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Journal Article
Vangala, Deepak B., Ladigan-Badura, Swetlana, Engel, Christoph ORCID: 0000-0002-7247-282X, Hueneburg, Robert, Perne, Claudia, Bucksch, Karolin
ORCID: 0000-0003-4586-4032, Nattermann, Jacob, Steinke-Lange, Verena
ORCID: 0000-0001-8491-3234, Rahner, Nils, Weitz, Juergen, Kloor, Matthias, Tomann, Judith, Canbay, Ali, Strassburg, Christian, Moeslein, Gabriele, Morak, Monika, Holinski-Feder, Elke, Buettner, Reinhard, Aretz, Stefan
ORCID: 0000-0002-5228-1890, Loeffler, Markus, Schmiegel, Wolff, Pox, Christian and Schulmann, Karsten
(2021).
Early detection of duodenal cancer by upper gastrointestinal-endoscopy in Lynch syndrome.
Int. J. Cancer, 149 (12).
S. 2052 - 2063.
HOBOKEN:
WILEY.
ISSN 1097-0215
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
Seppala, Toni T., Dominguez-Valentin, Mev, Crosbie, Emma J., Engel, Christoph ORCID: 0000-0002-7247-282X, Aretz, Stefan
ORCID: 0000-0002-5228-1890, Macrae, Finlay, Winship, Ingrid, Capella, Gabriel, Thomas, Huw, Hovig, Eivind
ORCID: 0000-0002-9103-1077, Nielsen, Maartje, Sijmons, Rolf H., Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria G., Cavestro, Giulia M., Mints, Miriam, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A., Green, Kate, Lalloo, Fiona, Hill, James, Schmiegel, Wolff, Vangala, Deepak
ORCID: 0000-0002-4175-5683, Perne, Claudia, Strauss, Hans-Georg, Tecklenburg, Johanna, Holinski-Feder, Elke, Steinke-Lange, Verena, Mecklin, Jukka-Pekka, Plazzer, John-Paul, Pineda, Marta, Navarro, Matilde, Vida, Joan B., Kariv, Revital, Rosner, Guy, Pinero, Tamara A., Pavicic, Walter, Kalfayan, Pablo, Ten Broeke, Sanne W., Jenkins, Mark A., Sunde, Lone
ORCID: 0000-0002-8479-165X, 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, Redler, Silke, Weitz, Jurgen, Pylvaenaeinen, Kirsi, Renkonen-Sinisalo, Laura, Lepisto, Anna, Hopper, John L., Win, Aung K., Lindor, Noralane M., Gallinger, Steven, Marchand, Loic Le, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Therkildsen, Christina, Wadt, Karin A. W., Mourits, Marian J. E., Ketabi, Zohreh, Denton, Oliver G., Rodland, Einar A., Vasen, Hans, Neffa, Florencia, Esperon, Patricia, Tjandra, Douglas, Moeslein, Gabriela, Rokkones, Erik, Sampson, Julian R., Evans, D. G. and Moller, Pal
(2021).
Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
Eur. J. Cancer, 148.
S. 124 - 134.
OXFORD:
ELSEVIER SCI LTD.
ISSN 1879-0852
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
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
Gallon, Richard ORCID: 0000-0002-5395-0099, Muehlegger, Barbara, Wenzel, Soeren-Sebastian, Sheth, Harsh, Hayes, Christine, Aretz, Stefan
ORCID: 0000-0002-5228-1890, Dahan, Karin, Foulkes, William, Kratz, Christian P., Ripperger, Tim, Azizi, Amedeo A., Feldman, Hagit Baris, Chong, Anne-Laure, Demirsoy, Ugur, Florkin, Benoit, Imschweiler, Thomas, Januszkiewicz-Lewandowska, Danuta
ORCID: 0000-0003-2332-2750, Lobitz, Stephan
ORCID: 0000-0001-5398-0610, Nathrath, Michaela, Pander, Hans-Juergen, Perez-Alonso, Vanesa, Perne, Claudia, Ragab, Iman, Rosenbaum, Thorsten, Rueda, Daniel
ORCID: 0000-0002-5377-8890, Seidel, Markus G.
ORCID: 0000-0003-0981-8661, Suerink, Manon, Taeubner, Julia, Zimmermann, Stefanie-Yvonne, Zschocke, Johannes, Borthwick, Gillian M., Burn, John, Jackson, Michael S., Santibanez-Koref, Mauro and Wimmer, Katharina
(2019).
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.
Hum. Mutat., 40 (5).
S. 649 - 656.
HOBOKEN:
WILEY.
ISSN 1098-1004
Kayser, Katrin, Degenhardt, Franziska, Holzapfel, Stefanie, Horpaopan, Sukanya, Peters, Sophia, Spier, Isabel, Morak, Monika, Vangala, Deepak, Rahner, Nils, von Knebel-Doeberitz, Magnus, Schackert, Hans K., Engel, Christoph ORCID: 0000-0002-7247-282X, Buettner, Reinhard, Wijnen, Juul, Doerks, Tobias, Bork, Peer, Moebus, Susanne, Herms, Stefan
ORCID: 0000-0002-2786-8200, Fischer, Sascha, Hoffmann, Per, Aretz, Stefan
ORCID: 0000-0002-5228-1890 and Steinke-Lange, Verena
(2018).
Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.
Int. J. Cancer, 143 (11).
S. 2800 - 2814.
HOBOKEN:
WILEY.
ISSN 1097-0215
Emons, Guenter, Steiner, Eric, Vordermark, Dirk, Uleer, Christoph, Bock, Nina, Paradies, Kerstin, Ortmann, Olaf, Aretz, Stefan ORCID: 0000-0002-5228-1890, Mallmann, Peter, Kurzeder, Christian, Hagen, Volker, van Oorschot, Birgitt, Hoecht, Stefan, Feyer, Petra, Egerer, Gerlinde, Friedrich, Michael, Cremer, Wolfgang, Prott, Franz-Josef, Horn, Lars-Christian, Prompeler, Heinrich, Langrehr, Jan, Leinung, Steffen, Beckmann, Matthias W., Kimmig, Rainer, Letsch, Anne, Reinhardt, Michael, Alt-Epping, Bernd, Kiesel, Ludwig, Menke, Jan, Gebhardt, Marion, Steinke-Lange, Verena, Rahner, Nils, Lichtenegger, Werner, Zeimet, Alain, Hanf, Volker, Weis, Joachim, Mueller, Michael, Henscher, Ulla, Schmutzler, Rita K., Meindl, Alfons, Hilpert, Felix, Panke, Joan Elisabeth, Strnad, Vratislav, Niehues, Christiane, Dauelsberg, Timm, Niehoff, Peter, Mayr, Doris, Grab, Dieter, Kreissl, Michael, Witteler, Ralf, Schorsch, Annemarie, Mustea, Alexander, Petru, Edgar, Huebner, Jutta, Rose, Anne Derke, Wight, Edward, Tholen, Reina, Bauerschmitz, Gerd J., Fleisch, Markus, Juhasz-Boess, Ingolf, Lax, Sigurd, Runnebaum, Ingo, Tempfer, Clemens
ORCID: 0000-0002-6904-3258, Nothacker, Monika J., Bloedt, Susanne, Follmann, Markus
ORCID: 0000-0003-3790-5578, Langer, Thomas, Raatz, Heike, Wesselmann, Simone and Erdogan, Saskia
(2018).
Interdisciplinary Diagnosis, Therapy and Follow-up of Patients with Endometrial Cancer. Guideline (S3-Level, AWMF Registry Number 032/034-OL, April 2018) - Part 2 with Recommendations on the Therapy and Follow-up of Endometrial Cancer, Palliative Care, Psycho-oncological/Psychosocial Care/Rehabilitation/Patient Information and Healthcare Facilities.
Geburtshilfe Frauenheilkd., 78 (11).
S. 1089 - 1110.
STUTTGART:
GEORG THIEME VERLAG KG.
ISSN 1438-8804
Emons, Guenter, Steiner, Eric, Vordermark, Dirk, Uleer, Christoph, Bock, Nina, Paradiess, Kerstin, Ortmann, Olaf, Aretz, Stefan ORCID: 0000-0002-5228-1890, Mallmann, Peter, Kurzeder, Christian, Hagen, Volker, van Oorschot, Birgitt, Hoecht, Stefan, Feyer, Petra, Egerer, Gerlinde, Friedrich, Michael, Cremer, Wolfgang, Prott, Franz-Josef, Horn, Lars-Christian, Proempeler, Heinrich, Langrehr, Jan, Leinung, Steffen, Beckmann, Matthias W., Kimmig, Rainer, Letsch, Anne, Reinhardt, Michael, Alt-Epping, Bernd, Kiesel, Ludwig, Menke, Jan, Gebhardt, Marion, Steinke-Lange, Verena, Rahner, Nils, Lichtenegger, Werner, Zeimet, Alain, Hanf, Volker, Weis, Joachim, Mueller, Michael, Henscher, Ulla, Schmutzler, Rita K., Meindl, Alfons, Hilpert, Felix, Panke, Joan Elisabeth, Strnad, Vratislav, Niehues, Christiane, Dauelsberg, Timm, Niehoff, Peter, Mayr, Doris, Grab, Dieter, Kreissl, Michael, Witteler, Ralf, Schorsch, Annemarie, Mustea, Alexander, Petru, Edgar, Huebner, Jutta, Rose, Anne Derke, Wight, Edward, Tholen, Reina, Bauerschmitz, Gerd J., Fleisch, Markus, Juhasz-Boess, Ingolf, Sigurd, Lax, Runnebaum, Ingo, Tempfer, Clemens
ORCID: 0000-0002-6904-3258, Nothacker, Monika J., Bloedt, Susanne, Follmann, Markus
ORCID: 0000-0003-3790-5578, Langer, Thomas, Raatz, Heike, Wesselmann, Simone and Erdogan, Saskia
(2018).
Interdisciplinary Diagnosis, Therapy and Follow-up of Patients with Endometrial Cancer. Guideline (S3-Level, AWMF Registry Nummer 032/034-OL, April 2018) - Part 1 with Recommendations on the Epidemiology, Screening, Diagnosis and Hereditary Factors of Endometrial Cancer.
Geburtshilfe Frauenheilkd., 78 (10).
S. 949 - 971.
STUTTGART:
GEORG THIEME VERLAG KG.
ISSN 1438-8804
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, Kirfel, Jutta, Peters, Sophia, Kloth, Michael, Hueneburg, Robert, Altmueller, Janine, Drichel, Dmitriy ORCID: 0000-0001-5978-3458, Odenthal, Margarete, Kristiansen, Glen, Strassburg, Christian, Nattermann, Jacob, Hoffmann, Per, Nuernberg, Peter, Buettner, Reinhard, Thiele, Holger, Kahl, Philip, Spier, Isabel and Aretz, Stefan
ORCID: 0000-0002-5228-1890
(2017).
Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS).
Hered. Cancer Clin. Pract., 15.
LONDON:
BIOMED CENTRAL LTD.
ISSN 1897-4287
Binder, Hans, Hopp, Lydia, Schweiger, Michal R., Hoffmann, Steve, Juehling, Frank, Kerick, Martin ORCID: 0000-0002-6298-4514, Timmermann, Bernd, Siebert, Susann, Grimm, Christina
ORCID: 0000-0002-4676-8870, Nersisyan, Lilit
ORCID: 0000-0001-8525-420X, Arakelyan, Arsen
ORCID: 0000-0002-6851-1056, Herberg, Maria, Buske, Peter, Loeffler-Wirth, Henry, Rosolowski, Maciej, Engel, Christoph
ORCID: 0000-0002-7247-282X, Przybilla, Jens, Peifer, Martin
ORCID: 0000-0002-5243-5503, Friedrichs, Nicolaus, Moeslein, Gabriela, Odenthal, Margarete, Hussong, Michelle, Peters, Sophia, Holzapfel, Stefanie, Nattermann, Jacob, Hueneburg, Robert, Schmiegel, Wolff, Royer-Pokora, Brigitte, Aretz, Stefan
ORCID: 0000-0002-5228-1890, Kloth, Michael, Kloor, Matthias, Buettner, Reinhard, Galle, Joerg and Loeffler, Markus
(2017).
Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome.
J. Pathol., 243 (2).
S. 242 - 255.
HOBOKEN:
WILEY.
ISSN 1096-9896
Kloth, Michael, Ruesseler, Vanessa, Engel, Christoph ORCID: 0000-0002-7247-282X, Koenig, Katharina, Peifer, Martin
ORCID: 0000-0002-5243-5503, Mariotti, Erika, Kuenstlinger, Helen, Florin, Alexandra, Rommerscheidt-Fuss, Ursula, Koitzsch, Ulrike, Wodtke, Claudia, Ueckeroth, Frank, Holzapfel, Stefanie, Aretz, Stefan
ORCID: 0000-0002-5228-1890, Propping, Peter, Loeffler, Markus, Merkelbach-Bruse, Sabine, Odenthal, Margarete, Friedrichs, Nicolaus, Heukamp, Lukas Carl, Zander, Thomas and Buettner, Reinhard
(2016).
Activating ERBB2/HER2 mutations indicate susceptibility to pan-HER inhibitors in Lynch and Lynch-like colorectal cancer.
Gut, 65 (8).
S. 1296 - 1306.
LONDON:
BMJ PUBLISHING GROUP.
ISSN 1468-3288
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
Spier, Isabel, Kerick, Martin ORCID: 0000-0002-6298-4514, Drichel, Dmitriy
ORCID: 0000-0001-5978-3458, Horpaopan, Sukanya, Altmueller, Janine, Laner, Andreas, Holzapfel, Stefanie, Peters, Sophia, Adam, Ronja, Zhao, Bixiao
ORCID: 0000-0002-1775-1690, Becker, Tim, Lifton, Richard P., Holinski-Feder, Elke, Perner, Sven, Thiele, Holger, Noethen, Markus M., Hoffmann, Per, Timmermann, Bernd, Schweiger, Michal R. and Aretz, Stefan
ORCID: 0000-0002-5228-1890
(2016).
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
Fam. Cancer, 15 (2).
S. 281 - 289.
DORDRECHT:
SPRINGER.
ISSN 1573-7292
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
Spier, Isabel, Holzapfel, Stefanie, Altmueller, Janine, Zhao, Bixiao ORCID: 0000-0002-1775-1690, Horpaopan, Sukanya, Vogt, Stefanie, Chen, Sophia, Morak, Monika, Raeder, Susanne, Kayser, Katrin, Stienen, Dietlinde, Adam, Ronja, Nuernberg, Peter, Plotz, Guido, Holinski-Feder, Elke, Lifton, Richard P., Thiele, Holger, Hoffmann, Per, Steinke, Verena and Aretz, Stefan
ORCID: 0000-0002-5228-1890
(2015).
Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas.
Int. J. Cancer, 137 (2).
S. 320 - 332.
HOBOKEN:
WILEY-BLACKWELL.
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
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