Disease-causing gene-flanking genomic rearrangements in HNPCC patients

od Morak, Monika, Massdorf, Trisari, Locher, Melanie, Holinski-Feder, Elke
Izdano 2011

MON-177 CAH-X Syndrome in a German Cohort of Patients with Congenital Adrenal Hyperplasia

od Sappl, Andrea, Lottspeich, Christian, Vill, Katharina, Morak, Monika, Bidlingmaier, Martin, Reisch, Nicole
izdano v J Endocr Soc (2020)

Targeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndrome

od Arnold, Anke Marie, Morak, Monika, Benet-Pagès, Anna, Laner, Andreas, Frishman, Dimitrij, Holinski-Feder, Elke
izdano v Eur J Hum Genet (2019)

Biallelic MUTYH mutations can mimic Lynch syndrome

od Morak, Monika, Heidenreich, Barbara, Keller, Gisela, Hampel, Heather, Laner, Andreas, de la Chapelle, Albert, Holinski-Feder, Elke
Izdano 2014

Serum antibodies against frameshift peptides in microsatellite unstable colorectal cancer patients with Lynch syndrome

od Reuschenbach, Miriam, Kloor, Matthias, Morak, Monika, Wentzensen, Nicolas, Germann, Anja, Garbe, Yvette, Tariverdian, Mirjam, Findeisen, Peter, Neumaier, Michael, Holinski-Feder, Elke, Doeberitz, Magnus von Knebel
Izdano 2010

Identification of genetic variants for clinical management of familial colorectal tumors

od Dominguez-Valentin, Mev, Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Martins, Alexandra, Møller, Pål, Hovig, Eivind
izdano v BMC Med Genet (2018)

Full-length transcript amplification and sequencing as universal method to test mRNA integrity and biallelic expression in mismatch repair genes

od Morak, Monika, Schaefer, Kerstin, Steinke-Lange, Verena, Koehler, Udo, Keinath, Susanne, Massdorf, Trisari, Mauracher, Brigitte, Rahner, Nils, Bailey, Jessica, Kling, Christiane, Haeusser, Tanja, Laner, Andreas, Holinski-Feder, Elke
izdano v Eur J Hum Genet (2019)

Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds

od Dominguez-Valentin, Mev, Evans, D. Gareth R., Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Martins, Alexandra, Møller, Pål, Hovig, Eivind
izdano v Hered Cancer Clin Pract (2018)

Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing

od Dominguez-Valentin, Mev, Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Holth, Arild, Capella, Gabriel, Davidson, Ben, Evans, D. Gareth, Martins, Alexandra, Møller, Pål, Hovig, Eivind
izdano v Sci Rep (2019)

An American Founder Mutation in MLH1

od Tomsic, Jerneja, Liyanarachchi, Sandya, Hampel, Heather, Morak, Monika, Thomas, Brittany C., Raymond, Victoria M., Chittenden, Anu, Schackert, Hans K., Gruber, Stephen B., Syngal, Sapna, Viel, Alessandra, Holinski-Feder, Elke, Thibodeau, Stephen N., de la Chapelle, Albert
Izdano 2011

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

od 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
Izdano 2010

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

od 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
Izdano 2011

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

od 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
izdano v BMC Cancer (2020)

Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications

od 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
Izdano 2010

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

od Møller, Pål, Seppälä, Toni, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paola, Evans, D Gareth, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf, Jeffries, Jacqueline, Vasen, Hans, Burn, John, Nakken, Sigve, Hovig, Eivind, Rødland, Einar Andreas, Tharmaratnam, Kukatharmini, de Vos tot Nederveen Cappel, Wouter H, Hill, James, Wijnen, Juul, Green, Kate, Lalloo, Fiona, Sunde, Lone, Mints, Miriam, Bertario, Lucio, Pineda, Marta, Navarro, Matilde, Morak, Monika, Renkonen-Sinisalo, Laura, Frayling, Ian M, Plazzer, John-Paul, Pylvanainen, Kirsi, Sampson, Julian R, Capella, Gabriel, Mecklin, Jukka-Pekka, Möslein, Gabriela
izdano v Gut (2017)

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

od Møller, Pål, Seppälä, Toni, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paola, Evans, D Gareth, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf, Jeffries, Jacqueline, Vasen, Hans, Burn, John, Nakken, Sigve, Hovig, Eivind, Rødland, Einar Andreas, Tharmaratnam, Kukatharmini, de Vos tot Nederveen Cappel, Wouter H, Hill, James, Wijnen, Juul, Jenkins, Mark, Green, Kate, Lalloo, Fiona, Sunde, Lone, Mints, Miriam, Bertario, Lucio, Pineda, Marta, Navarro, Matilde, Morak, Monika, Renkonen-Sinisalo, Laura, Frayling, Ian M, Plazzer, John-Paul, Pylvanainen, Kirsi, Genuardi, Maurizio, Mecklin, Jukka-Pekka, Möslein, Gabriela, Sampson, Julian R, Capella, Gabriel
izdano v Gut (2017)

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

od Seppälä, Toni, Pylvänäinen, Kirsi, Evans, Dafydd Gareth, Järvinen, Heikki, Renkonen-Sinisalo, Laura, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paola, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf, Jeffries, Jacqueline, Vasen, Hans, Burn, John, Nakken, Sigve, Hovig, Eivind, Rødland, Einar Andreas, Tharmaratnam, Kukatharmini, de Vos tot Nederveen Cappel, Wouter H., Hill, James, Wijnen, Juul, Jenkins, Mark, Genuardi, Maurizio, Green, Kate, Lalloo, Fiona, Sunde, Lone, Mints, Miriam, Bertario, Lucio, Pineda, Marta, Navarro, Matilde, Morak, Monika, Frayling, Ian M., Plazzer, John-Paul, Sampson, Julian R., Capella, Gabriel, Möslein, Gabriela, Mecklin, Jukka-Pekka, Møller, Pål
izdano v Hered Cancer Clin Pract (2017)

Application of a five-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants lodged on the InSiGHT locus-specific database

od Thompson, Bryony A., Spurdle, Amanda B., Plazzer, John-Paul, Greenblatt, Marc S., Akagi, Kiwamu, Al-Mulla, Fahd, Bapat, Bharati, Bernstein, Inge, Capellá, Gabriel, den Dunnen, Johan T., du Sart, Desiree, Fabre, Aurelie, Farrell, Michael P., Farrington, Susan M., Frayling, Ian M., Frebourg, Thierry, Goldgar, David E., Heinen, Christopher D., Holinski-Feder, Elke, Kohonen-Corish, Maija, Robinson, Kristina Lagerstedt, Leung, Suet Yi, Martins, Alexandra, Moller, Pal, Morak, Monika, Nystrom, Minna, Peltomaki, Paivi, Pineda, Marta, Qi, Ming, Ramesar, Rajkumar, Rasmussen, Lene Juel, Royer-Pokora, Brigitte, Scott, Rodney J., Sijmons, Rolf, Tavtigian, Sean V., Tops, Carli M., Weber, Thomas, Wijnen, Juul, Woods, Michael O., Macrae, Finlay, Genuardi, Maurizio
izdano v Nat Genet (2013)

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

od Møller, Pål, Seppälä, Toni T, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paulo, Gareth Evans, D, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf H, Jeffries, Jacqueline, Vasen, Hans F A, Burn, John, Nakken, Sigve, Hovig, Eivind, Rødland, Einar Andreas, Tharmaratnam, Kukatharmini, de Vos tot Nederveen Cappel, Wouter H, Hill, James, Wijnen, Juul T, Jenkins, Mark A, Green, Kate, Lalloo, Fiona, Sunde, Lone, Mints, Miriam, Bertario, Lucio, Pineda, Marta, Navarro, Matilde, Morak, Monika, Renkonen-Sinisalo, Laura, Valentin, Mev Dominguez, Frayling, Ian M, Plazzer, John-Paul, Pylvanainen, Kirsi, Genuardi, Maurizio, Mecklin, Jukka-Pekka, Moeslein, Gabriela, Sampson, Julian R, Capella, Gabriel
izdano v Gut (2018)

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

od 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
Izdano 2010