Natural history of the aortic root in Tetralogy of Fallot after repair by Yuli Y. Kim, Max T. Geisinger, Tanmay Bhamare, Melissa Wasserman, Jungwon Min, Elizabeth Goldmuntz

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Maternal effect genes as risk factors for congenital heart defects by Fadi I. Musfee, Omobola O. Oluwafemi, A.J. Agopian, Hakon Hakonarson, Elizabeth Goldmuntz, Laura E. Mitchell

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Genome-wide association study of maternal and inherited loci for conotruncal heart defects. by A J Agopian, Laura E Mitchell, Joseph Glessner, Angela D Bhalla, Anshuman Sewda, Hakon Hakonarson, Elizabeth Goldmuntz

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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. by Michelle Kaplinski, Deanne Taylor, Laura E Mitchell, Dorothy A Hammond, Elizabeth Goldmuntz, A J Agopian, Pediatric Cardiac Genomics Consortium

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

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Predictors of Length of Hospital Stay After Complete Repair for Tetralogy of Fallot: A Prospective Cohort Study by Laura Mercer‐Rosa, Okan U. Elci, Grace DeCost, Stacy Woyciechowski, Sharon M. Edman, Chitra Ravishankar, Christopher E. Mascio, Steven M. Kawut, Elizabeth Goldmuntz

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Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study by Thanh T. Hoang, Paulo Henrique Manso, Sharon Edman, Laura Mercer-Rosa, Laura E. Mitchell, Anshuman Sewda, Michael D. Swartz, Mark A. Fogel, A. J. Agopian, Elizabeth Goldmuntz

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Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects by Fadi I. Musfee, A. J. Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E. Morrow, Deanne M. Taylor, Martin Tristani-Firouzi, W. Scott Watkins, Mark Yandell, Laura E. Mitchell

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Resource Utilization in the First 2 Years Following Operative Correction for Tetralogy of Fallot: Study Using Data From the Optum's De‐Identified Clinformatics Data Mart Insurance... by Michael L. O'Byrne, Grace DeCost, Hannah Katcoff, Jill J. Savla, Joyce Chang, Elizabeth Goldmuntz, Peter W. Groeneveld, Joseph W. Rossano, Jennifer A. Faerber, Laura Mercer‐Rosa

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Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States by Omobola O. Oluwafemi, Fadi I. Musfee, Laura E. Mitchell, Elizabeth Goldmuntz, Hongbo M. Xie, Hakon Hakonarson, Bernice E. Morrow, Tingwei Guo, Deanne M. Taylor, Donna M. McDonald-McGinn, Beverly S. Emanuel, A. J. Agopian

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Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study by Hayley A. Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S. Emanuel, Douglas Ryba, James William Gaynor, Elaine H. Zackai, Hakon Hakonarson, Donna M. McDonald-McGinn

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P783: Two fetuses with hereditary hemorrhagic telangiectasia presenting with rare finding of arteriovenous malformations by Natalie Burrill, Christina Paidas Teefey, Nankee Kumar, Sonika Agarwal, Lauren Beslow, Edward Oliver, Minh-Huy Le Huynh, Elizabeth Goldmuntz, Bryan Pukenas, Alexandra Borst, Allison Britt, Arastoo Vossough, Stephanie Fuller, Shih-Shan Lang Chen, Erica Schindewolf, Lisa Pilchman, Renee Wright, Haley Crane

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

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

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Loss of RNA expression and allele-specific expression associated with congenital heart disease by David M. McKean, Jason Homsy, Hiroko Wakimoto, Neil Patel, Joshua Gorham, Steven R. DePalma, James S. Ware, Samir Zaidi, Wenji Ma, Nihir Patel, Richard P. Lifton, Wendy K. Chung, Richard Kim, Yufeng Shen, Martina Brueckner, Elizabeth Goldmuntz, Andrew J. Sharp, Christine E. Seidman, Bruce D. Gelb, J. G. Seidman

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

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Association of genetic and sulcal traits with executive function in congenital heart disease by Lara Maleyeff, Jane W. Newburger, David Wypij, Nina H. Thomas, Evdokia Anagnoustou, Martina Brueckner, Wendy K. Chung, John Cleveland, Sean Cunningham, Bruce D. Gelb, Elizabeth Goldmuntz, Donald J Hagler Jr, Hao Huang, Eileen King, Patrick McQuillen, Thomas A. Miller, Ami Norris‐Brilliant, George A. Porter Jr, Amy E. Roberts, P. Ellen Grant, Kiho Im, Sarah U. Morton

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Genetic and clinical variables act synergistically to impact neurodevelopmental outcomes in children with single ventricle heart disease by Thomas A. Miller, Edgar J. Hernandez, J. William Gaynor, Mark W. Russell, Jane W. Newburger, Wendy Chung, Elizabeth Goldmuntz, James F. Cnota, Sinai C. Zyblewski, William T. Mahle, Victor Zak, Chitra Ravishankar, Jonathan R. Kaltman, Brian W. McCrindle, Shanelle Clarke, Jodie K. Votava-Smith, Eric M. Graham, Mike Seed, Nancy Rudd, Daniel Bernstein, Teresa M. Lee, Mark Yandell, Martin Tristani-Firouzi

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EM-mosaic detects mosaic point mutations that contribute to congenital heart disease by Alexander Hsieh, Sarah U. Morton, Jon A. L. Willcox, Joshua M. Gorham, Angela C. Tai, Hongjian Qi, Steven DePalma, David McKean, Emily Griffin, Kathryn B. Manheimer, Daniel Bernstein, Richard W. Kim, Jane W. Newburger, George A. Porter, Deepak Srivastava, Martin Tristani-Firouzi, Martina Brueckner, Richard P. Lifton, Elizabeth Goldmuntz, Bruce D. Gelb, Wendy K. Chung, Christine E. Seidman, J. G. Seidman, Yufeng Shen

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Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome by Cristina E. Trevino, Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler, H. Richard Johnston, Benjamin L. Rambo-Martin, Jai Oberoi, Kenneth J. Dooley, George T. Capone, Roger H. Reeves, Heather J. Cordell, Bernard D. Keavney, A. J. Agopian, Elizabeth Goldmuntz, Peter J. Gruber, James E. O’Brien, Douglas C. Bittel, Lalita Wadhwa, Clifford L. Cua, Ivan P. Moskowitz, Jennifer G. Mulle, Michael P. Epstein, Stephanie L. Sherman, Michael E. Zwick

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