The single-nucleotide polymorphism 309 in the MDM2 gene contributes to the Li–Fraumeni syndrome and related phenotypes von Ruijs, Mariëlle W G, Schmidt, Marjanka K, Nevanlinna, Heli, Tommiska, Johanna, Aittomäki, Kristiina, Pruntel, Roelof, Verhoef, Senno, van't Veer, Laura J

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Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences von LAMMENS, Chantal R. M, AARONSON, Neil K, KLUIJT, Irma, NAGTEGAAL, Tanja, VERHOEF, Senno, BLEIKER, Eveline M. A, WAGNER, Anja, SIJMONS, Rolf H, AUSEMS, Margreet G. E. M, VRIENDS, Annette H. J. T, RUIJS, Mariëlle W. G, VAN OS, Theo A. M, SPRUIJT, Liesbeth, GOMEZ GARCIA, Encarna B

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An information-theoretic analysis of genetics, gender and age in cancer patients von Atwal, Gurinder Singh, Rabadán, Raúl, Lozano, Guillermina, Strong, Louise C, Ruijs, Mariëlle W G, Schmidt, Marjanka K, van't Veer, Laura J, Nevanlinna, Heli, Tommiska, Johanna, Aittomäki, Kristiina, Bougeard, Gaelle, Frebourg, Thierry, Levine, Arnold J, Bond, Gareth L

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TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes von Ruijs, Marielle W G, Verhoef, Senno, Rookus, Matti A, Pruntel, Roelof, van der Hout, Annemarie H, Hogervorst, Frans B L, Kluijt, I, Sijmons, Rolf H, Aalfs, Cora M, Wagner, Anja, Ausems, Margreet G E M, Hoogerbrugge, Nicoline, van Asperen, Christi J, Gomez Garcia, Encarna B, Meijers-Heijboer, Hanne, ten Kate, Leo P, Menko, Fred H, van 't Veer, Laura J

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Challenges in breast cancer genetic testing. A call for novel forms of multidisciplinary care and long-term evaluation von Menko, Fred H., Monkhorst, Kim, Hogervorst, Frans B.L., Rosenberg, Efraim H., Adank, Muriël, Ruijs, Mariëlle W.G., Bleiker, Eveline M.A., Sonke, Gabe S., Russell, Nicola S., Oldenburg, Hester S.A., van der Kolk, Lizet E.

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Impact of genetic counseling strategy on diagnostic yield and workload for genome-sequencing-based tumor diagnostics von Koster, Roelof, Schipper, Luuk J., Giesbertz, Noor A.A., van Beek, Daphne, Mendeville, Matías, Samsom, Kris G., Rosenberg, Efraim H., Hogervorst, Frans B.L., Roepman, Paul, Boelens, Mirjam C., Bosch, Linda J.W., van den Berg, Jose G., Meijer, Gerrit A., Voest, Emile E., Cuppen, Edwin, Ruijs, Marielle W.G., van Wezel, Tom, van der Kolk, Lizet, Monkhorst, Kim

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Long-term outcome of high-grade serous carcinoma established in risk-reducing salpingo-oophorectomy specimens in asymptomatic BRCA1/2 germline pathogenic variant carriers von Stroot, Iris A.S., Bart, Joost, Hollema, Harry, Jalving, Mathilde, Wagner, Marise M., Yigit, Refika, van Doorn, Helena C., de Hullu, Joanne A., Gaarenstroom, Katja N., van Beurden, Marc, van Lonkhuijzen, Luc R.C.W., Slangen, Brigitte F.M., Zweemer, Ronald P., Gómez García, Encarna B., Ausems, Margreet G.E.M., Boere, Ingrid A., van Hest, Liselotte P., Duijkers, Floor A.M., van Asperen, Christi J., Schmidt, Marjanka K., Wevers, Marijke R., Ruijs, Marielle W.G., Devilee, Peter, Collée, J. Margriet, HEBON investigators, de Bock, Geertruida H., Mourits, Marian J.E.

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The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype von Ruijs, Marielle W G, Broeks, Annegien, Menko, Fred H, Ausems, Margreet G E M, Wagner, Anja, Oldenburg, Rogier, Meijers-Heijboer, Hanne, van't Veer, Laura J, Verhoef, Senno

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Two TP53 germline mutations in a classical Li-Fraumeni syndrome family von van Hest, Liselotte P, Ruijs, Mariëlle W G, Wagner, Anja, van der Meer, Conny A, Verhoef, Senno, van't Veer, Laura J, Meijers-Heijboer, Hanne

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Late-onset common cancers in a kindred with an Arg213Gln TP53 germline mutation von Ruijs, Mariëlle W G, Verhoef, Senno, Wigbout, Gea, Pruntel, Roelof, Floore, Arno N, de Jong, Daphne, van T Veer, Laura J, Menko, Fred H

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Classic pseudoxanthoma elasticum in a patient with sickle cell disease von van Meurs, Tim, MD, van Hagen, Johanna M., MD, van de Scheur, Martijn R., MD, Vermaat, Hester, MD, Ruijs, Marielle W.G., MD, van den Hoogenband, Henk M., MD, Starink, Theo M., MD, PhD

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Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers von Page, Elizabeth, Bancroft, Elizabeth K, Brook, Mark N, Assel, Melissa, Al Battat, Mona Hassan, Thomas, Sarah, Taylor, Natalie, Chamberlain, Anthony, Ni Raghallaigh, Holly, Offman, Judith, Obeid, Elias, Dudderidge, Tim, Moynihan, Clare, Eeles, Rosalind A, Saya, Sibel, Castro, Elena, Arun, Banu K, Eyfjord, Jorunn E, Dias, Alexander, Ong, Kai Ren, Ardern Jones, Audrey, Bangma, Chris H, Dearnaley, David, Cybulski, Cezary, Falconer, Alison, Rennert, Gadi, Maehle, Lovise, Khoo, Vincent, Helfand, Brian T, Oosterwijk, Jan C, Lindeman, Geoffrey J, Cardoso, Marta, Mitra, Anita, Suri, Mohnish, Grindedal, Eli Marie, Rosario, Derek J, Azzabi, Ashraf, Vickers, Andrew, Wokolorczyk, Dominika, Ringelberg, Janneke, Mascarenhas, Lyon, Genova, Elena, Side, Lucy, Adank, Muriel A, Van Asperen, Christi, Domchek, Susan, Vasen, Hans, Ahmed, Munaza, Tischkowitz, Marc, Oldenburg, Rogier A, Huber, Camilla, Lam, Jimmy, Taylor, Louise, Ronlund, Karina, Ramón y Cajal, Teresa, Salinas Masdeu, Mònica, Van Randeraad, Heleen, Cook, Jackie, Foulkes, William D, Powers, Jacquelyn, Buys, Saundra S, O'toole, Karen, Izatt, Louise, Susman, Rachel, Greenhalgh, Lynn, Carlsson, Stefan, Tripathi, Vishakha, Cooke, Peter, Aprikian, Armen, Longmuir, Mark, Murthy, Vedang, Ruijs, Mariëlle W. G, Chen Shtoyerman, Rakefet, Helderman Van Den Enden, Apollonia T. J. M, Donaldson, Alan, Rothwell, Jeanette, Andrews, Lesley, Murphy, Declan G, Jobson, Irene, Morton, Catherine, Snape, Katie, Hamdy, Freddie C, McGrath, John J, Hanson, Helen, Barwell, Julian, Harris, Marion, Taylor, Amy, Kast, Karin, Kirk, Judy, Johannsson, Oskar, Spigelman, Allan, Pachter, Nicholas, Richardson, Kate, Tricker, Karen, Gadea, Neus, Brady, Angela F, Copakova, Lucia, Stefansdottir, Vigdis, Foster, Christopher, Friedman, Eitan

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Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers von Page, Elizabeth C., Bancroft, Elizabeth K., Brook, Mark N., Assel, Melissa, Hassan Al Battat, Mona, Thomas, Sarah, Taylor, Natalie, Raghallaigh, Holly Ni, Evans, D. Gareth, Maehle, Lovise, Grindedal, Eli Marie, James, Paul, Mascarenhas, Lyon, McKinley, Joanne, Thomas, Tessy, van Asperen, Christi, Vasen, Hans, Kiemeney, Lambertus A., Ringelberg, Janneke, Jensen, Thomas Dyrsø, Osther, Palle J.S., Helfand, Brian T., Genova, Elena, Oldenburg, Rogier A., Cybulski, Cezary, Ong, Kai-Ren, Lam, Jimmy, Taylor, Louise, Feliubadaló, Lidia, van Zelst-Stams, Wendy, Rosario, Derek J., Domchek, Susan, Powers, Jacquelyn, Buys, Saundra, O'Toole, Karen, Ausems, Margreet G.E.M., Schmutzler, Rita K., Rhiem, Kerstin, Izatt, Louise, Cardoso, Marta, Aprikian, Armen, van Randeraad, Heleen, Davidson, Rosemarie, Longmuir, Mark, Helderman van den Enden, Apollonia T.J.M., Adank, Muriel, Williams, Rachel, Andrews, Lesley, Murphy, Declan G., Halliday, Dorothy, Walker, Lisa, Liljegren, Annelie, Carlsson, Stefan, Morton, Catherine, Snape, Katie, Hanson, Helen, Tischkowitz, Marc, Taylor, Amy, Kirk, Judy, Susman, Rachel, Chen-Shtoyerman, Rakefet, Spigelman, Allan, Pachter, Nicholas, Ahmed, Munaza, Ramon y Cajal, Teresa, Brewer, Carole, Gadea, Neus, van Os, Theo, Gallagher, David, Johannsson, Oskar, Barwell, Julian, Nicolai, Nicola, Friedman, Eitan, Greenhalgh, Lynn, Murthy, Vedang, Saya, Sibel, McGrath, John, Rønlund, Karina, Teo, Soo H., Kast, Karin, Aaronson, Neil K., Ardern-Jones, Audrey, Bangma, Chris H., Dearnaley, David, Tricker, Karen, Eyfjord, Jorunn, Falconer, Alison, Foster, Christopher, Gronberg, Henrik, Hamdy, Freddie C., Stefansdottir, Vigdis, Khoo, Vincent, Lindeman, Geoffrey J., Lubinski, Jan, Mikropoulos, Christos, Mitra, Anita, Moynihan, Clare, Wilson, Penny, Dudderidge, Tim, Offman, Judith

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Classic pseudoxanthoma elasticum in a patient with sickle cell disease von van Meurs, Tim, van Hagen, Johanna M, van de Scheur, Martijn R, Vermaat, Hester, Ruijs, Marielle W G, van den Hoogenband, Henk M, Starink, Theo M

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