Cancer risks by gene, age, and gender in 6350 carriers ofpathogenic mismatch repair variants: findings from the Prospective Lynch SyndromeDatabase

by Dominguez-Valentin Mev, Sampson, Julian R, Seppälä, Toni T, ten Broeke Sanne W, John-Paul, Plazzer, Nakken Sigve, Engel, Christoph, Aretz, Stefan, Jenkins, Mark A, Sunde Lone, Bernstein, Inge, Capella, Gabriel, Balaguer Francesc, Thomas, Huw, Gareth, Evans D, 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-Köstner, Francisco, Gluck, Nathan, Katz, Lior H, Heinimann Karl, Vaccaro, Carlos A, Büttner Reinhard, Görgens Heike, Holinski-Feder Elke, Morak Monika, Holzapfel, Stefanie, Hüneburg, Robert, Knebel Doeberitz Magnus von, Loeffler, Markus, Rahner Nils, Schackert, Hans K, Steinke-Lange, Verena, Wolff, Schmiegel, Vangala Deepak, Pylvänäinen Kirsi, Renkonen-Sinisalo Laura, Hopper, John L, Win Aung Ko, Haile, Robert W, Lindor Noralane M, Gallinger, Steven, Le Marchand Loïc, Newcomb, Polly A, Figueiredo, Jane C, Thibodeau, Stephen N, Wadt Karin, Therkildsen, Christina, Okkels Henrik, Ketabi Zohreh, Moreira, Leticia, Sánchez 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, Rødland, Einar Andreas, Vasen Hans, Mints Miriam, Neffa Florencia, Esperon, Patricia, Alvarez, Karin, Kariv Revital, Rosner, Guy, Pinero, Tamara Alejandra, Gonzalez, María Laura, Kalfayan Pablo, Tjandra, Douglas, Winship, Ingrid M, Macrae Finlay, Möslein Gabriela, Jukka-Pekka, Mecklin, Nielsen Maartje, Møller Pål
Published in Genetics in medicine

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

by Dominguez-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, Capella, Gabriel, Balaguer, 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-Köstner, Francisco, Gluck, Nathan, Katz, Lior H, Heinimann, Karl, Vaccaro, Carlos A, Büttner, Reinhard, Görgens, Heike, Holinski-Feder, Elke, Morak, Monika, Holzapfel, Stefanie, Hüneburg, Robert, Knebel Doeberitz, Magnus von, Loeffler, Markus, Rahner, Nils, Schackert, Hans K, Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Hopper, John L, Win, Aung Ko, Haile, Robert W, Lindor, Noralane M, Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A, Figueiredo, Jane C, Thibodeau, Stephen N, Wadt, Karin, Therkildsen, Christina, Okkels, Henrik, Ketabi, Zohreh, Moreira, Leticia, Sánchez, 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, Rødland, Einar Andreas, Vasen, Hans, Mints, Miriam, Neffa, Florencia, Esperon, Patricia, Alvarez, Karin, Kariv, Revital, Rosner, Guy, Pinero, Tamara Alejandra, Gonzalez, María Laura, Kalfayan, Pablo, Tjandra, Douglas, Winship, Ingrid M, Macrae, Finlay, Möslein, Gabriela, Mecklin, Jukka-Pekka, Nielsen, Maartje, Møller, Pål
Published in Genetics in medicine

Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report

by Dominguez-Valentin, Mev, Seppälä, Toni T, Sampson, Julian R, Macrae, Finlay, Winship, Ingrid, Evans, D. G, Scott, Rodney J, Burn, John, Möslein, Gabriela, Bernstein, Inge, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Lindblom, Annika, Plazzer, John-Paul, Tjandra, Douglas, Thomas, Huw, Green, Kate, Lalloo, Fiona, Crosbie, Emma J, Hill, James, Capella, Gabriel, Pineda, Marta, Navarro, Matilde, Vidal, Joan B, Rønlund, Karina, Nielsen, Randi T, Yilmaz, Mette, Elvang, Louise L, Katz, Lior, Nielsen, Maartje, ten Broeke, Sanne W, Nakken, Sigve, Hovig, Eivind, Sunde, Lone, Kloor, Matthias, Knebel Doeberitz, Magnus v, Ahadova, Aysel, Lindor, Noralane, Steinke-Lange, Verena, Holinski-Feder, Elke, Mecklin, Jukka-Pekka, Møller, Pål

Mutational signature analysis reveals NTHL1 deficiency to cause a multi-tumor phenotype

by Grolleman, Judith E, de Voer, Richarda M, Elsayed, Fadwa A, Nielsen, Maartje, Weren, Robbert D.A, Palles, Claire, Ligtenberg, Marjolijn J.L, Vos, Janet R, ten Broeke, Sanne W, de Miranda, Noel F.C.C, Kuiper, Renske A, Kamping, Eveline J, Jansen, Erik A.M, Vink-Börger, M. Elisa, Popp, Isabell, Lang, Alois, Spier, Isabel, Hüneburg, Robert, James, Paul A, Li, Na, Staninova, Marija, Lindsay, Helen, Cockburn, David, Spasic-Boskovic, Olivera, Clendenning, Mark, Sweet, Kevin, Capellá, Gabriel, Sjursen, Wenche, Vetti, Hildegunn Høberg, Jongmans, Marjolijn C, Neveling, Kornelia, van Kessel, Ad Geurts, Morreau, Hans, Hes, Frederik J, Sijmons, Rolf H, Schackert, Hans K, Ruiz-Ponte, Clara, Dymerska, Dagmara, Lubiñski, Jan, Rivera, Barbara, Foulkes, William D, Tomlinson, Ian P, Valle, Laura, Buchanan, Daniel D, Kenwrick, Sue, Adlard, Julian, Dimovski, Aleksandar J, Campbell, Ian G, Aretz, Stefan, Schindler, Detlev, van Wezel, Tom, Hoogerbrugge, Nicoline, Kuiper, Roland P

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

by Seppälä, Toni T, Ahadova, Aysel, Dominguez-Valentin, Mev, Macrae, Finlay, Evans, D Gareth, Therkildsen, Christina, Sampson, Julian, Scott, Rodney, Burn, John, Möslein, Gabriela, Bernstein, Inge, Holinski-Feder, Elke, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Lautrup, Charlotte Kvist, Lindblom, Annika, Plazzer, John-Paul, Winship, Ingrid, Tjandra, Douglas, Katz, Lior H, Aretz, Stefan, Hüneburg, Robert, Holzapfel, Stefanie, Heinimann, Karl, Valle, Adriana Della, Neffa, Florencia, Gluck, Nathan, de Vos Tot Nederveen Cappel, Wouter H, 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, Møller, Pål
Published in Hereditary cancer in clinical practice