Publication

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

Dominguez-Valentin, M., Sampson, J. R., Seppälä, T. T., Ten Broeke, S. W., Plazzer, J-P., Nakken, S., Engel, C., Aretz, S., Jenkins, M. A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Thomas, H., Evans, D. G., Burn, J., Greenblatt, M., Hovig, E., de Vos Tot Nederveen Cappel, W. H., Sijmons, R. H., Bertario, L., Tibiletti, M. G., Cavestro, G. M., Lindblom, A., Della Valle, A., Lopez-Köstner, F., Gluck, N., Katz, L. H., Heinimann, K., Vaccaro, C. A., Büttner, R., Görgens, H., Holinski-Feder, E., Morak, M., Holzapfel, S., Hüneburg, R., Knebel Doeberitz, M. V., Loeffler, M., Rahner, N., Schackert, H. K., Steinke-Lange, V., Schmiegel, W., Vangala, D., Pylvänäinen, K., Renkonen-Sinisalo, L., Hopper, J. L., Win, A. K., Haile, R. W., Lindor, N. M., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J. C., Thibodeau, S. N., Wadt, K., Therkildsen, C., Okkels, H., Ketabi, Z., Moreira, L., Sánchez, A., Serra-Burriel, M., Pineda, M., Navarro, M., Blanco, I., Green, K., Lalloo, F., Crosbie, E. J., Hill, J., Denton, O. G., Frayling, I. M., Rødland, E. A., Vasen, H., Mints, M., Neffa, F., Esperon, P., Alvarez, K., Kariv, R., Rosner, G., Pinero, T. A., Gonzalez, M. L., Kalfayan, P., Tjandra, D., Winship, I. M., Macrae, F., Möslein, G., Mecklin, J-P., Nielsen, M. & Møller, P., 20-Jul-2020, In : Genetics in Medicine. 1 p.

Research output: Contribution to journalArticleAcademicpeer-review

  • Mev Dominguez-Valentin
  • Julian R Sampson
  • Toni T Seppälä
  • Sanne W Ten Broeke
  • John-Paul Plazzer
  • Sigve Nakken
  • Christoph Engel
  • Stefan Aretz
  • Mark A Jenkins
  • Lone Sunde
  • Inge Bernstein
  • Gabriel Capella
  • Francesc Balaguer
  • Huw Thomas
  • D Gareth Evans
  • John Burn
  • Marc Greenblatt
  • Eivind Hovig
  • Wouter H de Vos Tot Nederveen Cappel
  • Rolf H Sijmons
  • Lucio Bertario
  • Maria Grazia Tibiletti
  • Giulia Martina Cavestro
  • Annika Lindblom
  • Adriana Della Valle
  • Francisco Lopez-Köstner
  • Nathan Gluck
  • Lior H Katz
  • Karl Heinimann
  • Carlos A Vaccaro
  • Reinhard Büttner
  • Heike Görgens
  • Elke Holinski-Feder
  • Monika Morak
  • Stefanie Holzapfel
  • Robert Hüneburg
  • Magnus von Knebel Doeberitz
  • Markus Loeffler
  • Nils Rahner
  • Hans K Schackert
  • Verena Steinke-Lange
  • Wolff Schmiegel
  • Deepak Vangala
  • Kirsi Pylvänäinen
  • Laura Renkonen-Sinisalo
  • John L Hopper
  • Aung Ko Win
  • Robert W Haile
  • Noralane M Lindor
  • Steven Gallinger
  • Loïc Le Marchand
  • Polly A Newcomb
  • Jane C Figueiredo
  • Stephen N Thibodeau
  • Karin Wadt
  • Christina Therkildsen
  • Henrik Okkels
  • Zohreh Ketabi
  • Leticia Moreira
  • Ariadna Sánchez
  • Miquel Serra-Burriel
  • Marta Pineda
  • Matilde Navarro
  • Ignacio Blanco
  • Kate Green
  • Fiona Lalloo
  • Emma J Crosbie
  • James Hill
  • Oliver G Denton
  • Ian M Frayling
  • Einar Andreas Rødland
  • Hans Vasen
  • Miriam Mints
  • Florencia Neffa
  • Patricia Esperon
  • Karin Alvarez
  • Revital Kariv
  • Guy Rosner
  • Tamara Alejandra Pinero
  • María Laura Gonzalez
  • Pablo Kalfayan
  • Douglas Tjandra
  • Ingrid M Winship
  • Finlay Macrae
  • Gabriela Möslein
  • Jukka-Pekka Mecklin
  • Maartje Nielsen
  • Pål Møller

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Original languageEnglish
Number of pages1
JournalGenetics in Medicine
Publication statusE-pub ahead of print - 20-Jul-2020

ID: 130757491