Macrophage Sortilin Promotes LDL Uptake, Foam Cell Formation, and Atherosclerosis von Patel, Kevin M, Strong, Alanna, Tohyama, Junichiro, Jin, Xueting, Morales, Carlos R, Billheimer, Jeffery, Millar, John, Kruth, Howard, Rader, Daniel J

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CRISPR gene-editing therapies for hypertrophic cardiomyopathy von Strong, Alanna

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Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency von Pritchard, Amanda Barone, Strong, Alanna, Ficicioglu, Can

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From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus von Kathiresan, Sekar, Rader, Daniel J, Musunuru, Kiran, Strong, Alanna, Frank-Kamenetsky, Maria, Lee, Noemi E, Ahfeldt, Tim, Sachs, Katherine V, Li, Xiaoyu, Li, Hui, Kuperwasser, Nicolas, Ruda, Vera M, Pirruccello, James P, Muchmore, Brian, Prokunina-Olsson, Ludmila, Hall, Jennifer L, Schadt, Eric E, Morales, Carlos R, Lund-Katz, Sissel, Phillips, Michael C, Wong, Jamie, Cantley, William, Racie, Timothy, Ejebe, Kenechi G, Orho-Melander, Marju, Melander, Olle, Koteliansky, Victor, Fitzgerald, Kevin, Krauss, Ronald M, Cowan, Chad A

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Ocular manifestations of ectodermal dysplasia von Landau Prat, Daphna, Katowitz, William R, Strong, Alanna, Katowitz, James A

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Hepatic sortilin regulates both apolipoprotein B secretion and LDL catabolism von Strong, Alanna, Ding, Qiurong, Edmondson, Andrew C, Millar, John S, Sachs, Katherine V, Li, Xiaoyu, Kumaravel, Arthi, Wang, Margaret Ye, Ai, Ding, Guo, Liang, Alexander, Eric T, Nguyen, David, Lund-Katz, Sissel, Phillips, Michael C, Morales, Carlos R, Tall, Alan R, Kathiresan, Sekar, Fisher, Edward A, Musunuru, Kiran, Rader, Daniel J

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Revisiting Old Friends: Sortilin-1, Low-Density Lipoprotein Receptor, and Prorenin Receptor as Modulators of Lipoprotein and Energy Metabolism von Strong, Alanna

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Genome editing in cardiovascular diseases von Strong, Alanna, Musunuru, Kiran

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Early presentation of adult-onset conditions: A dual diagnosis of hereditary hemochromatosis and porphyria cutanea tarda von Strong, Alanna, Keller, Kierstin, Merves, Jamie

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Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort von Strong, Alanna, Behr, Meckenzie, Lott, Carina, Clark, Abigail J., Mentch, Frank, Da Silva, Renata Pellegrino, Rux, Danielle R., Campbell, Robert, Skraban, Cara, Wang, Xiang, Anari, Jason B., Sinder, Benjamin, Cahill, Patrick J., Sleiman, Patrick, Hakonarson, Hakon

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Revisiting Old Friends von Strong, Alanna

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Activation of ER stress and mTORC1 suppresses hepatic sortilin-1 levels in obese mice von Ai, Ding, Baez, Juan M, Jiang, Hongfeng, Conlon, Donna M, Hernandez-Ono, Antonio, Frank-Kamenetsky, Maria, Milstein, Stuart, Fitzgerald, Kevin, Murphy, Andrew J, Woo, Connie W, Strong, Alanna, Ginsberg, Henry N, Tabas, Ira, Rader, Daniel J, Tall, Alan R

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EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients von Cohen, Jennifer L., Schrier Vergano, Samantha A., Mazzola, Sarah, Strong, Alanna, Keena, Beth, McDougall, Carey, Ritter, Alyssa, Li, Dong, Bedoukian, Emma C., Burke, Leah W., Hoffman, Amber, Zurcher, Victoria, Krantz, Ian D., Izumi, Kosuke, Bhoj, Elizabeth, Zackai, Elaine H., Deardorff, Matthew A.

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Lessons Learned From the Long‐Term Use of Enzyme Replacement Therapy in the Treatment of Lysosomal Acid Lipase Deficiency von Strong, Alanna, Ficicioglu, Can

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P350: Variants in MED12 are associated with left ventricular non-compaction and arrhythmia von Weaver, Nicole, Shikany, Amy, Vieta, Emile, Russell, Bianca, Lerman, Bruce, Strong, Alanna, Li, Dong

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Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism von Li, Dong, Strong, Alanna, Hou, Cuiping, Downes, Helen, Pritchard, Amanda Barone, Mazzeo, Pamela, Zackai, Elaine H, Conlin, Laura K, Hakonarson, Hakon

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Introduction: Genetic Hepatobiliary Disease von Strong, Alanna

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Phenotypes of undiagnosed adults with actionable OTC and GLA variants von Gold, Jessica I., Madhavan, Sarina, Park, Joseph, Zouk, Hana, Perez, Emma, Strong, Alanna, Drivas, Theodore G., Karaa, Amel, Yudkoff, Marc, Rader, Daniel, Green, Robert C., Gold, Nina B.

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P408: Perspectives of rare disease experts on sequencing newborns for treatable genetic conditions von Shah, Nidhi, Gold, Nina, Adelson, Sophia, Williams, Shardae, Bick, Sarah, Gold, Jessica, Strong, Alanna, Ganetzky, Rebecca, Roberts, Amy, Walker, Melissa, Holtz, Alexander, Sankaran, Vijay, Delmonte, Ottavia, Tan, Weizhen, Holm, Ingrid, Thiagarajah, Jay, Kamihara, Junne, Comander, Jason, Place, Emily, Wiggs, Janey, Green, Robert

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Targeted treatment of migrating partial seizures of infancy with quinidine von Bearden, David, Strong, Alanna, Ehnot, Jessica, DiGiovine, Marissa, Dlugos, Dennis, Goldberg, Ethan M.

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