P155: Parsing autism heterogeneity: Phenotypic differences between individuals across genes of different effect sizes by Sarah Barns, Jessica Wright, Jacob Hall, Pamela Feliciano, Wendy Chung

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P258: Phenotypic predictors of dual genetic diagnosis in people with autism by Alexandra Goler, Jessica Wright, Jacob Hall, Pamela Feliciano, Wendy Chung

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P648: Automated reanalysis of clinical genomic data in undiagnosed patients by Shira Rockowitz, Wanqing Shao, Jacob Hagen, Courtney French, Alexa Geltzeiler, Piotr Sliz, Wendy Chung

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O24: Heterozygous de novo variants in CDKL1 and CDKL2 cause neuroregressive phenotypes in Human and Drosophila and are dominant negative alleles by Ali H. Bereshneh, Jonathan Andrews, Daniel Eberl, Guney Bademci, Nicholas Borja, Stephanie Bivona, Shinya Yamamoto, Michael F. Wangler, Shane McKee, Mustafa Tekin, Wendy Chung, Hugo Bellen, Oguz Kanca

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O52: Diagnostic benefits of long-read genome sequencing for short-read negative rare disease cases by Alan Beggs, Tina Truong, Wanqing Shao, Bryan Leland, Kshitij Amar, Mehmet Bugrahan Duz, Nathaniel Edisis, Casie Genetti, Médéric Jeanne, Pratiksha Pradhan, Priyesh Rughani, Luca Schierbaum, Shirlee Shril, Rebecca Stubbs, Malika Sud, Kenney Tuyen, Carly Tyer, Talia Tzadikario, Scott Hickey, Sissel Juul, Piotr Sliz, Monica Wojcik, Friedhelm Hildebrandt, Catherine Brownstein, Miten Jain, Wendy Chung

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O48: International Consortium on Newborn Sequencing (ICoNS) consensus guidelines for gene selection in genomic newborn screening programs by Nina Gold, Julie Yeo, Derek Ansel, Mei Baker, Jorune Balciuniene, Jonathan Berg, François Boemer, Wendy Chung, Heidi Cope, David Eckstein, Nicolas Encina, Laurence Faivre, Alessandra Ferlini, Judit Garcia-Villoria, Michael Gelb, Jose Manuel Gonzalez De Aledo Castillo, Katie Golden-Grant, Thomas Minten, Richard Parad, Nidhi Shah, Zornitza Stark, Kristen Sund, Petros Tsipouras, Meekai To, Lilian Downie

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