Assessing pathogenicity of mismatch repair variants of uncertain significance by molecular tumor analysis von van der Werf't Lam, Anne-Sophie, Helderman, Noah C., Boot, Arnoud, Terlouw, Diantha, Morreau, Hans, Mei, Hailian, Esveldt-van Lange, Rebecca E.E., Lakeman, Inge M.M., van Asperen, Christi J., Aten, Emmelien, Hofland, Nandy, de Koning Gans, Pia A.M., Rayner, Emily, Tops, Carli, de Wind, Niels, van Wezel, Tom, Nielsen, Maartje

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Next-Generation Diagnostics: Gene Panel, Exome, or Whole Genome? von Sun, Yu, Ruivenkamp, Claudia A.L., Hoffer, Mariëtte J.V., Vrijenhoek, Terry, Kriek, Marjolein, van Asperen, Christi J., den Dunnen, Johan T., Santen, Gijs W.E.

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Germline BRCA -Associated Endometrial Carcinoma Is a Distinct Clinicopathologic Entity von de Jonge, Marthe M, Ritterhouse, Lauren L, de Kroon, Cornelis D, Vreeswijk, Maaike P G, Segal, Jeremy P, Puranik, Rutika, Hollema, Harry, Rookus, Matti A, van Asperen, Christi J, van Leeuwen, Flora E, Smit, Vincent T H B M, Howitt, Brooke E, Bosse, Tjalling

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Progression-free survival and overall survival after BRCA1/2-associated epithelial ovarian cancer: A matched cohort study von Heemskerk-Gerritsen, Bernadette A. M, Hollestelle, Antoinette, van Asperen, Christi J, van den Beek, Irma, van Driel, Willemien J, van Engelen, Klaartje, Gómez Garcia, Encarna B, de Hullu, Joanne A, Koudijs, Marco J, Mourits, Marian J. E, Hooning, Maartje J, Boere, Ingrid A

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The functional impact of variants of uncertain significance in BRCA2 von Mesman, Romy L. S., Calléja, Fabienne M. G. R., Hendriks, Giel, Morolli, Bruno, Misovic, Branislav, Devilee, Peter, van Asperen, Christi J., Vrieling, Harry, Vreeswijk, Maaike P. G.

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Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles von Gracia-Aznarez, Francisco Javier, Fernandez, Victoria, Pita, Guillermo, Peterlongo, Paolo, Dominguez, Orlando, de la Hoya, Miguel, Duran, Mercedes, Osorio, Ana, Moreno, Leticia, Gonzalez-Neira, Anna, Rosa-Rosa, Juan Manuel, Sinilnikova, Olga, Mazoyer, Sylvie, Hopper, John, Lazaro, Conchi, Southey, Melissa, Odefrey, Fabrice, Manoukian, Siranoush, Catucci, Irene, Caldes, Trinidad, Lynch, Henry T, Hilbers, Florentine S M, van Asperen, Christi J, Vasen, Hans F A, Goldgar, David, Radice, Paolo, Devilee, Peter, Benitez, Javier

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Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk prediction von Tüchler, Anja, De Pauw, Antoine, Ernst, Corinna, Anota, Amélie, Lakeman, Inge M.M., Dick, Julia, van der Stoep, Nienke, van Asperen, Christi J., Maringa, Monika, Herold, Natalie, Blümcke, Britta, Remy, Robert, Westerhoff, Anke, Stommel-Jenner, Denise J., Frouin, Eléonore, Richters, Lisa, Golmard, Lisa, Kütting, Nadine, Colas, Chrystelle, Wappenschmidt, Barbara, Rhiem, Kerstin, Devilee, Peter, Stoppa-Lyonnet, Dominique, Schmutzler, Rita K., Hahnen, Eric

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Cohort profile: a nationwide study in Dutch CHEK2 c.1100delC families using the infrastructure of the HEreditary Breast and Ovarian cancer study Netherlands – Hebon-CHEK2 von Schreurs, Maartje A.C., Adank, Muriel A, Hollestelle, Antoinette, de Groot, Rosa, Stommel-Jenner, Denise J, Van Asperen, Christi J., Ausems, Margreet G.E.M., Berger, Lieke P V, Blok, Marinus J, van Engelen, Klaartje, Hogervorst, Frans B L, Geurts-Giele, Willemina, Gille, Johan J P, Wevers, Marijke R, Schmidt, Marjanka K, Hooning, Maartje J.

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Effects of chemotherapy on contralateral breast cancer risk in BRCA1 and BRCA2 mutation carriers: A nationwide cohort study von Akdeniz, Delal, van Barele, Mark, Heemskerk-Gerritsen, Bernadette A.M., Steyerberg, Ewout W., Hauptmann, Michael, van de Beek, Irma, van Engelen, Klaartje, Wevers, Marijke R., Gómez García, Encarnacion B., Ausems, Margreet G.E.M., Berger, Lieke P.V., van Asperen, Christi J., Adank, Muriel A., Collée, Margriet J., Stommel-Jenner, Denise J., Jager, Agnes, Schmidt, Marjanka K., Hooning, Maartje J.

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Correction: Alternative mRNA splicing can attenuate the pathogenicity of presumed loss-of-function variants in BRCA2 von Mesman, Romy L. S., Calléja, Fabienne M. G. R., de la Hoya, Miguel, Devilee, Peter, van Asperen, Christi J., Vrieling, Harry, Vreeswijk, Maaike P. G.

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Do Preferred Risk Formats Lead to Better Understanding? A Multicenter Controlled Trial on Communicating Familial Breast Cancer Risks Using Different Risk Formats von Henneman, Lidewij, van Asperen, Christi J., Oosterwijk, Jan C., Menko, Fred H., Claassen, Liesbeth, Timmermans, Danielle R. M.

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Effectiveness and cost-effectiveness of meaning-centered group psychotherapy in cancer survivors: protocol of a randomized controlled trial von van der Spek, Nadia, Vos, Joël, van Uden-Kraan, Cornelia F, Breitbart, William, Cuijpers, Pim, Knipscheer-Kuipers, Kitty, Willemsen, Vincent, Tollenaar, Rob A E M, van Asperen, Christi J, Verdonck-de Leeuw, Irma M

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Optimal age to start preventive measures in women with BRCA1/2 mutations or high familial breast cancer risk von Tilanus‐Linthorst, Madeleine M.A., Lingsma, Hester F., Evans, D. Gareth, Thompson, Deborah, Kaas, Reinoutje, Manders, Peggy, Asperen, Christi J., Adank, Muriel, Hooning, Maartje J., Kwan Lim, Gek E., Eeles, Rosalind, Oosterwijk, Jan C., Leach, Martin O., Steyerberg, Ewout W.

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Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies von Gonzalez-Neira, Anna, Rosa-Rosa, Juan Manuel, Osorio, Ana, Gonzalez, Emilio, Southey, Melissa, Sinilnikova, Olga, Lynch, Henry, Oldenburg, Rogier A, van Asperen, Christi J, Hoogerbrugge, Nicoline, Pita, Guillermo, Devilee, Peter, Goldgar, David, Benitez, Javier

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Exome sequencing of germline DNA from non-BRCA1/2 familial breast cancer cases selected on the basis of aCGH tumor profiling von Hilbers, Florentine S, Meijers, Caro M, Laros, Jeroen F J, van Galen, Michiel, Hoogerbrugge, Nicoline, Vasen, Hans F A, Nederlof, Petra M, Wijnen, Juul T, van Asperen, Christi J, Devilee, Peter

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CHEK21100delC homozygosity in the Netherlands--prevalence and risk of breast and lung cancer von Huijts, Petra E A, Hollestelle, Antoinette, Balliu, Brunilda, Houwing-Duistermaat, Jeanine J, Meijers, Caro M, Blom, Jannet C, Ozturk, Bahar, Krol-Warmerdam, Elly M M, Wijnen, Juul, Berns, Els M J J, Martens, John W M, Seynaeve, Caroline, Kiemeney, Lambertus A, van der Heijden, Henricus F, Tollenaar, Rob A E M, Devilee, Peter, van Asperen, Christi J

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Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers von Heemskerk-Gerritsen, Bernadette A. M., Jager, Agnes, Koppert, Linetta B., Obdeijn, A. Inge-Marie, Collée, Margriet, Meijers-Heijboer, Hanne E. J., Jenner, Denise J., Oldenburg, Hester S. A., van Engelen, Klaartje, de Vries, Jakob, van Asperen, Christi J., Devilee, Peter, Blok, Marinus J., Kets, C. Marleen, Ausems, Margreet G. E. M., Seynaeve, Caroline, Rookus, Matti A., Hooning, Maartje J.

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Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making von Reumkens, Kelly, Tummers, Marly H. E., Severijns, Yil, Gietel-Habets, Joyce J. G., van Kuijk, Sander M. J., Aalfs, Cora M., van Asperen, Christi J., Ausems, Margreet G. E. M., Collée, Margriet, Dommering, Charlotte J., Kets, Marleen, van der Kolk, Lizet E., Oosterwijk, Jan C., Tjan-Heijnen, Vivianne C. G., van der Weijden, Trudy, de Die-Smulders, Christine E. M., van Osch, Liesbeth A. D. M.

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Recommendations for reporting results of diagnostic genomic testing von Deans, Zandra C, Ahn, Joo Wook, Carreira, Isabel M, Dequeker, Elisabeth, Henderson, Mick, Lovrecic, Luca, Õunap, Katrin, Tabiner, Melody, Treacy, Rebecca, van Asperen, Christi J

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A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example von Mohammadi, Leila, Vreeswijk, Maaike P, Oldenburg, Rogier, van den Ouweland, Ans, Oosterwijk, Jan C, van der Hout, Annemarie H, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn, Ausems, Margreet G, van der Luijt, Rob B, Dommering, Charlotte J, Gille, Johan J, Verhoef, Senno, Hogervorst, Frans B, van Os, Theo A, Gómez García, Encarna, Blok, Marinus J, Wijnen, Juul T, Helmer, Quinta, Devilee, Peter, van Asperen, Christi J, van Houwelingen, Hans C

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