Phishing for Long Tails: Examining Organizational Repeat Clickers and Protective Stewards by Canham, Matthew, Posey, Clay, Strickland, Delainey, Constantino, Michael

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When Diversity in Training Improves Dyadic Problem Solving by Canham, Matthew S., Wiley, Jennifer, Mayer, Richard E.

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Developing Training Research to Improve Cyber Defense of Industrial Control Systems by Canham, Matthew, Fiore, Stephen M., Caulkins, Bruce D.

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Neurosecurity: Human Brain Electro-optical Signals as MASINT by Canham, Matthew, Sawyer, Ben D.

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Ambiguous Self-Induced Disinformation (ASID) Attacks: Weaponizing a Cognitive Deficiency by Canham, Matthew, Sütterlin, Stefan, Ask, Torvald Fossåen, Knox, Benjamin James, Glenister, Lauren, Lugo, Ricardo Gregorio

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Nonnative forest insects and pathogens in the United States: Impacts and policy options by Lovett, Gary M, Marissa Weiss, Andrew M. Liebhold, Thomas P. Holmes, Brian Leung, Kathy Fallon Lambert, David A. Orwig, Faith T. Campbell, Jonathan Rosenthal, Deborah G. McCullough, Radka Wildova, Matthew P. Ayres, Charles D. Canham, David R. Foster, Shannon L. LaDeau, Troy Weldy

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Reinforcement of flowable dental composites with titanium dioxide nanotubes by Dafar, Manal O, Grol, Matthew W, Canham, Peter B, Dixon, S. Jeffrey, Rizkalla, Amin S

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De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability by Grozeva, Detelina, Carss, Keren, Spasic-Boskovic, Olivera, Parker, Michael J., Archer, Hayley, Firth, Helen V., Park, Soo-Mi, Canham, Natalie, Holder, Susan E., Wilson, Meredith, Hackett, Anna, Field, Michael, Floyd, James A.B., Hurles, Matthew, Raymond, F. Lucy

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Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease by Stephens, Jonathan, Dewhurst, Eleanor, Malka, Samantha, Plagnol, Vincent, Rizzo, Roberta, Scott, Richard H., Henderson, Robert H.H., MacLaren, Robert E., Paterson, Joan, Aitman, Timothy, Ali, Sonia, Ambegaonkar, Gautum, Arno, Gavin, Astle, William, Attwood, Antony, Bennett, David, Bitner-Glindzicz, Maria, Bleda, Marta, Boggard, Harm, Carss, Keren, Clements-Brod, Naomi, DaCosta, Rosa, De Vries, Minka, Dewhurst, Eleanor, Drewe, Elizabeth, Egner, William, Erber, Wendy N., Everington, Tamara, Fletcher, Debra, Freson, Kathleen, Gale, Daniel, Ghali, Neeti, Ghurye, Rohit, Gräf, Stefan, Greene, Daniel, Grigoriadou, Sofia, Grozeva, Detelina, Hackett, Scott, Hadinnapola, Charaka, Hague, Rosie, Hammerton, Tracey, Heemskerk, Johan W.M., Holder, Muriel, Holder, Susan, Huissoon, Aarnoud, Hurst, Jane, Jolles, Stephen, Keeling, David, Kennedy, Fiona, Kiely, David, Lawrie, Allan, Lear, Sara, Lees, Melissa, Lentaigne, Claire, Lorenzo, Lorena, Mangles, Sarah, Mapeta, Rutendo, Masati, Larahmie, Mathias, Mary, Michaelides, Michel, Millar, Carolyn M., Moledina, Shahin, Moore, Anthony, Murng, Sai, Oksenhendler, Eric, Park, Soo-Mi, Patch, Chris, Paterson, Joan, Penkett, Christopher J., Pepke-Zaba, Joanna, Pollock, Val, Qasim, Waseem, Quinti, Isabella, Reid, Evan, Rondina, Matthew, Rosser, Elisabeth, Santra, Saikat, Sargur, Ravishankar, Savic, Sinisa, Scully, Marie, Sewell, Carrock, Smith, Kenneth, Southgate, Laura, Stauss, Hans, Stein, Penelope, Talks, Kate, Thomas, Ellen, Thrasher, Adrian, Tischkowitz, Marc, Titterton, Catherine, Turro, Ernest, von Ziegenweldt, Julie, Vonk Noordegraaf, Anton, Wakeling, Emma, Wanjiku, Ivy, Welch, Steve, Westbury, Sarah, Woods, Geoffrey, Yong, Patrick, Webster, Andrew R.

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The Impacts of ICD-10-CM on U.S. Army Injury Surveillance by Schuh-Renner, Anna, Inscore, Matthew C., Hauschild, Veronique D., Jones, Bruce H., Canham-Chervak, Michelle

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The effects of carbonate contamination on Ni-Cu-PGE deposit genesis in the Platreef, northern Bushveld Complex: A case study using Niggli numbers by Thompson, Erin S., Holwell, David A., McDonald, Iain, Reichow, Marc, Blenkinsop, Thomas G., Hughes, Hannah S.R., McFall, Katie, Canham, Kate R., Loader, Matthew A., Du Preez, Lara, Acheampong, Kofi, Lloyd, Andy

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122 Objective evaluation of plan quality in the PATHOS clinical trial using automated treatment planning by Berenato, Salvatore, Evans, Mererid, Webster, Richard, Palaniappan, Nachi, Nixon, Lisette, Higgins, Emma, Patel, Rush, Millin, Anthony E, Hurt, Christian, Heiberg, Christie, Canham, Joanna, Jones, Terence M, Miles, Elizabeth, Beasley, Matthew, Wheeler, Philip A

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49 Development of a Normal Tissue Complication Probability Model for Dysphagia in PATHOS trial patients by Higgins, Emma, Webster, Richard, Palaniappan, Nachi, Hurt, Chris, Nabi, Zohal, Rizos, Kostas, Elliott, Kate, Miles, Elizabeth, Patterson, Joanne, Hutcheson, Kate, Canham, Joanne, Nixon, Lisette, Heiberg, Christie, Beasley, Matthew, Jones, Terry M, Evans, Mererid

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A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders by King, Daniel A, Fitzgerald, Tomas W, Miller, Ray, Canham, Natalie, Clayton-Smith, Jill, Johnson, Diana, Mansour, Sahar, Stewart, Fiona, Vasudevan, Pradeep, Hurles, Matthew E

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Does variation in swallowing organs-at-risk (SWOAR) delineation impact on predicted swallowing dysfunction for PATHOS trial patients? by Higgins, Emma, Palaniappan, Nachi, Nabi, Zohal, Elliott, Kate, Miles, Liz, Lad, Rikki, Nixon, Lisette, Canham, Jo, Hurt, Chris, Heiberg, Christie, Beasley, Matthew, Jones, Terry, Webster, Richard, Evans, Mererid

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Lewis Acid Mediated Hydrosilylation on Porous Silicon Surfaces by Buriak, Jillian M, Stewart, Michael P, Geders, Todd W, Allen, Matthew J, Choi, Hee Cheul, Smith, Jay, Raftery, Daniel, Canham, Leigh T

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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes by West, Hannah, Carss, Keren, Shakeel, Hassan, Adlard, Julian, Cole, Trevor, Kwong, Ava, Paterson, Joan, Searle, Claire, Skytte, Anne-Bine, Aitman, Timothy, Ambegaonkar, Gautum, Antrobus, Richard, Arno, Gavin, Astle, William, Attwood, Antony, Austin, Steve, Bakchoul, Tamam, Bennett, David, Bitner-Glindzicz, Maria, Bleda, Marta, Bolton-Maggs, Paula, Booth, Claire, Clements-Brod, Naomi, Clowes, Virginia, Collins, Peter, Cookson, Victoria, Creaser-Myers, Amanda, DaCosta, Rosa, Davies, Sophie, Deegan, Patrick, Dewhurst, Eleanor, Doffinger, Rainer, Drewe, Elizabeth, Favier, Remi, Firth, Helen, Furie, Bruce, Furnell, Abigail, Gardham, Alice, Gissen, Paul, Gomez, Keith, Graf, Stefan, Gräf, Stefan, Greenhalgh, Alan, Hackett, Scott, Haimel, Matthias, Herwadkar, Archana, Holder, Muriel, Huissoon, Aarnoud, James, Roger, Kennedy, Fiona, Kingston, Nathalie, Kuijpers, Taco, Lawrie, Allan, Lentaigne, Claire, Machado, Rajiv, Maher, Eamonn, Mangles, Sarah, Manson, Ania, Matser, Vera, McDermott, Elizabeth, Megy, Karyn, Millar, Carolyn M., Morrell, Nicholas, Ouwehand, Willem H., Papadia, Sofia, Payne, Jeanette, Peacock, Andrew, Pollock, Val, Quinti, Isabella, Rayner-Matthews, Paula, Rehnstrom, Karola, Rhodes, Christopher J., Richardson, Sylvia, Richter, Alex, Rondina, Matthew, Rosser, Elisabeth, Rue-Albrecht, Kevin, Sargur, Ravishankar, Savic, Sinisa, Schotte, Gwen, Schulze, Harald, Seneviratne, Suranjith, Shamardina, Olga, Simeoni, Ilenia, Staines, Simon, Stark, Hannah, Stock, Sophie, Thaventhiran, James, Thompson, Dorothy, Toh, Cheng-Hock, Turek, Wojciech, Wassmer, Evangeline, Watt, Christopher, Wharton, John, Williamson, Catherine, Woods, Geoff, Wort, John, Yeatman, Nigel, Tischkowitz, Marc D., Maher, Eamonn R.

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Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth by Loveday, Chey, Tatton-Brown, Katrina, Clarke, Matthew, Westwood, Isaac, Renwick, Anthony, Ramsay, Emma, Nemeth, Andrea, Campbell, Jennifer, Joss, Shelagh, Gardner, McKinlay, Zachariou, Anna, Elliott, Anna, Ruark, Elise, van Montfort, Rob, Rahman, Nazneen

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Establishing a Role for Asthma Management As Adjuvant Therapy for Vaso-Occlusive Crisis: Pulmonary Risk Stratification and Proposed Interventions by Canham, Lorraine Elise, Ghosh, Taumoha, Grant, Matthew, Munchel, Ashley T., Macatangay, Regina A.

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De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures by Duarte, Sofia T., Charles, Perinne, Pfundt, Rolph, van Bokhoven, Hans, van Ravenswaaij-Arts, Conny, Morrell, Nicholas W., Thrasher, Adrian, Fletcher, Debra, Veltman, Marijke, Davis, John, Frary, Amy, Martin, Jennifer M., Collins, Janine, Favier, Remi, Hart, Daniel, Heemskerk, Johan W.M., Liesner, Ri, Mangles, Sarah, Roughley, Catherine, Tait, R. Campbell, Thachil, Jecko, Van Geet, Chris, De Vries, Minka, Warner, Timothy Q., Furnell, Abigail, Mapeta, Rutendo, Whitehorn, Deborah, Daugherty, Louise, Deevi, Sri V.V., Hu, Fengyuan, Matser, Vera, Megy, Karyn, Tuna, Salih, von Ziegenweldt, Julie, Haimel, Matthias, Richardson, Sylvia, Rankin, Stuart, Anderson, Julie, Stock, Sophie, Armstrong, Ruth, Bitner-Glindzicz, Maria, Brady, Angie, Clement, Emma, Firth, Helen, Flinter, Frances, French, Courtney, Holder, Muriel, Hurst, Jane, Josifova, Dragana, Krishnakumar, Deepa, Kurian, Manju A., Mehta, Sarju, Moore, Anthony, Rankin, Julia, Reid, Evan, Scott, Richard, Thomas, Ellen, Wassmer, Evangeline, Creaser-Myers, Amanda, Gall, Henning, Ghataorhe, Pavandeep K., Houweling, Arjan C., in’t Veld, Anna Huis, Ross, Rob V. Mackenzie, Rhodes, Christopher J., Soubrier, Florent, Treacy, Carmen M., Vonk Noordegraaf, Anton, Antrobus, Richard, Arumugakani, Gururaj, Bibi, Shahnaz, Devlin, Lisa, Ghurye, Rohit, Grigoriadou, Sofia, Harper, Lorraine, Herwadkar, Archana, Jolles, Stephen, Kumararatne, Dinakantha, Lorenzo, Lorena, Murng, Sai, Nejentsev, Sergey, Quinti, Isabella, Samarghitean, Crina, Savic, Sinisa, Yong, Patrick, Ancliff, Phil, Layton, Mark, Mead, Adam, Roy, Noémi, Chambers, Jenny, Estiu, Cecelia, Simpson, Michael, Emmerson, Ingrid, McCarthy, Mark, Van Zuydam, Natalie, Afzal, Maryam, Colby, Elizabeth, Boycott, Kym M., Majewski, Jacek, Dyment, David

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