Tsang, Michael, Lo, Cecilia W

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Trends in Pulmonary Valve Replacement in Children and Adults With Tetralogy of Fallot von O’Byrne, Michael L., MD, MSCE, Glatz, Andrew C., MD, MSCE, Mercer-Rosa, Laura, MD, MSCE, Gillespie, Matthew J., MD, Dori, Yoav, MD, PhD, Goldmuntz, Elizabeth, MD, Kawut, Steven, MD, MS, Rome, Jonathan J., MD

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Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiers von Unolt, Marta, Versacci, Paolo, Anaclerio, Silvia, Lambiase, Caterina, Calcagni, Giulio, Trezzi, Matteo, Carotti, Adriano, Crowley, Terrence Blaine, Zackai, Elaine H., Goldmuntz, Elizabeth, Gaynor, James William, Digilio, Maria Cristina, McDonald‐McGinn, Donna M., Marino, Bruno

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Automated Cmr-based Measurements Are Predictive of Pulmonic Valve Replacement in Repaired Tetralogy of Fallot von Thompson, Elizabeth, Kim, Jin-seo, Bhattaru, Abhijit, Vu, Phuong, Swago, Sophia, Donnelly, Elizabeth, zhang, Xuemei, Vuthuri, Lipika, Lanzilotta, Kristen, Loth, Annefleur, Whitehead, Kevin, Duda, Jeffrey, Gee, James, Almasy, Laura, Goldmuntz, Elizabeth, Fogel, Mark, Witschey, Walter

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Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles von Martin-Trujillo, Alejandro, Patel, Nihir, Richter, Felix, Jadhav, Bharati, Garg, Paras, Morton, Sarah U, McKean, David M, DePalma, Steven R, Goldmuntz, Elizabeth, Gruber, Dorota, Kim, Richard, Newburger, Jane W, Porter, Jr, George A, Giardini, Alessandro, Bernstein, Daniel, Tristani-Firouzi, Martin, Seidman, Jonathan G, Seidman, Christine E, Chung, Wendy K, Gelb, Bruce D, Sharp, Andrew J

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Mouse and Human CRKL Is Dosage Sensitive for Cardiac Outflow Tract Formation von Racedo, Silvia E., McDonald-McGinn, Donna M., Chung, Jonathan H., Goldmuntz, Elizabeth, Zackai, Elaine, Emanuel, Beverly S., Zhou, Bin, Funke, Birgit, Morrow, Bernice E.

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22q11.2 Deletion syndrome is associated with increased perioperative events and more complicated postoperative course in infants undergoing infant operative correction of truncus a... von O’Byrne, Michael L., MD, Yang, Wei, PhD, Mercer-Rosa, Laura, MD, MSCE, Parnell, Aimee S., MD, MSCE, Oster, Matthew E., MD, MPH, Levenbrown, Yosef, DO, Tanel, Ronn E., MD, Goldmuntz, Elizabeth, MD

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Identifying novel data-driven subgroups in congenital heart disease using multi-modal measures of brain structure von Vandewouw, Marlee M., Norris-Brilliant, Ami, Rahman, Anum, Assimopoulos, Stephania, Morton, Sarah U., Kushki, Azadeh, Cunningham, Sean, King, Eileen, Goldmuntz, Elizabeth, Miller, Thomas A., Thomas, Nina H., Adams, Heather R., Cleveland, John, Cnota, James F., Ellen Grant, P, Goldberg, Caren S., Huang, Hao, Li, Jennifer S., McQuillen, Patrick, Porter, George A., Roberts, Amy E., Russell, Mark W., Seidman, Christine E., Tivarus, Madalina E., Chung, Wendy K., Hagler, Donald J., Newburger, Jane W., Panigrahy, Ashok, Lerch, Jason P, Gelb, Bruce D., Anagnostou, Evdokia

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Exercise Performance and 22q11.2 Deletion Status Affect Quality of Life in Tetralogy of Fallot von Goldmuntz, Elizabeth, Cassedy, Amy, Mercer-Rosa, Laura, Fogel, Mark A., Paridon, Stephen M., Marino, Bradley S.

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GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm von Sharma, Arun, Wasson, Lauren K, Willcox, Jon Al, Morton, Sarah U, Gorham, Joshua M, DeLaughter, Daniel M, Neyazi, Meraj, Schmid, Manuel, Agarwal, Radhika, Jang, Min Young, Toepfer, Christopher N, Ward, Tarsha, Kim, Yuri, Pereira, Alexandre C, DePalma, Steven R, Tai, Angela, Kim, Seongwon, Conner, David, Bernstein, Daniel, Gelb, Bruce D, Chung, Wendy K, Goldmuntz, Elizabeth, Porter, George, Tristani-Firouzi, Martin, Srivastava, Deepak, Seidman, Jonathan G, Seidman, Christine E

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Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects von Sewda, Anshuman, Agopian, A J, Goldmuntz, Elizabeth, Hakonarson, Hakon, Morrow, Bernice E, Musfee, Fadi, Taylor, Deanne, Mitchell, Laura E

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The association of elevated maternal genetic risk scores for hypertension, type 2 diabetes and obesity and having a child with a congenital heart defect von Kaplinski, Michelle, Taylor, Deanne, Mitchell, Laura E, Hammond, Dorothy A, Goldmuntz, Elizabeth, Agopian, A J

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Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects von Sewda, Anshuman, Agopian, A J, Goldmuntz, Elizabeth, Hakonarson, Hakon, Morrow, Bernice E, Taylor, Deanne, Mitchell, Laura E

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