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Eine Ebene nach oben |
Gruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 31
2022
Scharf, Florentine; Silva, Rafaela Magalhaes Leal; Morak, Monika; Hastie, Alex; Pickl, Julia M. A.; Sendelbach, Kai; Gebhard, Christian; Locher, Melanie; Laner, Andreas; Steinke-Lange, Verena; Koehler, Udo; Holinski-Feder, Elke und Wolf, Dieter A.
(2022):
Constitutional chromothripsis of the APC locus as a cause of genetic predisposition to colon cancer.
In: Journal of Medical Genetics, Bd. 59, Nr. 10: S. 976-983
Morak, Monika; Pineda, Marta; Martins, Alexandra; Gaildrat, Pascaline; Tubeuf, Helene; Drouet, Aurelie; Gomez, Carolina; Damaso, Estela; Schäfer, Kerstin; Steinke-Lange, Verena; Koehler, Udo; Laner, Andreas; Hauchard, Julie; Chauris, Karine; Holinski-Feder, Elke und Capella, Gabriel
(2022):
Splicing analyses for variants in MMR genes: best practice recommendations from the European Mismatch Repair Working Group.
In: European Journal of Human Genetics, Bd. 30, Nr. 9: S. 1051-1059
Neuhann, Teresa M.; Haub, Katharina; Steinke-Lange, Verena; Morak, Monika; Laner, Andreas; Locher, Melanie und Holinski-Feder, Elke
(2022):
Long-term chemoprevention in patients with adenomatous polyposis coli: an observational study.
In: Familial Cancer, Bd. 21, Nr. 4: S. 463-472
2021
Vangala, Deepak B.; Ladigan-Badura, Swetlana; Engel, Christoph; Hueneburg, Robert; Perne, Claudia; Bucksch, Karolin; Nattermann, Jacob; Steinke-Lange, Verena; Rahner, Nils; Weitz, Jürgen; Kloor, Matthias; Tomann, Judith; Canbay, Ali; Huu-Phuc, Nguyen; Strassburg, Christian; Moeslein, Gabriele; Morak, Monika; Holinski-Feder, Elke; Buettner, Reinhard; Aretz, Stefan; Löffler, Markus; Schmiegel, Wolff; Pox, Christian und Schulmann, Karsten
(2021):
Early detection of duodenal cancer by upper gastrointestinal-endoscopy in Lynch syndrome.
In: International Journal of Cancer, Bd. 149, Nr. 12: S. 2052-2062
Seppälä, Toni T.; Dominguez-Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capella, Gabriel; Thomas, Huw; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria G.; Cavestro, Giulia M.; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauss, Hans-Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda, Marta; Navarro, Matilde; Vida, Joan B.; Kariv, Revital; Rosner, Guy; Pinero, Tamara A.; Pavicic, Walter; Kalfayan, Pablo; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; Cappel, Wouter H. de Vos Tot Nederveen; Della Valle, Adriana; Lopez-Koestner, Francisco; Alvarez, Karin; Büttner, Reinhard; Goergens, Heike; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; Knebel Doeberitz, Magnus von; Loeffler, Markus; Redler, Silke; Weitz, Jürgen; Pylvaenaeinen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Hopper, John L.; Win, Aung K.; Lindor, Noralane M.; Gallinger, Steven; Marchand, Loic Le; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Wadt, Karin A. W.; Mourits, Marian J. E.; Ketabi, Zohreh; Denton, Oliver G.; Rodland, Einar A.; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Rokkones, Erik; Sampson, Julian R.; Evans, D. G. und Moller, Pal
(2021):
Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
In: European Journal of Cancer, Bd. 148: S. 124-133
Dominguez-Valentin, Mev; Plazzer, John-Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capella, Gabriel; Balaguer, Francesc; Macrae, Finlay; Winship, Ingrid M.; Thomas, Huw; Evans, Dafydd Gareth; Burn, John; Greenblatt, Marc; Vos Tot Nederveen Cappel, Wouter H. de; Sijmons, Rolf H.; Nielsen, Maartje; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Della Valle, Adriana; Lopez-Kostner, Francisco; Alvarez, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans F. A.; Perne, Claudia; Büttner, Reinhard; Görgens, Heike; Holinski-Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; Knebel Doeberitz, Magnus von; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Crosbie, Emma J.; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Moreira, Leticia; Sanchez, Ariadna; Serra-Burriel, Miquel; Mints, Miriam; Kariv, Revital; Rosner, Guy; Pinero, Tamara Alejandra; Pavicic, Walter Hernan; Kalfayan, Pablo; Broeke, Sanne W. ten; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Peltomäki, Päivi; Hopper, John L.; Win, Aung Ko; Buchanan, Daniel D.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Hansen, Thomas V. O.; Lindberg, Lars; Rodland, Einar Andreas; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Seppälä, Toni T. und Moller, Pal
(2021):
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study.
In: Journal of Clinical Medicine, Bd. 10, Nr. 13, 2856
Bucksch, Karolin; Zachariae, Silke; Ahadova, Aysel; Aretz, Stefan; Buttner, Reinhard; Goergens, Heike; Holinski-Feder, Elke; Hueneburg, Robert; Kloor, Matthias; Doeberitz, Magnus Knebel; Ladigan-Badura, Swetlana; Moeslein, Gabriela; Morak, Monika; Nattermann, Jacob; Huu Phuc, Nguyen; Perne, Claudia; Redler, Silke; Schmetz, Ariane; Steinke-Lange, Verena; Surowy, Harald; Vangala, Deepak B.; Weitz, Jürgen; Loeffler, Markus und Engel, Christoph
(2021):
Adenoma and colorectal cancer risks in Lynch syndrome, Lynch-like syndrome and familial colorectal cancer type X.
In: International Journal of Cancer, Bd. 150, Nr. 1: S. 56-66
2020
Bucksch, Karolin; Zachariae, Silke; Aretz, Stefan; Buettner, Reinhard; Holinski-Feder, Elke; Holzapfel, Stefanie; Hueneburg, Robert; Kloor, Matthias; Knebel Doeberitz, Magnus von; 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 und Engel, Christoph
(2020):
Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study.
In: BMC Cancer, Bd. 20, Nr. 1
Engel, Christoph; Ahadova, Aysel; Seppala, Toni T.; Aretz, Stefan; Bigirwamungu-Bargeman, Marloes; Blaeker, Hendrik; Bucksch, Karolin; Buettner, Reinhard; Vos Tot Nederveen Cappel, Wouter T. De; Endris, Volker; Holinski-Feder, Elke; Holzapfel, Stefanie; Hueneburg, Robert; Jacobs, Maarten A. J. M.; Koornstra, Jan J.; Langers, Alexandra M.; episto, Anna; Morak, Monika; M oeslein, Gabriela; Peltomaeki, Paivi; Pylvaenaeinen, Kirsi; Rahner, Nils; Renkonen-Sinisalo, Laura; Schulmann, Karsten; Steinke-Lange, Verena; Stenzinger, Albrecht; Strassburg, Christian P.; Meeberg, Paul C. van de; Kouwen, Mariette van; Leerdam, Monique van; Vangala, Deepak B.; Vecht, Juda; Verhulst, Marie-Louise; Knebel Doeberitz, Magnus von; Weitz, Jürgen; Zachariae, Silke; Loeffler, Markus; Mecklin, Jukka-Pekka; Kloor, Matthias und Vasen, Hans F.
(2020):
Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome.
In: Gastroenterology, Bd. 158, Nr. 5: S. 1326-1333
Dominguez-Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capella, Gabriel; Thomas, Huw; Nakken, Sigve; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauss, Hans-Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda, Marta; Navarro, Matilde; Brunet Vidal, Joan; Kariv, Revital; Rosner, Guy; Alejandra Pinero, Tamara; Laura Gonzalez, Maria; Kalfayan, Pablo; Ryan, Neil; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; Vos tot Nederveen Cappel, Wouter H. de; Della Valle, Adriana; Lopez-Koestner, Francisco; Alvarez, Karin; Buettner, Reinhard; Goergens, Heike; Morak, Monika; Holzapfel, Stefanie; Hueneburg, Robert; Doeberitz, Magnus von Knebel; Loeffler, Markus; Rahner, Nils; Weitz, Jurgen; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Auranen, Annika; Hopper, John L.; Win, Aung Ko; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Denton, Oliver G.; Rodland, Einar Andreas; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Sampson, Julian R.; Evans, D. Gareth; Seppala, Toni T. und Moller, Pal
(2020):
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
In: Genetics in Medicine, Bd. 23, Nr. 4: S. 705-712
Dominguez-Valentin, Mev; Sampson, Julian R.; Seppala, Toni T.; ten Broeke, Sanne W.; Plazzer, John-Paul; Nakken, Sigve; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capella, Gabriel; Balaguer, Francesc; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; Hovig, Eivind; Vos Tot Nederveen Cappel, Wouter H. de; Sijmons, Rolf H.; Bertario, Lucio; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Della Valle, Adriana; Lopez-Kostner, Francisco; Gluck, Nathan; Katz, Lior H.; Heinimann, Karl; Vaccaro, Carlos A.; Buettner, Reinhard; Goergens, Heike; Holinski-Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hueneburg, Robert; Knebel Doeberitz, Magnus von; Loeffler, Markus; Rahner, Nils; Schackert, Hans K.; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Hopper, John L.; Win, Aung Ko; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Wadt, Karin; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Moreira, Leticia; Sanchez, Ariadna; Serra-Burriel, Miquel; Pineda, Marta; Navarro, Matilde; Blanco, Ignacio; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Denton, Oliver G.; Frayling, Ian M.; Rodland, Einar Andreas; Vasen, Hans; Mints, Miriam; Neffa, Florencia; Esperon, Patricia; Alvarez, Karin; Kariv, Revital; Rosner, Guy; Pinero, Tamara Alejandra; Gonzalez, Maria Laura; Kalfayan, Pablo; Tjandra, Douglas; Winship, Ingrid M.; Macrae, Finlay; Möslein, Gabriela; Mecklin, Jukka-Pekka; Nielsen, Maartje und Moller, Pal
(2020):
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.
In: Genetics in Medicine, Bd. 22, Nr. 1: S. 15-25
Arnold, Anke Marie; Morak, Monika; Benet-Pages, Anna; Laner, Andreas; Frishman, Dimitrij und Holinski-Feder, Elke
(2020):
Targeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndrome.
In: European Journal of Human Genetics, Bd. 28, Nr. 5: S. 597-608
Morak, Monika; Steinke-Lange, Verena; Massdorf, Trisari; Benet-Pages, Anna; Locher, Melanie; Laner, Andreas; Kayser, Katrin; Aretz, Stefan und Holinski-Feder, Elke
(2020):
Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics.
In: Familial Cancer, Bd. 19, Nr. 2: S. 161-167
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; Möslein, Gabriela; Strassburg, Christian; Morak, Monika; Holinski-Feder, Elke; Buettner, Reinhard; Aretz, Stefan; Loeffler, Markus; Schmiegel, Wolff; Pox, Christian und Schulmann, Karsten
(2020):
Value of uppergastrointestinalendoscopy for gastric cancer surveillance in patients with Lynch syndrome.
In: International Journal of Cancer, Bd. 148, Nr. 1: S. 106-114
Blaeker, Hendrik; Haupt, Saskia; Morak, Monika; Holinski-Feder, Elke; Arnold, Alexander; Horst, David; Sieber-Frank, Julia; Seidler, Florian; Winterfeld, Moritz von; Alwers, Elizabeth; Chang-Claude, Jenny; Brenner, Hermann; Roth, Wilfried; Engel, Christoph; Loeffler, Markus; Möslein, Gabriela; Schackert, Hans-Konrad; Weitz, Jürgen; Perne, Claudia; Aretz, Stefan; Hueneburg, Robert; Schmiegel, Wolff; Vangala, Deepak; Rahner, Nils; Steinke-Lange, Verena; Heuveline, Vincent; Knebel Doeberitz, Magnus von; Ahadova, Aysel; Hoffmeister, Michael und Kloor, Matthias
(2020):
Age-dependent performance of BRAF mutation testing in Lynch syndrome diagnostics.
In: International Journal of Cancer, Bd. 147, Nr. 10: S. 2801-2810
2019
Seppala, Toni T.; Ahadova, Aysel; Dominguez-Valentin, Mev; Macrae, Finlay; Evans, D. Gareth; Therkildsen, Christina; Sampson, Julian; Scott, Rodney; Burn, John; Moeslein, Gabriela; Bernstein, Inge; Holinski-Feder, Elke; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Lautrup, Charlotte Kvist; Lindblom, Annika; Plazzer, John-Paul; Winship, Ingrid; Tjandra, Douglas; Katz, Lior H.; Aretz, Stefan; Hueneburg, Robert; Holzapfel, Stefanie; Heinimann, Karl; Della Valle, Adriana; Neffa, Florencia; Gluck, Nathan; Cappel, Wouter H. de Vos Tot Nederveen; Vasen, Hans; Morak, Monika; Steinke-Lange, Verena; Engel, Christoph; Rahner, Nils; Schmiegel, Wolff; Vangala, Deepak; Thomas, Huw; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Capella, Gabriel; Pineda, Marta; Navarro, Matilde; Blanco, Ignacio; ten Broeke, Sanne; Nielsen, Maartje; Ljungmann, Ken; Nakken, Sigve; Lindor, Noralane; Frayling, Ian; Hovig, Eivind; Sunde, Lone; Kloor, Matthias; Mecklin, Jukka-Pekka; Kalager, Mette und Moller, Pal
(2019):
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis;a prospective Lynch syndrome database report.
In: Hereditary Cancer in Clinical Practice, Bd. 17, 8
Morak, Monika; Schäfer, Kerstin; Steinke-Lange, Verena; Köhler, Udo; Keinath, Susanne; Massdorf, Trisari; Mauracher, Brigitte; Rahner, Nils; Bailey, Jessica; Kling, Christiane; Haeusser, Tanja; Laner, Andreas und Holinski-Feder, Elke
(2019):
Full-length transcript amplification and sequencing as universal method to test mRNA integrity and biallelic expression in mismatch repair genes.
In: European Journal of Human Genetics, Bd. 27, Nr. 12: S. 1808-1820
Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Holth, Arild; Capella, Gabriel; Davidson, Ben; Evans, D. Gareth; Martins, Alexandra; Moller, Pal und Hovig, Eivind
(2019):
Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing.
In: Scientific Reports, Bd. 9, 18555
[PDF, 1MB]
2018
Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal und Hovig, Eivind
(2018):
Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families.
In: Familial Cancer, Bd. 17, Nr. 1: S. 141-153
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 und 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, Bd. 143, Nr. 11: S. 2800-2813
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 und 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, Bd. 155, Nr. 5: S. 1400-1409
Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal und Hovig, Eivind
(2018):
Identification of genetic variants for clinical management of familial colorectal tumors.
In: BMC Medical Genetics
19:26
[PDF, 652kB]
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 und Hovig, Eivind
(2018):
Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.
In: Hereditary Cancer in Clinical Practice
16:4
[PDF, 1MB]
2017
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 und 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, Bd. 66, Nr. 3: S. 464-472
[PDF, 764kB]
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. und 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, Bd. 66, Nr. 9: S. 1657-1664
[PDF, 769kB]
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 und Capella, Gabriel
(2017):
Elucidating the molecular basis of MSH2-deficienttumors by combined germline and somatic analysis.
In: International Journal of Cancer, Bd. 141, Nr. 7: S. 1365-1380
Morak, Monika; Käsbauer, Sarah; Kerscher, Martina; Massdorf, Trisari; Holinski-Feder, Elke; Laner, Andreas; Nissen, Anke M.; Benet-Pages, Anna; Schackert, Hans K. und Keller, Gisela
(2017):
Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6.
In: Familial Cancer, Bd. 16, Nr. 4: S. 491-500
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 und 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]
2011
Morak, Monika; Koehler, Udo; Schackert, Hans Konrad; Steinke, Verena; Royer-Pokora, Brigitte; Schulmann, Karsten; Kloor, Matthias; Höchter, Wilhelm; Weingart, Josef; Keiling, Cortina; Massdorf, Trisari und 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, Bd. 48, Nr. 8: S. 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 und 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]
In: PLOS ONE 6(6), e20464 [PDF, 112kB]
2010
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 und 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]