Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database-Reference-Cited by-同舟云学术

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

Published:2023-04 Issue: Volume:58 Page:101909
ISSN:2589-5370
Container-title:eClinicalMedicine
language:en
Short-container-title:eClinicalMedicine

Author:

Dominguez-Valentin Mev^ORCID,Haupt Saskia,Seppälä Toni T.,Sampson Julian R.,Sunde Lone,Bernstein Inge,Jenkins Mark A.,Engel Christoph,Aretz Stefan,Nielsen Maartje,Capella Gabriel^ORCID,Balaguer Francesc,Evans Dafydd Gareth,Burn John,Holinski-Feder Elke,Bertario Lucio,Bonanni Bernardo,Lindblom Annika,Levi Zohar,Macrae Finlay,Winship Ingrid,Plazzer John-Paul,Sijmons Rolf,Laghi Luigi,Della Valle Adriana,Heinimann Karl,Dębniak Tadeusz,Fruscio Robert,Lopez-Koestner Francisco,Alvarez-Valenzuela Karin,Katz Lior H.,Laish Ido,Vainer Elez,Vaccaro Carlos,Carraro Dirce Maria,Monahan Kevin,Half Elizabeth,Stakelum Aine,Winter Des,Kennelly Rory,Gluck Nathan,Sheth Harsh,Abu-Freha Naim,Greenblatt Marc,Rossi Benedito Mauro,Bohorquez Mabel,Cavestro Giulia Martina^ORCID,Lino-Silva Leonardo S.,Horisberger Karoline,Tibiletti Maria Grazia,Nascimento Ivana do,Thomas Huw,Rossi Norma Teresa,Apolinário da Silva Leandro,Zaránd Attila,Ruiz-Bañobre Juan^ORCID,Heuveline Vincent,Mecklin Jukka-Pekka,Pylvänäinen Kirsi,Renkonen-Sinisalo Laura,Lepistö Anna,Peltomäki Päivi,Therkildsen Christina,Madsen Mia Gebauer,Burgdorf Stefan Kobbelgaard,Hopper John L.,Win Aung Ko,Haile Robert W.,Lindor Noralane,Gallinger Steven,Le Marchand Loïc,Newcomb Polly A.,Figueiredo Jane,Buchanan Daniel D.,Thibodeau Stephen N.,von Knebel Doeberitz Magnus,Loeffler Markus,Rahner Nils,Schröck Evelin,Steinke-Lange Verena,Schmiegel Wolff,Vangala Deepak,Perne Claudia,Hüneburg Robert,Redler Silke,Büttner Reinhard,Weitz Jürgen,Pineda Marta,Duenas Nuria,Vidal Joan Brunet,Moreira Leticia,Sánchez Ariadna,Hovig Eivind,Nakken Sigve,Green Kate,Lalloo Fiona,Hill James,Crosbie Emma^ORCID,Mints Miriam,Goldberg Yael,Tjandra Douglas,ten Broeke Sanne W.,Kariv Revital,Rosner Guy,Advani Suresh H.,Thomas Lidiya,Shah Pankaj,Shah Mithun,Neffa Florencia,Esperon Patricia,Pavicic Walter,Torrezan Giovana Tardin,Bassaneze Thiago,Martin Claudia Alejandra,Moslein Gabriela,Moller Pål

Publisher

Elsevier BV

Subject

General Medicine

Reference27 articles.

1. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1;Ligtenberg;Nat Genet,2009

2. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts;Vasen;Gut,2013

3. Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report;Dominguez-Valentin;Genet Med,2021

4. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database;Dominguez-Valentin;Genet Med,2019

5. Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report;Seppala;Hered Cancer Clin Pract,2017

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2. Benign Adenomyoepithelioma: An Unrecognised Precursor of Ductal Carcinoma in Situ in Patient With Lynch Syndrome;International Journal of Surgical Pathology;2024-01-31

3. The Role of Capsule Endoscopy in the Diagnosis and Management of Small Bowel Tumors: A Narrative Review;Cancers;2024-01-07

4. Precision Healthcare and Interventions in Hereditary Breast and Ovarian Cancer and Lynch Syndrome;Cancers;2023-11-27

5. Estimating cancer risk in carriers of Lynch syndrome variants in UK Biobank;2023-11-10