Cultures of the Marine Bacterium Pseudovibrio denitrificans Ab134 Produce Bromotyrosine-Derived Alkaloids Previously Only Isolated from Marine Sponges von Nicacio, Karen J, Ióca, Laura P, Fróes, Adriana M, Leomil, Luciana, Appolinario, Luciana R, Thompson, Christiane C, Thompson, Fabiano L, Ferreira, Antonio G, Williams, David E, Andersen, Raymond J, Eustaquio, Alessandra S, Berlinck, Roberto G. S

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The Coral Bleaching Vibrio shiloi Kushmaro et al. 2001 is a Later Synonym of Vibrio mediterranei Pujalte and Garay 1986 von Thompson, Fabiano L., Hoste, Bart, Thompson, Cristiane C., Huys, Geert, Swings, Jean

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Regional hippocampal damage in heart failure von Woo, Mary A., Ogren, Jennifer A., Abouzeid, Christiane M., Macey, Paul M., Sairafian, Kevin G., Saharan, Priya S., Thompson, Paul M., Fonarow, Gregg C., Hamilton, Michele A., Harper, Ronald M., Kumar, Rajesh

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Sequence and comparative analysis of the maize NB mitochondrial genome von Clifton, S.W, Minx, P, Fauron, C.M.R, Gibson, M, Allen, J.O, Sun, H, Thompson, M, Barbazuk, W.B, Kanuganti, S, Tayloe, C

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Macroergonomic factors in the patient work system: examining the context of patients with chronic illness von Holden, Richard J., Valdez, Rupa S., Schubert, Christiane C., Thompson, Morgan J., Hundt, Ann S.

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A 23-year retrospective investigation of Salmonella Typhi and Salmonella Paratyphi isolated in a tertiary Kathmandu hospital von Zellweger, Raphaël M, Basnyat, Buddha, Shrestha, Poojan, Prajapati, Krishna G, Dongol, Sabina, Sharma, Paban K, Koirala, Samir, Darton, Thomas C, Dolecek, Christiane, Thompson, Corinne N, Thwaites, Guy E, Baker, Stephen G, Karkey, Abhilasha

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In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2 von Morison, LD, Meffert, E, Stampfer, M, Steiner-Wilke, I, Vollmer, B, Schulze, K, Briggs, T, Braden, R, Vogel, A, Thompson-Lake, D, Patel, C, Blair, E, Goel, H, Turner, S, Moog, U, Riess, A, Liegeois, F, Koolen, DA, Amor, DJ, Kleefstra, T, Fisher, SE, Zweier, C, Morgan, AT

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Genetic variants in the Fat and Obesity Associated (FTO) gene and risk of Alzheimer's disease von Reitz, Christiane, Tosto, Giuseppe, Mayeux, Richard, Luchsinger, Jose A

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Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults von Hofer, Edith, Roshchupkin, Gennady V., Adams, Hieab H. H., Knol, Maria J., Lin, Honghuang, Li, Shuo, Zare, Habil, Ahmad, Shahzad, Armstrong, Nicola J., Satizabal, Claudia L., Bernard, Manon, Bis, Joshua C., Gillespie, Nathan A., Luciano, Michelle, Mishra, Aniket, Scholz, Markus, Teumer, Alexander, Xia, Rui, Jian, Xueqiu, Mosley, Thomas H., Saba, Yasaman, Pirpamer, Lukas, Seiler, Stephan, Becker, James T., Carmichael, Owen, Rotter, Jerome I., Psaty, Bruce M., Lopez, Oscar L., Amin, Najaf, van der Lee, Sven J., Yang, Qiong, Himali, Jayandra J., Maillard, Pauline, Beiser, Alexa S., DeCarli, Charles, Karama, Sherif, Lewis, Lindsay, Harris, Mat, Bastin, Mark E., Deary, Ian J., Veronica Witte, A., Beyer, Frauke, Loeffler, Markus, Mather, Karen A., Schofield, Peter R., Thalamuthu, Anbupalam, Kwok, John B., Wright, Margaret J., Ames, David, Trollor, Julian, Jiang, Jiyang, Brodaty, Henry, Wen, Wei, Vernooij, Meike W., Hofman, Albert, Uitterlinden, André G., Niessen, Wiro J., Wittfeld, Katharina, Bülow, Robin, Völker, Uwe, Pausova, Zdenka, Bruce Pike, G., Maingault, Sophie, Crivello, Fabrice, Tzourio, Christophe, Amouyel, Philippe, Mazoyer, Bernard, Neale, Michael C., Franz, Carol E., Lyons, Michael J., Panizzon, Matthew S., Andreassen, Ole A., Dale, Anders M., Logue, Mark, Grasby, Katrina L., Jahanshad, Neda, Painter, Jodie N., Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P., Lind, Penelope A., Pizzagalli, Fabrizio, Stein, Jason L., Thompson, Paul M., Medland, Sarah E., Sachdev, Perminder S., Kremen, William S., Wardlaw, Joanna M., Villringer, Arno, van Duijn, Cornelia M., Grabe, Hans J., Longstreth, William T., Fornage, Myriam, Paus, Tomas, Debette, Stephanie, Ikram, M. Arfan, Schmidt, Helena, Schmidt, Reinhold, Seshadri, Sudha

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Children and adolescents are not small adults: toward a better understanding of multimorbidity in younger populations von van den Akker, Marjan, Dieckelmann, Mirjam, Hussain, Mohammad Akhtar, Bond-Smith, Daniela, Muth, Christiane, Pati, Sanghamitra, Saxena, Sonia, Silva, Desiree, Skoss, Rachel, Straker, Leon, Thompson, Sandra C., Katzenellenbogen, Judith M.

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A study of spin chemistry in weak magnetic fields von Thompson, J. M. T., Timmel, Christiane R., Henbest, Kevin B.

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Structure-Based Design of Potent and Orally Active Isoindolinone Inhibitors of MDM2-p53 Protein–Protein Interaction von Chessari, Gianni, Hardcastle, Ian R, Ahn, Jong Sook, Anil, Burcu, Anscombe, Elizabeth, Bawn, Ruth H, Bevan, Luke D, Blackburn, Timothy J, Buck, Ildiko, Cano, Celine, Carbain, Benoit, Castro, Juan, Cons, Ben, Cully, Sarah J, Endicott, Jane A, Fazal, Lynsey, Golding, Bernard T, Griffin, Roger J, Haggerty, Karen, Harnor, Suzannah J, Hearn, Keisha, Hobson, Stephen, Holvey, Rhian S, Howard, Steven, Jennings, Claire E, Johnson, Christopher N, Lunec, John, Miller, Duncan C, Newell, David R, Noble, Martin E. M, Reeks, Judith, Revill, Charlotte H, Riedinger, Christiane, St. Denis, Jeffrey D, Tamanini, Emiliano, Thomas, Huw, Thompson, Neil T, Vinković, Mladen, Wedge, Stephen R, Williams, Pamela A, Wilsher, Nicola E, Zhang, Bian, Zhao, Yan

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Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease von Serra, Eva Gonçalves, Schwerd, Tobias, Moutsianas, Loukas, Cavounidis, Athena, Fachal, Laura, Pandey, Sumeet, Kammermeier, Jochen, Croft, Nicholas M., Posovszky, Carsten, Rodrigues, Astor, Russell, Richard K., Barakat, Farah, Auth, Marcus K. H., Heuschkel, Robert, Zilbauer, Matthias, Fyderek, Krzysztof, Braegger, Christian, Travis, Simon P., Satsangi, Jack, Parkes, Miles, Thapar, Nikhil, Ferry, Helen, Matte, Julie C., Gilmour, Kimberly C., Wedrychowicz, Andrzej, Sullivan, Peter, Moore, Carmel, Sambrook, Jennifer, Ouwehand, Willem, Roberts, David, Danesh, John, Baeumler, Toni A., Fulga, Tudor A., Carrami, Eli M., Ahmed, Ahmed, Wilson, Rachel, Barrett, Jeffrey C., Elkadri, Abdul, Griffiths, Anne M., Snapper, Scott B., Shah, Neil, Muise, Aleixo M., Wilson, David C., Uhlig, Holm H., Anderson, Carl A.

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Children and adolescents are not small adults: toward a better understanding of multimorbidity in younger populations von van den Akker, Marjan, Dieckelmann, Mirjam, Hussain, Mohammad Akhtar, Bond-Smith, Daniela, Muth, Christiane, Pati, Sanghamitra, Saxena, Sonia, Silva, Desiree, Skoss, Rachel, Straker, Leon, Thompson, Sandra C, Katzenellenbogen, Judith M

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Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan von Hollis, Ben, Day, Felix R., Busch, Alexander S., Thompson, Deborah J., Soares, Ana Luiza G., Timmers, Paul R. H. J., Kwong, Alex, Easton, Doug F., Joshi, Peter K., Timpson, Nicholas J., Ong, Ken K., Perry, John R. B.

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Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia von Vijayakrishnan, Jayaram, Studd, James, Broderick, Peter, Kinnersley, Ben, Holroyd, Amy, Law, Philip J., Kumar, Rajiv, Allan, James M., Harrison, Christine J., Moorman, Anthony V., Vora, Ajay, Roman, Eve, Rachakonda, Sivaramakrishna, Kinsey, Sally E., Sheridan, Eamonn, Thompson, Pamela D., Irving, Julie A., Koehler, Rolf, Hoffmann, Per, Nöthen, Markus M., Heilmann-Heimbach, Stefanie, Jöckel, Karl-Heinz, Easton, Douglas F., Pharaoh, Paul D. P., Dunning, Alison M., Peto, Julian, Canzian, Frederico, Swerdlow, Anthony, Eeles, Rosalind A., Kote-Jarai, ZSofia, Muir, Kenneth, Pashayan, Nora, Greaves, Mel, Zimmerman, Martin, Bartram, Claus R., Schrappe, Martin, Stanulla, Martin, Hemminki, Kari, Houlston, Richard S.

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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders von Gillentine, Madelyn A, Wang, Tianyun, Hoekzema, Kendra, Rosenfeld, Jill, Liu, Pengfei, Guo, Hui, Kim, Chang N, De Vries, Bert B A, Vissers, Lisenka E L M, Nordenskjold, Magnus, Kvarnung, Malin, Lindstrand, Anna, Nordgren, Ann, Gecz, Jozef, Iascone, Maria, Cereda, Anna, Scatigno, Agnese, Maitz, Silvia, Zanni, Ginevra, Bertini, Enrico, Zweier, Christiane, Schuhmann, Sarah, Wiesener, Antje, Pepper, Micah, Panjwani, Heena, Torti, Erin, Abid, Farida, Anselm, Irina, Srivastava, Siddharth, Atwal, Paldeep, Bacino, Carlos A, Bhat, Gifty, Cobian, Katherine, Bird, Lynne M, Friedman, Jennifer, Wright, Meredith S, Callewaert, Bert, Petit, Florence, Mathieu, Sophie, Afenjar, Alexandra, Christensen, Celenie K, White, Kerry M, Elpeleg, Orly, Berger, Itai, Espineli, Edward J, Fagerberg, Christina, Brasch-Andersen, Charlotte, Hansen, Lars Kjærsgaard, Feyma, Timothy, Hughes, Susan, Thiffault, Isabelle, Sullivan, Bonnie, Yan, Shuang, Keller, Kory, Keren, Boris, Mignot, Cyril, Kooy, Frank, Meuwissen, Marije, Basinger, Alice, Kukolich, Mary, Philips, Meredith, Ortega, Lucia, Drummond-Borg, Margaret, Lauridsen, Mathilde, Sorensen, Kristina, Lehman, Anna, Lopez-Rangel, Elena, Levy, Paul, Lessel, Davor, Lotze, Timothy, Madan-Khetarpal, Suneeta, Sebastian, Jessica, Vento, Jodie, Vats, Divya, Benman, L Manace, Mckee, Shane, Mirzaa, Ghayda M, Muss, Candace, Pappas, John, Peeters, Hilde, Romano, Corrado, Elia, Maurizio, Galesi, Ornella, Simon, Marleen E H, van Gassen, Koen L I, Simpson, Kara, Stratton, Robert, Syed, Sabeen, Thevenon, Julien, Palafoll, Irene Valenzuela, Vitobello, Antonio, Bournez, Marie, Faivre, Laurence, Xia, Kun, Earl, Rachel K, Nowakowski, Tomasz, Bernier, Raphael A, Eichler, Evan E

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Action to Control Cardiovascular Risk in Diabetes (ACCORD) Trial: Design and Methods von Buse, John B., MD, PhD

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Common variants at 12q14 and 12q24 are associated with hippocampal volume von Bis, Joshua C, DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M, Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F J, DeStefano, Anita L, Lambert, Jean-Charles, Jack, Jr, Clifford R, Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A, Fleischman, Debra, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H, Enzinger, Christian, Danoy, Patrick, Amin, Najaf, Arfanakis, Konstantinos, van Buchem, Mark A, de Bruijn, Renée F A G, Beiser, Alexa, Dufouil, Carole, Huang, Juebin, Cavalieri, Margherita, Thomson, Russell, Niessen, Wiro J, Chibnik, Lori B, Gislason, Gauti K, Hofman, Albert, Pikula, Aleksandra, Amouyel, Philippe, Freeman, Kevin B, Phan, Thanh G, Oostra, Ben A, Stein, Jason L, Medland, Sarah E, Vasquez, Alejandro Arias, Hibar, Derrek P, Wright, Margaret J, Franke, Barbara, Martin, Nicholas G, Thompson, Paul M, Nalls, Michael A, Uitterlinden, Andre G, Au, Rhoda, Elbaz, Alexis, Beare, Richard J, van Swieten, John C, Lopez, Oscar L, Harris, Tamara B, Chouraki, Vincent, Breteler, Monique M B, De Jager, Philip L, Becker, James T, Vernooij, Meike W, Knopman, David, Fazekas, Franz, Wolf, Philip A, van der Lugt, Aad, Gudnason, Vilmundur, Longstreth, Jr, W T, Brown, Matthew A, Bennett, David A, van Duijn, Cornelia M, Mosley, Thomas H, Schmidt, Reinhold, Tzourio, Christophe, Launer, Lenore J, Ikram, M Arfan, Seshadri, Sudha

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De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay von Ha, Thoa, Morgan, Angela, Bartos, Meghan N., Beatty, Katelyn, Cogné, Benjamin, Braun, Dominique, Gerber, Céline B., Gaspar, Harald, Kopps, Anna M., Rieubland, Claudine, Hurst, Anna C. E., Amor, David J., Nizon, Mathilde, Pasquier, Laurent, Pfundt, Rolph, Reis, André, Siu, Victoria Mok, Tessarech, Marine, Thompson, Michelle L., Vincent, Marie, Vries, Bert B. A., Walsh, Matthew B., Wechsler, Stephanie Burns, Zweier, Christiane, Schnur, Rhonda E., Guillen Sacoto, Maria J., Margot, Henri, Masotto, Barbara, Palafoll, Maria Irene Valenzuela, Nawaz, Urwah, Voineagu, Irina, Slavotinek, Anne

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