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Publications by Moller, Pal

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Number of items: 6.

Journal article

Broeke, Sanne W. ten; Klift, Heleen M. van der; Tops, Carli M. J.; Aretz, Stefan; Bernstein, Inge; Buchanan, Daniel D.; Chapelle, Albert de la; Capella, Gabriel; Clendenning, Mark; Engel, Christoph; Gallinger, Steven; Gomez Garcia, Encarna; Figueiredo, Jane C.; Haile, Robert; Hampel, Heather L.; Hopper, John L.; Hoogerbrugge, Nicoline; Knebel Doeberitz, Magnus von; Le Marchand, Loic; Lettebör, Tom G. W.; Jenkins, Mark A.; Lindblom, Annika; Lindor, Noralane M.; Mensenkamp, Arjen R.; Moller, Pal; Newcomb, Polly A.; Os, Theo A. M. van; Pearlman, Rachel; Pineda, Marta; Rahner, Nils; Redeker, Egbert J. W.; Olderode-Berends, Maran J. W.; Rosty, Christophe; Schackert, Hans K.; Scott, Rodney; Senter, Leigha; Spruijt, Liesbeth; Steinke-Lange, Verena; Suerink, Manon; Thibodeau, Stephen; Vos, Yvonne J.; Wagner, Anja; Winship, Ingrid; Hes, Frederik J.; Vasen, Hans F. A.; Wijnen, Juul T.; Nielsen, Maartje; Win, Aung Ko (2018): Cancer Risks for PMS2-Associated Lynch Syndrome. In: Journal of Clinical Oncology, Vol. 36, No. 29: pp. 2961-2968

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]

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]

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

This list was generated on Fri Aug 14 02:55:09 2020 CEST.