Current Interruption Using Electromagnetically Convolved Electric Arcs in Gases von Shpanin, L.M., Jones, G.R., Humphries, J.E., Spencer, J.W.

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RLC-Induced Current Oscillations in Convoluted Arcs With Independently Activated Magnetic Fields von Shpanin, Leonid M., Jones, Gordon R., Humphries, Jim E., Spencer, Joseph W., Shammas, Noel Y. A., Tennakoon, Sarath B.

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Electromagnetically convoluted arcs for the interruption of quasi direct current von Shpanin, L. M., Jones, G. R., Shammas, N. Y. A., Humphries, J. E., Tennakoon, S. B., Spencer, J. W.

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RCP-driven α5β1 recycling suppresses Rac and promotes RhoA activity via the RacGAP1-IQGAP1 complex von Jacquemet, Guillaume, Green, David M, Bridgewater, Rebecca E, von Kriegsheim, Alexander, Humphries, Martin J, Norman, Jim C, Caswell, Patrick T

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Long-term Mortality, Readmission, and Resource Utilization Among Hospital Survivors of Out-of-Hospital Cardiac Arrest von Fordyce, Christopher B., Grunau, Brian E., Guan, Meijiao, Hawkins, Nathaniel M., Lee, May K., Helmer, Jennie S., Wong, Graham C., Humphries, Karin H., Christenson, Jim

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Predictors of neurological outcome after out-of-hospital cardiac arrest: sex-based analysis: do males derive greater benefit from hypothermia management than females? von Awad, Emad M., Humphries, Karin H., Grunau, Brian E., Norris, Colleen M., Christenson, Jim M.

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Premenopausal-aged females have no neurological outcome advantage after out-of-hospital cardiac arrest: A multilevel analysis of North American populations von Awad, Emad M., Humphries, Karin H., Grunau, Brian E., Christenson, Jim M.

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Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes von Pazoki, Raha, Vujkovic, Marijana, Elliott, Joshua, Evangelou, Evangelos, Gill, Dipender, Ghanbari, Mohsen, van der Most, Peter J., Pinto, Rui Climaco, Wielscher, Matthias, Farlik, Matthias, Zuber, Verena, de Knegt, Robert J., Snieder, Harold, Uitterlinden, André G., Lynch, Julie A., Jiang, Xiyun, Said, Saredo, Kaplan, David E., Lee, Kyung Min, Serper, Marina, Carr, Rotonya M., Tsao, Philip S., Atkinson, Stephen R., Dehghan, Abbas, Tzoulaki, Ioanna, Ikram, M. Arfan, Herzig, Karl-Heinz, Järvelin, Marjo-Riitta, Alizadeh, Behrooz Z., O’Donnell, Christopher J., Saleheen, Danish, Voight, Benjamin F., Chang, Kyong-Mi, Thursz, Mark R., Elliott, Paul

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An organelle-specific protein landscape identifies novel diseases and molecular mechanisms von Boldt, Karsten, van Reeuwijk, Jeroen, Lu, Qianhao, Koutroumpas, Konstantinos, Nguyen, Thanh-Minh T., Texier, Yves, van Beersum, Sylvia E. C., Horn, Nicola, Willer, Jason R., Mans, Dorus A., Dougherty, Gerard, Lamers, Ideke J. C., Coene, Karlien L. M., Arts, Heleen H., Betts, Matthew J., Beyer, Tina, Bolat, Emine, Gloeckner, Christian Johannes, Haidari, Khatera, Hetterschijt, Lisette, Iaconis, Daniela, Jenkins, Dagan, Klose, Franziska, Knapp, Barbara, Latour, Brooke, Letteboer, Stef J. F., Marcelis, Carlo L., Mitic, Dragana, Morleo, Manuela, Oud, Machteld M., Riemersma, Moniek, Rix, Susan, Terhal, Paulien A., Toedt, Grischa, van Dam, Teunis J. P., de Vrieze, Erik, Wissinger, Yasmin, Wu, Ka Man, Apic, Gordana, Beales, Philip L., Blacque, Oliver E., Gibson, Toby J., Huynen, Martijn A., Katsanis, Nicholas, Kremer, Hannie, Omran, Heymut, van Wijk, Erwin, Wolfrum, Uwe, Kepes, François, Davis, Erica E., Franco, Brunella, Giles, Rachel H., Ueffing, Marius, Russell, Robert B., Roepman, Ronald

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Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies von Fang, Huaying, Hui, Qin, Lynch, Julie, Honerlaw, Jacqueline, Assimes, Themistocles L., Huang, Jie, Vujkovic, Marijana, Damrauer, Scott M., Pyarajan, Saiju, Gaziano, J. Michael, DuVall, Scott L., O’Donnell, Christopher J., Cho, Kelly, Chang, Kyong-Mi, Wilson, Peter W.F., Tsao, Philip S., Gaziano, J. Michael, Ramoni, Rachel, Breeling, Jim, Chang, Kyong-Mi, Huang, Grant, Muralidhar, Sumitra, O’Donnell, Christopher J., Tsao, Philip S., Moser, Jennifer, Whitbourne, Stacey B., Brewer, Jessica V., Warren, Stuart, Argyres, Dean P., Stephens, Brady, Brophy, Mary T., Humphries, Donald E., Do, Nhan, Shayan, Shahpoor, Nguyen, Xuan-Mai T., Pyarajan, Saiju, Cho, Kelly, Hauser, Elizabeth, Sun, Yan, Zhao, Hongyu, Wilson, Peter, McArdle, Rachel, Dellitalia, Louis, Harley, John, Whittle, Jeffrey, Beckham, Jean, Wells, John, Gutierrez, Salvador, Gibson, Gretchen, Kaminsky, Laurence, Villareal, Gerardo, Kinlay, Scott, Xu, Junzhe, Hamner, Mark, Haddock, Kathlyn Sue, Bhushan, Sujata, Iruvanti, Pran, Godschalk, Michael, Ballas, Zuhair, Buford, Malcolm, Mastorides, Stephen, Klein, Jon, Ratcliffe, Nora, Florez, Hermes, Swann, Alan, Murdoch, Maureen, Sriram, Peruvemba, Yeh, Shing Shing, Washburn, Ronald, Jhala, Darshana, Aguayo, Samuel, Cohen, David, Sharma, Satish, Callaghan, John, Oursler, Kris Ann, Whooley, Mary, Ahuja, Sunil, Gutierrez, Amparo, Schifman, Ronald, Greco, Jennifer, Rauchman, Michael, Servatius, Richard, Oehlert, Mary, Wallbom, Agnes, Fernando, Ronald, Stapley, Todd, Sherman, Scott, Anderson, Gwenevere, Sonel, Elif, Boyko, Edward, Meyer, Laurence, Gupta, Samir, Fayad, Joseph, Hung, Adriana, Lichy, Jack, Hurley, Robin, Robey, Brooks, Striker, Robert, Sun, Yan V., Tang, Hua

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X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3 von Olcese, Chiara, Patel, Mitali P., Shoemark, Amelia, Kiviluoto, Santeri, Legendre, Marie, Williams, Hywel J., Vaughan, Cara K., Hayward, Jane, Goldenberg, Alice, Emes, Richard D., Munye, Mustafa M., Dyer, Laura, Cahill, Thomas, Bevillard, Jeremy, Gehrig, Corinne, Guipponi, Michel, Chantot, Sandra, Duquesnoy, Philippe, Thomas, Lucie, Jeanson, Ludovic, Copin, Bruno, Tamalet, Aline, Thauvin-Robinet, Christel, Papon, Jean- François, Garin, Antoine, Pin, Isabelle, Vera, Gabriella, Aurora, Paul, Fassad, Mahmoud R., Jenkins, Lucy, Boustred, Christopher, Cullup, Thomas, Dixon, Mellisa, Onoufriadis, Alexandros, Bush, Andrew, Chung, Eddie M. K., Antonarakis, Stylianos E., Loebinger, Michael R., Wilson, Robert, Armengot, Miguel, Escudier, Estelle, Hogg, Claire, Amselem, Serge, Sun, Zhaoxia, Bartoloni, Lucia, Blouin, Jean-Louis, Mitchison, Hannah M.

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Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program von Klarin, Derek, Verma, Shefali Setia, Judy, Renae, Dikilitas, Ozan, Wolford, Brooke N., Paranjpe, Ishan, Levin, Michael G., Pan, Cuiping, Tcheandjieu, Catherine, Spin, Joshua M., Lynch, Julie, Assimes, Themistocles L., Åldstedt Nyrønning, Linn, Mattsson, Erney, Edwards, Todd L., Denny, Josh, Larson, Eric, Lee, Ming Ta Michael, Carrell, David, Zhang, Yanfei, Jarvik, Gail P., Gharavi, Ali G., Harley, John, Mentch, Frank, Pacheco, Jennifer A., Hakonarson, Hakon, Skogholt, Anne Heidi, Thomas, Laurent, Gabrielsen, Maiken Elvestad, Hveem, Kristian, Nielsen, Jonas Bille, Zhou, Wei, Fritsche, Lars, Huang, Jie, Natarajan, Pradeep, Sun, Yan V., DuVall, Scott L., Rader, Daniel J., Cho, Kelly, Chang, Kyong-Mi, Wilson, Peter W.F., O’Donnell, Christopher J., Kathiresan, Sekar, Scali, Salvatore T., Berceli, Scott A., Willer, Cristen, Jones, Gregory T., Bown, Matthew J., Nadkarni, Girish, Kullo, Iftikhar J., Ritchie, Marylyn, Damrauer, Scott M., Tsao, Philip S.

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Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry von OLBRICH, Heike, SCHMIDTS, Miriam, HURLES, Matthew E, CONSORTIUM, Ukk, KÖHLER, Gabriele, SCHROEDER, Josef, NÜRNBERG, Gudrun, NÜRNBERG, Peter, CHUNG, Eddie M. K, REINHARDT, Richard, MARTHIN, June K, NIELSEN, Kim G, WERNER, Claudius, MITCHISON, HannahM, OMRAN, Heymut, ONOUFRIADIS, Alexandros, LOGES, Niki T, RAIDT, Johanna, FANNI BANKI, Nora, SHOEMARK, Amelia, BURGOYNE, Tom, AL TURKI, Saeed

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Long-term outcomes among out-of-hospital cardiac arrest survivors with reversible vs. non-reversible causes von Barcella, Carlo Alberto, Grunau, Brian E, Guan, Meijiao, Hawkins, Nathaniel M, Deyell, Marc W, Andrade, Jason G, Helmer, Jennie S, Wong, Graham C, Kragholm, Kristian H, Humphries, Karin H, Christenson, Jim, Fordyce, Christopher B

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Machine Learning Characterization of COPD Subtypes: Insights From the COPDGene Study von Castaldi, Peter J, Boueiz, Adel, Yun, Jeong, Estepar, Raul San Jose, Ross, James C, Washko, George, Cho, Michael H, Hersh, Craig P, Kinney, Gregory L, Young, Kendra A, Regan, Elizabeth A, Lynch, David A, Criner, Gerald J, Dy, Jennifer G, Rennard, Stephen I, Casaburi, Richard, Make, Barry J, Crapo, James, Silverman, Edwin K, Hokanson, John E

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Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: A randomized controlled trial von Marteau, Theresa, Senior, Victoria, Humphries, Steve E., Bobrow, Martin, Cranston, Treena, Crook, Martin A., Day, Lorna, Fernandez, Maryam, Horne, Rob, Iversen, Andrew, Jackson, Zoe, Lynas, Jacqui, Middleton-Price, Helen, Savine, Richard, Sikorski, Jim, Watson, Melanie, Weinman, John, Wierzbicki, Anthony S., Wray, Richard

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A small molecule with anticancer and antimetastatic activities induces rapid mitochondrial-associated necrosis in breast cancer von Bastian, Anja, Thorpe, Jessica E, Disch, Bryan C, Bailey-Downs, Lora C, Gangjee, Aleem, Devambatla, Ravi K V, Henthorn, Jim, Humphries, Kenneth M, Vadvalkar, Shraddha S, Ihnat, Michael A

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Abstract 332: Long-term Post-discharge Survival and Healthcare Utilization Following Out-of-hospital Cardiac Arrest: Insights From a Novel Province-wide Linkage von Fordyce, Christopher B, Grunau, Brian E, Guan, Meijiao, Lee, May K, Hawkins, Nathaniel M, Helmer, Jennie, Wong, Graham C, Humphries, Karin H, Christenson, Jim

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Mutations in CCDC39 and CCDC40 are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms von Antony, Dinu, Becker-Heck, Anita, Zariwala, Maimoona A., Schmidts, Miriam, Onoufriadis, Alexandros, Forouhan, Mitra, Wilson, Robert, Taylor-Cox, Theresa, Dewar, Ann, Jackson, Claire, Goggin, Patricia, Loges, Niki T., Olbrich, Heike, Jaspers, Martine, Jorissen, Mark, Leigh, Margaret W., Wolf, Whitney E., Daniels, M. Leigh Anne, Noone, Peadar G., Ferkol, Thomas W., Sagel, Scott D., Rosenfeld, Margaret, Rutman, Andrew, Dixit, Abhijit, O'Callaghan, Christopher, Lucas, Jane S., Hogg, Claire, Scambler, Peter J., Emes, Richard D., UK10K, Chung, Eddie M.K., Shoemark, Amelia, Knowles, Michael R., Omran, Heymut, Mitchison, Hannah M.

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Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects von Williamson, Kathleen A., Rainger, Joe, Floyd, James A.B., Ansari, Morad, Meynert, Alison, Aldridge, Kishan V., Rainger, Jacqueline K., Anderson, Carl A., Moore, Anthony T., Hurles, Matthew E., Clarke, Angus, van Heyningen, Veronica, Verloes, Alain, Taylor, Martin S., Wilkie, Andrew O.M., FitzPatrick, David R.

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