Opinion on moderate/low cancer genetic risk markers in medical practice

por Aretz, Stefan, Friedl, Waltraut
Publicado 2008

Familial Adenomatous Polyposis: Experience from a Study of 1164 Unrelated German Polyposis Patients

por Friedl, Waltraut, Aretz, Stefan
Publicado 2005

MEDB-61. Genetic alterations ofTP53 andOTX2 indicate increased risk of relapse in WNT medulloblastomas

por Goschzik, Tobias, Mynarek, Martin, Dörner, Evelyn, Aretz, Stefan, Rutkowski, Stefan, Pietsch, Torsten
Publicado 2022

Overview of the Clinical Features of Li-Fraumeni Syndrome and the Current European ERN GENTURIS Guideline

por Kratz, Christian Peter, Steinke-Lange, Verena, Spier, Isabel, Aretz, Stefan, Schröck, Evelin, Holinski-Feder, Elke
Publicado 2021

Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes

por Henn, Jonas, Spier, Isabel, Adam, Ronja S., Holzapfel, Stefanie, Uhlhaas, Siegfried, Kayser, Katrin, Plotz, Guido, Peters, Sophia, Aretz, Stefan
Publicado 2019

Hereditary Diffuse Gastric Cancer: A Comparative Cohort Study According to Pathogenic Variant Status

por Marwitz, Tim, Hüneburg, Robert, Spier, Isabel, Lau, Jan-Frederic, Kristiansen, Glen, Lingohr, Philipp, Kalff, Jörg C., Aretz, Stefan, Nattermann, Jacob, Strassburg, Christian P.
Publicado 2020

Effects of common haplotypes of the ileal sodium dependent bile acid transporter gene on the development of sporadic and familial colorectal cancer: A case control study

por Grünhage, Frank, Jungck, Matthias, Lamberti, Christoph, Keppeler, Hildegard, Becker, Ursula, Schulte-Witte, Hildegard, Plassmann, Dominik, Friedrichs, Nicolaus, Buettner, Reinhard, Aretz, Stefan, Sauerbruch, Tilman, Lammert, Frank
Publicado 2008

Real‐time use of artificial intelligence (CADEYE) in colorectal cancer surveillance of patients with Lynch syndrome—A randomized controlled pilot trial (CADLY)

por Hüneburg, Robert, Bucksch, Karolin, Schmeißer, Friederike, Heling, Dominik, Marwitz, Tim, Aretz, Stefan, Kaczmarek, Dominik J., Kristiansen, Glen, Hommerding, Oliver, Strassburg, Christian P., Engel, Christoph, Nattermann, Jacob
Publicado 2022

Chromoendoscopy in combination with random biopsies does not improve detection of gastric cancer foci in CDH1 mutation positive patients

por Hüneburg, Robert, Marwitz, Tim, van Heteren, Peer, Weismüller, Tobias J., Trebicka, Jonel, Adam, Ronja, Aretz, Stefan, Perez Bouza, Alberto, Pantelis, Dimitrios, Kalff, Jörg C., Nattermann, Jacob, Strassburg, Cristian P.
Publicado 2016

Genetic alterations of TP53 and OTX2 indicate increased risk of relapse in WNT medulloblastomas

por Goschzik, Tobias, Mynarek, Martin, Doerner, Evelyn, Schenk, Alina, Spier, Isabel, Warmuth-Metz, Monika, Bison, Brigitte, Obrecht, Denise, Struve, Nina, Kortmann, Rolf-Dieter, Schmid, Matthias, Aretz, Stefan, Rutkowski, Stefan, Pietsch, Torsten
Publicado 2022

Survival of MUTYH-Associated Polyposis Patients With Colorectal Cancer and Matched Control Colorectal Cancer Patients

por Nielsen, Maartje, van Steenbergen, Liza N., Jones, Natalie, Vogt, Stefanie, Vasen, Hans F. A., Morreau, Hans, Aretz, Stefan, Sampson, Julian R., Dekkers, Olaf M., Janssen-Heijnen, Maryska L. G., Hes, Frederik J.
Publicado 2010

Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS)

por Horpaopan, Sukanya, Kirfel, Jutta, Peters, Sophia, Kloth, Michael, Hüneburg, Robert, Altmüller, Janine, Drichel, Dmitriy, Odenthal, Margarete, Kristiansen, Glen, Strassburg, Christian, Nattermann, Jacob, Hoffmann, Per, Nürnberg, Peter, Büttner, Reinhard, Thiele, Holger, Kahl, Philip, Spier, Isabel, Aretz, Stefan
Publicado 2017

The Management of Peutz–Jeghers Syndrome: European Hereditary Tumour Group (EHTG) Guideline †

por Wagner, Anja, Aretz, Stefan, Auranen, Annika, Bruno, Marco J., Cavestro, Giulia M., Crosbie, Emma J., Goverde, Anne, Jelsig, Anne Marie, Latchford, Andrew R., van Leerdam, Monique E., Lepisto, Anna H., Puzzono, Marta, Winship, Ingrid, Zuber, Veronica, Möslein, Gabriela
Publicado 2021

Variant profiling of colorectal adenomas from three patients of two families with MSH3-related adenomatous polyposis

por Perne, Claudia, Peters, Sophia, Cartolano, Maria, Horpaopan, Sukanya, Grimm, Christina, Altmüller, Janine, Sommer, Anna K., Hillmer, Axel M., Thiele, Holger, Odenthal, Margarete, Möslein, Gabriela, Adam, Ronja, Sivalingam, Sugirthan, Kirfel, Jutta, Schweiger, Michal R., Peifer, Martin, Spier, Isabel, Aretz, Stefan
Publicado 2021

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

por Hassanin, Emadeldin, Spier, Isabel, Bobbili, Dheeraj R., Aldisi, Rana, Klinkhammer, Hannah, David, Friederike, Dueñas, Nuria, Hüneburg, Robert, Perne, Claudia, Brunet, Joan, Capella, Gabriel, Nöthen, Markus M., Forstner, Andreas J., Mayr, Andreas, Krawitz, Peter, May, Patrick, Aretz, Stefan, Maj, Carlo
Publicado 2023

MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome

por Wiik, Mariann Unhjem, Negline, Mia, Beisvåg, Vidar, Clapham, Matthew, Holliday, Elizabeth, Dueñas, Nuria, Brunet, Joan, Pineda, Marta, Bonifaci, Nuria, Aretz, Stefan, Klinkhammer, Hannah, Spier, Isabel, Perne, Claudia, Mayr, Andreas, Valle, Laura, Lubinski, Jan, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A.
Publicado 2023

Disease expression in juvenile polyposis syndrome: a retrospective survey on a cohort of 221 European patients and comparison with a literature-derived cohort of 473 SMAD4/BMPR1A p...

por Blatter, Robert, Tschupp, Benjamin, Aretz, Stefan, Bernstein, Inge, Colas, Chrystelle, Evans, D. Gareth, Genuardi, Maurizio, Hes, Frederik J., Hüneburg, Robert, Järvinen, Heikki, Lalloo, Fiona, Moeslein, Gabriela, Renkonen-Sinisalo, Laura, Resta, Nicoletta, Spier, Isabel, Varvara, Dora, Vasen, Hans, Latchford, Andrew R., Heinimann, Karl
Publicado 2020

mTOR inhibitors reduce enteropathy, intestinal bleeding and colectomy rate in patients with juvenile polyposis of infancy with PTEN-BMPR1A deletion

por Taylor, Henry, Yerlioglu, Dilay, Phen, Claudia, Ballauff, Antje, Nedelkopoulou, Natalia, Spier, Isabel, Loverdos, Inés, Busoni, Veronica B, Heise, Jürgen, Dale, Peter, de Meij, Tim, Sweet, Kevin, Cohen, Marta C, Fox, Victor L, Mas, Emmanuel, Aretz, Stefan, Eng, Charis, Buderus, Stephan, Thomson, Mike, Rojas, Isabel, Uhlig, Holm H
Publicado 2021

Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study

por Bucksch, Karolin, Zachariae, Silke, Aretz, Stefan, Büttner, Reinhard, Holinski-Feder, Elke, Holzapfel, Stefanie, Hüneburg, Robert, Kloor, Matthias, von Knebel Doeberitz, Magnus, Morak, Monika, Möslein, Gabriela, Nattermann, Jacob, Perne, Claudia, Rahner, Nils, Schmiegel, Wolff, Schulmann, Karsten, Steinke-Lange, Verena, Strassburg, Christian P., Vangala, Deepak B., Weitz, Jürgen, Loeffler, Markus, Engel, Christoph
Publicado 2020

Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin

por Förster, Alisa, Brand, Frank, Banan, Rouzbeh, Hüneburg, Robert, Weber, Christine A. M., Ewert, Wiebke, Kronenberg, Jessica, Previti, Christopher, Elyan, Natalie, Beyer, Ulrike, Martens, Helge, Hong, Bujung, Bräsen, Jan H., Erbersdobler, Andreas, Krauss, Joachim K., Stangel, Martin, Samii, Amir, Wolf, Stephan, Preller, Matthias, Aretz, Stefan, Wiese, Bettina, Hartmann, Christian, Weber, Ruthild G.
Publicado 2021