Ryanodine Receptor–Mediated Calcium Leak Drives Progressive Development of an Atrial Fibrillation Substrate in a Transgenic Mouse Model von Li, Na, Chiang, David Y, Wang, Sufen, Wang, Qiongling, Sun, Liang, Voigt, Niels, Respress, Jonathan L, Ather, Sameer, Skapura, Darlene G, Jordan, Valerie K, Horrigan, Frank T, Schmitz, Wilhelm, Müller, Frank U, Valderrabano, Miguel, Nattel, Stanley, Dobrev, Dobromir, Wehrens, Xander H.T

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De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions von Fregeau, Brieana, Kim, Bum Jun, Hernández-García, Andrés, Jordan, Valerie K., Cho, Megan T., Schnur, Rhonda E., Monaghan, Kristin G., Juusola, Jane, Rosenfeld, Jill A., Bhoj, Elizabeth, Zackai, Elaine H., Sacharow, Stephanie, Barañano, Kristin, Bosch, Daniëlle G.M., de Vries, Bert B.A., Lindstrom, Kristin, Schroeder, Audrey, James, Philip, Kulch, Peggy, Lalani, Seema R., van Haelst, Mieke M., van Gassen, Koen L.I., van Binsbergen, Ellen, Barkovich, A. James, Scott, Daryl A., Sherr, Elliott H.

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RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects von Kim, Bum Jun, Zaveri, Hitisha P, Jordan, Valerie K, Hernandez-Garcia, Andres, Jacob, Daron J, Zamora, Diana L, Yu, Wei, Schwartz, Robert J, Scott, Daryl A

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Running a successful STEMM summer program: A week-by-week guide von Beasley, Heather K, Vue, Zer, McReynolds, Melanie R, Garza-Lopez, Edgar, Neikirk, Kit, Mungai, Margaret, Marshall, Andrea G, Shao, Bryanna, Benjamin, Jazmine I, Wanjalla, Celestine N, Williams, Clintoria R, Murray, Sandra A, Jordan, Valerie K, Shuler, Haysetta D, Kirabo, Annet, Hinton, Jr, Antentor

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RERE deficiency contributes to the development of orofacial clefts in humans and mice von Kim, Bum Jun, Zaveri, Hitisha P, Kundert, Peter N, Jordan, Valerie K, Scott, Tiana M, Carmichael, Jenny, Scott, Daryl A

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SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2 von Hernández-García, Andrés, Pendleton, Katherine E, Kim, Sangbae, Li, Yumei, Kim, Bum J, Zaveri, Hitisha P, Jordan, Valerie K, Berry, Aliska M, Ljungberg, M Cecilia, Chen, Rui, Lanz, Rainer B, Scott, Daryl A

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1p36 deletion syndrome: an update von Jordan, Valerie K, Zaveri, Hitisha P, Scott, Daryl A

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Genotype–phenotype correlations in individuals with pathogenic RERE variants von Jordan, Valerie K., Fregeau, Brieana, Ge, Xiaoyan, Giordano, Jessica, Wapner, Ronald J., Balci, Tugce B., Carter, Melissa T., Bernat, John A., Moccia, Amanda N., Srivastava, Anshika, Martin, Donna M., Bielas, Stephanie L., Pappas, John, Svoboda, Melissa D., Rio, Marlène, Boddaert, Nathalie, Cantagrel, Vincent, Lewis, Andrea M., Scaglia, Fernando, Kohler, Jennefer N., Bernstein, Jonathan A., Dries, Annika M., Rosenfeld, Jill A., DeFilippo, Colette, Thorson, Willa, Yang, Yaping, Sherr, Elliott H., Bi, Weimin, Scott, Daryl A.

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The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia von Jordan, Valerie K, Beck, Tyler F, Hernandez-Garcia, Andres, Kundert, Peter N, Kim, Bum-Jun, Jhangiani, Shalini N, Gambin, Tomasz, Starkovich, Molly, Punetha, Jaya, Paine, Ingrid S, Posey, Jennifer E, Li, Alexander H, Muzny, Donna, Hsu, Chih-Wei, Lashua, Amber J, Sun, Xin, Fernandes, Caraciolo J, Dickinson, Mary E, Lally, Kevin P, Gibbs, Richard A, Boerwinkle, Eric, Lupski, James R, Scott, Daryl A

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Duplication of HEY2 in cardiac and neurologic development von Jordan, Valerie K., Rosenfeld, Jill A., Lalani, Seema R., Scott, Daryl A.

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FBN1 contributing to familial congenital diaphragmatic hernia von Beck, Tyler F., Campeau, Philippe M., Jhangiani, Shalini N., Gambin, Tomasz, Li, Alexander H., Abo-Zahrah, Reem, Jordan, Valerie K., Hernandez-Garcia, Andres, Wiszniewski, Wojciech K., Muzny, Donna, Gibbs, Richard A., Boerwinkle, Eric, Lupski, James R., Lee, Brendan, Reardon, Willie, Scott, Daryl A.

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De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions von Fregeau, Brieana, Kim, Bum Jun, Hernández-García, Andrés, Jordan, Valerie K, Cho, Megan T, Schnur, Rhonda E, Monaghan, Kristin G, Juusola, Jane, Rosenfeld, Jill A, Bhoj, Elizabeth, Zackai, Elaine H, Sacharow, Stephanie, Barañano, Kristin, Bosch, Daniëlle G M, de Vries, Bert B A, Lindstrom, Kristin, Schroeder, Audrey, James, Philip, Kulch, Peggy, Lalani, Seema R, van Haelst, Mieke M, van Gassen, Koen L I, van Binsbergen, Ellen, Barkovich, A James, Scott, Daryl A, Sherr, Elliott H

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A More Connected Future: How Social Connection, Interdisciplinary Approaches, and New Technology Will Shape the Affective Science of Loneliness, a Commentary on the Special Issue von Pierce, Jordan E., Jones, Valerie K., Neta, Maital

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Predictive value and diagnostic accuracy of F-18-fluoro-deoxy-glucose positron emission tomography treated grade 1 and 2 follicular lymphoma von Bishu, Shrinivas, Quigley, Joanna M., Bishu, Shreenath R., Olsasky, Sarah M., Stem, Richard A., Shostrom, Valerie K., Holdeman, Karen P., Paknikar, Subash, Armitage, James O., Hankins, Jordan H.

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