Testing Rare-Variant Association without Calling Genotypes Allows for Systematic Differences in Sequencing between Cases and Controls. by Yi-Juan Hu, Peizhou Liao, H Richard Johnston, Andrew S Allen, Glen A Satten

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Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders by Trenell J. Mosley, H. Richard Johnston, David J. Cutler, Michael E. Zwick, Jennifer G. Mulle

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HIV, asymptomatic STI, and the rectal mucosal immune environment among young men who have sex with men. by Vanessa E Van Doren, S Abigail Smith, Yi-Juan Hu, Gregory Tharp, Steven Bosinger, Cassie G Ackerley, Phillip M Murray, Rama R Amara, Praveen K Amancha, Robert A Arthur, H Richard Johnston, Colleen F Kelley

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Novel Missense CNTNAP2 Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior by Noor Badshah, Noor Badshah, Kari A. Mattison, Kari A. Mattison, Sohail Ahmad, Pankaj Chopra, H. Richard Johnston, Shakoor Ahmad, Sher Hayat Khan, Muhammad Tahir Sarwar, David J. Cutler, Micheal Taylor, Gayatri Vadlamani, Michael E. Zwick, Andrew Escayg

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Two New Aspergillus flavus Reference Genomes Reveal a Large Insertion Potentially Contributing to Isolate Stress Tolerance and Aflatoxin Production by Jake C. Fountain, Josh P. Clevenger, Brian Nadon, Ramey C. Youngblood, Walid Korani, Perng-Kuang Chang, Dakota Starr, Hui Wang, Benjamin Isett, H. Richard Johnston, Raegan Wiggins, Gaurav Agarwal, Ye Chu, Robert C. Kemerait, Manish K. Pandey, Deepak Bhatnagar, Peggy Ozias-Akins, Rajeev K. Varshney, Brian E. Scheffler, Justin N. Vaughn, Baozhu Guo

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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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Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS by Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M. McDonald-McGinn, T. Blaine Crowley, Daniel E. McGinn, Oanh T. Tran, Daniella Miller, Jhih-Rong Lin, Elaine Zackai, H. Richard Johnston, Eva W. C. Chow, Jacob A. S. Vorstman, Claudia Vingerhoets, Therese van Amelsvoort, Doron Gothelf, Ann Swillen, Jeroen Breckpot, Joris R. Vermeesch, Stephan Eliez, Maude Schneider, Marianne B. M. van den Bree, Michael J. Owen, Wendy R. Kates, Gabriela M. Repetto, Vandana Shashi, Kelly Schoch, Carrie E. Bearden, M. Cristina Digilio, Marta Unolt, Carolina Putotto, Bruno Marino, Maria Pontillo, Marco Armando, Stefano Vicari, Kathleen Angkustsiri, Linda Campbell, Tiffany Busa, Damian Heine-Suñer, Kieran C. Murphy, Declan Murphy, Sixto García-Miñaúr, Luis Fernández, International 22q11.2 Brain and Behavior Consortium (IBBC), Zhengdong D. Zhang, Elizabeth Goldmuntz, Raquel E. Gur, Beverly S. Emanuel, Deyou Zheng, Christian R. Marshall, Anne S. Bassett, Tao Wang, Bernice E. Morrow

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