MITF reprograms the extracellular matrix and focal adhesion in melanoma von Dilshat, Ramile, Fock, Valerie, Kenny, Colin, Gerritsen, Ilse, Lasseur, Romain Maurice Jacques, Travnickova, Jana, Eichhoff, Ossia M., Cerny, Philipp, Moller, Katrin, Sigurbjornsdottir, Sara, Kirty, Kritika, Einarsdottir, Berglind Osk, Cheng, Phil F., Levesque, Mitchell, Cornell, Robert A., Patton, E. Elizabeth, Larue, Lionel, de Tayrac, Marie, Magnusdottir, Erna, Ogmundsdottir, Margret Helga, Steingrimsson, Eirikur

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DNA methylation in glioblastoma: impact on gene expression and clinical outcome von Etcheverry, Amandine, Aubry, Marc, de Tayrac, Marie, Vauleon, Elodie, Boniface, Rachel, Guenot, Frederique, Saikali, Stephan, Hamlat, Abderrahmane, Riffaud, Laurent, Menei, Philippe, Quillien, Veronique, Mosser, Jean

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Du cyclope à la réalité: Un nouveau regard sur la génétique de l’holoprosencéphalie von Dupé, Valérie, Dubourg, Christèle, de Tayrac, Marie, David, Véronique

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Automated Analysis of 1p/19q Status by FISH in Oligodendroglial Tumors: Rationale and Proposal of an Algorithm von Duval, Céline, de Tayrac, Marie, Michaud, Karine, Cabillic, Florian, Paquet, Claudie, Gould, Peter Vincent, Saikali, Stéphan

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Contribution of 1p, 19q, 9p and 10q Automated Analysis by FISH to the Diagnosis and Prognosis of Oligodendroglial Tumors According to WHO 2016 Guidelines von Michaud, Karine, de Tayrac, Marie, D'Astous, Myreille, Duval, Céline, Paquet, Claudie, Samassekou, Oumar, Gould, Peter Vincent, Saikali, Stéphan

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Implementation of a molecular tumor board at a regional level to improve access to targeted therapy von Bourien, Héloïse, Lespagnol, Alexandra, Campillo-Gimenez, Boris, Felten-Vinot, Ingrid, Metges, Jean-Philippe, Corre, Romain, Lesimple, Thierry, le Marechal, Cédric, Boussemart, Lise, Kammerer-Jacquet, Solène-Florence, le Gall, Edouard, Denoual, Florent, de Tayrac, Marie, Galibert, Marie-Dominique, Mosser, Jean, Edeline, Julien

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ImmunoFISH is a reliable technique for the assessment of 1p and 19q status in oligodendrogliomas von Duval, Céline, de Tayrac, Marie, Sanschagrin, François, Michaud, Karine, Gould, Peter Vincent, Saikali, Stéphan

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GNPAT Variant associated with severe iron overload in HFE hemochromatosis von Bardou‐Jacquet, Edouard, de Tayrac, Marie, Mosser, Jean, Deugnier, Yves

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Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway von Dubourg, Christèle, Carré, Wilfrid, Hamdi-Rozé, Houda, Mouden, Charlotte, Roume, Joëlle, Abdelmajid, Benmansour, Amram, Daniel, Baumann, Clarisse, Chassaing, Nicolas, Coubes, Christine, Faivre-Olivier, Laurence, Ginglinger, Emmanuelle, Gonzales, Marie, Levy-Mozziconacci, Annie, Lynch, Sally-Ann, Naudion, Sophie, Pasquier, Laurent, Poidvin, Amélie, Prieur, Fabienne, Sarda, Pierre, Toutain, Annick, Dupé, Valérie, Akloul, Linda, Odent, Sylvie, de Tayrac, Marie, David, Véronique

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Characterizing the peritumoral brain zone in glioblastoma: a multidisciplinary analysis von Lemée, Jean-Michel, Clavreul, Anne, Aubry, Marc, Com, Emmanuelle, de Tayrac, Marie, Eliat, Pierre-Antoine, Henry, Cécile, Rousseau, Audrey, Mosser, Jean, Menei, Philippe

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Five distinct biological processes and 14 differentially expressed genes characterize TEL/AML1-positive leukemia von Gandemer, Virginie, Rio, Anne-Gaëlle, de Tayrac, Marie, Sibut, Vonnick, Mottier, Stéphanie, Ly Sunnaram, Béatrice, Henry, Catherine, Monnier, Annabelle, Berthou, Christian, Le Gall, Edouard, Le Treut, André, Schmitt, Claudine, Le Gall, Jean-Yves, Mosser, Jean, Galibert, Marie-Dominique

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Depicting the genetic architecture of pediatric cancers through an integrative gene network approach von Savary, Clara, Kim, Artem, Lespagnol, Alexandra, Gandemer, Virginie, Pellier, Isabelle, Andrieu, Charlotte, Pagès, Gilles, Galibert, Marie-Dominique, Blum, Yuna, de Tayrac, Marie

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Disrupted Hypothalamo-Pituitary Axis in Association With Reduced SHH Underlies the Pathogenesis of NOTCH-Deficiency von Hamdi-Rozé, Houda, Ware, Michelle, Guyodo, Hélène, Rizzo, Aurélie, Ratié, Leslie, Rupin, Maïlys, Carré, Wilfrid, Kim, Artem, Odent, Sylvie, Dubourg, Christèle, David, Véronique, de Tayrac, Marie, Dupé, Valérie

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A framework for validating AI in precision medicine: considerations from the European ITFoC consortium von Tsopra, Rosy, Fernandez, Xose, Luchinat, Claudio, Alberghina, Lilia, Lehrach, Hans, Vanoni, Marco, Dreher, Felix, Sezerman, O. Ugur, Cuggia, Marc, de Tayrac, Marie, Miklasevics, Edvins, Itu, Lucian Mihai, Geanta, Marius, Ogilvie, Lesley, Godey, Florence, Boldisor, Cristian Nicolae, Campillo-Gimenez, Boris, Cioroboiu, Cosmina, Ciusdel, Costin Florian, Coman, Simona, Cubelos, Oliver Hijano, Itu, Alina, Lange, Bodo, Le Gallo, Matthieu, Lespagnol, Alexandra, Mauri, Giancarlo, Soykam, H. Okan, Rance, Bastien, Turano, Paola, Tenori, Leonardo, Vignoli, Alessia, Wierling, Christoph, Benhabiles, Nora, Burgun, Anita

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Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis von de Tayrac, Marie, Roth, Marie-Paule, Jouanolle, Anne-Marie, Coppin, Hélène, le Gac, Gérald, Piperno, Alberto, Férec, Claude, Pelucchi, Sara, Scotet, Virginie, Bardou-Jacquet, Edouard, Ropert, Martine, Bouvet, Régis, Génin, Emmanuelle, Mosser, Jean, Deugnier, Yves

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Simultaneous analysis of distinct Omics data sets with integration of biological knowledge: Multiple Factor Analysis approach von de Tayrac, Marie, Lê, Sébastien, Aubry, Marc, Mosser, Jean, Husson, François

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Impact of 9p deletion and p16, Cyclin D1, and Myc hyperexpression on the outcome of anaplastic oligodendrogliomas von Michaud, Karine, de Tayrac, Marie, D'Astous, Myreille, Paquet, Claudie, Gould, Peter Vincent, Saikali, Stéphan

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Prognostic significance of EDN/RB, HJURP, p60/CAF-1 and PDLI4, four new markers in high-grade gliomas von de Tayrac, Marie, Saikali, Stephan, Aubry, Marc, Bellaud, Pascale, Boniface, Rachel, Quillien, Véronique, Mosser, Jean

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Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings von Mouden, Charlotte, de Tayrac, Marie, Dubourg, Christèle, Rose, Sophie, Carré, Wilfrid, Hamdi-Rozé, Houda, Babron, Marie-Claude, Akloul, Linda, Héron-Longe, Bénédicte, Odent, Sylvie, Dupé, Valérie, Giet, Régis, David, Véronique

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IGHV segment utilization in immunoglobulin gene rearrangement differentiates patients with anti-myelin-associated glycoprotein neuropathy from others immunoglobulin M-gammopathies von Allain, Jean-Sebastien, Thonier, Florian, Pihan, Morgane, Boulland, Marie-Laure, de Guibert, Sophie, Launay, Vincent, Doncker, Anne-Violaine, Ganard, Michel, Aliouat, Amyra, Pangault, Céline, Houot, Roch, De Tayrac, Marie, Lamy, Thierry, Roussel, Mikael, Fest, Thierry, Decaux, Olivier, Pastoret, Cedric

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