Air medical transport safety von Fallat, Mary E, Overton, Jr, John W

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Experience with generally accepted centrifugal pumps: Personal and collective experience von Joyce, Lyle D., Kiser, Joseph C., Eales, Frazier, King, R. Michael, Overton, John W., Toninato, Carol J.

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Successful Management of Left Ventricular Rupture Following Myocardial Revascularization von Bojar, Robert M., Overton, John W., Madoff, Irving M.

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NPOESS direct readout mission von Overton, J.W., Coronado, P., van de Wouw, J.A.

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Temporary antenna support von OVERTON JOHN W

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In Vivo Antagonism between Gentamicin and Chloramphenicol in Neutropenic Mice von Sande, Merle A., Overton, John W.

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Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism von Scholl, Ute I, Goh, Gerald, Stölting, Gabriel, de Oliveira, Regina Campos, Choi, Murim, Overton, John D, Fonseca, Annabelle L, Korah, Reju, Starker, Lee F, Kunstman, John W, Prasad, Manju L, Hartung, Erum A, Mauras, Nelly, Benson, Matthew R, Brady, Tammy, Shapiro, Jay R, Loring, Erin, Nelson-Williams, Carol, Libutti, Steven K, Mane, Shrikant, Hellman, Per, Westin, Gunnar, Åkerström, Göran, Björklund, Peyman, Carling, Tobias, Fahlke, Christoph, Hidalgo, Patricia, Lifton, Richard P

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Whole-Exome Sequencing Characterizes the Landscape of Somatic Mutations and Copy Number Alterations in Adrenocortical Carcinoma von Juhlin, C. Christofer, Goh, Gerald, Healy, James M, Fonseca, Annabelle L, Scholl, Ute I, Stenman, Adam, Kunstman, John W, Brown, Taylor C, Overton, John D, Mane, Shrikant M, Nelson-Williams, Carol, Bäckdahl, Martin, Suttorp, Anna-Carinna, Haase, Matthias, Choi, Murim, Schlessinger, Joseph, Rimm, David L, Höög, Anders, Prasad, Manju L, Korah, Reju, Larsson, Catharina, Lifton, Richard P, Carling, Tobias

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Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development von Owens, Nick D.L., Blitz, Ira L., Lane, Maura A., Patrushev, Ilya, Overton, John D., Gilchrist, Michael J., Cho, Ken W.Y., Khokha, Mustafa K.

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Oil Impacts on Coastal Wetlands: Implications for the Mississippi River Delta Ecosystem after the Deepwater Horizon Oil Spill von Mendelssohn, Irving A, Andersen, Gary L, Baltz, Donald M, Caffey, Rex H, Carman, Kevin R, Fleeger, John W, Joye, Samantha B, Lin, Qianxin, Maltby, Edward, Overton, Edward B, Rozas, Lawrence P

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How Visual Stimuli Activate Dopaminergic Neurons at Short Latency von Dommett, Eleanor, Coizet, Véronique, Blaha, Charles D, Martindale, John, Lefebvre, Véronique, Walton, Natalie, Mayhew, John E. W, Overton, Paul G, Redgrave, Peter

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De novo mutations in histone-modifying genes in congenital heart disease von Zaidi, Samir, Choi, Murim, Wakimoto, Hiroko, Ma, Lijiang, Jiang, Jianming, Overton, John D., Romano-Adesman, Angela, Bjornson, Robert D., Breitbart, Roger E., Brown, Kerry K., Carriero, Nicholas J., Cheung, Yee Him, Deanfield, John, DePalma, Steve, Fakhro, Khalid A., Glessner, Joseph, Hakonarson, Hakon, Italia, Michael J., Kaltman, Jonathan R., Kaski, Juan, Kim, Richard, Kline, Jennie K., Lee, Teresa, Leipzig, Jeremy, Lopez, Alexander, Mane, Shrikant M., Mitchell, Laura E., Newburger, Jane W., Parfenov, Michael, Pe’er, Itsik, Porter, George, Roberts, Amy E., Sachidanandam, Ravi, Sanders, Stephan J., Seiden, Howard S., State, Mathew W., Subramanian, Sailakshmi, Tikhonova, Irina R., Wang, Wei, Warburton, Dorothy, White, Peter S., Williams, Ismee A., Zhao, Hongyu, Seidman, Jonathan G., Brueckner, Martina, Chung, Wendy K., Gelb, Bruce D., Goldmuntz, Elizabeth, Seidman, Christine E., Lifton, Richard P.

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De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder von Dong, Shan, Walker, Michael F, Carriero, Nicholas J, DiCola, Michael, Willsey, A Jeremy, Ye, Adam Y, Waqar, Zainulabedin, Gonzalez, Luis E, Overton, John D, Frahm, Stephanie, Keaney, 3rd, John F, Teran, Nicole A, Dea, Jeanselle, Mandell, Jeffrey D, Hus Bal, Vanessa, Sullivan, Catherine A, DiLullo, Nicholas M, Khalil, Rehab O, Gockley, Jake, Yuksel, Zafer, Sertel, Sinem M, Ercan-Sencicek, A Gulhan, Gupta, Abha R, Mane, Shrikant M, Sheldon, Michael, Brooks, Andrew I, Roeder, Kathryn, Devlin, Bernie, State, Matthew W, Wei, Liping, Sanders, Stephan J

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Pathways for avian influenza virus spread: GPS reveals wild waterfowl in commercial livestock facilities and connectivity with the natural wetland landscape von McDuie, Fiona, Matchett, Elliott L, Prosser, Diann J, Takekawa, John Y, Pitesky, Maurice E, Lorenz, Austen A, McCuen, Madeline M, T, Overton Cory, Ackerman, Joshua T, De La Cruz, Susan E. W., Casazza, Michael L

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Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO von Clark, Victoria E., Erson-Omay, E. Zeynep, Serin, Akdes, Yin, Jun, Cotney, Justin, Özduman, Koray, Avşar, Timuçin, Li, Jie, Murray, Phillip B., Henegariu, Octavian, Yilmaz, Saliha, Günel, Jennifer Moliterno, Carrión-Grant, Geneive, Yılmaz, Baran, Grady, Conor, Tanrıkulu, Bahattin, Bakırcıoǧlu, Mehmet, Kaymakçalan, Hande, Caglayan, Ahmet Okay, Sencar, Leman, Ceyhun, Emre, Atik, A. Fatih, Bayri, Yaşar, Bai, Hanwen, Kolb, Luis E., Hebert, Ryan M., Omay, S. Bulent, Mishra-Gorur, Ketu, Choi, Murim, Overton, John D., Holland, Eric C., Mane, Shrikant, State, Matthew W., Bilgüvar, Kaya, Baehring, Joachim M., Gutin, Philip H., Piepmeier, Joseph M., Vortmeyer, Alexander, Brennan, Cameron W., Pamir, M. Necmettin, Kılıç, Türker, Lifton, Richard P., Noonan, James P., Yasuno, Katsuhito, Günel, Murat

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Effect of HIV Antibody VRC01 on Viral Rebound after Treatment Interruption von Bar, Katharine J, Sneller, Michael C, Harrison, Linda J, Justement, J. Shawn, Overton, Edgar T, Petrone, Mary E, Salantes, D. Brenda, Seamon, Catherine A, Scheinfeld, Benjamin, Kwan, Richard W, Learn, Gerald H, Proschan, Michael A, Kreider, Edward F, Blazkova, Jana, Bardsley, Mark, Refsland, Eric W, Messer, Michael, Clarridge, Katherine E, Tustin, Nancy B, Madden, Patrick J, Oden, KaSaundra, O’Dell, Sijy J, Jarocki, Bernadette, Shiakolas, Andrea R, Tressler, Randall L, Doria-Rose, Nicole A, Bailer, Robert T, Ledgerwood, Julie E, Capparelli, Edmund V, Lynch, Rebecca M, Graham, Barney S, Moir, Susan, Koup, Richard A, Mascola, John R, Hoxie, James A, Fauci, Anthony S, Tebas, Pablo, Chun, Tae-Wook

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Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity von Akbari, Parsa, Gilani, Ankit, Sosina, Olukayode, Kosmicki, Jack A, Khrimian, Lori, Fang, Yi-Ya, Persaud, Trikaldarshi, Garcia, Victor, Sun, Dylan, Li, Alexander, Mbatchou, Joelle, Locke, Adam E, Benner, Christian, Verweij, Niek, Lin, Nan, Hossain, Sakib, Agostinucci, Kevin, Pascale, Jonathan V, Dirice, Ercument, Dunn, Michael, Kraus, William E, Shah, Svati H, Chen, Yii-Der I, Rotter, Jerome I, Rader, Daniel J, Melander, Olle, Still, Christopher D, Mirshahi, Tooraj, Carey, David J, Berumen-Campos, Jaime, Kuri-Morales, Pablo, Alegre-Díaz, Jesus, Torres, Jason M, Emberson, Jonathan R, Collins, Rory, Balasubramanian, Suganthi, Hawes, Alicia, Jones, Marcus, Zambrowicz, Brian, Murphy, Andrew J, Paulding, Charles, Coppola, Giovanni, Overton, John D, Reid, Jeffrey G, Shuldiner, Alan R, Cantor, Michael, Kang, Hyun M, Abecasis, Goncalo R, Karalis, Katia, Economides, Aris N, Marchini, Jonathan, Yancopoulos, George D, Sleeman, Mark W, Altarejos, Judith, Della Gatta, Giusy, Tapia-Conyer, Roberto, Schwartzman, Michal L, Baras, Aris, Ferreira, Manuel A R, Lotta, Luca A

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Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease von Zhu, Na, Welch, Carrie L, Wang, Jiayao, Allen, Philip M, Gonzaga-Jauregui, Claudia, Ma, Lijiang, King, Alejandra K, Krishnan, Usha, Rosenzweig, Erika B, Ivy, D Dunbar, Austin, Eric D, Hamid, Rizwan, Pauciulo, Michael W, Lutz, Katie A, Nichols, William C, Reid, Jeffrey G, Overton, John D, Baras, Aris, Dewey, Frederick E, Shen, Yufeng, Chung, Wendy K

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism von Sanders, Stephan J., Murtha, Michael T., Gupta, Abha R., Murdoch, John D., Raubeson, Melanie J., Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, DiLullo, Nicholas M., Parikshak, Neelroop N., Stein, Jason L., Walker, Michael F., Ober, Gordon T., Teran, Nicole A., Song, Youeun, El-Fishawy, Paul, Murtha, Ryan C., Choi, Murim, Overton, John D., Bjornson, Robert D., Carriero, Nicholas J., Meyer, Kyle A., Bilguvar, Kaya, Mane, Shrikant M., Šestan, Nenad, Lifton, Richard P., Günel, Murat, Roeder, Kathryn, Geschwind, Daniel H., Devlin, Bernie, State, Matthew W.

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Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome von Lemaire, Mathieu, Frémeaux-Bacchi, Véronique, Schaefer, Franz, Choi, Murim, Tang, Wai Ho, Le Quintrec, Moglie, Fakhouri, Fadi, Taque, Sophie, Nobili, François, Martinez, Frank, Ji, Weizhen, Overton, John D, Mane, Shrikant M, Nürnberg, Gudrun, Altmüller, Janine, Thiele, Holger, Morin, Denis, Deschenes, Georges, Baudouin, Véronique, Llanas, Brigitte, Collard, Laure, Majid, Mohammed A, Simkova, Eva, Nürnberg, Peter, Rioux-Leclerc, Nathalie, Moeckel, Gilbert W, Gubler, Marie Claire, Hwa, John, Loirat, Chantal, Lifton, Richard P

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