Continuing professional development for public health: An andragogical approach von Bennetts, C, Elliston, K, Maconachie, M

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Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration von Melamed, Ze’ev, López-Erauskin, Jone, Baughn, Michael W., Zhang, Ouyang, Drenner, Kevin, Sun, Ying, Freyermuth, Fernande, McMahon, Moira A., Beccari, Melinda S., Artates, Jon W., Ohkubo, Takuya, Rodriguez, Maria, Lin, Nianwei, Wu, Dongmei, Bennett, C. Frank, Rigo, Frank, Da Cruz, Sandrine, Ravits, John, Lagier-Tourenne, Clotilde, Cleveland, Don W.

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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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In Situ Visualization for Computational Science von Childs, Hank, Bennett, Janine C, Garth, Christoph

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Unlocking Large Scale Uncertainty Quantification with In Transit Iterative Statistics von Ribés, Alejandro, Terraz, Théophile, Fournier, Yvan, Iooss, Bertrand, Raffin, Bruno

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In Situ Visualization for Computational Science: Background and Foundational Topics von Childs, Hank, Bennett, Janine C., Garth, Christoph

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The Adaptable IO System (ADIOS) von Pugmire, David, Podhorszki, Norbert, Klasky, Scott, Wolf, Matthew, Kress, James, Kim, Mark, Thompson, Nicholas, Logan, Jeremy, Wang, Ruonan, Mehta, Kshitij, Suchyta, Eric, Godoy, William, Choi, Jong, Ostrouchov, George, Wan, Lipeng, Chen, Jieyang, Atkins, Berk Geveci Chuck, Ross, Caitlin, Eisenhauer, Greg, Gu, Junmin, Wu, John, Huebl, Axel, Tsutsumi, Seiji

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A comparison of lamellar and penetrating keratoplasty outcomes: a registry study von Coster, Douglas J, Lowe, Marie T, Keane, Miriam C, Williams, Keryn A

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Resource-Aware Optimal Scheduling of In Situ Analysis von Malakar, Preeti, Vishwanath, Venkatram, Knight, Christopher, Munson, Todd, Papka, Michael E.

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A Simulation-Oblivious Data Transport Model for Flexible In Transit Visualization von Usher, Will, Park, Hyungman, Lee, Myoungkyu, Navrátil, Paul, Fussell, Donald, Pascucci, Valerio

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Proximity Portability and in Transit, M-to-N Data Partitioning and Movement in SENSEI von Bethel, E. Wes, Loring, Burlen, Ayachit, Utkarsh, Duque, Earl P. N., Ferrier, Nicola, Insley, Joseph, Gu, Junmin, Kress, James, O’Leary, Patrick, Pugmire, Dave, Rizzi, Silvio, Thompson, David, Usher, Will, Weber, Gunther H., Whitlock, Brad, Wolf, Matthew, Wu, Kesheng

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The SENSEI Generic In Situ Interface: Tool and Processing Portability at Scale von Bethel, E. Wes, Loring, Burlen, Ayachit, Utkarsh, Camp, David, Duque, Earl P. N., Ferrier, Nicola, Insley, Joseph, Gu, Junmin, Kress, James, O’Leary, Patrick, Pugmire, David, Rizzi, Silvio, Thompson, David, Weber, Gunther H., Whitlock, Brad, Wolf, Matthew, Wu, Kesheng

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Osmium isotopic constraints on the age of lithospheric mantle beneath northeastern China von Wu, Fu-yuan, Walker, Richard J., Ren, Xiang-wen, Sun, De-you, Zhou, Xin-hua

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Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability von Grozeva, Detelina, Carss, Keren, Spasic-Boskovic, Olivera, Tejada, Maria-Isabel, Gecz, Jozef, Shaw, Marie, Corbett, Mark, Haan, Eric, Thompson, Elizabeth, Friend, Kathryn, Hussain, Zaamin, Hackett, Anna, Field, Michael, Renieri, Alessandra, Stevenson, Roger, Schwartz, Charles, Floyd, James A.B., Bentham, Jamie, Cosgrove, Catherine, Keavney, Bernard, Bhattacharya, Shoumo, Hurles, Matthew, Raymond, F. Lucy

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Highly siderophile elements in chondrites von Horan, M.F., Walker, R.J., Morgan, J.W., Grossman, J.N., Rubin, A.E.

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Molecular pathogenesis and heterogeneity in type 3 VWD families in U.S. Zimmerman program von Christopherson, Pamela A., Haberichter, Sandra L., Flood, Veronica H., Perry, Crystal L., Sadler, Brooke E., Bellissimo, Daniel B., Di Paola, Jorge, Montgomery, Robert R., Abshire, T, Weiler, H, Lillicrap, D, James, P, O’Donnell, J, Ng, C, Bennett, C, Sidonio, R, Manco‐Johnson, M, Journeycake, J, Zia, A, Lusher, J, Rajpurkar, M, Shapiro, A, Lentz, S, Gill, J, Leissinger, C, Ragni, M, Tarantino, M, Roberts, J, Hord, J, Strouse, J, Ma, A, Valentino, L, Boggio, L, Sharathkumar, A, Gruppo, R, Kerlin, B, Kulkarni, R, Green, D, Hoots, K, Brown, D, Mahoney, D, Mathias, L, Bedros, A, Diamond, C, Neff, A, DiMichele, D, Giardina, P, Cohen, A, Paidas, M, Werner, E, Matsunaga, A, Shafer, F, Konkle, B, Cuker, A, Kouides, P, Stein, D

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Crucial role for the VWF A1 domain in binding to type IV collagen von Flood, Veronica H., Schlauderaff, Abraham C., Haberichter, Sandra L., Slobodianuk, Tricia L., Jacobi, Paula M., Bellissimo, Daniel B., Christopherson, Pamela A., Friedman, Kenneth D., Gill, Joan Cox, Hoffmann, Raymond G., Montgomery, Robert R.

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Rapid discrimination of the phenotypic variants of von Willebrand disease von Roberts, Jonathan C., Morateck, Patti A., Christopherson, Pamela A., Yan, Ke, Hoffmann, Raymond G., Gill, Joan Cox, Montgomery, Robert R.

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Laboratory variability in the diagnosis of type 2 VWD variants von DiGiandomenico, Stefanie, Christopherson, Pamela A., Haberichter, Sandra L., Abshire, Thomas C., Montgomery, Robert R., Flood, Veronica H., Valentino, L., Abshire, T., Dunn, A., Bennett, C., Lusher, J., Rajpurkar, M., Hoots, W. K., Brown, D., Shapiro, A., Paola, J. Di, Lentz, S., Gill, J., Leissinger, C., Ragni, M., Hord, J., Manco‐Johnson, M., Ma, A., Boggio, L., Sharathkumar, A., Gruppo, R., Kerlin, B., Journeycake, J., Kulkarni, R., Mahoney, D, Mathias, L., Bedros, A., Diamond, C., Neff, A., Paroskie, A., DiMichele, D., Giardina, P., Cohen, A., Paidas, M., Werner, E., Matsunaga, A., Singer, T., Tarantino, M., Roberts, J., Shafer, F., Konkle, B., Cuker, A., Kouides, P., Stein, D., Manco‐Johnson, M., Dunn, A., Bennett, C., Journeycake, J., Lusher, J., Rajpurkar, M., Shapiro, A., Lentz, S., Lillicrap, D., James, P., Leissinger, C., Roberts, J., Ragni, M.

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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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