CHEK2*1100delC homozygosity in the Netherlands—prevalence and risk of breast and lung cancer
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Title
CHEK2*1100delC homozygosity in the Netherlands—prevalence and risk of breast and lung cancer
Authors
Keywords
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Journal
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 22, Issue 1, Pages 46-51
Publisher
Springer Nature
Online
2013-05-08
DOI
10.1038/ejhg.2013.85
References
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Related references
Note: Only part of the references are listed.- Detecting differential allelic expression using high-resolution melting curve analysis: application to the breast cancer susceptibility gene CHEK2
- (2011) Tú Nguyen-Dumont et al. BMC Medical Genomics
- Gene expression profiling assigns CHEK2 1100delC breast cancers to the luminal intrinsic subtypes
- (2011) Jord H. A. Nagel et al. BREAST CANCER RESEARCH AND TREATMENT
- Meta-analysis of CHEK2 1100delC variant and colorectal cancer susceptibility
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- Gene–gene interactions in breast cancer susceptibility
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- CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women
- (2011) M. A. Adank et al. JOURNAL OF MEDICAL GENETICS
- Prevalence of the variant allele rs61764370 T>G in the 3′UTR of KRAS among Dutch BRCA1, BRCA2 and non-BRCA1/BRCA2 breast cancer families
- (2010) Antoinette Hollestelle et al. BREAST CANCER RESEARCH AND TREATMENT
- A variant in the CHEK2 promoter at a methylation site relieves transcriptional repression and confers reduced risk of lung cancer
- (2010) Shuyu Zhang et al. CARCINOGENESIS
- Discovering moderate-risk breast cancer susceptibility genes
- (2010) Antoinette Hollestelle et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Evaluating Cancer Epidemiologic Risk Factors Using Multiple Primary Malignancies
- (2010) Ekatherina Kuligina et al. EPIDEMIOLOGY
- Genetics of lung-cancer susceptibility
- (2010) Paul Brennan et al. LANCET ONCOLOGY
- The associations of sequence variants in DNA-repair and cell-cycle genes with cancer risk: genotype–phenotype correlations
- (2009) Janet Hall et al. BIOCHEMICAL SOCIETY TRANSACTIONS
- Family History, Genetic Testing, and Clinical Risk Prediction: Pooled Analysis of CHEK2*1100delC in 1,828 Bilateral Breast Cancers and 7,030 Controls
- (2009) O. Fletcher et al. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
- Sequence variants at the TERT-CLPTM1L locus associate with many cancer types
- (2009) Thorunn Rafnar et al. NATURE GENETICS
- Mice with the CHEK2*1100delC SNP are predisposed to cancer with a strong gender bias
- (2009) E. M. Bahassi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Risk for contralateral breast cancer among carriers of the CHEK2*1100delC mutation in the WECARE Study
- (2008) L Mellemkjær et al. BRITISH JOURNAL OF CANCER
- Frequency of the CHEK2 1100delC Mutation among Women with Breast Cancer: An International Study
- (2008) S. Zhang et al. CANCER RESEARCH
- Constitutional CHEK2 mutations are associated with a decreased risk of lung and laryngeal cancers
- (2008) C. Cybulski et al. CARCINOGENESIS
- CHEK2*1100delC Genotyping for Clinical Assessment of Breast Cancer Risk: Meta-Analyses of 26,000 Patient Cases and 27,000 Controls
- (2008) Maren Weischer et al. JOURNAL OF CLINICAL ONCOLOGY
- Common variants of DNA repair genes and malignant melanoma
- (2007) T. Dębniak et al. EUROPEAN JOURNAL OF CANCER
- Does the nonsense-mediated mRNA decay mechanism prevent the synthesis of truncated BRCA1, CHK2, and p53 proteins?
- (2007) Olga Anczuków et al. HUMAN MUTATION
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