Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families von Osher, D J, De Leeneer, K, Michils, G, Hamel, N, Tomiak, E, Poppe, B, Leunen, K, Legius, E, Shuen, A, Smith, E, Arseneau, J, Tonin, P, Matthijs, G, Claes, K, Tischkowitz, M D, Foulkes, W D

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Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testing von De Leeneer, K., Van Bockstal, M., De Brouwer, S., Swietek, N., Schietecatte, P., Sabbaghian, N., Van den Ende, J., Willocx, S., Storm, K., Blaumeiser, B., Van Asperen, C. J., Wijnen, J. T., Leunen, K., Legius, E., Michils, G., Matthijs, G., Blok, M. J., Gomez-Garcia, E., De Paepe, A., Tischkowitz, M., Poppe, B., Claes, K.

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Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk... von Garcia-Pelaez, José, Barbosa-Matos, Rita, Lobo, Silvana, Dias, Alexandre, Garrido, Luzia, Castedo, Sérgio, Sousa, Sónia, Pinheiro, Hugo, Sousa, Liliana, Monteiro, Rita, Maqueda, Joaquin J, Fernandes, Susana, Carneiro, Fátima, Pinto, Nádia, Lemos, Carolina, Pinto, Carla, Teixeira, Manuel R, Aretz, Stefan, Bajalica-Lagercrantz, Svetlana, Balmaña, Judith, Blatnik, Ana, Benusiglio, Patrick R, Blanluet, Maud, Bours, Vincent, Brems, Hilde, Brunet, Joan, Calistri, Daniele, Capellá, Gabriel, Carrera, Sergio, Colas, Chrystelle, Dahan, Karin, de Putter, Robin, Desseignés, Camille, Domínguez-Garrido, Elena, Egas, Conceição, Evans, D Gareth, Feret, Damien, Fewings, Eleanor, Fitzgerald, Rebecca C, Coulet, Florence, Garcia-Barcina, María, Genuardi, Maurizio, Golmard, Lisa, Hackmann, Karl, Hanson, Helen, Holinski-Feder, Elke, Hüneburg, Robert, Krajc, Mateja, Lagerstedt-Robinson, Kristina, Lázaro, Conxi, Ligtenberg, Marjolijn J L, Martínez-Bouzas, Cristina, Merino, Sonia, Michils, Geneviève, Novaković, Srdjan, Patiño-García, Ana, Ranzani, Guglielmina Nadia, Schröck, Evelin, Silva, Inês, Silveira, Catarina, Soto, José L, Spier, Isabel, Steinke-Lange, Verena, Tedaldi, Gianluca, Tejada, María-Isabel, Woodward, Emma R, Tischkowitz, Marc, Hoogerbrugge, Nicoline, Oliveira, Carla

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Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor) von TEJPAR, S, NOLLET, F, ALMAN, B. A, LI, C, WUNDER, J. S, MICHILS, G, CIN, P. D, VAN CUTSEM, E, BAPAT, B, VAN ROY, F, CASSIMAN, J. J

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Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk... von Garcia-Pelaez, J, Barbosa-Matos, R, Lobo, S, Dias, A, Garrido, L, Castedo, S, Sousa, SP, Pinheiro, H, Sousa, L, Monteiro, AR, Maqueda, J, Fernandes, S, Carneiro, F, Pinto, N, Lemos, C, Pinto, C, Teixeira, M, Aretz, S, Lagercrantz, SB, Balmana, J, Blatnik, A, Benusiglio, P, Blanluet, M, Bours, V, Brems, H, Brunet, J, Calistri, D, Capella, G, Revilla, SC, Colas, C, Dahan, K, de Putter, R, Desseignes, C, Dominguez-Garrido, E, Egas, C, Evans, G, Feret, D, Fewings, E, Fitzgerald, R, Coulet, F, Garcia-Barcina, M, Genuardi, M, Lisa, G, Hackmann, K, Hanson, H, Holinski-Feder, E, Huneburg, R, Krajc, M, Lagerstedt-Robinson, K, Lazaro, C, Ligtenberg, M, Bouzas, MCM, Merino, S, Michils, G, Novakovic, S, Patino, A, Ranzani, G, Schrock, E, Silva, I, Silveira, C, Soto, JL, Spier, I, Steinke-Lange, V, Tedaldi, G, Tejada, I, Woodward, E, Tischkowitz, M, Hoogerbrugge, N, Oliveira, C

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GENOTYPE-PHENOTYPE ASSOCIATIONS PROVIDE A RATIONAL TO IDENTIFY POTENTIALLY ACTIONABLE VUS von Pelaez, J, Monteiro, R, Lobo, S, Sousa, L, Pinheiro, H, Castedo, S, Garrido, L, Teixeira, M, Michils, G, Bours, V, de Putter, R, Golmard, L, Blanluet, M, Colas, C, Benusiglio, P, Desseignes, C, Florence, C, Aretz, S, Spier, I, Huneburg, R, Gieldon, L, Schrock, E, Holinski-Feder, E, Steinke, V, Calistri, D, Tedaldi, G, Ranzani, G, Genuardi, M, Silveira, C, Silva, I, Krajc, M, Blatnik, A, Novacovik, S, Patino-Garcia, A, Soto, JL, Lazaro, C, Capella, G, Brunet-Vidal, J, Balmana, J, Dominguez-Garrido, E, Ligtenberg, M, Fewings, E, Fitzgerald, R, Woodward, E, Evans, G, Hanson, H, Lagerstedt-Robinson, K, Bajalica-Lagercrantz, S, Egas, C, Tejada, MI, Dahan, K, Feret, D, Hoogerbrugge, N, Tischkowitz, M, Oliveira, C

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The first genotype-phenotype study on European carriers of CDH1 germline mutations von Garcia-Pelaez, J, Monteiro, R, Sousa, L, Pinheiro, H, Castedo, S, Garrido, L, Teixeira, M, Michils, G, Bours, V, de Putter, R, Golmard, L, Blanluet, M, Colas, C, Benusiglio, P, Aretz, S, Spier, I, Huneburg, R, Gieldon, L, Schrock, E, Holinski-Feder, E, Steinke, V, Calistri, D, Tedaldi, G, Ranzani, G, Genuardi, M, Silveira, C, Silva, I, Krajc, M, Blatnik, A, Novakovic, S, Patino-Garcia, A, Soto, J, Lazaro, C, Capella, G, Brunet-Vidal, J, Balmana, J, Dominguez-Garrido, E, Ligtenberg, M, Fewings, E, Fitzgerald, R, Woodward, E, Evans, G, Hanson, H, Lagerstedt-Robinson, K, Bajalica-Lagercrantz, S, Egas, C, Martinez-Bouzas, C, Dahan, K, Feret, D, Hoogerbrugge, N, Tischkowitz, M, Oliveira, C

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Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families von Osher, D.J, De Leeneer, K, Michils, G, Hamel, N, Tomiak, E, Poppe, B, Leunen, K, Legius, Eric, Shuen, A, Smith, E, Arseneau, J, Tonin, P, Matthijs, Gert, Claes, K, Tischkowitz, M.D, Foulkes, W.D

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European Landscape of CDH1 germline mutations: a new tool to understand hereditary diffuse gastric cancer (HDGC) von Pelaez, JG, Monteiro, A, Sousa, L, Castedo, S, Garrido, L, Michils, G, Bours, V, de Putter, R, Golmard, L, Blanluet, M, Colas, C, Benusiglio, P, Aretz, S, Spier, I, Huneburg, R, Gieldon, L, Schrock, E, Holinski-Feder, E, Steinke, V, Calistri, D, Tedaldi, G, Nadia-Ranzani, G, Genuardi, M, Silveira, C, Krajc, M, Blatnik, A, Novakovic, S, Patino-Garcia, A, Soto, J, Lazaro, C, Capella, G, Brunet-Vidal, J, Balmana, J, Dominguez-Garrido, E, Ligtenberg, M, Fewings, E, Fitzgerald, R, Woodward, E, Evans, G, Hanson, H, Lagerstedt-Robinson, K, Bajalica-Lagercrantz, S, Teixeira, M, Hoogerbrugge, N, Tischkowitz, M, Oliveira, C

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Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testing von De Leeneer, K, Van Bockstal, M, De Brouwer, S, Swietek, N, Schietecatte, P, Sabbaghian, N, Van den Ende, J, Willocx, S, Storm, K, Blaumeiser, B, Van Asperen, C.J, Wijnen, J.T, Leunen, K, Legius, Eric, Michils, G, Matthijs, Gert, Blok, M.J, Gomez-Garcia, E, De Paepe, A, Tischkowitz, M, Poppe, B, Claes, K

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Diagnostic DHPLC Quality Assurance (DDQA): A collaborative approach to the generation of validated and standardized methods for DHPLC‐based mutation screening in clinical genetics... von Schollen, Els, Dequeker, Elisabeth, McQuaid, Shirley, Vankeirsbilck, Bruno, Michils, Geneviève, Harvey, John, van den Akker, Eric, van Schooten, Ron, Clark, Zandra, Schrooten, Stephan, Matthijs, Gert

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Duplication of the VHL and IRAK2 genes in a patient with mental retardation/multiple congenital anomalies, epilepsy and ectomorphic habitus von Chabchoub, Elyes, Michils, G, Vermeesch, Joris, De Cock, Paul, Lagae, L, Fryns, Jean-Pierre

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Pathogenic mutations and rare variants of the APC gene identified in 75 Belgian patients with familial adenomatous polyposis by fluorescent enzymatic mutation detection (EMD) von Michils, Geneviève, Tejpar, Sabine, Fryns, Jean-Pierre, Legius, Eric, Van Cutsem, Eric, Cassiman, Jean-Jacques, Matthijs, Gert

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Analysis of Wnt/beta catenin signalling in desmoid tumors von TEJPAR, S, MICHILS, G, DENYS, H, VAN DAM, K, NIK, S. A, JADIDIZADEH, A, CASSIMAN, J. J

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Novel germline mutations in the APC gene and their phenotypic spectrum in familial adenomatous polyposis kindreds von WALON, C, KARTHEUSER, A, MICHILS, G, SMAERS, M, LANNOY, N, NGOUNOU, P, MERTENS, G, VERELLEN-DUMOULIN, C

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Chronic oral corticosteroids use and persistent eosinophilia in severe asthmatics from the Belgian severe asthma registry von Graff, S., Vanwynsberghe, S., Brusselle, G., Hanon, S., Sohy, C., Dupont, L. J., Peche, R., Michils, A., Pilette, C., Joos, G., Louis, R. E., Schleich, F. N.

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impact of concomitant rhinitis on asthma-related quality of life and asthma control von Vandenplas, O, Dramaix, M, Joos, G, Louis, R, Michils, A, Verleden, G, Vincken, W, Vints, A.-M, Herbots, E, Bachert, C

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“Real-life” effectiveness of omalizumab in patients with severe persistent allergic asthma: The PERSIST study von Brusselle, G, Michils, A, Louis, R, Dupont, L, Van de Maele, B, Delobbe, A, Pilette, C, Lee, C.S, Gurdain, S, Vancayzeele, S, Lecomte, P, Hermans, C, MacDonald, K, Song, M, Abraham, I

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Variability in total serum IgE over 1 year in severe asthmatics von Louis, Renaud, Pilette, Charles, Michel, Olivier, Michils, Alain, Brusselle, Guy, Poskin, Antoine, Van Schoor, Jan, Denhaerynck, Kris, Vancayzeele, Stefaan, Abraham, Ivo, Gurdain, Sandra

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Heterogeneity of phenotypes in severe asthmatics. The Belgian Severe Asthma Registry (BSAR) von Schleich, F, Brusselle, G, Louis, R, Vandenplas, O, Michils, A, Pilette, C, Peche, R, Manise, M, Joos, G

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