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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Family History, Surgery, and APC Mutation Are Risk Factors for Desmoid Tumors in Familial Adenomatous Polyposis: An International Cohort Study von Nieuwenhuis, Marry H, Lefevre, Jérémie H, Bülow, Steffen, Järvinen, Heikki, Bertario, Lucio, Kernéis, Solen, Parc, Yann, Vasen, Hans F. A

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A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants von Wiik, Mariann Unhjem, Evans, Tiffany-Jane, Belhadj, Sami, Bolton, Katherine A., Dymerska, Dagmara, Jagmohan-Changur, Shantie, Capellá, Gabriel, Kurzawski, Grzegorz, Wijnen, Juul T., Valle, Laura, Vasen, Hans F. A., Lubinski, Jan, Scott, Rodney J., Talseth-Palmer, Bente A.

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Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers von Pijpe, Anouk, Manders, Peggy, Brohet, Richard M., Collée, J. Margriet, Verhoef, Senno, Vasen, Hans F. A., Hoogerbrugge, Nicoline, van Asperen, Christi J., Dommering, Charlotte, Ausems, Margreet G. E. M., Aalfs, Cora M., Gomez-Garcia, Encarna B., van‘t Veer, Laura J., van Leeuwen, Flora E., Rookus, Matti A.

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Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘Care for CMMRD’ (C4CMMRD) von Wimmer, Katharina, Kratz, Christian P, Vasen, Hans F A, Caron, Olivier, Colas, Chrystelle, Entz-Werle, Natacha, Gerdes, Anne-Marie, Goldberg, Yael, Ilencikova, Denisa, Muleris, Martine, Duval, Alex, Lavoine, Noémie, Ruiz-Ponte, Clara, Slavc, Irene, Burkhardt, Brigit, Brugieres, Laurence

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In Memoriam: Steffen Bülow (1943–2023) von Vasen, Hans F. A.

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Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts von Vasen, Hans F A, Blanco, Ignacio, Aktan-Collan, Katja, Gopie, Jessica P, Alonso, Angel, Aretz, Stefan, Bernstein, Inge, Bertario, Lucio, Burn, John, Capella, Gabriel, Colas, Chrystelle, Engel, Christoph, Frayling, Ian M, Genuardi, Maurizio, Heinimann, Karl, Hes, Frederik J, Hodgson, Shirley V, Karagiannis, John A, Lalloo, Fiona, Lindblom, Annika, Mecklin, Jukka-Pekka, Møller, Pal, Myrhoj, Torben, Nagengast, Fokko M, Parc, Yann, Ponz de Leon, Maurizio, Renkonen-Sinisalo, Laura, Sampson, Julian R, Stormorken, Astrid, Sijmons, Rolf H, Tejpar, Sabine, Thomas, Huw J W, Rahner, Nils, Wijnen, Juul T, Järvinen, Heikki Juhani, Möslein, Gabriela

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Progress Report: New insights into the prevention of CRC by colonoscopic surveillance in Lynch syndrome von Vasen, Hans F. A.

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MUTYH-associated polyposis (MAP) von Nielsen, Maartje, Morreau, Hans, Vasen, Hans F.A, Hes, Frederik J

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Body weight and risk of breast cancer in BRCA1/2 mutation carriers von Manders, Peggy, Pijpe, Anouk, Hooning, Maartje J, Kluijt, Irma, Vasen, Hans F. A, Hoogerbrugge, Nicoline, van Asperen, Christi J, Meijers-Heijboer, Hanne, Ausems, Margreet G. E. M, van Os, Theo A, Gomez-Garcia, Encarna B, Brohet, Richard M, van Leeuwen, Flora E, Rookus, Matti A

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Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome von ENGEL, Christoph, LOEFFLER, Markus, SCHMIEGEL, Wolff, BUETTNER, Reinhard, MOESLEIN, Gabriela, LETTEBOER, Tom G. W, GOMEZ GARCIA, Encarna, HES, Frederik J, HOOGERBRUGGE, Nicoline, MENKO, Fred H, VAN OS, Theo A. M, SIJMONS, Rolf H, STEINKE, Verena, WAGNER, Anja, KLUIJT, Irma, PROPPING, Peter, VASEN, Hans F. A, RAHNER, Nils, HOLINSKI-FEDER, Elke, DIETMAIER, Wolfgang, SCHACKERT, Hans K, GOERGENS, Heike, VON KNEBEL DOEBERITZ, Magnus, GOECKE, Timm O

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Enrichment of Low Penetrance Susceptibility Loci in a Dutch Familial Colorectal Cancer Cohort von MIDDELDORP, Anneke, JAGMOHAN-CHANGUR, Shantie, WIJNEN, Juul T, MORREAU, Hans, VAN WEDEL, Tom, VAN EIJK, Ronald, TOPS, Carli, DEVILEE, Peter, VASEN, Hans F. A, HES, Frederik J, HOULSTON, Richard, TOMLINSON, Ian, HOUWING-DUISTERMAAT, Jeanine J

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The risk of extra‐colonic, extra‐endometrial cancer in the Lynch syndrome von Watson, Patrice, Vasen, Hans F.A., Mecklin, Jukka‐Pekka, Bernstein, Inge, Aarnio, Markku, Järvinen, Heikki J., Myrhøj, Torben, Sunde, Lone, Wijnen, Juul T., Lynch, Henry T.

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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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Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer von DE JONG, Andrea E, VAN PUIJENBROEK, Marjo, VASEN, Hans F. A, MORREAU, Hans, HENDRIKS, Yvonne, TOPS, Carli, WIJNEN, Juul, AUSEMS, Margreet G. E. M, MEIJERS-HEIJBOER, Hanne, WAGNER, Anja, VAN OS, Theo A. M, BRÖCKER-VRIENDS, Annette H. J. T

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Equivalent Helicobacter pylori infection rates in Lynch syndrome mutation carriers with and without a first-degree relative with gastric cancer von Soer, Eline C., Leicher, Laura W., Langers, Alexandra M. J., van de Meeberg, Paul C., van der Wouden, Egbert-Jan, Koornstra, Jan Jakob, Bigirwamungu-Bargeman, Marloes, Vasen, Hans F. A., de Vos tot Nederveen Cappel, Wouter H.

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A nation‐wide study comparing sporadic and familial adenomatous polyposis‐related desmoid‐type fibromatoses von Nieuwenhuis, Marry H., Casparie, Mariel, Mathus‐Vliegen, Lisbeth M.H., Dekkers, Olaf M., Hogendoorn, Pancras C.W., Vasen, Hans F.A.

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Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers von Talseth‐Palmer, Bente A., Wijnen, Juul T., Brenne, Ingvild S., Jagmohan‐Changur, Shantie, Barker, Daniel, Ashton, Katie A., Tops, Carli M., Evans, Tiffany‐Jane, McPhillips, Mary, Groombridge, Claire, Suchy, Janina, Kurzawski, Grzegorz, Spigelman, Allan, Møller, Pål, Morreau, Hans M., Van Wezel, Tom, Lubinski, Jan, Vasen, Hans F.A., Scott, Rodney J.

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Surveillance for hereditary cancer: Does the benefit outweigh the psychological burden?—A systematic review von Gopie, Jessica P, Vasen, Hans F.A, Tibben, Aad

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Infiltration of Lynch Colorectal Cancers by Activated Immune Cells Associates with Early Staging of the Primary Tumor and Absence of Lymph Node Metastases von DE MIRANDA, Noel F. C. C, GOUDKADE, Danny, JORDANOVA, Ekaterina S, TOPS, Carli M. J, HES, Frederik J, VASEN, Hans F. A, VAN WEZEL, Tom, MORREAU, Hans

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