Plasma membrane nanodeformations promote actin polymerization through CIP4/CDC42 recruitment and regulate type II IFN signaling von Ledoux, Benjamin, Zanin, Natacha, Yang, Jinsung, Mercier, Vincent, Coster, Charlotte, Dupont-Gillain, Christine, Alsteens, David, Morsomme, Pierre, Renard, Henri-François

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Universal input device von Coster Charlotte, van Hengel Johan, Feiz Khodayar, Thong Jerry, Helwig Marten

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Keyboard von Jun Shu, Jasper Phua, Bril, Tom Michael, Feiz, Khodayar, Thong, Jerry, Helwig, Marten, Cathelijn Coster, Charlotte Alexandra, van Hengel, Johan, Brümmer, Bengt Gunnar

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Universal input device von FEIZ KHODAYAR, VAN HENGEL JOHAN, HELWIG MARTEN, THONG JERRY, COSTER CHARLOTTE

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Automatic Imitation: A Meta-Analysis von Cracco, Emiel, Bardi, Lara, Desmet, Charlotte, Genschow, Oliver, Rigoni, Davide, De Coster, Lize, Radkova, Ina, Deschrijver, Eliane, Brass, Marcel

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PAX5-ELN oncoprotein promotes multistep B-cell acute lymphoblastic leukemia in mice von Jamrog, Laura, Chemin, Guillaume, Fregona, Vincent, Coster, Lucie, Pasquet, Marlène, Oudinet, Chloé, Rouquié, Nelly, Prade, Naïs, Lagarde, Stéphanie, Cresson, Charlotte, Hébrard, Sylvie, Huu, Ngoc Sa Nguyen, Bousquet, Marina, Quelen, Cathy, Brousset, Pierre, Mancini, Stéphane J. C., Delabesse, Eric, Khamlichi, Ahmed Amine, Gerby, Bastien, Broccardo, Cyril

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Clinical, biochemical, and genetic spectrum of seven new patients with NFU1 deficiency von Uwe eAhting, Johannes A Mayr, Arnaud V Vanlander, Steven A Hardy, Saikat eSantra, Christine eMakowski, Charlotte L Alston, Franz A Zimmermann, Lucia eAbela, Barbara ePlecko, Marianne eRohrbach, Stephanie eSpranger, Sara eSeneka, Boris eRolinski, Angela eHagendorff, Maja eHempel, Wolfgang eSperl, Thomas eMeitinger, Thomas eMeitinger, Joél eSmet, Robert W Taylor, Rudy eVan Coster, Peter eFreisinger, Holger eProkisch, Holger eProkisch, Tobias Bernd Haack, Tobias Bernd Haack

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Clinical implementation of RNA sequencing for Mendelian disease diagnostics von Yépez, Vicente A, Gusic, Mirjana, Kopajtich, Robert, Mertes, Christian, Smith, Nicholas H, Alston, Charlotte L, Ban, Rui, Beblo, Skadi, Berutti, Riccardo, Blessing, Holger, Ciara, Elżbieta, Distelmaier, Felix, Freisinger, Peter, Häberle, Johannes, Hayflick, Susan J, Hempel, Maja, Itkis, Yulia S, Kishita, Yoshihito, Klopstock, Thomas, Krylova, Tatiana D, Lamperti, Costanza, Lenz, Dominic, Makowski, Christine, Mosegaard, Signe, Müller, Michaela F, Muñoz-Pujol, Gerard, Nadel, Agnieszka, Ohtake, Akira, Okazaki, Yasushi, Procopio, Elena, Schwarzmayr, Thomas, Smet, Joél, Staufner, Christian, Stenton, Sarah L, Strom, Tim M, Terrile, Caterina, Tort, Frederic, Van Coster, Rudy, Vanlander, Arnaud, Wagner, Matias, Xu, Manting, Fang, Fang, Ghezzi, Daniele, Mayr, Johannes A, Piekutowska-Abramczuk, Dorota, Ribes, Antonia, Rötig, Agnès, Taylor, Robert W, Wortmann, Saskia B, Murayama, Kei, Meitinger, Thomas, Gagneur, Julien, Prokisch, Holger

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Impact of Check of Medication Appropriateness (CMA) in optimizing analgesic prescribing: An interrupted time series analysis von Quintens, Charlotte, De Coster, Johan, Van der Linden, Lorenz, Morlion, Bart, Nijns, Egon, Van den Bosch, Bart, Peetermans, Willy E., Spriet, Isabel

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Impact of Check of Medication Appropriateness (CMA) in optimizing analgesic prescribing: An interrupted time series analysis von Quintens, Charlotte, De Coster, Johan, Van der Linden, Lorenz, Morlion, Bart, Nijns, Egon, Van den Bosch, Bart, Peetermans, Willy E, Spriet, Isabel

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Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype von Alston, Charlotte L., Compton, Alison G., Formosa, Luke E., Strecker, Valentina, Oláhová, Monika, Haack, Tobias B., Smet, Joél, Stouffs, Katrien, Diakumis, Peter, Ciara, Elżbieta, Cassiman, David, Romain, Nadine, Yarham, John W., He, Langping, De Paepe, Boel, Vanlander, Arnaud V., Seneca, Sara, Feichtinger, René G., Płoski, Rafal, Rokicki, Dariusz, Pronicka, Ewa, Haller, Ronald G., Van Hove, Johan L.K., Bahlo, Melanie, Mayr, Johannes A., Van Coster, Rudy, Prokisch, Holger, Wittig, Ilka, Ryan, Michael T., Thorburn, David R., Taylor, Robert W.

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Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective? von Repp, Birgit M, Mastantuono, Elisa, Alston, Charlotte L, Schiff, Manuel, Haack, Tobias B, Rötig, Agnes, Ardissone, Anna, Lombès, Anne, Catarino, Claudia B, Diodato, Daria, Schottmann, Gudrun, Poulton, Joanna, Burlina, Alberto, Jonckheere, An, Munnich, Arnold, Rolinski, Boris, Ghezzi, Daniele, Rokicki, Dariusz, Wellesley, Diana, Martinelli, Diego, Wenhong, Ding, Lamantea, Eleonora, Ostergaard, Elsebet, Pronicka, Ewa, Pierre, Germaine, Smeets, Hubert J M, Wittig, Ilka, Scurr, Ingrid, de Coo, Irenaeus F M, Moroni, Isabella, Smet, Joél, Mayr, Johannes A, Dai, Lifang, de Meirleir, Linda, Schuelke, Markus, Zeviani, Massimo, Morscher, Raphael J, McFarland, Robert, Seneca, Sara, Klopstock, Thomas, Meitinger, Thomas, Wieland, Thomas, Strom, Tim M, Herberg, Ulrike, Ahting, Uwe, Sperl, Wolfgang, Nassogne, Marie-Cecile, Ling, Han, Fang, Fang, Freisinger, Peter, Van Coster, Rudy, Strecker, Valentina, Taylor, Robert W, Häberle, Johannes, Vockley, Jerry, Prokisch, Holger, Wortmann, Saskia

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Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency von Ahting, Uwe, Mayr, Johannes A, Vanlander, Arnaud V, Hardy, Steven A, Santra, Saikat, Makowski, Christine, Alston, Charlotte L, Zimmermann, Franz A, Abela, Lucia, Plecko, Barbara, Rohrbach, Marianne, Spranger, Stephanie, Seneca, Sara, Rolinski, Boris, Hagendorff, Angela, Hempel, Maja, Sperl, Wolfgang, Meitinger, Thomas, Smet, Joél, Taylor, Robert W, Van Coster, Rudy, Freisinger, Peter, Prokisch, Holger, Haack, Tobias B

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Newborn Hearing Screening vs Later Hearing Screening and Developmental Outcomes in Children With Permanent Childhood Hearing Impairment von Korver, Anna M. H, Konings, Saskia, Dekker, Friedo W, Beers, Mieke, Wever, Capi C, Frijns, Johan H. M, Oudesluys-Murphy, Anne M, DECIBEL Collaborative Study Group, for the

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Tolerance to Water Stress and Shade in the Invasive Impatiens parviflora von Quinet, Muriel, Descamps, Charlotte, Coster, Quentin, Lutts, Stanley, Jacquemart, Anne-Laure, Mazer, Susan J.

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“Accelerated phase” chronic lymphocytic leukemia: Still an intermediate risk disease in the era of targeted therapies von Lapierre, Léopoldine, Syrykh, Charlotte, Largeaud, Laetitia, Cabarrou, Bastien, Filleron, Thomas, Oberic, Lucie, Kanoun, Salim, Coster, Lucie, Laurent, Camille, Branco, Benoît, Gadaud, Noémie, Récher, Christian, Brechemier, Delphine, Balardy, Laurent, Vergez, François, Ysebaert, Loïc, Gauthier, Martin

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Tolerance to Water Stress and Shade in the InvasiveImpatiens parviflora von Quinet, Muriel, Descamps, Charlotte, Coster, Quentin, Lutts, Stanley, Jacquemart, Anne-Laure

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Clinical implementation of RNA sequencing for Mendelian disease diagnostics von Yépez, Vincente A, Gusic, Mirjana, Kopajtich, Robert, Mertes, Christian, Smith, Nicholas H, Alston, Charlotte L, Ban, Rui, Beblo, Skadi, Berutti, Riccardo, Blessing, Holger, Ciara, Elzbieta, Distelmaier, Felix, Freisinger, Peter, Häberle, Johannes, Hayflick, Susan J, Hempel, Marja, Itkis, Yulia S, Kishita, Yoshihito, Klopstock, Thomas, Krylova, Tatiana D, Lamperti, Costanza, Lenz, Dominic, Makowski, Christine, Mosegaard, Signe, Müller, Michalea F, Muñoz-Pujol, Gerard, Nadel, Agnieszka, Ohtake, Akira, Okazaki, Yasushi, Procopio, Elena, Schwarzmayr, Thomas, Smet, Joél, Staufner, Christian, Stenton, Sarah L, Strom, Tim M, Terrile, Caterina, Tort, Frederic, Van Coster, Rudy, Vanlander, Arnaud, Wagner, Matias, Xu, Manting, Fang, Fang, Ghezzi, Daniele, Mayr, Johannes A, Piekutowska-Abramczuk, Dorota, Ribes, Antonia, Rötig, Agnès, Taylor, Robert W, Wortmann, Saskia B, Murayama, Kei, Meitinger, Thomas, Gagneur, Julien, Prokisch, Holger

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Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype von Alston, Charlotte L, Compton, Alison G, Formosa, Luke E, Strecker, Valentina, Oláhová, Monika, Haack, Tobias B, Smet, Joél, Stouffs, Katrien, Diakumis, Peter, Ciara, Elżbieta, Cassiman, David, Romain, Nadine, Yarham, John W, He, Langping, De Paepe, Boel, Vanlander, Arnaud V, Seneca, Sara, Feichtinger, René G, Płoski, Rafal, Rokicki, Dariusz, Pronicka, Ewa, Haller, Ronald G, Van Hove, Johan L.K, Bahlo, Melanie, Mayr, Johannes A, Van Coster, Rudy, Prokisch, Holger, Wittig, Ilka, Ryan, Michael T, Thorburn, David R, Taylor, Robert W

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Biallelic mutations in TMEM126B cause severe complex I deficiency with a variable clinical phenotype von Alston, Charlotte L, Compton, Alison G, Formosa, Luke E, Strecker, Valentina, Oláhová, Monika, Haack, Tobias B, Smet, Joél, Stouffs, Katrien, Diakumis, Peter, Ciara, Elżbieta, Cassiman, David, Romain, Nadine, Yarham, John W, He, Langping, De Paepe, Boel, Vanlander, Arnaud, Seneca, Sara, Feichtinger, René G, Płoski, Rafal, Rokicki, Dariusz, Pronicka, Ewa, Haller, Ronald G, Van Hove, Johan LK, Bahlo, Melanie, Mayr, Johannes A, Van Coster, Rudy, Prokisch, Holger, Wittig, Ilka, Ryan, Michael T, Thorburn, David R, Taylor, Robert W

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