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Issue DateTitleAuthor(s)
1-Jan-2020Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseDominguez Valentin, Mev; Sampson, Julian R.; Seppälä, Toni T.; ten Broeke, Sanne W.; Plazzer, John Paul; Nakken, Sigve; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; Hovig, Eivind; de Vos Tot Nederveen Cappel, Wouter H.; 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; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Schackert, Hans K.
10-Jul-2020Association of ionizing radiation dose from common medical diagnostic procedures and lymphoma risk in the Epilymph case-control studyPasqual, Elisa; Turner, Michelle C.; Gracia Lavedan, Esther; Casabonne, Delphine; Benavente, Yolanda; Thierry-Chef, Isabelle; Maynadié, Marc; Cocco, Pierluigi; Staines, Anthony; Foretova, Lenka; Nieters, Alexandra; Boffetta, Paolo; Brennan, Paul; Cardis, Elisabeth; Sanjosé Llongueras, Silvia de
15-Feb-2021Genetically Raised Circulating Bilirubin Levels and Risk of Ten Cancers: A Mendelian Randomization StudySeyed Khoei, Nazlisadat; Carreras Torres, Robert; Murphy, Neil; Gunter, Marc J.; Brennan, Paul; Smith-Byrne, Karl; Mariosa, Daniela; McKay, James D.; O’Mara, Tracy; Jarrett, Ruth; Hjalgrim, Henrik; Smedby, Karin E.; Cozen, Wendy; Onel, Kenan; Diepstra, Arjan; Wagner, Karl-Heinz; Freisling, Heinz; ECAC Group
7-Apr-2021A comparison of complementary measures of vitamin B6 status, function, and metabolism in the European Prospective Investigation into Cancer and Nutrition (EPIC) studyClasen, Joanna L.; Heath, Alicia K.; Van Puyvelde, Heleen; Huybrechts, Inge; Park, Jing Young; Ferrari, Pietro; Johansson, Mattias; Scelo, Ghislaine; Ulvik, Arve; Midttun, Øivind; Ueland, Per Magne; Dahm, Christina C.; Halkjær, Jytte; Olsen, Anja; Johnson, Theron; Katzke, Verena; Schulze, Matthias B.; Masala, Giovanna; Segrado, Francesco; Santucci de Magistris, Maria; Sacerdote, Carlotta; Ocké, Marga C.; Luján Barroso, Leila; Ching López, Ana; Huerta, José María; Ardanaz, Eva; Amiano, Pilar; Ericson, Ulrika; Manjer, Jonas; Gylling, Björn; Johansson, Ingegerd; Schmidt, Julie; Weiderpass, Elisabete; Riboli, Elio; Cross, Amanda J.; Muller, David C.
28-Jun-2021No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database StudyDominguez Valentin, Mev; Plazzer, John Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Macrae, Finlay; Winship, Ingrid M.; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Sijmons, Rolf H.; Nielsen, Maartje; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Valle, Adriana Della; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans; Perne, Claudia; Büttner, Reinhard; Görgens, Heike; Holinski Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Steinke Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Crosbie, Emma J.; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Moreira, Leticia; Sánchez, Ariadna; Serra Burriel, Miquel; Mints, Miriam; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; Pavicic, Walter Hernán; Kalfayan, Pablo; ten Broeke, Sanne W.; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Peltomäki, Päivi; Hopper, John L.; Ko Win, Aung; Buchanan, Daniel D.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Hansen, Thomas V. O.; Lindberg, Lars; Rødland, Einar Andreas; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Seppälä, Toni T.; Møller, Pål
31-May-2021A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variantsUnhjem Wiik, Mariann; Evans, Tiffany Jane; Belhadj, Sami; Bolton, Katherine A.; Dymerska, Dagmara; Jagmohan Changur, Shantie; Capellá, G. (Gabriel); Kurzawski, Grzegorz; Wijnen, Juul T.; Valle, Laura; Vasen, Hans; Lubinski, Jan; Scott, Rodney J.; Talseth-Palmer, Bente A.