Morphological responses of Pinus laricio in Corsican island to prescribed burning von Cannac, M., Syx, G., Voron, E., Ferrat, L., Santoni, P.-A., Planelles, G., Pasqualini, V.

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Kinetics of Xist -induced gene silencing can be predicted from combinations of epigenetic and genomic features von Barros de Andrade E Sousa, Lisa, Jonkers, Iris, Syx, Laurène, Dunkel, Ilona, Chaumeil, Julie, Picard, Christel, Foret, Benjamin, Chen, Chong-Jian, Lis, John T, Heard, Edith, Schulz, Edda G, Marsico, Annalisa

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Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa von Van Damme, Tim, Gardeitchik, Thatjana, Mohamed, Miski, Guerrero-Castillo, Sergio, Freisinger, Peter, Guillemyn, Brecht, Kariminejad, Ariana, Dalloyaux, Daisy, van Kraaij, Sanne, Lefeber, Dirk J., Syx, Delfien, Steyaert, Wouter, De Rycke, Riet, Hoischen, Alexander, Kamsteeg, Erik-Jan, Wong, Sunnie Y., van Scherpenzeel, Monique, Jamali, Payman, Brandt, Ulrich, Nijtmans, Leo, Korenke, G. Christoph, Chung, Brian H.Y., Mak, Christopher C.Y., Hausser, Ingrid, Kornak, Uwe, Fischer-Zirnsak, Björn, Strom, Tim M., Meitinger, Thomas, Alanay, Yasemin, Utine, Gulen E., Leung, Peter K.C., Ghaderi-Sohi, Siavash, Coucke, Paul, Symoens, Sofie, De Paepe, Anne, Thiel, Christian, Haack, Tobias B., Malfait, Fransiska, Morava, Eva, Callewaert, Bert, Wevers, Ron A.

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Relative calibration of the LIGO and Virgo detectors using astrophysical events from their third observing run von Alléné, C, Andres, N, Assiduo, M, Aubin, F, Buskulic, D, Chierici, R, Estevez, D, Faedi, F, Guidi, G M, Juste, V, Marion, F, Mours, B, Nitoglia, E, Sordini, V, Syx, A

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Prognostic value of tumor mutational burden in patients with oral cavity squamous cell carcinoma treated with upfront surgery von Moreira, A., Poulet, A., Masliah-Planchon, J., Lecerf, C., Vacher, S., Larbi Chérif, L., Dupain, C., Marret, G., Girard, E., Syx, L., Hoffmann, C., Jeannot, E., Klijanienko, J., Guillou, I., Mariani, O., Dubray-Vautrin, A., Badois, N., Lesnik, M., Choussy, O., Calugaru, V., Borcoman, E., Baulande, S., Legoix, P., Albaud, B., Servant, N., Bieche, I., Le Tourneau, C., Kamal, M.

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Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa von Van Damme, Tim, Gardeitchik, Thatjana, Mohamed, Miski, Guerrero-Castillo, Sergio, Freisinger, Peter, Guillemyn, Brecht, Kariminejad, Ariana, Dalloyaux, Daisy, van Kraaij, Sanne, Lefeber, Dirk J., Syx, Delfien, Steyaert, Wouter, De Rycke, Riet, Hoischen, Alexander, Kamsteeg, Erik-Jan, Wong, Sunnie Y., van Scherpenzeel, Monique, Jamali, Payman, Brandt, Ulrich, Nijtmans, Leo, Korenke, G. Christoph, Chung, Brian H.Y., Mak, Christopher C.Y., Hausser, Ingrid, Kornak, Uwe, Fischer-Zirnsak, Björn, Strom, Tim M., Meitinger, Thomas, Alanay, Yasemin, Utine, Gulen E., Leung, Kai Ching Peter, Ghaderi-Sohi, Siavash, Coucke, Paul, Symoens, Sofie, De Paepe, Anne, Thiel, Christian, Haack, Tobias B., Malfait, Fransiska, Morava, Eva, Callewaert, Bert, Wevers, Ron A.

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Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa von Van Damme, Tim, Gardeitchik, Thatjana, Mohamed, Miski, Guerrero-Castillo, Sergio, Freisinger, Peter, Guillemyn, Brecht, Kariminejad, Ariana, Dalloyaux, Daisy, van Kraaij, Sanne, Lefeber, Dirk J, Syx, Delfien, Steyaert, Wouter, De Rycke, Riet, Hoischen, Alexander, Kamsteeg, Erik-Jan, Wong, Sunnie Y, van Scherpenzeel, Monique, Jamali, Payman, Brandt, Ulrich, Nijtmans, Leo, Korenke, G. Christoph, Chung, Brian H.Y, Mak, Christopher C.Y, Hausser, Ingrid, Kornak, Uwe, Fischer-Zirnsak, Björn, Strom, Tim M, Meitinger, Thomas, Alanay, Yasemin, Utine, Gulen E, Leung, Peter K.C, Ghaderi-Sohi, Siavash, Coucke, Paul, Symoens, Sofie, De Paepe, Anne, Thiel, Christian, Haack, Tobias B, Malfait, Fransiska, Morava, Eva, Wevers, Ron A, Callewaert, Bert

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Relative calibration of the LIGO and Virgo detectors using astrophysical events from their third observing run von Alléné, C, Andres, N, Assiduo, M, Aubin, F, Buskulic, D, Chierici, R, Estevez, D, Faedi, F, Guidi, G M, Juste, V, Marion, F, Mours, B, Nitoglia, E, Sordini, V, Syx, A

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Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14) von Minatogawa, M., Unzaki, A., Morisaki, H., Syx, D., Sonoda, T., Janecke, A.R., Slavotinek, A., Voermans, N.C., Lacassie, Y., Mendoza-Londono, R., Wierenga, K.J., Jayakar, P., Gahl, W.A., Tifft, C.J., Figuera, L.E., Hilhorst-Hofstee, Y., Maugeri, A., Ishikawa, K., Kobayashi, T., Aoki, Y., Ohura, T., Kawame, H., Kono, M., Mochida, K., Tokorodani, C., Kikkawa, K., Morisaki, T., Nakane, T., Kubo, A., Ranells, J.D., Migita, O., Sobey, G., Kaur, A., Ishikawa, M., Yamaguchi, T., Matsumoto, N., Malfait, F., Miyake, N., Kosho, T.

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