A High Percentage of NSCLC With Germline CHEK2 Mutation Harbors Actionable Driver Alterations: Survey of a Cancer Genomic Database and Review of Literature-Reference-Cited by-同舟云学术

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A High Percentage of NSCLC With Germline CHEK2 Mutation Harbors Actionable Driver Alterations: Survey of a Cancer Genomic Database and Review of Literature

Published:2022-09 Issue:9 Volume:3 Page:100387
ISSN:2666-3643
Container-title:JTO Clinical and Research Reports
language:en
Short-container-title:JTO Clinical and Research Reports

Author:

Zhang Shannon S.,Lee Jessica K.,Tukachinsky Hanna,Schrock Alexa B.,Nagasaka Misako,Ou Sai-Hong Ignatius

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Oncology

Reference11 articles.

1. CHEK2 germline variants in cancer predisposition: stalemate rather than checkmate;Stolarova;Cells,2020

2. A computational approach to distinguish somatic vs. germline origin of genomic alterations from deep sequencing of cancer specimens without a matched normal;Sun;PLoS Comput Biol,2018

3. The common thread: a case of synchronous lung cancers and a germline CHEK2 mutation;Carey;Clin Lung Cancer,2022

4. Should we test cancer susceptibility genes in routinely used multigene panels? A case of synchronous lung adenocarcinoma and breast cancer associated with germline CHEK2 mutation;Federico;Clin Lung Cancer,2022

5. Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs;Kukita;Cold Spring Harb Mol Case Stud,2016

Cited by 1 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. In Response to Dr. Steven Sorscher;JTO Clinical and Research Reports;2023-01

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