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Publications by Morak, Monika

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Number of items: 14.

Journal article

Morak, Monika; Ibisler, Ayseguel; Keller, Gisela; Jessen, Ellen; Laner, Andreas; Gonzales-Fassrainer, Daniela; Locher, Melanie; Massdorf, Trisari; Nissen, Anke M.; Benet-Pages, Anna; Holinski-Feder, Elke (2018): Comprehensive analysis of the MLH1 promoter region in 480 patients with colorectal cancer and 1150 controls reveals new variants including one with a heritable constitutional MLH1 epimutation. In: Journal of Medical Genetics, Vol. 55, No. 4: pp. 240-248

Dominguez-Valentin, Mev; Evans, D. Gareth R.; Nakken, Sigve; Tubeuf, HLsne; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal; Hovig, Eivind (2018): Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds. In: Hereditary Cancer in Clinical Practice 16:4 [PDF, 1MB]

Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal; Hovig, Eivind (2018): Identification of genetic variants for clinical management of familial colorectal tumors. In: BMC Medical Genetics 19:26 [PDF, 652kB]

Engel, Christoph; Vasen, Hans F.; Seppala, Toni; Aretz, Stefan; Bigirwamungu-Bargeman, Marloes; Bör, Sybrand Y. de; Bucksch, Karolin; Buttner, Reinhard; Holinski-Feder, Elke; Holzapfel, Stefanie; Hueneburg, Robert; Jacobs, Maarten A. J. M.; Jarvinen, Heikki; Kloor, Matthias; Knebel Doeberitz, Magnus von; Koornstra, Jan J.; Kouwen, Mariette van; Langers, Alexandra M.; Meeberg, Paul C. van de; Morak, Monika; Moeslein, Gabriela; Nagengast, Fokko M.; Pylvanainen, Kirsi; Rahner, Nils; Renkonen-Sinisalo, Laura; Sanduleanu, Silvia; Schackert, Hans K.; Schmiegel, Wolff; Schulmann, Karsten; Steinke-Lange, Verena; Strassburg, Christian P.; Vecht, Juda; Verhulst, Marie-Louise; Vos Tot Nederveen Cappel, Wouter de; Zachariae, Silke; Mecklin, Jukka-Pekka; Löffler, Markus (2018): No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies. In: Gastroenterology, Vol. 155, No. 5: pp. 1400-1409

Kayser, Katrin; Degenhardt, Franziska; Holzapfel, Stefanie; Horpaopan, Sukanya; Peters, Sophia; Spier, Isabel; Morak, Monika; Vangala, Deepak; Rahner, Nils; Knebel Doeberitz, Magnus von; Schackert, Hans K.; Engel, Christoph; Büttner, Reinhard; Wijnen, Juul; Doerks, Tobias; Bork, Peer; Moebus, Susanne; Herms, Stefan; Fischer, Sascha; Hoffmann, Per; Aretz, Stefan; Steinke-Lange, Verena (2018): Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes. In: International Journal of Cancer, Vol. 143, No. 11: pp. 2800-2813

Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal; Hovig, Eivind (2018): Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families. In: Familial Cancer, Vol. 17, No. 1: pp. 141-153

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; Rodland, Einar Andreas; Tharmaratnam, Kukatharmini; Vos tot Nederveen Cappel, Wouter H. de; 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; Moller, Pal (2017): Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report. In: Hereditary Cancer in Clinical Practice 15:18 [PDF, 621kB]

Morak, Monika; Käsbauer, Sarah; Kerscher, Martina; Massdorf, Trisari; Holinski-Feder, Elke; Laner, Andreas; Nissen, Anke M.; Benet-Pages, Anna; Schackert, Hans K.; Keller, Gisela (2017): Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6. In: Familial Cancer, Vol. 16, No. 4: pp. 491-500

Vargas-Parra, Gardenia M.; Gonzalez-Acosta, Maribel; Thompson, Bryony A.; Gomez, Carolina; Fernandez, Anna; Damaso, Estela; Pons, Tirso; Morak, Monika; Valle, Jesus del; Iglesias, Silvia; Velasco, Angela; Solanes, Ares; Sanjuan, Xavier; Padilla, Natalia; Cruz, Xavier de la; Valencia, Alfonso; Holinski-Feder, Elke; Brunet, Joan; Feliubadalo, Lidia; Lazaro, Conxi; Navarro, Matilde; Pineda, Marta; Capella, Gabriel (2017): Elucidating the molecular basis of MSH2-deficienttumors by combined germline and somatic analysis. In: International Journal of Cancer, Vol. 141, No. 7: pp. 1365-1380

Moller, Pal; Seppala, 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; Rodland, Einar Andreas; Tharmaratnam, Kukatharmini; Vos Tot Nederveen Cappel, Wouter H. de; 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; Moslein, Gabriela; Sampson, Julian R.; Capella, Gabriel (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. In: Gut, Vol. 66, No. 9: pp. 1657-1664

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; Rodland, Einar Andreas; Tharmaratnam, Kukatharmini; Vos Tot Nederveen Cappel, Wouter H. de; 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 (2017): Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database. In: Gut, Vol. 66, No. 3: pp. 464-472

Morak, Monika; Koehler, Udo; Schackert, Hans Konrad; Steinke, Verena; Royer-Pokora, Brigitte; Schulmann, Karsten; Kloor, Matthias; Höchter, Wilhelm; Weingart, Josef; Keiling, Cortina; Massdorf, Trisari; Holinski-Feder, Elke (August 2011): Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome. In: Journal of medical genetics, Vol. 48, No. 8: pp. 513-519 [PDF, 917kB]

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 (2011): Association between TAS2R38 gene polymorphisms and colorectal cancer risk. A case-control study in two independent populations of Caucasian origin.
In: PLOS ONE 6(6), e20464 [PDF, 112kB]

Campa, Daniele; Pardini, Barbara; Naccarati, Alessio; Vodickova, Ludmila; Novotny, Jan; Steinke, Verena; Rahner, Nils; Holinski-Feder, Elke; Morak, Monika; Schackert, Hans K.; Goergens, Heike; Koetting, Judith; Betz, Beate; Kloor, Matthias; Engel, Christoph; Buettner, Reinhard; Propping, Peter; Foersti, Asta; Hemminki, Kari; Barale, Roberto; Vodicka, Pavel; Canzian, Federico (2010): Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study. In: BMC Gastroenterology 10:112 [PDF, 235kB]

This list was generated on Sat Aug 8 02:15:44 2020 CEST.