Associated Papers
Predisposition of an Intronic Duplication in CHEK2 Gene in the Cases of Breast Cancer from Balochistan.
Baloch AH et al.
Asian Pacific Journal of Cancer Prevention : Apjcp, 2025
Feasibility of long-read sequencing to identify molecular alterations in an Indonesian cohort of locally advanced to advanced nasopharyngeal cancer.
Handoko et al.
Scientific Reports, 2025
40594369 (PubMed )
Supplement: 41598_2025_6096_MOESM8_ESM.zip › Supp_Data_6 › S5_SNV.xlsx › CHEK2
A case report of biallelic CHEK2 heterozygous variant presenting with breast cancer.
Soleimani T et al.
Clinical Case Reports, 2023
Association of Germline CHEK2 Gene Variants with Risk and Prognosis of Non-Hodgkin Lymphoma.
Havranek O et al.
Plos One, 2015
Constitutional CHEK2 mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan.
Rashid MU et al.
Bmc Cancer, 2013
Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals.
Kuusisto KM et al.
Breast Cancer Research : Bcr, 2011
21356067 (PubMed )
Supplement: bcr2832-S1.PDF
CHEK2 variant I157T may be associated with increased breast cancer risk.
Kilpivaara O et al.
International Journal of Cancer, 2004
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