Molecular Dissection of the Munc18c/Syntaxin4 Interaction: Implications for Regulation of Membrane Trafficking von Latham, Catherine F., Lopez, Jamie A., Hu, Shu‐Hong, Gee, Christine L., Westbury, Elizabeth, Blair, Duncan H., Armishaw, Chris J., Alewood, Paul F., Bryant, Nia J., James, David E., Martin, Jennifer L.

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Abnormalities in brain biochemistry associated with lack of dystrophin: studies of the mdx mouse von Rae, Caroline, Griffin, Julian L, Blair, Duncan H, Bothwell, John H, Bubb, William A, Maitland, Annie, Head, Stewart

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Differential sensitivity to calcium and osmotic pressure of fast and slow ATP currents at sympathetic varicosities in mouse vas deferens von Blair, Duncan H, Lin, Yong Q, Bennett, Maxwell R

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Randomized Pragmatic Trial of Stroke Transitional Care: The COMPASS Study von Duncan, Pamela W., Bushnell, Cheryl D., Jones, Sara B., Psioda, Matthew A., Gesell, Sabina B., D'Agostino, Ralph B., Sissine, Mysha E., Coleman, Sylvia W., Johnson, Anna M., Barton-Percival, Blair F., Prvu-Bettger, Janet, Calhoun, Adrienne G., Cummings, Doyle M., Freburger, Janet K., Halladay, Jacqueline R., Kucharska-Newton, Anna M., Lundy-Lamm, Gladys, Lutz, Barbara J., Mettam, Laurie H., Pastva, Amy M., Xenakis, James G., Ambrosius, Walter T., Radman, Meghan D., Vetter, Betsy, Rosamond, Wayne D.

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A Person‐Centered Approach to Poststroke Care: The COMprehensive Post‐Acute Stroke Services Model von Bushnell, Cheryl D., Duncan, Pamela W., Lycan, Sarah L., Condon, Christina N., Pastva, Amy M., Lutz, Barbara J., Halladay, Jacqueline R., Cummings, Doyle M., Arnan, Martinson K., Jones, Sara B., Sissine, Mysha E., Coleman, Sylvia W., Johnson, Anna M., Gesell, Sabina B., Mettam, Laurie H., Freburger, Janet K., Barton‐Percival, Blair, Taylor, Karen M., Prvu‐Bettger, Janet, Lundy‐Lamm, Gladys, Rosamond, Wayne D.

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Large-scale discovery of novel genetic causes of developmental disorders von van Kogelenberg, M, Goudie, D, Gray, E, Harrison, L, Hawkins, R, Henderson, A, Holder, S, Irving, M, Bayzetinova, T, Jones, D, Kini, U, Kinning, E, Kirby, G, Kirk, C, Kumar, D, Lachlan, K, Lees, M, Lim, D, Coomber, E L, Lowther, G, Lynch, S A, Maher, E, Mansour, S, Maye, U, McCann, E, McMullan, D J, McNerlan, S, Metcalfe, K, Mohammed, S, Jones, P, Moore, D, Morton, J, Mugalaasi, H, Newbury-Ecob, R, Ogilvie, C, Park, S, Parker, M J, Patel, C, Porteous, D, Mason, L E, Ragge, N, Rankin, J, Raymond, L, Rosser, E, Miller, R, Sarkar, A, Scott, C, Scott, R, Selby, A, Shannon, N, Simpkin, D, Singzon, R, Skitt, Z, Rajan, D, Splitt, M, Stewart, F, Swaminathan, G J, Tatton-Brown, K, Temple, I K, Torokwa, A, Turner, C, Turnpenny, P, Tysoe, C, Vandersteen, A, Walker, D, Ahmed, M, Widaa, S, Williams, N, Wragg, C, Yau, M, FitzPatrick, D R, Anjum, U, Balasubramanian, M, Banerjee, R, Baralle, D, Baty, D, Bennett, C, Berg, J, Bevan, A P, Bourdon, L, Brady, A, Burton, J, Chandler, K, Cooper, N, Cross, G, D'Alessandro, M, Dabir, T, Davidson, R, Davies, S, Dean, J, Deshpande, C, Donnelly, C, Douglas, A, Eason, J, Edkins, S, Foulds, N, Fryer, A, Gardiner, C, Pereira, S L Gomes, Goodship, J

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Incorporation of Biological Knowledge Into the Study of Gene-Environment Interactions von Ritchie, Marylyn D, Davis, Joe R, Aschard, Hugues, Battle, Alexis, Conti, David, Du, Mengmeng, Eskin, Eleazar, Fallin, M Daniele, Hsu, Li, Kraft, Peter, Moore, Jason H, Pierce, Brandon L, Bien, Stephanie A, Thomas, Duncan C, Wei, Peng, Montgomery, Stephen B

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The Comprehensive Post-Acute Stroke Services (COMPASS) study: design and methods for a cluster-randomized pragmatic trial von Duncan, Pamela W, Bushnell, Cheryl D, Rosamond, Wayne D, Jones Berkeley, Sara B, Gesell, Sabina B, D'Agostino, Jr, Ralph B, Ambrosius, Walter T, Barton-Percival, Blair, Bettger, Janet Prvu, Coleman, Sylvia W, Cummings, Doyle M, Freburger, Janet K, Halladay, Jacqueline, Johnson, Anna M, Kucharska-Newton, Anna M, Lundy-Lamm, Gladys, Lutz, Barbara J, Mettam, Laurie H, Pastva, Amy M, Sissine, Mysha E, Vetter, Betsy

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The conservation status of the world’s reptiles von Böhm, Monika, Collen, Ben, Baillie, Jonathan E.M., Chanson, Janice, Livingstone, Suzanne R., Ram, Mala, Ajtic, Rastko, Akarsu, Ferdi, Anderson, Steve, Baker, Patrick J., Barrio-Amorós, César L., Bates, Michael F., Bauer, Aaron, Bennett, Daniel, Broadley, Don, Brown, Rafe, Catenazzi, Alessandro, Chapple, David G., Cheylan, Marc, Cisneros-Heredia, Diego F., Cogalniceanu, Dan, Corti, Claudia, Costa, Gabriel C., de Silva, Anslem, Doan, Tiffany M., El Mouden, El Hassan, Feng, Xie, Feng, Zhao-Jun, Flores-Villela, Oscar, Ganesh, S.R., Gaulke, Maren, Geniez, Philippe, Georges, Arthur, Hamilton, Alison M., Hare, Kelly, Hedges, S. Blair, Hilton-Taylor, Craig, Ineich, Ivan, Jaksic, Fabian M., Joger, Ulrich, Jose, Reizl, Kaska, Yakup, Keogh, J. Scott, Köhler, Gunther, La Marca, Enrique, Lane, Amanda, Lardner, Bjorn, Latta, Gabrielle, Lavin, Pablo, Lehr, Edgar, Limpus, Duncan, Lundberg, Mikael, Macey, Robert, Magnusson, William E., Malhotra, Anita, Mariaux, Jean, Maritz, Bryan, Marques, Otavio A.V., Márquez, Rafael, Martins, Marcio, Mathew, Rosamma, Mathews, Nixon, Mayer, Gregory, Mendoza-Quijano, Fernando, Métrailler, Sébastien, Morato, Sérgio A.A., Muñoz-Alonso, Antonio, Murphy, John, Nogueira, Cristiano, Núñez, Herman, Papenfuss, Theodore, Pauwels, Olivier S.G., Pérez-Mellado, Valentín, Pleguezuelos, Juan, Ponce-Campos, Paulino, Quintero Díaz, Gustavo E., Roosenburg, Willem M., Ross, James P., Schleich, Hermann H., Schmidt, Benedikt R., Schmitz, Andreas, Shine, Richard, Sindaco, Roberto, Slimani, Tahar, Somaweera, Ruchira, Sy, Emerson, Tolley, Krystal, Üzüm, Nazan, Van Sluys, Monique, Velasco, Alvaro, Vinke, Sabine, Vogel, Gernot, Vogrin, Milan, Vogt, Richard C., Werner, Yehudah L., Whiting, Martin J., Wiewandt, Thomas, Wilkinson, John, Wilson, Byron, Wren, Sally

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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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SARS-CoV-2 Genomic Surveillance Reveals Little Spread From a Large University Campus to the Surrounding Community von Valesano, Andrew L, Fitzsimmons, William J, Blair, Christopher N, Woods, Robert J, Gilbert, Julie, Rudnik, Dawn, Mortenson, Lindsey, Friedrich, Thomas C, O’Connor, David H, MacCannell, Duncan R, Petrie, Joshua G, Martin, Emily T, Lauring, Adam S

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Short-term risk prediction after major lower limb amputation: PERCEIVE study von Gwilym, Brenig L, Pallmann, Philip, Waldron, Cherry-Ann, Thomas-Jones, Emma, Milosevic, Sarah, Brookes-Howell, Lucy, Harris, Debbie, Massey, Ian, Burton, Jo, Stewart, Phillippa, Samuel, Katie, Jones, Sian, Cox, David, Clothier, Annie, Edwards, Adrian, Twine, Christopher P, Bosanquet, David C

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Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects von Mircsof, Dennis, Langouët, Maéva, Rio, Marlène, Moutton, Sébastien, Siquier-Pernet, Karine, Bole-Feysot, Christine, Cagnard, Nicolas, Nitschke, Patrick, Gaspar, Ludmila, Žnidarič, Matej, Alibeu, Olivier, Fritz, Ann-Kristina, Wolfer, David P, Schröter, Aileen, Bosshard, Giovanna, Rudin, Markus, Koester, Christina, Crestani, Florence, Seebeck, Petra, Boddaert, Nathalie, Prescott, Katrina, Hines, Rochelle, Moss, Steven J, Fritschy, Jean-Marc, Munnich, Arnold, Amiel, Jeanne, Brown, Steven A, Tyagarajan, Shiva K, Colleaux, Laurence

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Development of a decision-making tool for reporting drivers with mild dementia and mild cognitive impairment to transportation administrators von Cameron, Duncan H., Zucchero Sarracini, Carla, Rozmovits, Linda, Naglie, Gary, Herrmann, Nathan, Molnar, Frank, Jordan, John, Byszewski, Anna, Tang-Wai, David, Dow, Jamie, Frank, Christopher, Henry, Blair, Pimlott, Nicholas, Seitz, Dallas, Vrkljan, Brenda, Taylor, Rebecca, Masellis, Mario, Rapoport, Mark J.

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Kinetics and basic understanding: general discussion von Angerhofer, Alexander, Auvray, Thomas, Balema, Viktor, Balá, Matej, Batteas, James D, Blair, Richard G, Boldyreva, Elena, Bolm, Carsten, Borchardt, Lars, Borchers, Tristan H, Braunschweig, Adam B, Browne, Duncan L, Carpick, Robert W, Ciaccia, Maria, Craig, Stephen, Emmerling, Franziska, Ferguson, Michael, Fiore, Cecilia, Friš i, Tomislav, Grätz, Sven, Halasz, Ivan, Hamzehpoor, Ehsan, Ito, Hajime, James, Stuart, Kim, Jeung Gon, Lamaty, Frédéric, Lampronti, Giulio I, Laurencin, Danielle, Leitch, Jamie, Lu, Erli, Lukin, Stipe, Mack, James, Maini, Lucia, Martini, Ashlie, Mazzeo, Paolo P, Michalchuk, Adam A. L, Mittelette, Sébastien, Mohamed, Sharmarke, Moores, Audrey, Mortera-Carbonell, Aldo de Jesús, Nagapudi, Karthik, Niidu, Allan, Puccetti, Francesco, Stahorský, Martin, Vugrin, Leonarda

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Identification of reference genes for RT-qPCR in ovine mammary tissue during late pregnancy and lactation and in response to maternal nutritional programming von Paten, A M, Pain, S J, Peterson, S W, Blair, H T, Kenyon, P R, Dearden, P K, Duncan, E J

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cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing von Uggenti, Carolina, Lepelley, Alice, Depp, Marine, Badrock, Andrew P, Rodero, Mathieu P, El-Daher, Marie-Therese, Rice, Gillian I, Dhir, Somdutta, Wheeler, Ann P, Dhir, Ashish, Albawardi, Waad, Fremond, Marie-Louise, Seabra, Luis, Doig, Jennifer, Blair, Natalie, Martin-Niclos, Maria Jose, Della Mina, Erika, Rubio-Roldan, Alejandro, Garcia-Perez, Jose L, Sproul, Duncan, Rehwinkel, Jan, Hertzog, Jonny, Boland-Auge, Anne, Olaso, Robert, Deleuze, Jean-Francois, Baruteau, Julien, Brochard, Karine, Buckley, Jonathan, Cavallera, Vanessa, Cereda, Cristina, De Waele, Liesbeth M. H, Dobbie, Angus, Doummar, Diane, Elmslie, Frances, Koch-Hogrebe, Margarete, Kumar, Ram, Lamb, Kate, Livingston, John H, Majumdar, Anirban, Lorenco, Charles Marques, Orcesi, Simona, Peudenier, Sylviane, Rostasy, Kevin, Salmon, Caroline A, Scott, Christiaan, Tonduti, Davide, Touati, Guy, Valente, Marialuisa, van der Linden, Helio, Jr, Van Esch, Hilde, Vermelle, Marie, Webb, Kate, Jackson, Andrew P, Reijns, Martin A. M, Gilbert, Nick, Crow, Yanick J

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cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing von Uggenti, Carolina, Lepelley, Alice, Depp, Marine, Badrock, Andrew P, Rodero, Mathieu P, El-Daher, Marie-Therese, Rice, Gillian I, Dhir, Somdutta, Wheeler, Ann P, Dhir, Ashish, Albawardi, Waad, Fremond, Marie-Louise, Seabra, Luis, Doig, Jennifer, Blair, Natalie, Martin-Niclos, Maria Jose, Della Mina, Erika, Rubio-Roldan, Alejandro, Garcia-Perez, Jose L, Sproul, Duncan, Rehwinkel, Jan, Hertzog, Jonny, Boland-Auge, Anne, Olaso, Robert, Deleuze, Jean-Francois, Baruteau, Julien, Brochard, Karine, Buckley, Jonathan, Cavallera, Vanessa, Cereda, Cristina, De Waele, Liesbeth M.H, Dobbie, Angus, Doummar, Diane, Elmslie, Frances, Koch-Hogrebe, Margarete, Kumar, Ram, Lamb, Kate, Livingston, John H, Majumdar, Anirban, Lorenco, Charles Marques, Orcesi, Simona, Peudenier, Sylviane, Rostasy, Kevin, Salmon, Caroline A, Scott, Christiaan, Tonduti, Davide, Touati, Guy, Valente, Marialuisa, van der Linden, Helio, Van Esch, Hilde, Vermelle, Marie, Webb, Kate, Jackson, Andrew P, Reijns, Martin A.M, Gilbert, Nick, Crow, Yanick J

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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An unusually strong Einstein ring in the radio source PKS1830 - 211 von Jauncey, D. L., Reynolds, J. E., Tzioumis, A. K., Murphy, D. W., Preston, R. A., Jones, D. L., Meier, D. L., Hoard, D. W., Lobdell, E. T., Skjerve, L.

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