Dominguez-Valentin, Mev http://orcid.org/0000-0001-7856-0057
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
Funding for this research was provided by:
Kreftforeningen (194751)
This article is maintained by: Elsevier
Article Title: Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-020-01029-1
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics