Is the dark triad always detrimental to firm performance? Testing different performance outcomes and the moderating effects of competitive rivalry von Haar, Jarrod, de Jong, Kirsty

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Giving Science Innovation Systems a 'Nudge' von de Jong, Kirsty, Daellenbach, Urs, Davenport, Sally, Haar, Jarrod, Leitch, Shirley

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Computation-Aided Engineering of Cytochrome P450 for the Production of Pravastatin von Ashworth, Mark A., Bombino, Elvira, de Jong, René M., Wijma, Hein J., Janssen, Dick B., McLean, Kirsty J., Munro, Andrew W.

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Antimicrobial susceptibility monitoring of respiratory tract pathogens isolated from diseased cattle and pigs across Europe: The VetPath study von de Jong, Anno, Thomas, Valérie, Simjee, Shabbir, Moyaert, Hilde, El Garch, Farid, Maher, Kirsty, Morrissey, Ian, Butty, Pascal, Klein, Ulrich, Marion, Hervé, Rigaut, Delphine, Vallé, Michel

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Epidemiological investigation of foot-and-mouth disease outbreaks in a Vietnamese bear rescue centre von Ludi, Anna B, Baker, Hannah, Sanki, Rachel, De Jong, Rosanne M F, Maryan, Julie, Walker, Martin, King, Donald P, Gubbins, Simon, Limon, Georgina, Officer, Kirsty

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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Sound Change and Speaker Identity: An Acoustic Study von de Jong, Gea, McDougall, Kirsty, Nolan, Francis

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The International Bathymetric Chart of the Southern Ocean Version 2 (IBCSO v2) von Dorschel, Boris, Hehemann, Laura, Viquerat, Sacha, Warnke, Fynn, Dreutter, Simon, Schulze Tenberge, Yvonne, Accettella, Daniela, An, Lu, Barrios, Felipe, Bazhenova, Evgenia A, Black, Jenny, Bohoyo, Fernando, Davey, Craig, de Santis, Laura, Escutia Dotti, Carlota, Frémand, Alice C, Fretwell, Peter T, Gales, Jenny A, Gao, Jinyao, Gasperini, Luca, Greenbaum, Jamin S, Henderson Jencks, Jennifer, Hogan, Kelly A, Hong, Jong Kuk, Jakobsson, Martin, Jensen, Laura, Kool, Johnathan, Larin, Sergei, Larter, Robert D, Leitchenkov, German L, Loubrieu, Benoît, Mackay, Kevin, Mayer, Larry, Millan, Romain, Morlighem, Mathieu, Navidad, Francisco, Nitsche, Frank-Oliver, Nogi, Yoshifumi, Pertuisot, Cécile, Post, Alexandra L, Pritchard, Hamish D, Purser, Autun, Rebesco, Michele, Rignot, Eric, Roberts, Jason L, Rovere, Marzia, Ryzhov, Ivan, Sauli, Chiara, Schmitt, Thierry, Silvano, Alessandro, Smith, Jodie E, Snaith, Helen, Tate, Alex J, Tinto, Kirsty, Vandenbossche, Philippe, Weatherall, Pauline, Wintersteller, Paul, Yang, Chunguo, Zhang, Tao, Arndt, Jan Erik

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A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder von Casey, Jillian P

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