Hereditary Cancer Syndromes

Por Rahner, Nils, Steinke, Verena
Publicado em 2008

Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2)

Por Rahner, Nils, Steinke, Verena, Schlegelberger, Brigitte, Olschwang, Sylviane, Eisinger, François, Hutter, Pierre
Publicado em 2010

Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012

Por Rahner, Nils, Steinke, Verena, Schlegelberger, Brigitte, Eisinger, Francois, Hutter, Pierre, Olschwang, Sylviane
Publicado em 2013

Constitutional mismatch repair deficiency and childhood leukemia/lymphoma – report on a novel biallelic MSH6 mutation

Por Ripperger, Tim, Beger, Carmela, Rahner, Nils, Sykora, Karl W., Bockmeyer, Clemens L., Lehmann, Ulrich, Kreipe, Hans H., Schlegelberger, Brigitte
Publicado em 2010

A Complex Rearrangement in the APC Gene Uncovered by Multiplex Ligation-Dependent Probe Amplification

Por Pagenstecher, Constanze, Gadzicki, Dorothea, Stienen, Dietlinde, Uhlhaas, Siegfried, Mangold, Elisabeth, Rahner, Nils, Arslan-Kirchner, Mine, Propping, Peter, Friedl, Waltraut, Aretz, Stefan
Publicado em 2007

Functional PMS2 Hybrid Alleles Containing a Pseudogene-Specific Missense Variant Trace Back to a Single Ancient Intrachromosomal Recombination Event

Por Ganster, Christina, Wernstedt, Annekatrin, Kehrer-Sawatzki, Hildegard, Messiaen, Ludwine, Schmidt, Konrad, Rahner, Nils, Heinimann, Karl, Fonatsch, Christa, Zschocke, Johannes, Wimmer, Katharina
Publicado em 2010

Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study

Por Campa, Daniele, Pardini, Barbara, Naccarati, Alessio, Vodickova, Ludmila, Novotny, Jan, Steinke, Verena, Rahner, Nils, Holinski-Feder, Elke, Morak, Monika, Schackert, Hans K, Görgens, Heike, Kötting, Judith, Betz, Beate, Kloor, Matthias, Engel, Christoph, Büttner, Reinhard, Propping, Peter, Försti, Asta, Hemminki, Kari, Barale, Roberto, Vodicka, Pavel, Canzian, Federico
Publicado em 2010

Association Between TAS2R38 Gene Polymorphisms and Colorectal Cancer Risk: A Case-Control Study in Two Independent Populations of Caucasian Origin

Por Carrai, Maura, Steinke, Verena, Vodicka, Pavel, Pardini, Barbara, Rahner, Nils, Holinski-Feder, Elke, Morak, Monika, Schackert, Hans K., Görgens, Heike, Stemmler, Susanne, Betz, Beate, Kloor, Matthias, Engel, Christoph, Büttner, Reinhard, Naccarati, Alessio, Vodickova, Ludmila, Novotny, Jan, Stein, Angelika, Hemminki, Kari, Propping, Peter, Försti, Asta, Canzian, Federico, Barale, Roberto, Campa, Daniele
Publicado em 2011

Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications

Por Huhn, Stefanie, Ingelfinger, Dierk, Bermejo, Justo Lorenzo, Bevier, Melanie, Pardini, Barbara, Naccarati, Alessio, Steinke, Verena, Rahner, Nils, Holinski-Feder, Elke, Morak, Monika, Schackert, Hans K, Görgens, Heike, Pox, Christian P, Goecke, Timm, Kloor, Matthias, Loeffler, Markus, Büttner, Reinhard, Vodickova, Ludmila, Novotny, Jan, Demir, Kubilay, Cruciat, Cristina-Maria, Renneberg, Rebecca, Huber, Wolfgang, Niehrs, Christof, Boutros, Michael, Propping, Peter, Vodička, Pavel, Hemminki, Kari, Försti, Asta
Publicado em 2010

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

Por Vasen, Hans F A, Blanco, Ignacio, Aktan-Collan, Katja, Gopie, Jessica P, Alonso, Angel, Aretz, Stefan, Bernstein, Inge, Bertario, Lucio, Burn, John, Capella, Gabriel, Colas, Chrystelle, Engel, Christoph, Frayling, Ian M, Genuardi, Maurizio, Heinimann, Karl, Hes, Frederik J, Hodgson, Shirley V, Karagiannis, John A, Lalloo, Fiona, Lindblom, Annika, Mecklin, Jukka-Pekka, Møller, Pal, Myrhoj, Torben, Nagengast, Fokko M, Parc, Yann, Ponz de Leon, Maurizio, Renkonen-Sinisalo, Laura, Sampson, Julian R, Stormorken, Astrid, Sijmons, Rolf H, Tejpar, Sabine, Thomas, Huw J W, Rahner, Nils, Wijnen, Juul T, Järvinen, Heikki Juhani, Möslein, Gabriela
Publicado em 2013

HIGH COLORECTAL AND LOW ENDOMETRIAL CANCER RISK IN EPCAM DELETION-POSITIVE LYNCH SYNDROME: A COHORT STUDY

Por Kempers, Marlies JE, Kuiper, Roland P, Ockeloen, Charlotte W, Chappuis, Pierre O, Hutter, Pierre, Rahner, Nils, Schackert, Hans K, Steinke, Verena, Holinski-Feder, Elke, Morak, Monika, Kloor, Matthias, Büttner, Reinhard, Verwiel, Eugene TP, van Krieken, J. Han, Nagtegaal, Iris D, Goossens, Monique, van der Post, Rachel S., Niessen, Renée C, Sijmons, Rolf H, Kluijt, Irma, Hogervorst, Frans BL, Leter, Edward M, Gille, Johan JP, Aalfs, Cora M, Redeker, Egbert JW, Hes, Frederik J, Tops, Carli MJ, van Nesselrooij, Bernadette PM, van Gijn, Marielle E, García, Encarna B Gómez, Eccles, Diana M, Bunyan, David J, Syngal, Sapna, Stoffel, Elena M, Culver, Julie O, Palomares, Melanie R, Graham, Tracy, Velsher, Lea, Papp, Janos, Oláh, Edith, Chan, Tsun L, Leung, Suet Y, van Kessel, Ad Geurts, Kiemeney, Lambertus ALM, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn JL
Publicado em 2010