Burden of comorbidities: Osteoporotic vertebral fracture during non-small cell lung cancer - the BONE study von Ebstein, E., Brocard, P., Soussi, G., Khoury, R., Forien, M., Khalil, A., Vauchier, C., Juge, P.A., Léger, B., Ottaviani, S., Dieudé, P., Zalcman, G., Gounant, V.

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Incidence and severeness of COVID-19 hospitalization in patients with inflammatory rheumatic disease: a nationwide cohort study from Denmark von Cordtz, René, Lindhardsen, Jesper, Soussi, Bolette G, Vela, Jonathan, Uhrenholt, Line, Westermann, Rasmus, Kristensen, Salome, Nielsen, Henrik, Torp-Pedersen, Christian, Dreyer, Lene

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Temporal trends in mortality in patients with rheumatoid arthritis: a Danish population-based matched cohort study von Soussi, Bolette G, Duch, Kirsten, Cordtz, René L, Lindhardsen, Jesper, Kristensen, Salome, Bork, Christian S, Linauskas, Asta, Schmidt, Erik B, Dreyer, Lene

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EP01.01-16 Osteoporotic Vertebral Fractures in Non-small Cell Lung Cancer: A Cracking Connection von Soussi, G., Ebstein, E., Brocard, P., Khoury, R., Zalcman, G., Dieudé, P., Gounant, V.

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EP06.03-15 Predicting ROS1 Fusions and Targetable Mutations in Non-small Cell Lung Cancer through H-score Pathological Analysis von Soussi, G., Hercent, A., Gounant, V., Lupo, A., Cazes, A., Lamoril, J., Guyard, A., Théou-Anton, N.

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Maladie d’Addison rentrant dans le cadre d’un syndrome parathymique von Soussi, G, Aydi, Z, Ben Dhaou, B, Baili, L, Boussema, F, Rokbani, L

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Incidence and severeness of COVID-19 hospitalization in patients with inflammatory rheumatic disease: a nationwide cohort study from Denmark von Cordtz, Rene, Lindhardsen, Jesper, Soussi, Bolette G., Vela, Jonathan, Uhrenholt, Line, Westermann, Rasmus, Kristensen, Salome, Nielsen, Henrik, Torp-Pedersen, Christian, Dreyer, Lene

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Prévalence des fractures vertébrales ostéoporotiques au cours du Cancers Bronchique Non à Petites Cellules (CBNPC) : analyse d’une cohorte de 289 patients von Ebstein, E., Brocard, P., Soussi, G., Khoury, R., Bizot, A., Juge, P.A., Léger, B., Forien, M., Vauchier, C., Ottaviani, S., Zalcman, G., Dieudé, P., Gounant, V.

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Tamponnade et myocardite aiguë au cours d’un syndrome de Churg-Strauss von Baili, L., Aydi, Z., Soussi, G., Ben Dhaou B, B., Zidi, A., Berraies, A., Boussema, F., Kammoun, S., Hamzaoui, A., Kraiem, S., Ben Miled M’rad, K., Rokbani, L.

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TP53: an oncogene in disguise von Soussi, T, Wiman, K G

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Shaping Genetic Alterations in Human Cancer: The p53 Mutation Paradigm von Soussi, Thierry, Wiman, Klas G.

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Identification of cancer sex-disparity in the functional integrity of p53 and its X chromosome network von Haupt, Sue, Caramia, Franco, Herschtal, Alan, Soussi, Thierry, Lozano, Guillermina, Chen, Hu, Liang, Han, Speed, Terence P., Haupt, Ygal

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Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene von Doffe, Flora, Carbonnier, Vincent, Tissier, Manon, Leroy, Bernard, Martins, Isabelle, Mattsson, Johanna S. M., Micke, Patrick, Pavlova, Sarka, Pospisilova, Sarka, Smardova, Jana, Joerger, Andreas C., Wiman, Klas G., Kroemer, Guido, Soussi, Thierry

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p53 mutation heterogeneity in cancer von Soussi, T., Lozano, G.

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ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia—update on methodological approaches and results interpretation von Malcikova, J., Tausch, E., Rossi, D., Sutton, L. A., Soussi, T., Zenz, T., Kater, A. P., Niemann, C. U., Gonzalez, D., Davi, F., Gonzalez Diaz, M., Moreno, C., Gaidano, G., Stamatopoulos, K., Rosenquist, R., Stilgenbauer, S., Ghia, P., Pospisilova, S.

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TP53 Mutations in Human Cancer: Database Reassessment and Prospects for the Next Decade von Soussi, Thierry

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Mutations in TP53 are exclusively associated with del(17p) in multiple myeloma von LODE, Laurence, EVEILLARD, Marion, GUILHOT, François, CAILLOT, Denis, MARIT, Gérald, MATHIOT, Claire, FACON, Thierry, ATTAL, Michel, HAROUSSEAU, Jean-Luc, MOREAU, Philippe, MINVIELLE, Stéphane, AVET-LOISEAU, Hervé, TRICHET, Valérie, SOUSSI, Thierry, WUILLEME, Soraya, RICHEBOURG, Steven, MAGRANGEAS, Florence, IFRAH, Norbert, CAMPION, Loic, TRAULLE, Catherine

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Evolutionary history of the p53 family DNA-binding domain: insights from an Alvinella pompejana homolog von Zhang, Qiang, Balourdas, Dimitrios-Ilias, Baron, Bruno, Senitzki, Alon, Haran, Tali E., Wiman, Klas G., Soussi, Thierry, Joerger, Andreas C.

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Fam83F induces p53 stabilisation and promotes its activity von Salama, Mohammed, Benitez-Riquelme, Diego, Elabd, Seham, Munoz, Leonel, Zhang, Ping, Glanemann, Matthias, Mione, Maria Caterina, Goldin, Robert, Soussi, Thierry, Davidson, Gary, Blattner, Christine

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Mutations in HECW2 are associated with intellectual disability and epilepsy von Halvardson, Jonatan, Zhao, Jin J, Zaghlool, Ammar, Wentzel, Christian, Georgii-Hemming, Patrik, Månsson, Else, Ederth Sävmarker, Helena, Brandberg, Göran, Soussi Zander, Cecilia, Thuresson, Ann-Charlotte, Feuk, Lars

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