Universität zu Köln

Journal Article

Adam, Ronja, Spier, Isabel, Zhao, Bixiao ORCID: 0000-0002-1775-1690, Kloth, Michael, Marquez, Jonathan, Hinrichsen, Inga, Kirfel, Jutta, Tafazzoli, Aylar, Horpaopan, Sukanya, Uhlhaas, Siegfried, Stienen, Dietlinde, Friedrichs, Nicolaus, Altmueller, Janine, Laner, Andreas, Holzapfel, Stefanie, Peters, Sophia, Kayser, Katrin, Thiele, Holger, Holinski-Feder, Elke, Marra, Giancarlo, Kristiansen, Glen, Noethen, Markus M., Buettner, Reinhard, Moeslein, Gabriela, Betz, Regina C., Brieger, Angela, Lifton, Richard P. and Aretz, Stefan ORCID: 0000-0002-5228-1890 (2016). Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis. Am. J. Hum. Genet., 99 (2). S. 337 - 352. CAMBRIDGE: CELL PRESS. ISSN 1537-6605

Bucksch, Karolin ORCID: 0000-0003-4586-4032, Zachariae, Silke, Ahadova, Aysel, Aretz, Stefan, Buttner, Reinhard, Goergens, Heike, Holinski-Feder, Elke, Hueneburg, Robert, Kloor, Matthias, Doeberitz, Magnus Knebel, Ladigan-Badura, Swetlana, Moeslein, Gabriela, Morak, Monika, Nattermann, Jacob, Perne, Claudia, Redler, Silke, Schmetz, Ariane, Steinke-Lange, Verena, Surowy, Harald, Vangala, Deepak B., Weitz, Juergen, Loeffler, Markus and Engel, Christoph ORCID: 0000-0002-7247-282X (2022). Adenoma and colorectal cancer risks in Lynch syndrome, Lynch-like syndrome and familial colorectal cancer type X. Int. J. Cancer, 150 (1). S. 56 - 67. HOBOKEN: WILEY. ISSN 1097-0215

Bucksch, Karolin, Zachariae, Silke, Aretz, Stefan, Buettner, Reinhard, Holinski-Feder, Elke, Holzapfel, Stefanie, Hueneburg, Robert, Kloor, Matthias, Doeberitz, Magnus von Knebel, Morak, Monika, Moeslein, Gabriela, Nattermann, Jacob, Perne, Claudia, Rahner, Nils, Schmiegel, Wolff, Schulmann, Karsten, Steinke-Lange, Verena, Strassburg, Christian P., Vangala, Deepak B., Weitz, Juergen, Loeffler, Markus and Engel, Christoph ORCID: 0000-0002-7247-282X (2020). Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study. BMC Cancer, 20 (1). LONDON: BMC. ISSN 1471-2407

Dominguez-Valentin, Mev ORCID: 0000-0001-7856-0057, Crosbie, Emma J., Engel, Christoph, Aretz, Stefan, Macrae, Finlay, Winship, Ingrid, Capella, Gabriel, Thomas, Huw, Nakken, Sigve ORCID: 0000-0001-8468-2050, Hovig, Eivind, Nielsen, Maartje, Sijmons, Rolf H., Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Mints, Miriam, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A., Green, Kate, Lalloo, Fiona, Hill, James, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Strauss, Hans-Georg, Tecklenburg, Johanna, Holinski-Feder, Elke, Steinke-Lange, Verena, Mecklin, Jukka-Pekka, Plazzer, John-Paul, Pineda, Marta, Navarro, Matilde, Brunet Vidal, Joan, Kariv, Revital, Rosner, Guy, Alejandra Pinero, Tamara, Laura Gonzalez, Maria, Kalfayan, Pablo, Ryan, Neil, Ten Broeke, Sanne W., Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Burn, John, Greenblatt, Marc, Cappel, Wouter H. de Vos tot Nederveen, Della Valle, Adriana, Lopez-Koestner, Francisco, Alvarez, Karin, Buettner, Reinhard, Goergens, Heike, Morak, Monika, Holzapfel, Stefanie, Hueneburg, Robert, Doeberitz, Magnus von Knebel, Loeffler, Markus, Rahner, Nils, Weitz, Jurgen, Pylvanainen, Kirsi ORCID: 0000-0003-4399-9283, Renkonen-Sinisalo, Laura, Lepisto, Anna, Auranen, Annika, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loic, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Therkildsen, Christina, Okkels, Henrik, Ketabi, Zohreh, Denton, Oliver G., Rodland, Einar Andreas, Vasen, Hans, Neffa, Florencia, Esperon, Patricia, Tjandra, Douglas, Moeslein, Gabriela, Sampson, Julian R., Evans, D. Gareth, Seppala, Toni T. and Moller, Pal . Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report. Genet. Med.. LONDON: SPRINGERNATURE. ISSN 1530-0366

Dominguez-Valentin, Mev ORCID: 0000-0001-7856-0057, Plazzer, John-Paul ORCID: 0000-0001-5114-4301, Sampson, Julian R., Engel, Christoph ORCID: 0000-0002-7247-282X, Aretz, Stefan ORCID: 0000-0002-5228-1890, Jenkins, Mark A., Sunde, Lone ORCID: 0000-0002-8479-165X, Bernstein, Inge, Capella, Gabriel ORCID: 0000-0002-4669-7320, Balaguer, Francesc ORCID: 0000-0002-0206-0539, Macrae, Finlay, Winship, Ingrid M., Thomas, Huw, Evans, Dafydd Gareth, Burn, John, Greenblatt, Marc, Cappel, Wouter H. de Vos Tot Nederveen, Sijmons, Rolf H., Nielsen, Maartje, Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Lindblom, Annika, Della Valle, Adriana, Lopez-Kostner, Francisco, Alvarez, Karin, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A., Nakken, Sigve ORCID: 0000-0001-8468-2050, Hovig, Eivind ORCID: 0000-0002-9103-1077, Green, Kate, Lalloo, Fiona, Hill, James, Vasen, Hans F. A., Perne, Claudia, Buettner, Reinhard, Goergens, Heike, Holinski-Feder, Elke, Morak, Monika, Holzapfel, Stefanie, Hueneburg, Robert, Doeberitz, Magnus von Knebel, Loeffler, Markus, Rahner, Nils, Weitz, Juergen, Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak ORCID: 0000-0002-4175-5683, Crosbie, Emma J., Pineda, Marta, Navarro, Matilde, Brunet, Joan, Moreira, Leticia ORCID: 0000-0002-4518-8591, Sanchez, Ariadna ORCID: 0000-0003-0409-1328, Serra-Burriel, Miquel ORCID: 0000-0001-8595-1224, Mints, Miriam, Kariv, Revital, Rosner, Guy, Pinero, Tamara Alejandra, Pavicic, Walter Hernan, Kalfayan, Pablo, ten Broeke, Sanne W., Mecklin, Jukka-Pekka, Pylvanainen, Kirsi, Renkonen-Sinisalo, Laura, Lepisto, Anna, Peltomaki, Paivi ORCID: 0000-0001-8819-2980, Hopper, John L., Win, Aung Ko, Buchanan, Daniel D., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loic, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Therkildsen, Christina, Hansen, Thomas V. O., Lindberg, Lars, Rodland, Einar Andreas, Neffa, Florencia, Esperon, Patricia, Tjandra, Douglas, Moslein, Gabriela, Seppala, Toni T. and Moller, Pal (2021). No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study. J. Clin. Med., 10 (13). BASEL: MDPI. ISSN 2077-0383

Dominguez-Valentin, Mev ORCID: 0000-0001-7856-0057, Sampson, Julian R., Seppala, Toni T. ORCID: 0000-0002-4940-3498, ten Broeke, Sanne W., Plazzer, John-Paul, Nakken, Sigve ORCID: 0000-0001-8468-2050, Engel, Christoph ORCID: 0000-0002-7247-282X, Aretz, Stefan, Jenkins, Mark A., Sunde, Lone ORCID: 0000-0002-8479-165X, Bernstein, Inge ORCID: 0000-0003-4095-432X, Capella, Gabriel ORCID: 0000-0002-4669-7320, Balaguer, Francesc, Thomas, Huw, Evans, D. Gareth, Burn, John ORCID: 0000-0002-9823-2322, Greenblatt, Marc, Hovig, Eivind, de Vos Tot Nederveen Cappel, Wouter H., Sijmons, Rolf H., Bertario, Lucio, Tibiletti, Maria Grazia, Cavestro, Giulia Martina ORCID: 0000-0003-1947-9368, Lindblom, Annika, Della Valle, Adriana, Lopez-Kostner, Francisco, Gluck, Nathan, Katz, Lior H., Heinimann, Karl, Vaccaro, Carlos A., Buettner, Reinhard, Goergens, Heike, Holinski-Feder, Elke, Morak, Monika, Holzapfel, Stefanie, Hueneburg, Robert, von Knebel Doeberitz, Magnus, Loeffler, Markus, Rahner, Nils, Schackert, Hans K., Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Pylvanainen, Kirsi ORCID: 0000-0003-4399-9283, Renkonen-Sinisalo, Laura, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loic, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Wadt, Karin, Therkildsen, Christina, Okkels, Henrik, Ketabi, Zohreh, Moreira, Leticia, Sanchez, Ariadna, Serra-Burriel, Miquel ORCID: 0000-0001-8595-1224, Pineda, Marta, Navarro, Matilde, Blanco, Ignacio ORCID: 0000-0002-7414-7481, Green, Kate, Lalloo, Fiona, Crosbie, Emma J., Hill, James, Denton, Oliver G., Frayling, Ian M., Rodland, Einar Andreas, Vasen, Hans, Mints, Miriam, Neffa, Florencia, Esperon, Patricia, Alvarez, Karin ORCID: 0000-0001-5349-0267, Kariv, Revital, Rosner, Guy, Pinero, Tamara Alejandra, Gonzalez, Maria Laura, Kalfayan, Pablo, Tjandra, Douglas, Winship, Ingrid M., Macrae, Finlay, Moeslein, Gabriela, Mecklin, Jukka-Pekka ORCID: 0000-0003-4895-2249, Nielsen, Maartje ORCID: 0000-0002-5351-1870 and Moller, Pal (2020). Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database. Genet. Med., 22 (1). S. 15 - 26. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1530-0366

Engel, Christoph ORCID: 0000-0002-7247-282X, Ahadova, Aysel, Seppala, Toni T. ORCID: 0000-0002-4940-3498, Aretz, Stefan ORCID: 0000-0002-5228-1890, Bigirwamungu-Bargeman, Marloes, Blaeker, Hendrik, Bucksch, Karolin, Buettner, Reinhard, Cappel, Wouter T. De Vos Tot Nederveen, Endris, Volker, Holinski-Feder, Elke, Holzapfel, Stefanie, Hueneburg, Robert, Jacobs, Maarten A. J. M., Koornstra, Jan J., Langers, Alexandra M., Lepisto, Anna, Morak, Monika, Moeslein, Gabriela, Peltomaeki, Paivi, Pylvaenaeinen, Kirsi, Rahner, Nils, Renkonen-Sinisalo, Laura, Schulmann, Karsten, Steinke-Lange, Verena, Stenzinger, Albrecht, Strassburg, Christian P., van de Meeberg, Paul C., van Kouwen, Mariette, van Leerdam, Monique ORCID: 0000-0002-5719-3208, Vangala, Deepak B., Vecht, Juda, Verhulst, Marie-Louise, Doeberitz, Magnus von Knebel, Weitz, Juergen, Zachariae, Silke, Loeffler, Markus, Mecklin, Jukka-Pekka ORCID: 0000-0003-4895-2249, Kloor, Matthias and Vasen, Hans F. (2020). Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome. Gastroenterology, 158 (5). S. 1326 - 1334. PHILADELPHIA: W B SAUNDERS CO-ELSEVIER INC. ISSN 1528-0012

Engel, Christoph ORCID: 0000-0002-7247-282X, Loeffler, Markus, Steinke, Verena, Rahner, Nils, Holinski-Feder, Elke, Dietmaier, Wolfgang, Schackert, Hans K., Goergens, Heike, Doeberitz, Magnus von Knebel, Goecke, Timm O., Schmiegel, Wolff, Buettner, Reinhard, Moeslein, Gabriela, Letteboer, Tom G. W., Garcia, Encarna Gomez, Hes, Frederik J., Hoogerbrugge, Nicoline ORCID: 0000-0003-2393-8141, Menko, Fred H., van Os, Theo A. M., Sijmons, Rolf H., Wagner, Anja, Kluijt, Irma, Propping, Peter and Vasen, Hans F. A. (2012). Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome. J. Clin. Oncol., 30 (35). S. 4409 - 4416. ALEXANDRIA: AMER SOC CLINICAL ONCOLOGY. ISSN 0732-183X

Engel, Christoph ORCID: 0000-0002-7247-282X, Vasen, Hans F., Seppala, Toni, Aretz, Stefan ORCID: 0000-0002-5228-1890, Bigirwamungu-Bargeman, Marloes, de Boer, Sybrand Y., Bucksch, Karolin, Buttner, Reinhard, Holinski-Feder, Elke, Holzapfel, Stefanie, Hueneburg, Robert, Jacobs, Maarten A. J. M., Jarvinen, Heikki, Kloor, Matthias, Doeberitz, Magnus von Knebel, Koornstra, Jan J., van Kouwen, Mariette, Langers, Alexandra M., van de Meeberg, Paul C., Morak, Monika, Moeslein, Gabriela, Nagengast, Fokko M., Pylvanainen, Kirsi ORCID: 0000-0003-4399-9283, Rahner, Nils, Renkonen-Sinisalo, Laura, Sanduleanu, Silvia, Schackert, Hans K., Schmiegel, Wolff, Schulmann, Karsten, Steinke-Lange, Verena, Strassburg, Christian P., Vecht, Juda, Verhulst, Marie-Louise, Cappel, Wouter de Vos Tot Nederveen, Zachariae, Silke, Mecklin, Jukka-Pekka ORCID: 0000-0003-4895-2249 and Loeffler, Markus (2018). No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies. Gastroenterology, 155 (5). S. 1400 - 1412. PHILADELPHIA: W B SAUNDERS CO-ELSEVIER INC. ISSN 1528-0012

Horpaopan, Sukanya, Spier, Isabel, Zink, Alexander M., Altmueller, Janine, Holzapfel, Stefanie, Laner, Andreas, Vogt, Stefanie, Uhlhaas, Siegfried, Heilmann, Stefanie, Stienen, Dietlinde, Pasternack, Sandra M., Keppler, Kathleen, Adam, Ronja, Kayser, Katrin, Moebus, Susanne, Draaken, Markus ORCID: 0000-0002-4546-0786, Degenhardt, Franziska, Engels, Hartmut, Hofmann, Andrea, Noethen, Markus M., Steinke, Verena, Perez-Bouza, Alberto, Herms, Stefan ORCID: 0000-0002-2786-8200, Holinski-Feder, Elke, Froehlich, Holger, Thiele, Holger, Hoffmann, Per and Aretz, Stefan ORCID: 0000-0002-5228-1890 (2015). Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis. Int. J. Cancer, 136 (6). S. E578 - 12. HOBOKEN: WILEY. ISSN 1097-0215

Horpaopan, Sukanya, Spier, Isabel, Zink, Alexander M., Altmueller, Janine, Holzapfel, Stefanie, Laner, Andreas, Vogt, Stefanie, Uhlhaas, Siegfried, Heilmann, Stefanie, Stienen, Dietlinde, Pasternack, Sandra M., Keppler, Kathleen, Adam, Ronja, Kayser, Katrin, Moebus, Susanne, Draaken, Markus ORCID: 0000-0002-4546-0786, Degenhardt, Franziska, Engels, Hartmut, Hofmann, Andrea, Noethen, Markus M., Steinke, Verena, Perez-Bouza, Alberto, Herms, Stefan ORCID: 0000-0002-2786-8200, Holinski-Feder, Elke, Froehlich, Holger, Thiele, Holger, Hoffmann, Per and Aretz, Stefan ORCID: 0000-0002-5228-1890 (2015). Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis. Int. J. Cancer, 136 (6). S. E578 - 12. HOBOKEN: WILEY. ISSN 1097-0215

Hueneburg, Robert, Aretz, Stefan ORCID: 0000-0002-5228-1890, Buettner, Reinhard, Daum, Severin, Engel, Christoph ORCID: 0000-0002-7247-282X, Fechner, Guido, Habermann, Jens K., Heling, Dominik, Hoffmann, Katrin, Holinski-Feder, Elke, Kloor, Matthias, von Knebel-Doeberitz, Magnus, Loeffler, Markus, Moeslein, Gabriela, Perne, Claudia, Redler, Silke, Riess, Olaf, Schmiegel, Wolff, Seufferlein, Thomas, Siebers-Renelt, Ulrike, Steinke-Lange, Verena, Tecklenburg, Johanna, Vangala, Deepak, Vilz, Tim, Weitz, Juergen, Wiedenmann, Bertram, Strassburg, Christian P. and Nattermann, Jacob (2019). Current recommendations for surveillance, risk reduction and therapy in Lynch syndrome patients. Z. Gastroent., 57 (11). S. 1309 - 1321. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-7803

Ladigan, Swetlana, Vangala, Deepak B., Kuhlkamp, Judith, Pox, Christian, Engel, Christoph, Hueneburg, Robert, Perne, Claudia, Nattermann, Jacob, Steinke-Lange, Verena, Rahner, Nils, Schackert, Hans K., Kloor, Matthias, Strassburg, Christian, Morak, Monika, Holinski-Feder, Elke, Buttner, Reinhard, Aretz, Stefan, Loeffler, Markus, Schmiegel, Wolff H. and Schulmann, Karsten (2018). Value of EGD for gastric cancer surveillance in patients with hereditary non-polyposis colorectal cancer (HNPCC) or Lynch syndrome (LS). J. Clin. Oncol., 36 (15). ALEXANDRIA: AMER SOC CLINICAL ONCOLOGY. ISSN 1527-7755

Ladigan-Badura, Swetlana, Vangala, Deepak B., Engel, Christoph ORCID: 0000-0002-7247-282X, Bucksch, Karolin, Hueneburg, Robert, Perne, Claudia, Nattermann, Jacob, Steinke-Lange, Verena, Rahner, Nils, Schackert, Hans K., Weitz, Juergen, Kloor, Matthias, Kuhlkamp, Judith, Moeslein, Gabriela, Strassburg, Christian, Morak, Monika, Holinski-Feder, Elke, Buettner, Reinhard, Aretz, Stefan, Loeffler, Markus, Schmiegel, Wolff, Pox, Christian and Schulmann, Karsten (2021). Value of uppergastrointestinalendoscopy for gastric cancer surveillance in patients with Lynch syndrome. Int. J. Cancer, 148 (1). S. 106 - 115. HOBOKEN: WILEY. ISSN 1097-0215

Moller, Pal, Seppala, Toni, Dowty, James G., Haupt, Saskia ORCID: 0000-0001-7537-9439, Dominguez-Valentin, Mev, Sunde, Lone ORCID: 0000-0002-8479-165X, Bernstein, Inge, Engel, Christoph ORCID: 0000-0002-7247-282X, Aretz, Stefan, Nielsen, Maartje, Capella, Gabriel, Evans, Dafydd Gareth, Burn, John, Holinski-Feder, Elke, Bertario, Lucio, Bonanni, Bernardo, Lindblom, Annika, Levi, Zohar, Macrae, Finlay, Winship, Ingrid, Plazzer, John-Paul, Sijmons, Rolf, Laghi, Luigi ORCID: 0000-0003-4187-1059, Della Valle, Adriana, Heinimann, Karl, Half, Elizabeth, Lopez-Koestner, Francisco, Alvarez-Valenzuela, Karin, Scott, Rodney J., Katz, Lior, Laish, Ido, Vainer, Elez, Vaccaro, Carlos Alberto, Carraro, Dirce Maria, Gluck, Nathan, Abu-Freha, Naim, Stakelum, Aine, Kennelly, Rory, Winter, Des, Rossi, Benedito Mauro, Greenblatt, Marc, Bohorquez, Mabel, Sheth, Harsh ORCID: 0000-0001-9626-0971, Tibiletti, Maria Grazia, Lino-Silva, Leonardo S., Horisberger, Karoline, Portenkirchner, Carmen, Nascimento, Ivana, Rossi, Norma Teresa, da Silva, Leandro Apolinario, Thomas, Huw, Zarand, Attila, Mecklin, Jukka-Pekka ORCID: 0000-0003-4895-2249, Pylvanainen, Kirsi, Renkonen-Sinisalo, Laura, Lepisto, Anna, Peltomaki, Paivi, Therkildsen, Christina, Lindberg, Lars Joachim, Thorlacius-Ussing, Ole ORCID: 0000-0003-4963-1551, von Knebel Doeberitz, Magnus, Loeffler, Markus, Rahner, Nils, Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Hueneburg, Robert, de Vargas, Aida Falcon, Latchford, Andrew, Gerdes, Anne-Marie, Backman, Ann-Sofie ORCID: 0000-0002-6054-6692, Guillen-Ponce, Carmen, Snyder, Carrie, Lautrup, Charlotte K., Amor, David ORCID: 0000-0001-7191-8511, Palmero, Edenir ORCID: 0000-0003-1904-2158, Stoffel, Elena, Duijkers, Floor, Hall, Michael J., Hampel, Heather, Williams, Heinric, Okkels, Henrik, Lubinski, Jan, Reece, Jeanette, Ngeow, Joanne, Guillem, Jose G., Arnold, Julie, Wadt, Karin, Monahan, Kevin ORCID: 0000-0002-7918-4003, Senter, Leigha, Rasmussen, Lene J., van Hest, Liselotte P., Ricciardiello, Luigi, Kohonen-Corish, Maija R. J., Ligtenberg, Marjolijn J. L., Southey, Melissa, Aronson, Melyssa, Zahary, Mohd N., Samadder, N. Jewel, Poplawski, Nicola, Hoogerbrugge, Nicoline, Morrison, Patrick J., James, Paul, Lee, Grant, Chen-Shtoyerman, Rakefet, Ankathil, Ravindran, Pai, Rish, Ward, Robyn, Parry, Susan, Debniak, Tadeusz, John, Thomas, van Overeem Hansen, Thomas, Caldes, Trinidad, Yamaguchi, Tatsuro ORCID: 0000-0001-8454-1995, Barca-Tierno, Veronica, Garre, Pilar, Cavestro, Giulia Martina, Weitz, Juergen, Redler, Silke, Buettner, Reinhard, Heuveline, VincentZ, Hopper, John L., Win, Aung Ko, Lindor, Noralane, Gallinger, Steven, Le Marchand, Loic, Newcomb, Polly A., Figueiredo, Jane, Buchanan, Daniel D., Thibodeau, Stephen N., ten Broeke, Sanne W., Hovig, Eivind, Nakken, Sigve ORCID: 0000-0001-8468-2050, Pineda, Marta, Duenas, Nuria, Brunet, Joan ORCID: 0000-0003-1945-3512, Green, Kate, Lalloo, Fiona, Newton, Katie, Crosbie, Emma J., Mints, Miriam, Tjandra, Douglas, Neffa, Florencia, Esperon, Patricia, Kariv, Revital, Rosner, Guy, Pavicic, Walter Hernan, Kalfayan, Pablo, Torrezan, Giovana Tardin, Bassaneze, Thiago, Martin, Claudia, Moslein, Gabriela, Ahadova, Aysel, Kloor, Matthias, Sampson, Julian R. and Jenkins, Mark A. (2022). Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium. Hered. Cancer Clin. Pract., 20 (1). LONDON: BMC. ISSN 1897-4287

Rump, Andreas ORCID: 0000-0001-7116-6364, Benet-Pages, Anna, Schubert, Steffen, Kuhlmann, Jan Dominik, Janavicius, Ramunas, Machackova, Eva ORCID: 0000-0002-0246-1471, Foretov, Lenka, Kleibl, Zdenek ORCID: 0000-0003-2050-9667, Lhota, Filip, Zemankova, Petra, Betcheva-Krajcir, Elitza, Mackenroth, Luisa, Hackmann, Karl, Lehmann, Janin, Nissen, Anke, DiDonato, Nataliya, Opitz, Romy, Thiele, Holger, Kast, Karin, Wimberger, Pauline, Holinski-Feder, Elke, Emmert, Steffen, Schroeck, Evelin and Klink, Barbara (2016). Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer. PLoS Genet., 12 (8). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1553-7404

Schrock, Evelin, Benet-Pages, Anna, Schuber, Steffen, Janavicius, Ramunas, Hackmann, Karl, Betcheva-Krajcir, Elitza, Mackenroth, Luisa, Lehmann, Janin, Nissen, Am, Altmueller, Janine, Thiele, Holger, Di Donato, Nataliya ORCID: 0000-0001-9439-4677, Klink, Barbara, Kuhlmann, Jan D., Tzschach, Andreas ORCID: 0000-0002-6840-965X, Kast, Karin, Wimberger, Pauline, Holinski-Feder, Elke, Meind, Alfons, Emmert, Steffen and Rump, Andreas (2015). Germline mutations in patients with hereditary breast and ovarian cancer establish ERCC2 as a cancer susceptibility gene. Cancer Res., 75. PHILADELPHIA: AMER ASSOC CANCER RESEARCH. ISSN 1538-7445

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Spier, Isabel, Drichel, Dmitriy ORCID: 0000-0001-5978-3458, Kerick, Martin ORCID: 0000-0002-6298-4514, Kirfel, Jutta, Horpaopan, Sukanya, Laner, Andreas, Holzapfel, Stefanie, Peters, Sophia, Adam, Ronja, Zhao, Bixiao ORCID: 0000-0002-1775-1690, Becker, Tim, Lifton, Richard P., Perner, Sven, Hoffmann, Per, Kristiansen, Glen, Timmermann, Bernd, Noethen, Markus M., Holinski-Feder, Elke, Schweiger, Michal R. and Aretz, Stefan ORCID: 0000-0002-5228-1890 (2016). Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. J. Med. Genet., 53 (3). S. 172 - 180. LONDON: BMJ PUBLISHING GROUP. ISSN 1468-6244

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