Point-of-Care Analysis of Blood Ammonia with a Gas-Phase Sensor von Veltman, Thomas R, Tsai, Chun J, Gomez-Ospina, Natalia, Kanan, Matthew W, Chu, Gilbert

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Carbon Monoxide Gas Diffusion Electrolysis that Produces Concentrated C2 Products with High Single-Pass Conversion von Ripatti, Donald S., Veltman, Thomas R., Kanan, Matthew W.

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Directed Synthesis of Noncentrosymmetric Molybdates Using Composition Space Analysis von Veltman, Thomas R, Stover, Adam K, Narducci Sarjeant, Amy, Ok, Kang Min, Halasyamani, P. Shiv, Norquist, Alexander J

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Carbon Monoxide Gas Diffusion Electrolysis that Produces Concentrated C2 Products with High Single-Pass Conversion von Ripatti, Donald S., Veltman, Thomas R., Kanan, Matthew W.

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Electrochemical cells and cathodes for the production of concentrated product streams from the reduction of CO and/or CO2 von Ripatti, Donald Stephen, Kanan, Matthew W, Veltman, Thomas R

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ELECTROCHEMICAL CELLS AND CATHODES FOR THE PRODUCTION OF CONCENTRATED PRODUCT STREAMS FROM THE REDUCTION OF CO AND/OR CO2 von VELTMAN, Thomas R, RIPATTI, Donald Stephen, KANAN, Matthew W

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Rapid and efficient genetic engineering of both wild type and axenic strains of Dictyostelium discoideum von Paschke, Peggy, Knecht, David A, Silale, Augustinas, Traynor, David, Williams, Thomas D, Thomason, Peter A, Insall, Robert H, Chubb, Jonathan R, Kay, Robert R, Veltman, Douwe M

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A plasma membrane template for macropinocytic cups von Veltman, Douwe M, Williams, Thomas D, Bloomfield, Gareth, Chen, Bi-Chang, Betzig, Eric, Insall, Robert H, Kay, Robert R

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Transcriptome and genome sequencing uncovers functional variation in humans von Lappalainen, Tuuli, Sammeth, Michael, Friedländer, Marc R., ‘t Hoen, Peter A. C., Monlong, Jean, Rivas, Manuel A., Gonzàlez-Porta, Mar, Kurbatova, Natalja, Griebel, Thasso, Ferreira, Pedro G., Barann, Matthias, Wieland, Thomas, Greger, Liliana, van Iterson, Maarten, Almlöf, Jonas, Ribeca, Paolo, Pulyakhina, Irina, Esser, Daniela, Giger, Thomas, Tikhonov, Andrew, Sultan, Marc, Bertier, Gabrielle, MacArthur, Daniel G., Lek, Monkol, Lizano, Esther, Buermans, Henk P. J., Padioleau, Ismael, Schwarzmayr, Thomas, Karlberg, Olof, Ongen, Halit, Kilpinen, Helena, Beltran, Sergi, Gut, Marta, Kahlem, Katja, Amstislavskiy, Vyacheslav, Stegle, Oliver, Pirinen, Matti, Montgomery, Stephen B., Donnelly, Peter, McCarthy, Mark I., Flicek, Paul, Strom, Tim M., Lehrach, Hans, Schreiber, Stefan, Sudbrak, Ralf, Carracedo, Ángel, Antonarakis, Stylianos E., Häsler, Robert, Syvänen, Ann-Christine, van Ommen, Gert-Jan, Brazma, Alvis, Meitinger, Thomas, Rosenstiel, Philip, Guigó, Roderic, Gut, Ivo G., Estivill, Xavier, Dermitzakis, Emmanouil T.

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ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation von Jansen, Eric J. R., Timal, Sharita, Ryan, Margret, Ashikov, Angel, van Scherpenzeel, Monique, Graham, Laurie A., Mandel, Hanna, Hoischen, Alexander, Iancu, Theodore C., Raymond, Kimiyo, Steenbergen, Gerry, Gilissen, Christian, Huijben, Karin, van Bakel, Nick H. M., Maeda, Yusuke, Rodenburg, Richard J., Adamowicz, Maciej, Crushell, Ellen, Koenen, Hans, Adams, Darius, Vodopiutz, Julia, Greber-Platzer, Susanne, Müller, Thomas, Dueckers, Gregor, Morava, Eva, Sykut-Cegielska, Jolanta, Martens, Gerard J. M., Wevers, Ron A., Niehues, Tim, Huynen, Martijn A., Veltman, Joris A., Stevens, Tom H., Lefeber, Dirk J.

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Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype von Milner, Katja M., Craig, Ellen E., Thompson, Russell J., Veltman, Marijcke W.M., Simon Thomas, N., Roberts, Sian, Bellamy, Margaret, Curran, Sarah R., Sporikou, Caroline M.J., Bolton, Patrick F.

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Hidden Rice Diversity in the Guianas von Van Andel, Tinde, Veltman, Margaretha A., Bertin, Alice, Maat, Harro, Polime, Thomas, Hille Ris Lambers, Derk, Tjoe Awie, Jerry, De Boer, Hugo, Manzanilla, Vincent

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Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease von Pottier, Cyril, Bieniek, Kevin F., Finch, NiCole, van de Vorst, Maartje, Baker, Matt, Perkersen, Ralph, Brown, Patricia, Ravenscroft, Thomas, van Blitterswijk, Marka, Nicholson, Alexandra M., DeTure, Michael, Knopman, David S., Josephs, Keith A., Parisi, Joseph E., Petersen, Ronald C., Boylan, Kevin B., Boeve, Bradley F., Graff-Radford, Neill R., Veltman, Joris A., Gilissen, Christian, Murray, Melissa E., Dickson, Dennis W., Rademakers, Rosa

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The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders von Bolton, Patrick Farrar, Dennis, N.R., Browne, C.E., Thomas, N.S., Veltman, M.W.M., Thompson, R.J., Jacobs, P.

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White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group von van Velzen, Laura S., Kelly, Sinead, Isaev, Dmitry, Aleman, Andre, Aftanas, Lyubomir I., Bauer, Jochen, Baune, Bernhard T., Brak, Ivan V., Carballedo, Angela, Connolly, Colm G., Couvy-Duchesne, Baptiste, Cullen, Kathryn R., Danilenko, Konstantin V., Dannlowski, Udo, Enneking, Verena, Filimonova, Elena, Förster, Katharina, Frodl, Thomas, Gotlib, Ian H., Groenewold, Nynke A., Grotegerd, Dominik, Harris, Mathew A., Hatton, Sean N., Hawkins, Emma L., Hickie, Ian B., Ho, Tiffany C., Jansen, Andreas, Kircher, Tilo, Klimes-Dougan, Bonnie, Kochunov, Peter, Krug, Axel, Lagopoulos, Jim, Lee, Renick, Lett, Tristram A., Li, Meng, MacMaster, Frank P., Martin, Nicholas G., McIntosh, Andrew M., McLellan, Quinn, Meinert, Susanne, Nenadić, Igor, Osipov, Evgeny, Penninx, Brenda W. J. H., Portella, Maria J., Repple, Jonathan, Roos, Annerine, Sacchet, Matthew D., Sämann, Philipp G., Schnell, Knut, Shen, Xueyi, Sim, Kang, Stein, Dan J., van Tol, Marie-Jose, Tomyshev, Alexander S., Tozzi, Leonardo, Veer, Ilya M., Vermeiren, Robert, Vives-Gilabert, Yolanda, Walter, Henrik, Walter, Martin, van der Wee, Nic J. A., van der Werff, Steven J. A., Schreiner, Melinda Westlund, Whalley, Heather C., Wright, Margaret J., Yang, Tony T., Zhu, Alyssa, Veltman, Dick J., Thompson, Paul M., Jahanshad, Neda, Schmaal, Lianne

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Identification of common variants associated with human hippocampal and intracranial volumes von Vasquez, Alejandro Arias, Toro, Roberto, Bartecek, Richard, Bergmann, Ørjan, Bernard, Manon, Chakravarty, M Mallar, Grimm, Oliver, Homuth, Georg, Lopez, Lorna M, Hansell, Narelle K, Kim, Sungeun, Laje, Gonzalo, Lee, Phil H, Liu, Xinmin, Loth, Eva, Lourdusamy, Anbarasu, Mattingsdal, Morten, Mohnke, Sebastian, Maniega, Susana Muñoz, O'Brien, Carol, Pütz, Benno, Rasmussen, Jerod, Risacher, Shannon L, Rose, Emma J, Ryten, Mina, Sprooten, Emma, Teumer, Alexander, Trabzuni, Daniah, Turner, Jessica, van Eijk, Kristel, van Erp, Theo G M, van Tol, Marie-Jose, Wolf, Christiane, Aleman, Andre, Alhusaini, Saud, Binder, Elisabeth B, Brohawn, David G, Cantor, Rita M, Czisch, Michael, de Almeida, Marcio A A, Delanty, Norman, Dyer, Thomas D, Erk, Susanne, Fox, Peter T, Freimer, Nelson B, Hagler, Donald J, Hoogman, Martine, Johnson, Matthew P, Kasperaviciute, Dalia, Kent, Jack W, Kochunov, Peter, Lancaster, Jack L, Liewald, David C, Matarin, Mar, Mattheisen, Manuel, Moses, Eric K, Mühleisen, Thomas W, Nöthen, Markus M, Puls, Ralf, Reinvang, Ivar, Savitz, Jonathan, Schnack, Hugo G, Seiferth, Nina, Valdés Hernández, Maria C, Van Haren, Neeltje E M, Veltman, Joris A, Völzke, Henry, Westlye, Lars T, Whelan, Christopher D, Cavalleri, Gianpiero L, Dale, Anders M, Drevets, Wayne C, Heinz, Andreas, Le Hellard, Stephanie, Macciardi, Fabio, Montgomery, Grant W, Starr, John M, Gudnason, Vilmundur, Tzourio, Christophe, Vernooij, Meike W, Launer, Lenore J, Andreassen, Ole A, Bastin, Mark E, Blangero, John, Brunner, Han G, Buckner, Randy L, Coppola, Giovanni, de Zubicaray, Greig I, Fernández, Guillén, Glahn, David C, Hardy, John, Kahn, René S, McIntosh, Andrew M, Nichols, Thomas E, Ophoff, Roel A, Pausova, Zdenka, Potkin, Steven G, Smoller, Jordan W, Martin, Nicholas G, Thompson, Paul M

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Modelling survival: exposure pattern, species sensitivity and uncertainty von Ashauer, Roman, Albert, Carlo, Augustine, Starrlight, Cedergreen, Nina, Charles, Sandrine, Ducrot, Virginie, Focks, Andreas, Gabsi, Faten, Gergs, André, Goussen, Benoit, Jager, Tjalling, Kramer, Nynke I., Nyman, Anna-Maija, Poulsen, Veronique, Reichenberger, Stefan, Schäfer, Ralf B., Van den Brink, Paul J., Veltman, Karin, Vogel, Sören, Zimmer, Elke I., Preuss, Thomas G.

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Brain structural abnormalities in obesity: relation to age, genetic risk, and common psychiatric disorders: Evidence through univariate and multivariate mega-analysis including 642... von Opel, Nils, Thalamuthu, Anbupalam, Milaneschi, Yuri, Grotegerd, Dominik, Flint, Claas, Leenings, Ramona, Goltermann, Janik, Richter, Maike, Hahn, Tim, Woditsch, Georg, Berger, Klaus, Hermesdorf, Marco, McIntosh, Andrew, Whalley, Heather C., Harris, Mathew A., MacMaster, Frank P., Walter, Henrik, Veer, Ilya M., Frodl, Thomas, Carballedo, Angela, Krug, Axel, Nenadic, Igor, Kircher, Tilo, Aleman, Andre, Groenewold, Nynke A., Stein, Dan J., Soares, Jair C., Zunta-Soares, Giovana B., Mwangi, Benson, Wu, Mon-Ju, Walter, Martin, Li, Meng, Harrison, Ben J., Davey, Christopher G., Cullen, Kathryn R., Klimes-Dougan, Bonnie, Mueller, Bryon A., Sämann, Philipp G., Penninx, Brenda, Nawijn, Laura, Veltman, Dick J., Aftanas, Lyubomir, Brak, Ivan V., Filimonova, Elena A., Osipov, Evgeniy A., Reneman, Liesbeth, Schrantee, Anouk, Grabe, Hans J., Van der Auwera, Sandra, Wittfeld, Katharina, Hosten, Norbert, Völzke, Henry, Sim, Kang, Gotlib, Ian H., Sacchet, Matthew D., Lagopoulos, Jim, Hatton, Sean N., Hickie, Ian, Pozzi, Elena, Thompson, Paul M., Jahanshad, Neda, Schmaal, Lianne, Baune, Bernhard T., Dannlowski, Udo

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Examining the association between posttraumatic stress disorder and disruptions in cortical networks identified using data-driven methods von Yang, Jin, Huggins, Ashley A, Sun, Delin, Baird, C Lexi, Haswell, Courtney C, Frijling, Jessie L, Olff, Miranda, van Zuiden, Mirjam, Koch, Saskia B J, Nawijn, Laura, Veltman, Dick J, Suarez-Jimenez, Benjamin, Zhu, Xi, Neria, Yuval, Hudson, Anna R, Mueller, Sven C, Baker, Justin T, Lebois, Lauren A M, Kaufman, Milissa L, Qi, Rongfeng, Lu, Guang Ming, Říha, Pavel, Rektor, Ivan, Dennis, Emily L, Ching, Christopher R K, Thomopoulos, Sophia I, Salminen, Lauren E, Jahanshad, Neda, Thompson, Paul M, Stein, Dan J, Koopowitz, Sheri M, Ipser, Jonathan C, Seedat, Soraya, du Plessis, Stefan, van den Heuvel, Leigh L, Wang, Li, Zhu, Ye, Li, Gen, Sierk, Anika, Manthey, Antje, Walter, Henrik, Daniels, Judith K, Schmahl, Christian, Herzog, Julia I, Liberzon, Israel, King, Anthony, Angstadt, Mike, Davenport, Nicholas D, Sponheim, Scott R, Disner, Seth G, Straube, Thomas, Hofmann, David, Grupe, Daniel W, Nitschke, Jack B, Davidson, Richard J, Larson, Christine L, deRoon-Cassini, Terri A, Blackford, Jennifer U, Olatunji, Bunmi O, Gordon, Evan M, May, Geoffrey, Nelson, Steven M, Abdallah, Chadi G, Levy, Ifat, Harpaz-Rotem, Ilan, Krystal, John H, Morey, Rajendra A, Sotiras, Aristeidis

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Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13 von Dennis, N.R., Veltman, M.W.M., Thompson, R., Craig, E., Bolton, P.F., Thomas, N.S.

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