The comprehensive English National Lynch Syndrome Registry: development and description of a new genomics data resource-Reference-Cited by-同舟云学术

The comprehensive English National Lynch Syndrome Registry: development and description of a new genomics data resource

Published:2024-03 Issue: Volume:69 Page:102465
ISSN:2589-5370
Container-title:eClinicalMedicine
language:en
Short-container-title:eClinicalMedicine

Author:

Huntley Catherine,Loong Lucy,Mallinson Corinne,Bethell Rachel,Rahman Tameera,Alhaddad Neelam,Tulloch Oliver,Zhou Xue,Lee Jason,Eves Paul,Cook Jacqueline,Armstrong Ruth,Ahmed Munaza,McVeigh Terri,DeSouza Bianca,Kulkarni Anjana,Bezuidenhout Heirdre,Martin Richard,Holliday Debbie,Hart Rachel,Lalloo Fiona,Donaldson Alan,Cleaver Ruth,Willis Catherine,Kiesel Victoria,O'Reilly Marie-Anne,Halliday Dorothy,Solomons Joyce,Ong Kai Ren,McRonald Fiona,Torr Bethany,Burn John,Shaw Adam,Morris Eva J.A.^ORCID,Monahan Kevin,Hardy Steven,Turnbull Clare^ORCID

Funder

Wellcome Trust

Cancer Research UK

Publisher

Elsevier BV

Reference15 articles.

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3. Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch Syndrome Registry;Vasen;Fam Cancer,2016

4. Outcome of 24 years national surveillance in different hereditary colorectal cancer subgroups leading to more individualised surveillance;Lindberg;J Med Genet,2017

5. Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial;Burn;Lancet,2020

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