Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome
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Published in Journal of clinical oncology (10.12.2012)
Published in Journal of clinical oncology (10.12.2012)
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Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism
Rauch, Anita, Thiel, Christian T, Schindler, Detlev, Wick, Ursula, Crow, Yanick J, Ekici, Arif B, van Essen, Anthonie J, Goecke, Timm O, Al-Gazali, Lihadh, Chrzanowska, Krystyna H, Zweier, Christiane, Brunner, Han G, Becker, Kristin, Curry, Cynthia J, Dallapiccola, Bruno, Devriendt, Koenraad, Dörfler, Arnd, Kinning, Esther, Megarbane, André, Meinecke, Peter, Semple, Robert K, Spranger, Stephanie, Toutain, Annick, Trembath, Richard C, Voss, Egbert, Wilson, Louise, Hennekam, Raoul, de Zegher, Francis, Dörr, Helmuth-Günther, Reis, André
Published in Science (American Association for the Advancement of Science) (08.02.2008)
Published in Science (American Association for the Advancement of Science) (08.02.2008)
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Efficacy of Annual Colonoscopic Surveillance in Individuals With Hereditary Nonpolyposis Colorectal Cancer
Engel, Christoph, Rahner, Nils, Schulmann, Karsten, Holinski–Feder, Elke, Goecke, Timm O, Schackert, Hans K, Kloor, Matthias, Steinke, Verena, Vogelsang, Holger, Möslein, Gabriela, Görgens, Heike, Dechant, Stefan, von Knebel Doeberitz, Magnus, Rüschoff, Josef, Friedrichs, Nicolaus, Büttner, Reinhard, Loeffler, Markus, Propping, Peter, Schmiegel, Wolff
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MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases
Engert, Stefanie, Wappenschmidt, Barbara, Betz, Beate, Kast, Karin, Kutsche, Michael, Hellebrand, Heide, Goecke, Timm O, Kiechle, Marion, Niederacher, Dieter, Schmutzler, Rita K, Meindl, Alfons
Published in Human mutation (01.07.2008)
Published in Human mutation (01.07.2008)
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Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical management
Heidemann, Simone, Fischer, Christine, Engel, Christoph, Fischer, Barbara, Harder, Lana, Schlegelberger, Brigitte, Niederacher, Dieter, Goecke, Timm O., Doelken, Sandra C., Dikow, Nicola, Jonat, Walter, Morlot, Susanne, Schmutzler, Rita C., Arnold, Norbert K.
Published in Breast cancer research and treatment (01.08.2012)
Published in Breast cancer research and treatment (01.08.2012)
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Genotype-Phenotype Comparison of German MLH1 and MSH2 Mutation Carriers Clinically Affected With Lynch Syndrome: A Report by the German HNPCC Consortium
GOECKE, Timm, SCHULMANN, Karsten, DIETMAIER, Wolfgang, MANGOLD, Elisabeth, FRIEDRICHS, Nicolaus, PROPPING, Peter, KRÜGER, Stefan, GEBERT, Johannes, SCHMIEGEL, Wolff, RUESCHOFF, Josef, LOEFFLER, Markus, MOESLEIN, Gabriela, ENGEL, Christoph, HOLINSKI-FEDER, Eike, PAGENSTECHER, Constanze, SCHACKERT, Hans K, KLOOR, Matthias, KUNSTMANN, Erdmute, VOGELSANG, Holger, KELLER, Gisela
Published in Journal of clinical oncology (10.09.2006)
Published in Journal of clinical oncology (10.09.2006)
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Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome
NEUMANN, Thomas E, ALLANSON, Judith, HOELTZENBEIN, Maria, GOECKE, Timm O, GERD KEHL, Hans, ALBRECHT, Beate, LUCZAK, Klaudiusz, SASIADEK, Maria M, MUSANTE, Luciana, LAURIE, Rohan, PETERS, Hartmut, TARTAGLIA, Marco, KAVAMURA, Ines, ZENKER, Martin, KALSCHEUER, Vera, KERR, Bronwyn, NERI, Giovanni, NOONAN, Jacqueline, CORDEDDU, Viviana, GIBSON, Kate, TZSCHACH, Andreas, KRÜGER, Gabriele
Published in European journal of human genetics : EJHG (01.04.2009)
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Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9
Czeschik, Johanna Christina, Voigt, Claudia, Goecke, Timm O., Lüdecke, Hermann-Josef, Wagner, Nicholas, Kuechler, Alma, Wieczorek, Dagmar
Published in American journal of medical genetics. Part A (01.02.2013)
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Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers
Salloch, Heidi, Reinacher-Schick, Anke, Schulmann, Karsten, Pox, Christian, Willert, Jörg, Tannapfel, Andrea, Heringlake, Stefan, Goecke, Timm O., Aretz, Stefan, Stemmler, Susanne, Schmiegel, Wolff
Published in International journal of colorectal disease (2010)
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Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2
Betz, Beate, Theiss, Stephan, Aktas, Murat, Konermann, Carolin, Goecke, Timm O, Möslein, Gabriela, Schaal, Heiner, Royer-Pokora, Brigitte
Published in Journal of cancer research and clinical oncology (2010)
Published in Journal of cancer research and clinical oncology (2010)
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Congenital central hypoventilation syndrome with hyperinsulinism in a preterm infant
Hennewig, Ulrike, Hadzik, Berit, Vogel, Markus, Meissner, Thomas, Goecke, Timm, Peters, Hartmut, Selzer, Georg, Mayatepek, Ertan, Hoehn, Thomas
Published in Journal of human genetics (01.06.2008)
Published in Journal of human genetics (01.06.2008)
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Gene expression in acute Stanford type A dissection: a comparative microarray study
Weis-Müller, Barbara Theresia, Modlich, Olga, Drobinskaya, Irina, Unay, Derya, Huber, Rita, Bojar, Hans, Schipke, Jochen D, Feindt, Peter, Gams, Emmeran, Müller, Wolfram, Goecke, Timm, Sandmann, Wilhelm
Published in Journal of translational medicine (06.07.2006)
Published in Journal of translational medicine (06.07.2006)
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New mutations in the ATM gene and clinical data of 25 AT patients
Demuth, Ilja, Dutrannoy, Véronique, Marques, Wilson, Neitzel, Heidemarie, Schindler, Detlev, Dimova, Petja S., Chrzanowska, Krystyna H., Bojinova, Veneta, Gregorek, Hanna, Graul-Neumann, Luitgard M., von Moers, Arpad, Schulze, Ilka, Nicke, Marion, Bora, Elcin, Cankaya, Tufan, Oláh, Éva, Kiss, Csongor, Bessenyei, Beáta, Szakszon, Katalin, Gruber-Sedlmayr, Ursula, Kroisel, Peter Michael, Sodia, Sigrun, Goecke, Timm O., Dörk, Thilo, Digweed, Martin, Sperling, Karl, de Sá, Joaquim, Lourenco, Charles Marques, Varon, Raymonda
Published in Neurogenetics (01.11.2011)
Published in Neurogenetics (01.11.2011)
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Deciphering the genetics of hereditary non-syndromic colorectal cancer
PAPAEMMANUIL, Eli, CARVAJAL-CARMONA, Luis, VIJAYAKRISHNAN, Jayaram, BRODERICK, Peter, GORMAN, Maggie, MARTIN, Lynn, LUCASSEN, Anneke, BISHOP, D. Timothy, EVANS, D. Gareth, MAHER, Eamonn R, STEINKE, Verena, RAHNER, Nils, SELLICK, Gabrielle S, SCHACKERT, Hans K, GOECKE, Timm O, HOLINSKI-FEDER, Elke, PROPPING, Peter, VAN WEZEL, Tom, WIJNEN, Juul, CAZIER, Jean-Baptiste, THOMAS, Huw, HOULSTON, Richard S, TOMLINSON, Ian, KEMP, Zoe, WEBB, Emily, SPAIN, Sarah, SULLIVAN, Kate, BARCLAY, Ella, LUBBE, Steven, JAEGER, Emma
Published in European journal of human genetics : EJHG (01.12.2008)
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Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1
Schwabe, Georg C., Türkmen, Seval, Leschik, Gundula, Palanduz, Sukru, Stöver, Brigitte, Goecke, Timm O., Mundlos, Stefan
Published in American journal of medical genetics. Part A (01.02.2004)
Published in American journal of medical genetics. Part A (01.02.2004)
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Age of uptake of early cancer detection facilities by low-risk and high-risk patients with familial breast and ovarian cancer
Lux, Michael Patrick, Ackermann, Sven, Bani, Mayada R, Nestle-Krämling, Caroline, Goecke, Timm O, Niederacher, Dieter, Bodden-Heidrich, R, Bender, Hans-Georg, Beckmann, Matthias Wilhelm, Fasching, Peter Andreas
Published in European journal of cancer prevention (01.12.2005)
Published in European journal of cancer prevention (01.12.2005)
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Spectrum and frequencies of mutations inMSH2 andMLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer
Mangold, Elisabeth, Pagenstecher, Constanze, Friedl, Waltraut, Mathiak, Micaela, Buettner, Reinhard, Engel, Christoph, Loeffler, Markus, Holinski-Feder, Elke, Müller-Koch, Yvonne, Keller, Gisela, Schackert, Hans K., Krüger, Stefan, Goecke, Timm, Moeslein, Gabriela, Kloor, Matthias, Gebert, Johannes, Kunstmann, Erdmute, Schulmann, Karsten, Rüschoff, Josef, Propping, Peter
Published in International journal of cancer (20.09.2005)
Published in International journal of cancer (20.09.2005)
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Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects
WUYTS, Wim, WAEBER, Gerard, MEINECKE, Peter, SCHÜLER, Herdit, GOECKE, Timm O, VAN HUL, Wim, BARTSCH, Oliver
Published in European journal of human genetics : EJHG (01.05.2004)
Published in European journal of human genetics : EJHG (01.05.2004)
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Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility
Lascorz, Jesús, Försti, Asta, Chen, Bowang, Buch, Stephan, Steinke, Verena, Rahner, Nils, Holinski-Feder, Elke, Morak, Monika, Schackert, Hans K., Görgens, Heike, Schulmann, Karsten, Goecke, Timm, Kloor, Matthias, Engel, Cristoph, Büttner, Reinhard, Kunkel, Nelli, Weires, Marianne, Hoffmeister, Michael, Pardini, Barbara, Naccarati, Alessio, Vodickova, Ludmila, Novotny, Jan, Schreiber, Stefan, Krawczak, Michael, Bröring, Clemens D., Völzke, Henry, Schafmayer, Clemens, Vodicka, Pavel, Chang-Claude, Jenny, Brenner, Hermann, Burwinkel, Barbara, Propping, Peter, Hampe, Jochen, Hemminki, Kari
Published in Carcinogenesis (New York) (01.09.2010)
Published in Carcinogenesis (New York) (01.09.2010)
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Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer
Mangold, Elisabeth, Pagenstecher, Constanze, Friedl, Waltraut, Mathiak, Micaela, Buettner, Reinhard, Engel, Christoph, Loeffler, Markus, Holinski‐Feder, Elke, Müller‐Koch, Yvonne, Keller, Gisela, Schackert, Hans K., Krüger, Stefan, Goecke, Timm, Moeslein, Gabriela, Kloor, Matthias, Gebert, Johannes, Kunstmann, Erdmute, Schulmann, Karsten, Rüschoff, Josef, Propping, Peter
Published in International journal of cancer (20.09.2005)
Published in International journal of cancer (20.09.2005)
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