Glycolytic Enzymes Localize to Synapses under Energy Stress to Support Synaptic Function von Jang, SoRi, Nelson, Jessica C., Bend, Eric G., Rodríguez-Laureano, Lucelenie, Tueros, Felipe G., Cartagenova, Luis, Underwood, Katherine, Jorgensen, Erik M., Colón-Ramos, Daniel A.

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Axons Degenerate in the Absence of Mitochondria in C. elegans von Rawson, Randi L., Yam, Lung, Weimer, Robby M., Bend, Eric G., Hartwieg, Erika, Horvitz, H. Robert, Clark, Scott G., Jorgensen, Erik M.

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Syntaxin N-terminal peptide motif is an initiation factor for the assembly of the SNARE—Sec1/Munc18 membrane fusion complex von Rathore, Shailendra S., Bend, Eric G., Yu, Haijia, Hammarlund, Marc, Jorgensen, Erik M., Shen, Jingshi, Wickner, William T.

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Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome von Bend, Eric G, Aref-Eshghi, Erfan, Everman, David B, Rogers, R Curtis, Cathey, Sara S, Prijoles, Eloise J, Lyons, Michael J, Davis, Heather, Clarkson, Katie, Gripp, Karen W, Li, Dong, Bhoj, Elizabeth, Zackai, Elaine, Mark, Paul, Hakonarson, Hakon, Demmer, Laurie A, Levy, Michael A, Kerkhof, Jennifer, Stuart, Alan, Rodenhiser, David, Friez, Michael J, Stevenson, Roger E, Schwartz, Charles E, Sadikovic, Bekim

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PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation von Truong, Brittany T, Shull, Lomeli C, Lencer, Ezra, Bend, Eric G, Field, Michael, Blue, Elizabeth E, Bamshad, Michael J, Skinner, Cindy, Everman, David, Schwartz, Charles E, Flanagan-Steet, Heather, Artinger, Kristin B

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Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions von Aref-Eshghi, Erfan, Bend, Eric G., Colaiacovo, Samantha, Caudle, Michelle, Chakrabarti, Rana, Napier, Melanie, Brick, Lauren, Brady, Lauren, Carere, Deanna Alexis, Levy, Michael A., Kerkhof, Jennifer, Stuart, Alan, Saleh, Maha, Beaudet, Arthur L., Li, Chumei, Kozenko, Maryia, Karp, Natalya, Prasad, Chitra, Siu, Victoria Mok, Tarnopolsky, Mark A., Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Krantz, Ian D., Deardorff, Matthew A., Schwartz, Charles E., Sadikovic, Bekim

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BAFopathies’ DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin–Siris and Nicolaides–Baraitser syndromes von Aref-Eshghi, Erfan, Bend, Eric G., Hood, Rebecca L., Schenkel, Laila C., Carere, Deanna Alexis, Chakrabarti, Rana, Nagamani, Sandesh C. S., Cheung, Sau Wai, Campeau, Philippe M., Prasad, Chitra, Siu, Victoria Mok, Brady, Lauren, Tarnopolsky, Mark A., Callen, David J., Innes, A. Micheil, White, Susan M., Meschino, Wendy S., Shuen, Andrew Y., Paré, Guillaume, Bulman, Dennis E., Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Hennekam, Raoul C., Boycott, Kym M., Schwartz, Charles E., Sadikovic, Bekim

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NALCN channelopathies: Distinguishing gain-of-function and loss-of-function mutations von Bend, Eric G, Si, Yue, Stevenson, David A, Bayrak-Toydemir, Pinar, Newcomb, Tara M, Jorgensen, Erik M, Swoboda, Kathryn J

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Reactions with Dye Free Radicals Reveal Weak Redox Properties of Drugs von Marinov, Benjamin S., Bend, Eric G., Abramson, Jonathan J.

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De novo missense variants in the PP2A regulatory subunit PPP2R2B in a neurodevelopmental syndrome: potential links to mitochondrial dynamics and spinocerebellar ataxias von Sandal, Priyanka, Jong, Chian Ju, Merrill, Ronald A, Kollman, Grace J, Paden, Austin H, Bend, Eric G, Sullivan, Jennifer, Spillmann, Rebecca C, Shashi, Vandana, Vulto-van Silfhout, Anneke T, Pfundt, Rolph, de Vries, Bert B A, Li, Pan P, Bicknell, Louise S, Strack, Stefan

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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis von Mak, Christopher C.Y, Doherty, Dan, Lin, Angela E, Vegas, Nancy, Cho, Megan T, Viot, Geraldine, Dimartino, Clemantine, Weisfeld-Adams, James D, Lessel, Davor, Joss, Shelagh, Li, Chumei, Gonzaga-Jauregui, Claudia, Zarate, Yuri A, Ehmke, Nadja, Horn, Denise, Troyer, Caitlin, Kant, Sarina G, Lee, Youngha, Ishak, Gisele E, Leung, Gordon, Pritchard, Amanda Barone, Yang, Sandra, Bend, Eric G, Filippini, Francesca, Roadhouse, Chelsea, Lebrun, Nicolas, Mehaffey, Michele G, Martin, Pierre-Marie, Apple, Benjamin, Millan, Francisca, Puk, Oliver, Hoffer, Mariette J.V, Henderson, Lindsay B, McGowan, Ruth, Wentzensen, Ingrid M, Pei, Steven, Zahir, Farah R, Yu, Mullin, Gibson, William T, Seman, Ann, Steeves, Marcie, Murrell, Jill R, Luettgen, Sabine, Francisco, Elizabeth, Strom, Tim M, Amlie-Wolf, Louise, Kaindl, Angela M, Wilson, William G, Halbach, Sara, Basel-Salmon, Lina, Lev-El, Noa, Denecke, Jonas, Vissers, Lisenka E.L.M, Radtke, Kelly, Chelly, Jamel, Zackai, Elaine, Friedman, Jan M, Bamshad, Michael J, Nickerson, Deborah A, Reid, Russell R, Devriendt, Koenraad, Chae, Jong-Hee, Stolerman, Elliot, McDougall, Carey, Powis, Zoe, Bienvenu, Thierry, Tan, Tiong Y, Orenstein, Naama, Dobyns, William B, Shieh, Joseph T, Choi, Murim, Waggoner, Darrel, Gripp, Karen W, Parker, Michael J, Stoler, Joan, Lyonnet, Stanislas, Cormier-Daire, Valerie, Viskochil, David, Hoffman, Trevor L, Amiel, Jeanne, Chung, Brian H.Y, Gordon, Christopher T

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Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders von Levy, Michael A, McConkey, Haley, Kerkhof, Jennifer, Barat-Houari, Mouna, Bargiacchi, Sara, Biamino, Elisa, Bralo, María Palomares, Cappuccio, Gerarda, Ciolfi, Andrea, Clarke, Angus, DuPont, Barbara R, Elting, Mariet W, Faivre, Laurence, Fee, Timothy, Fletcher, Robin S, Cherik, Florian, Foroutan, Aidin, Friez, Michael J, Gervasini, Cristina, Haghshenas, Sadegheh, Hilton, Benjamin A, Jenkins, Zandra, Kaur, Simranpreet, Lewis, Suzanne, Louie, Raymond J, Maitz, Silvia, Milani, Donatella, Morgan, Angela T, Oegema, Renske, Østergaard, Elsebet, Pallares, Nathalie Ruiz, Piccione, Maria, Pizzi, Simone, Plomp, Astrid S, Poulton, Cathryn, Reilly, Jack, Relator, Raissa, Rius, Rocio, Robertson, Stephen, Rooney, Kathleen, Rousseau, Justine, Santen, Gijs W E, Santos-Simarro, Fernando, Schijns, Josephine, Squeo, Gabriella Maria, St John, Miya, Thauvin-Robinet, Christel, Traficante, Giovanna, van der Sluijs, Pleuntje J, Vergano, Samantha A, Vos, Niels, Walden, Kellie K, Azmanov, Dimitar, Balci, Tugce, Banka, Siddharth, Gecz, Jozef, Henneman, Peter, Mannens, Marcel M A M, Roscioli, Tony, Siu, Victoria, Amor, David J, Baynam, Gareth, Bend, Eric G, Boycott, Kym, Brunetti-Pierri, Nicola, Campeau, Philippe M, Christodoulou, John, Dyment, David, Esber, Natacha, Fahrner, Jill A, Fleming, Mark D, Genevieve, David, Kerrnohan, Kristin D, McNeill, Alisdair, Menke, Leonie A, Merla, Giuseppe, Prontera, Paolo, Rockman-Greenberg, Cheryl, Schwartz, Charles, Skinner, Steven A, Stevenson, Roger E, Vitobello, Antonio, Tartaglia, Marco, Alders, Marielle, Tedder, Matthew L, Sadikovic, Bekim

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Reactions with Dye Free Radicals Reveal Weak Redox Properties of Drugs von Marinov, Benjamin S., Bend, Eric G., Abramson, Jonathan J.

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Cardiac surgeons' concerns, perceptions, and responses during the COVID‐19 pandemic von Luc, Jessica G.Y., Ad, Niv, Nguyen, Tom C., Arora, Rakesh C., Balkhy, Husam H., Bender, Edward M., Bethencourt, Daniel M., Bisleri, Gianluigi, Boyd, Douglas, Chu, Michael W.A., Cruz, Kim I., DeAnda, Abe, Engelman, Daniel T., Farkas, Emily A., Fedoruk, Lynn M., Fiocco, Michael, Forcillo, Jessica, Fradet, Guy, Fremes, Stephen E., Gammie, James S., Geirsson, Arnar, Gerdisch, Marc W., Girard, Leonard N., Kaiser, Clayton A., Kaneko, Tsuyoshi, Kent, William D.T., Khabbaz, Kamal R., Khoynezhad, Ali, Kiaii, Bob, Lee, Richard, Legare, Jean‐Francois, Lehr, Eric J., MacArthur, Roderick G.G., McCarthy, Patrick M., Mehall, John R., Merrill, Walter H., Moon, Marc R., Ouzounian, Maral, Peltz, Matthias, Perrault, Louis P., Preventza, Ourania, Ramchandani, Mahesh, Ramlawi, Basel, Salenger, Rawn, Sekela, Michael E., Sellke, Frank W., Stulak, John M., Sutter, Francis P., Timek, Tomasz A., Whitman, Glenn, Williams, Judson B., Wong, Daniel R., Yanagawa, Bobby, Ye, Jian, Zeigler, Sanford M.

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Feeding behavior, toe count, and the phylogenetic relationships among alcedinine kingfishers (Alcedininae) von G. Moyle, Robert, Fuchs, Jérôme, Pasquet, Eric, D. Marks, Ben

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