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

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

Genetics in medicine, 2020-01, Vol.22 (1), p.15-25 [Periódico revisado por pares]

United States: Elsevier Limited

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2
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
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Artigo
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Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

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 ; Vidal, Joan Brunet ; Kariv, Revital ; Rosner, Guy ; Piñero, Tamara Alejandra ; Gonzalez, María Laura ; Kalfayan, Pablo ; Ryan, Neil ; ten Broeke, Sanne W. ; Jenkins, Mark A. ; Sunde, Lone ; Bernstein, Inge ; Burn, John ; Greenblatt, Marc ; de Vos tot Nederveen Cappel, Wouter H. ; Della Valle, Adriana ; Lopez-Koestner, Francisco ; Alvarez, Karin ; Büttner, Reinhard ; Görgens, Heike ; Morak, Monika ; Holzapfel, Stefanie ; Hüneburg, Robert ; von Knebel Doeberitz, Magnus ; Loeffler, Markus ; Rahner, Nils ; Weitz, Jürgen ; Pylvänäinen, Kirsi ; Renkonen-Sinisalo, Laura ; Lepistö, Anna ; Auranen, Annika ; 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. ; Therkildsen, Christina ; Okkels, Henrik ; Ketabi, Zohreh ; Denton, Oliver G. ; Rødland, Einar Andreas ; Vasen, Hans ; Neffa, Florencia ; Esperon, Patricia ; Tjandra, Douglas ; Möslein, Gabriela ; Sampson, Julian R. ; Evans, D. Gareth ; Seppälä, Toni T. ; Møller, Pål

Genetics in medicine, 2021-04, Vol.23 (4), p.705-712 [Periódico revisado por pares]

United States: Elsevier Inc

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