Transiently elevated plasma methionine, S‐adenosylmethionine and S‐adenosylhomocysteine: Unreported laboratory findings in a patient with NGLY1 deficiency, a congenital disorder of... von Chang, Caitlin A., Wei, Xing‐Chang, Martin, Steven R., Sinasac, David S., Al‐Hertani, Walla

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An ACSL4 Hemizygous Intragenic Deletion in a Patient With Childhood Stroke von Chang, Caitlin A., Lauzon, Julie, Kirton, Adam, Argiropoulos, Bob

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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome von Alharatani, Reham, Ververi, Athina, Beleza-Meireles, Ana, Ji, Weizhen, Mis, Emily, Patterson, Quinten T., Griffin, John N., Bhujel, Nabina, Chang, Caitlin A., Dixit, Abhijit, Konstantino, Monica, Healy, Christopher, Hannan, Sumayyah, Neo, Natsuko, Cash, Alex, Li, Dong, Bhoj, Elizabeth, Zackai, Elaine H., Cleaver, Ruth, Baralle, Diana, McEntagart, Meriel, Newbury-Ecob, Ruth, Scott, Richard, Hurst, Jane A., Au, Ping Yee Billie, Hosey, Marie Therese, Khokha, Mustafa, Marciano, Denise K., Lakhani, Saquib A., Liu, Karen J.

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Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variants von Chang, Caitlin A., Perrier, Renee, Kurek, Kyle C., Estrada‐Veras, Juvianee, Lehman, Anna, Yip, Stephen, Hendson, Glenda, Diamond, Carol, Pinchot, Jason W., Tran, Jennifer M., Arkin, Lisa M., Drolet, Beth A., Napier, Melanie P., O'Neill, Sarah A., Balci, Tugce B., Keppler‐Noreuil, Kim M.

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Bilateral Nephroblastic Tumors and a Complex Renal Vascular Anomaly in a Patient With a Mosaic RASopathy: Novel Histopathologic Features and Molecular Insights von Slack, Jonathan C, Bründler, Marie-Anne, Chang, Caitlin A, Perrier, Renee, Lafay-Cousin, Lucie, Kurek, Kyle C

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Congenital hiatal hernia segregating with a duplication in 9q22.31q22.32 in two families von Chang, Caitlin A., Di Donato, Nataliya, Hackmann, Karl, Argiropoulos, Bob, Ferreira, Patrick, Innes, A. Micheil, Thomas, Mary Ann

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Mechanical stretch upregulates connexin43 in human trabecular meshwork cells von Tellios, Nikoleta, Feng, Mary, Chen, Nancy, Liu, Hong, Tellios, Vasiliki, Wang, Mary, Li, Xiangji, Chang, Caitlin A., Hutnik, Cindy

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Pathogenic heterozygous TRPM7 variants and hypomagnesemia with developmental delay von Bosman, Willem, Butler, Kameryn M, Chang, Caitlin A, Ganapathi, Mythily, Guzman, Edwin, Latta, Femke, Chung, Wendy K, Claverie-Martin, Felix, Davis, Jessica M, Hoenderop, Joost G J, de Baaij, Jeroen H F

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Isolated Horner Syndrome From an Elongated Styloid Process (Eagle Syndrome) von Chang, Caitlin A, Lin, Tony, Fung, Kevin, Sharma, Manas, Fraser, J Alexander

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The seventh international RASopathies symposium: Pathways to a cure—expanding knowledge, enhancing research, and therapeutic discovery von Kontaridis, Maria I., Roberts, Amy E., Schill, Lisa, Schoyer, Lisa, Stronach, Beth, Andelfinger, Gregor, Aoki, Yoko, Axelrad, Marni E., Bakker, Annette, Bennett, Anton M., Broniscer, Alberto, Castel, Pau, Chang, Caitlin A., Cyganek, Lukas, Das, Tirtha K., Hertog, Jeroen, Galperin, Emilia, Garg, Shruti, Gelb, Bruce D., Gordon, Kristiana, Green, Tamar, Gripp, Karen W., Itkin, Maxim, Kiuru, Maija, Korf, Bruce R., Livingstone, Jeff R., López‐Juárez, Alejandro, Magoulas, Pilar L., Mansour, Sahar, Milner, Theresa, Parker, Elisabeth, Pierpont, Elizabeth I., Plouffe, Kevin, Rauen, Katherine A., Shankar, Suma P., Smith, Shane B., Stevenson, David A., Tartaglia, Marco, Van, Richard, Wagner, Morgan E., Ware, Stephanie M., Zenker, Martin

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The seventh international RASopathies symposium: Pathways to a cure—expanding knowledge, enhancing research, and therapeutic discovery von Kontaridis, Maria I, Roberts, Amy E, Schill, Lisa, Schoyer, Lisa, Stronach, Beth, Andelfinger, Gregor, Aoki, Yoko, Axelrad, Marni E, Bakker, Annette, Bennett, Anton M, Broniscer, Alberto, Castel, Pau, Chang, Caitlin A, Cyganek, Lukas, Das, Tirtha K, den Hertog, Jeroen, Galperin, Emilia, Garg, Shruti, Gelb, Bruce D, Gordon, Kristiana, Green, Tamar, Gripp, Karen W, Itkin, Maxim, Kiuru, Maija, Korf, Bruce R, Livingstone, Jeff R, López-Juárez, Alejandro, Magoulas, Pilar L, Mansour, Sahar, Milner, Theresa, Parker, Elisabeth, Pierpont, Elizabeth I, Plouffe, Kevin, Rauen, Katherine A, Shankar, Suma P, Smith, Shane B, Stevenson, David A, Tartaglia, Marco, Van, Richard, Wagner, Morgan E, Ware, Stephanie M, Zenker, Martin

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An ACSL4 Hemizygous Intragenic Deletion in a Patient With Childhood Stroke von Chang, Caitlin A, Lauzon, Julie, Kirton, Adam, Argiropoulos, Bob

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Transiently elevated plasma methionine, S-adenosylmethionine and S-adenosylhomocysteine: Unreported laboratory findings in a patient with NGLY1 deficiency, a congenital disorder of... von Chang, Caitlin A, Wei, Xing-Chang, Martin, Steven R, Sinasac, David S, Al-Hertani, Walla

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Congenital hiatal hernia segregating with a duplication in 9q22.31q22.32 in two families von Chang, Caitlin A, Di Donato, Nataliya, Hackmann, Karl, Argiropoulos, Bob, Ferreira, Patrick, Innes, A Micheil, Thomas, Mary Ann

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The Landmark Series: Multimodal Therapy for Esophageal Cancer von Demarest, Caitlin T., Chang, Andrew C.

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An engineered human Fc domain that behaves like a pH-toggle switch for ultra-long circulation persistence von Lee, Chang-Han, Kang, Tae Hyun, Godon, Ophélie, Watanabe, Makiko, Delidakis, George, Gillis, Caitlin M., Sterlin, Delphine, Hardy, David, Cogné, Michel, Macdonald, Lynn E., Murphy, Andrew J., Tu, Naxin, Lee, Jiwon, McDaniel, Jonathan R., Makowski, Emily, Tessier, Peter M., Meyer, Aaron S., Bruhns, Pierre, Georgiou, George

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Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of Microglia von Oosterhof, Nynke, Chang, Irene J., Karimiani, Ehsan Ghayoor, Kuil, Laura E., Jensen, Dana M., Daza, Ray, Young, Erica, Astle, Lee, van der Linde, Herma C., Shivaram, Giridhar M., Demmers, Jeroen, Latimer, Caitlin S., Keene, C. Dirk, Loter, Emily, Maroofian, Reza, van Ham, Tjakko J., Hevner, Robert F., Bennett, James T.

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Endocytic proteins with prion-like domains form viscoelastic condensates that enable membrane remodeling von Bergeron-Sandoval, Louis-Philippe, Kumar, Sandeep, Heris, Hossein Khadivi, Chang, Catherine L. A., Cornell, Caitlin E., Keller, Sarah L., François, Paul, Hendricks, Adam G., Ehrlicher, Allen J., Pappu, Rohit V., Michnick, Stephen W.

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Preliminary Findings of mRNA Covid-19 Vaccine Safety in Pregnant Persons von Shimabukuro, Tom T, Kim, Shin Y, Myers, Tanya R, Moro, Pedro L, Oduyebo, Titilope, Panagiotakopoulos, Lakshmi, Marquez, Paige L, Olson, Christine K, Liu, Ruiling, Chang, Karen T, Ellington, Sascha R, Burkel, Veronica K, Smoots, Ashley N, Green, Caitlin J, Licata, Charles, Zhang, Bicheng C, Alimchandani, Meghna, Mba-Jonas, Adamma, Martin, Stacey W, Gee, Julianne M, Meaney-Delman, Dana M

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Phenotypes of macrophages present in the intestine are impacted by stage of disease in cattle naturally infected with Mycobacterium avium subsp. paratuberculosis von Jenvey, Caitlin J, Shircliff, Adrienne L, Bannantine, John P, Stabel, Judith R

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