P586: The qMini assay identifies an overlooked class of splice variants by Bin Guan, Chelsea Bender, Robert Hufnagel

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P657: Structural variants identified by short-read genome sequencing solves missing heritability in retinal dystrophies by Ehsan Ullah, Amelia Naik, Chelsea Bender, Delphine Blain, Laryssa Huryn, Robert Hufnagel, Bin Guan

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P336: Resolving missing heritability by iterative multidisciplinary and organ-specific reanalysis by Ehsan Ullah, Bin Guan, Amelia Naik, Chelsea Bender, Ranya Al Rawi, Delphine Blain, Aime Agather, Laryssa Huryn, Wadih Zein, Catherine Cukras, Brian Brooks, Robert Hufnagel

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Predominant Founder Effect among Recurrent Pathogenic Variants for an X-Linked Disorder by Chelsea Bender, Elizabeth Geena Woo, Bin Guan, Ehsan Ullah, Eric Feng, Amy Turriff, Santa J. Tumminia, Paul A. Sieving, Catherine A. Cukras, Robert B. Hufnagel

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Widespread subclinical cellular changes revealed across a neural-epithelial-vascular complex in choroideremia using adaptive optics by Nancy Aguilera, Tao Liu, Andrew J. Bower, Joanne Li, Sarah Abouassali, Rongwen Lu, John Giannini, Maximilian Pfau, Chelsea Bender, Margery G. Smelkinson, Amelia Naik, Bin Guan, Owen Schwartz, Andrei Volkov, Alfredo Dubra, Zhuolin Liu, Daniel X. Hammer, Dragan Maric, Robert Fariss, Robert B. Hufnagel, Brett G. Jeffrey, Brian P. Brooks, Wadih M. Zein, Laryssa A. Huryn, Johnny Tam

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