Value of upper gastrointestinal endoscopy for gastric cancer surveillance in patients with Lynch syndrome
Ladigan‐Badura, Swetlana, Vangala, Deepak B., Engel, Christoph, Bucksch, Karolin, Hueneburg, Robert, Perne, Claudia, Nattermann, Jacob, Steinke‐Lange, Verena, Rahner, Nils, Schackert, Hans K., Weitz, Jürgen, Kloor, Matthias, Kuhlkamp, Judith, Nguyen, Huu Phuc, Moeslein, Gabriela, Strassburg, Christian, Morak, Monika, Holinski‐Feder, Elke, Buettner, Reinhard, Aretz, Stefan, Loeffler, Markus, Schmiegel, Wolff, Pox, Christian, Schulmann, Karsten
Published in International journal of cancer (01.01.2021)
Published in International journal of cancer (01.01.2021)
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Early detection of duodenal cancer by upper gastrointestinal‐endoscopy in Lynch syndrome
Vangala, Deepak B., Ladigan‐Badura, Swetlana, Engel, Christoph, Hüneburg, Robert, Perne, Claudia, Bucksch, Karolin, Nattermann, Jacob, Steinke‐Lange, Verena, Rahner, Nils, Weitz, Jürgen, Kloor, Matthias, Tomann, Judith, Canbay, Ali, Nguyen, Huu‐Phuc, Strassburg, Christian, Möslein, Gabriele, Morak, Monika, Holinski‐Feder, Elke, Büttner, Reinhard, Aretz, Stefan, Löffler, Markus, Schmiegel, Wolff, Pox, Christian, Schulmann, Karsten
Published in International journal of cancer (15.12.2021)
Published in International journal of cancer (15.12.2021)
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Age‐dependent performance of BRAF mutation testing in Lynch syndrome diagnostics
Bläker, Hendrik, Haupt, Saskia, Morak, Monika, Holinski‐Feder, Elke, Arnold, Alexander, Horst, David, Sieber‐Frank, Julia, Seidler, Florian, Winterfeld, Moritz, Alwers, Elizabeth, Chang‐Claude, Jenny, Brenner, Hermann, Roth, Wilfried, Engel, Christoph, Löffler, Markus, Möslein, Gabriela, Schackert, Hans‐Konrad, Weitz, Jürgen, Perne, Claudia, Aretz, Stefan, Hüneburg, Robert, Schmiegel, Wolff, Vangala, Deepak, Rahner, Nils, Steinke‐Lange, Verena, Heuveline, Vincent, von Knebel Doeberitz, Magnus, Ahadova, Aysel, Hoffmeister, Michael, Kloor, Matthias
Published in International journal of cancer (15.11.2020)
Published in International journal of cancer (15.11.2020)
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Adenoma and colorectal cancer risks in Lynch syndrome, Lynch‐like syndrome and familial colorectal cancer type X
Bucksch, Karolin, Zachariae, Silke, Ahadova, Aysel, Aretz, Stefan, Büttner, Reinhard, Görgens, Heike, Holinski‐Feder, Elke, Hüneburg, Robert, Kloor, Matthias, Knebel Doeberitz, Magnus, Ladigan‐Badura, Swetlana, Moeslein, Gabriela, Morak, Monika, Nattermann, Jacob, Nguyen, Huu Phuc, Perne, Claudia, Redler, Silke, Schmetz, Ariane, Steinke‐Lange, Verena, Surowy, Harald, Vangala, Deepak B., Weitz, Jürgen, Loeffler, Markus, Engel, Christoph
Published in International journal of cancer (01.01.2022)
Published in International journal of cancer (01.01.2022)
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Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis
Vargas-Parra, Gardenia M, González-Acosta, Maribel, Thompson, Bryony A, Gómez, Carolina, Fernández, Anna, Dámaso, Estela, Pons, Tirso, Morak, Monika, Del Valle, Jesús, Iglesias, Silvia, Velasco, Àngela, Solanes, Ares, Sanjuan, Xavier, Padilla, Natàlia, de la Cruz, Xavier, Valencia, Alfonso, Holinski-Feder, Elke, Brunet, Joan, Feliubadaló, Lídia, Lázaro, Conxi, Navarro, Matilde, Pineda, Marta, Capellá, Gabriel
Published in International journal of cancer (01.10.2017)
Published in International journal of cancer (01.10.2017)
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Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families
Steinke, Verena, Holzapfel, Stefanie, Loeffler, Markus, Holinski‐Feder, Elke, Morak, Monika, Schackert, Hans K., Görgens, Heike, Pox, Christian, Royer‐Pokora, Brigitte, Knebel‐Doeberitz, Magnus, Büttner, Reinhard, Propping, Peter, Engel, Christoph
Published in International journal of cancer (01.07.2014)
Published in International journal of cancer (01.07.2014)
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Mitochondrial and nuclear disease panel (Mito‐aND‐Panel): Combined sequencing of mitochondrial and nuclear DNA by a cost‐effective and sensitive NGS‐based method
Abicht, Angela, Scharf, Florentine, Kleinle, Stephanie, Schön, Ulrike, Holinski‐Feder, Elke, Horvath, Rita, Benet‐Pagès, Anna, Diebold, Isabel
Published in Molecular genetics & genomic medicine (01.11.2018)
Published in Molecular genetics & genomic medicine (01.11.2018)
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Extending the critical regions for mutations in the non‐coding gene RNU4ATAC in another patient with Roifman Syndrome
Hallermayr, Ariane, Graf, Janine, Koehler, Udo, Laner, Andreas, Schönfeld, Brigitte, Benet‐Pagès, Anna, Holinski‐Feder, Elke
Published in Clinical case reports (01.11.2018)
Published in Clinical case reports (01.11.2018)
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Guidelines for the Li-Fraumeni and heritable TP53-related cancer syndromes
Frebourg, Thierry, Bajalica Lagercrantz, Svetlana, Oliveira, Carla, Magenheim, Rita, Evans, D Gareth
Published in European journal of human genetics : EJHG (01.10.2020)
Published in European journal of human genetics : EJHG (01.10.2020)
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Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas
Spier, Isabel, Holzapfel, Stefanie, Altmüller, Janine, Zhao, Bixiao, Horpaopan, Sukanya, Vogt, Stefanie, Chen, Sophia, Morak, Monika, Raeder, Susanne, Kayser, Katrin, Stienen, Dietlinde, Adam, Ronja, Nürnberg, Peter, Plotz, Guido, Holinski‐Feder, Elke, Lifton, Richard P., Thiele, Holger, Hoffmann, Per, Steinke, Verena, Aretz, Stefan
Published in International journal of cancer (15.07.2015)
Published in International journal of cancer (15.07.2015)
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The “unnatural” history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance
Ahadova, Aysel, Seppälä, Toni T., Engel, Christoph, Gallon, Richard, Burn, John, Holinski‐Feder, Elke, Steinke‐Lange, Verena, Möslein, Gabriela, Nielsen, Maartje, Broeke, Sanne W., Laghi, Luigi, Dominguez‐Valentin, Mev, Capella, Gabriel, Macrae, Finlay, Scott, Rodney, Hüneburg, Robert, Nattermann, Jacob, Hoffmeister, Michael, Brenner, Hermann, Bläker, Hendrik, Knebel Doeberitz, Magnus, Sampson, Julian R., Vasen, Hans, Mecklin, Jukka‐Pekka, Møller, Pål, Kloor, Matthias
Published in International journal of cancer (15.02.2021)
Published in International journal of cancer (15.02.2021)
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Intrafamilial variability in fragile X-associated tremor/ataxia syndrome
Peters, Nils, Kamm, Christoph, Asmus, Friedrich, Holinski-Feder, Elke, Kraft, Eduard, Dichgans, Martin, Brüning, Roland, Gasser, Thomas, Bötzel, Kai
Published in Movement disorders (01.01.2006)
Published in Movement disorders (01.01.2006)
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Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
Zurek, Birte, Ellwanger, Kornelia, Vissers, Lisenka E L M, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, de Voer, Richarda M, Laurie, Steven, Matalonga, Leslie, Gilissen, Christian, Ossowski, Stephan, 't Hoen, Peter A C, Vitobello, Antonio, Schulze-Hentrich, Julia M, Riess, Olaf, Brunner, Han G, Brookes, Anthony J, Rath, Ana, Bonne, Gisèle, Gumus, Gulcin, Verloes, Alain, Hoogerbrugge, Nicoline, Evangelista, Teresinha, Harmuth, Tina, Swertz, Morris, Spalding, Dylan, Hoischen, Alexander, Beltran, Sergi, Graessner, Holm
Published in European journal of human genetics : EJHG (01.09.2021)
Published in European journal of human genetics : EJHG (01.09.2021)
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Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome
Tischkowitz, Marc, Colas, Chrystelle, Pouwels, Sjaak, Hoogerbrugge, Nicoline
Published in European journal of human genetics : EJHG (01.10.2020)
Published in European journal of human genetics : EJHG (01.10.2020)
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Microsatellite Instability in Pediatric and Adult High-grade Gliomas
Eckert, Anika, Kloor, Matthias, Giersch, Antje, Ahmadi, Rezvan, Herold-Mende, Christel, Hampl, Jürgen A., Heppner, Frank L., Zoubaa, Saida, Holinski-Feder, Elke, Pietsch, Torsten, Wiestler, Otmar D., Von Knebel Doeberitz, Magnus, Roth, Wilfried, Gebert, Johannes
Published in Brain pathology (Zurich, Switzerland) (01.04.2007)
Published in Brain pathology (Zurich, Switzerland) (01.04.2007)
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Targeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndrome
Arnold, Anke Marie, Morak, Monika, Benet-Pagès, Anna, Laner, Andreas, Frishman, Dimitrij, Holinski-Feder, Elke
Published in European journal of human genetics : EJHG (01.05.2020)
Published in European journal of human genetics : EJHG (01.05.2020)
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Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome
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
Published in Journal of clinical oncology (10.12.2012)
Published in Journal of clinical oncology (10.12.2012)
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Somatic copy number alteration and fragmentation analysis in circulating tumor DNA for cancer screening and treatment monitoring in colorectal cancer patients
Hallermayr, Ariane, Wohlfrom, Tobias, Steinke-Lange, Verena, Benet-Pagès, Anna, Scharf, Florentine, Heitzer, Ellen, Mansmann, Ulrich, Haberl, Christopher, de Wit, Maike, Vogelsang, Holger, Rentsch, Markus, Holinski-Feder, Elke, Pickl, Julia M. A
Published in Journal of hematology and oncology (02.09.2022)
Published in Journal of hematology and oncology (02.09.2022)
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Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study
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
Published in BMC cancer (24.05.2020)
Published in BMC cancer (24.05.2020)
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