Functional analysis identifies damaging CHEK2 missense variants associated with increased cancer risk-Reference-Cited by-同舟云学术

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Functional analysis identifies damaging CHEK2 missense variants associated with increased cancer risk

Published:2021-12-13 Issue: Volume: Page:canres.1845.2021
ISSN:0008-5472
Container-title:Cancer Research
language:en
Short-container-title:Cancer Res

Author:

Boonen Rick ACM,Wiegant Wouter W,Celosse Nandi,Vroling Bas,Heijl Stephan^ORCID,Kote-Jarai Zsofia,Mijuskovic Martina,Cristea Simona,Solleveld-Westerink Nienke,van Wezel Tom^ORCID,Beerenwinkel Niko,Eeles Rosalind^ORCID,Devilee Peter^ORCID,Vreeswijk Maaike PG^ORCID,Marra Giancarlo^ORCID,van Attikum Haico^ORCID

Funder

Giulio and Georgio Stafnini foundation

KWF Kankerbestrijding

EC | Horizon Europe

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

Cited by 36 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. Germline variant profiling of CHEK2 sequencing variants in breast cancer patients;Cancer Genetics;2024-11

2. Protein-truncating and rare missense variants inATMandCHEK2and associations with cancer in UK Biobank whole-exome sequence data;Journal of Medical Genetics;2024-08-29

3. Comprehensive analysis of the functional impact of single nucleotide variants of human CHEK2;PLOS Genetics;2024-08-15

4. Cytomorphologic and molecular characterization of spindle cell carcinoid tumors of the lung;Cancer Cytopathology;2024-07-18

5. Comparing Cancer Risk Management between Females with Truncating CHEK2 1100delC versus Missense CHEK2 I157T Variants;Genes;2024-07-05

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