Plasma ALS and Gal-3BP differentiate early from advanced liver fibrosis in MASLD patients by Pérez Compte, David, Etourneau, Lucas, Hesse, Anne-Marie, Kraut, Alexandra, Barthelon, Justine, Sturm, Nathalie, Borges, Hélène, Biennier, Salomé, Courçon, Marie, de Saint Loup, Marc, Mignot, Victoria, Costentin, Charlotte, Burger, Thomas, Couté, Yohann, Bruley, Christophe, Decaens, Thomas, Jaquinod, Michel, Boursier, Jérôme, Brun, Virginie

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FrzS acts as a polar beacon to recruit SgmX, a central activator of type IV pili during Myxococcus xanthus motility by Bautista, Sarah, Schmidt, Victoria, Guiseppi, Annick, Mauriello, Emillia M F, Attia, Bouchra, Elantak, Latifa, Mignot, Tâm, Mercier, Romain

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Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities by Carmignac, Virginie, Mignot, Cyril, Blanchard, Emmanuelle, Kuentz, Paul, Aubriot-Lorton, Marie-Hélène, Parker, Victoria E.R., Sorlin, Arthur, Fraitag, Sylvie, Courcet, Jean-Benoît, Duffourd, Yannis, Rodriguez, Diana, Knox, Rachel G., Polubothu, Satyamaanasa, Boland, Anne, Olaso, Robert, Delepine, Marc, Darmency, Véronique, Riachi, Melissa, Quelin, Chloé, Rollier, Paul, Goujon, Louise, Grotto, Sarah, Capri, Yline, Jacquemont, Marie-Line, Odent, Sylvie, Amram, Daniel, Chevarin, Martin, Vincent-Delorme, Catherine, Catteau, Benoît, Guibaud, Laurent, Arzimanoglou, Alexis, Keddar, Malika, Sarret, Catherine, Callier, Patrick, Bessis, Didier, Geneviève, David, Deleuze, Jean-François, Thauvin, Christel, Semple, Robert K., Philippe, Christophe, Rivière, Jean-Baptiste, Kinsler, Veronica A., Faivre, Laurence, Vabres, Pierre

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BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms by Barish, Scott, Barakat, Tahsin Stefan, Michel, Brittany C., Mashtalir, Nazar, Phillips, Jennifer B., Valencia, Alfredo M., Ugur, Berrak, Wegner, Jeremy, Scott, Tiana M., Bostwick, Brett, Murdock, David R., Dai, Hongzheng, Perenthaler, Elena, Nikoncuk, Anita, van Slegtenhorst, Marjon, Brooks, Alice S., Keren, Boris, Nava, Caroline, Mignot, Cyril, Douglas, Jessica, Rodan, Lance, Nowak, Catherine, Ellard, Sian, Stals, Karen, Lynch, Sally Ann, Faoucher, Marie, Lesca, Gaetan, Edery, Patrick, Engleman, Kendra L., Zhou, Dihong, Thiffault, Isabelle, Herriges, John, Gass, Jennifer, Louie, Raymond J., Stolerman, Elliot, Washington, Camerun, Vetrini, Francesco, Otsubo, Aiko, Pratt, Victoria M., Conboy, Erin, Treat, Kayla, Shannon, Nora, Camacho, Jose, Wakeling, Emma, Yuan, Bo, Chen, Chun-An, Rosenfeld, Jill A., Westerfield, Monte, Wangler, Michael, Yamamoto, Shinya, Kadoch, Cigall, Scott, Daryl A., Bellen, Hugo J.

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A molecular switch controls assembly of bacterial focal adhesions by Attia, Bouchra, My, Laetitia, Castaing, Jean Philippe, Dinet, Céline, Le Guenno, Hugo, Schmidt, Victoria, Espinosa, Leon, Anantharaman, Vivek, Aravind, L, Sebban-Kreuzer, Corinne, Nouailler, Matthieu, Bornet, Olivier, Viollier, Patrick, Elantak, Latifa, Mignot, Tâm

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Deep brain stimulation is effective in pediatric patients with GNAO1 associated severe hyperkinesia by Koy, Anne, Cirak, Sebahattin, Gonzalez, Victoria, Becker, Kerstin, Roujeau, Thomas, Milesi, Christophe, Baleine, Julien, Cambonie, Gilles, Boularan, Alain, Greco, Frederic, Perrigault, Pierre-Francois, Cances, Claude, Dorison, Nathalie, Doummar, Diane, Roubertie, Agathe, Beroud, Christophe, Körber, Friederike, Stüve, Burkhard, Waltz, Stephan, Mignot, Cyril, Nava, Caroline, Maarouf, Mohammad, Coubes, Philippe, Cif, Laura

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Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities by Carmignac, Virginie, Mignot, Cyril, Blanchard, Emmanuelle, Kuentz, Paul, Aubriot-Lorton, Marie-Hélène, Parker, Victoria E.R., Sorlin, Arthur, Fraitag, Sylvie, Courcet, Jean-Benoît, Duffourd, Yannis, Rodriguez, Diana, Knox, Rachel G., Polubothu, Satyamaanasa, Boland, Anne, Olaso, Robert, Delepine, Marc, Darmency, Véronique, Riachi, Melissa, Quelin, Chloé, Rollier, Paul, Goujon, Louise, Grotto, Sarah, Capri, Yline, Jacquemont, Marie-Line, Odent, Sylvie, Amram, Daniel, Chevarin, Martin, Vincent-Delorme, Catherine, Catteau, Benoît, Guibaud, Laurent, Arzimanoglou, Alexis, Keddar, Malika, Sarret, Catherine, Callier, Patrick, Bessis, Didier, Geneviève, David, Deleuze, Jean-François, Thauvin, Christel, Semple, Robert K., Philippe, Christophe, Rivière, Jean-Baptiste, Kinsler, Veronica A., Faivre, Laurence, Vabres, Pierre

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Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders by Aref-Eshghi, Erfan, Kerkhof, Jennifer, Pedro, Victor P., France, Groupe DI, Barat-Houari, Mouna, Ruiz-Pallares, Nathalie, Andrau, Jean-Christophe, Lacombe, Didier, Van-Gils, Julien, Fergelot, Patricia, Dubourg, Christéle, Cormier-Daire, Valerie, Rondeau, Sophie, Lecoquierre, François, Saugier-Veber, Pascale, Nicolas, Gaël, Lesca, Gaetan, Chatron, Nicolas, Sanlaville, Damien, Vitobello, Antonio, Faivre, Laurence, Thauvin-Robinet, Christel, Laumonnier, Frederic, Raynaud, Martine, Alders, Mariëlle, Mannens, Marcel, Henneman, Peter, Hennekam, Raoul C., Velasco, Guillaume, Francastel, Claire, Ulveling, Damien, Ciolfi, Andrea, Pizzi, Simone, Tartaglia, Marco, Heide, Solveig, Héron, Delphine, Mignot, Cyril, Keren, Boris, Whalen, Sandra, Afenjar, Alexandra, Bienvenu, Thierry, Campeau, Philippe M., Rousseau, Justine, Levy, Michael A., Brick, Lauren, Kozenko, Mariya, Balci, Tugce B., Siu, Victoria Mok, Stuart, Alan, Kadour, Mike, Masters, Jennifer, Takano, Kyoko, Kleefstra, Tjitske, de Leeuw, Nicole, Field, Michael, Shaw, Marie, Gecz, Jozef, Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Friez, Michael J., Tedder, Matt, Lee, Jennifer A., DuPont, Barbara R., Stevenson, Roger E., Skinner, Steven A., Schwartz, Charles E., Genevieve, David, Sadikovic, Bekim

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Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmentalabnormalities by Carmignac Virginie, Mignot Cyril, Blanchard, Emmanuelle, Kuentz, Paul, Marie-Hélène, Aubriot-Lorton, Parker, Victoria E, Sorlin Arthur, Fraitag Sylvie, Jean-Benoît, Courcet, Duffourd Yannis, Rodriguez, Diana, Knox, Rachel G, Satyamaanasa, Polubothu, Boland, Anne, Olaso, Robert, Delepine, Marc, Darmency Véronique, Riachi, Melissa, Quelin Chloé, Rollier, Paul, Goujon Louise, Grotto, Sarah, Capri Yline, Marie-Line, Jacquemont, Odent Sylvie, Amram, Daniel, Chevarin Martin, Vincent-Delorme, Catherine, Catteau Benoît, Guibaud Laurent, Arzimanoglou Alexis, Keddar Malika, Sarret, Catherine, Callier, Patrick, Bessis Didier, David, Geneviève, Deleuze Jean-François, Thauvin Christel, Semple, Robert K, Christophe, Philippe, Rivière Jean-Baptiste, Kinsler, Veronica A, Faivre, Laurence, Vabres Pierre

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Protective association of HLA‐DRB1 04 subtypes in neurodegenerative diseases implicates acetylated tau PHF6 sequences by Guen, Yann Le, Luo, Guo, Ambati, Aditya, Damotte, Vincent, Jansen, Iris E, Nicolas, Aude, de Rojas, Itziar, Leal, Thiago Peixoto, Miyashita, Akinori, Bellenguez, Céline, Lian, Michelle Mulan, Parveen, Kayenat, Grenier‐Boley, Benjamin, Naito, Tatsuhiko, Küçükali, Fahri, Talyansky, Seth D., Yogeshwar, Selina Marie, Sempere, Vicente, Satake, Wataru, Álvarez‐Martínez, Victoria, Belloy, Michael E, Benussi, Luisa, Borroni, Barbara, Bullido, María J., Clarimon, Jordi, Daniele, Antonio, Darling, Daniel, During, Emmanuel, Duzel, Emrah, Galimberti, Daniela, García‐Ribas, Guillermo, García‐González, Pablo, Giedraitis, Vilmantas, Goldhardt, Oliver, Graff, Caroline, Grunblatt, Edna, Hausner, Lucrezia, Heilmann‐Heimbach, Stefanie, Holstege, Henne, Hort, Jakub, Jung, Yoo Jin, Jurgen, Deckert, Kern, Silke, Kuulasmaa, Teemu, Lee, Kun Ho, Ling, Ling, Masullo, Carlo, Mecocci, Patrizia, Mehrabian, Shima, de Mendonça, Alexandre, Mir, Pablo, Moebus, Susanne, Moreno, Fermin, Nacmias, Benedetta, Nicolas, Gaël, Niida, Shumpei, Papenberg, Goran, Papma, Janne M., Peters, Oliver, Pijnenburg, Yolande A.L., Piñol‐Ripoll, Gerard, Popp, Julius, Pérez‐Tur, Jordi, Real, Luis Miguel, Riedel‐Heller, Steffi G., Rodríguez, Eloy Rodríguez, Royo, José Luís, Scarmeas, Nikolaos, Scherbaum, Norbert, Schneider, Anja, Skoog, Ingmar, Solfrizzi, Vincenzo, Squassina, Alessio, van Swieten, John C, Sanchez‐Valle, Raquel, Tan, Eng‐King, Tegos, Thomas, Teunissen, Charlotte E., Thomassen, Jesper Qvist, Tremolizzo, Lucio, Vyhnalek, Martin, Wiltfang, Jens, Zhang, Jing, Zetterberg, Henrik, Blennow, Kaj, Williams, Julie, Amouyel, Philippe, Jessen, Frank, Andreassen, Ole, Frikke‐Schmidt, Ruth, Sleegers, Kristel, Toda, Tatsushi, Zettergren, Anna, Ingelsson, Martin, Okada, Yukinori, Hiltunen, Mikko, Gim, Jungsoo, van der Flier, Wiesje M., Greicius, Michael D, Mignot, Emmanuel

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Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish by Patterson, Victoria, Ullah, Farid, Bryant, Laura, Griffin, John N, Sidhu, Alpa, Saliganan, Sheila, Blaile, Mackenzie, Saenz, Margarita S, Smith, Rosemarie, Ellingwood, Sara, Grange, Dorothy K, Hu, Xuyun, Mireguli, Maimaiti, Luo, Yanfei, Shen, Yiping, Mulhern, Maureen, Zackai, Elaine, Ritter, Alyssa, Izumi, Kosaki, Hoefele, Julia, Wagner, Matias, Riedhammer, Korbinian M, Seitz, Barbara, Robin, Nathaniel H, Goodloe, Dana, Mignot, Cyril, Keren, Boris, Cox, Helen, Jarvis, Joanna, Hempel, Maja, Gibson, Cynthia Forster, Tran Mau-Them, Frederic, Vitobello, Antonio, Bruel, Ange-Line, Sorlin, Arthur, Mehta, Sarju, Raymond, F Lucy, Gilmore, Kelly, Powell, Bradford C, Weck, Karen, Li, Chumei, Vulto-van Silfhout, Anneke T, Giacomini, Thea, Mancardi, Maria Margherita, Accogli, Andrea, Salpietro, Vincenzo, Zara, Federico, Vora, Neeta L, Davis, Erica E, Burdine, Rebecca, Bhoj, Elizabeth

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