Exome sequencing in a Swedish family with PMS2 mutation with varying penetrance of colorectal cancer: investigating the presence of genetic risk modifiers in colorectal cancer risk-Reference-Cited by-同舟云学术

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Exome sequencing in a Swedish family with PMS2 mutation with varying penetrance of colorectal cancer: investigating the presence of genetic risk modifiers in colorectal cancer risk

Published:2022-12-06 Issue:2 Volume:32 Page:113-118
ISSN:0959-8278
Container-title:European Journal of Cancer Prevention
language:en
Short-container-title:

Author:

Bryant Patrick,Walton Bernstedt Sophie,Thutkawkorapin Jessada,Backman Ann-Sofie,Lindblom Annika,Lagerstedt-Robinson Kristina

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cancer Research,Public Health, Environmental and Occupational Health,Oncology,Epidemiology

Reference47 articles.

1. A method and server for predicting damaging missense mutations.;Adzhubei;Nat Methods,2010

2. SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population.;Ameur;Eur J Hum Genet,2017

3. A global reference for human genetic variation.;Auton;Nature,2015

4. Nuclear BAG-1 expression inhibits apoptosis in colorectal adenoma-derived epithelial cells.;Barnes;Apoptosis,2005

5. Identification of deleterious mutations within three human genomes.;Chun;Genome Res,2009

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. WITHDRAWN: The Molecular Signature Associated with Oxaliplatin Induced Peripheral Neuropathy in Colorectal Cancer;2024-01-24

2. Lynch syndrome: toward an increasingly complex picture. The case of PMS2;European Journal of Cancer Prevention;2023-03-21

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